Title of Invention

"A PROCESS FOR THE ISOLATION OF A MAJOR HARMFUL OXIDANT FORM CIGARETTE SMOKE,P-BENZOSEMIQUINONE"

Abstract

The components of cigarette smoke, known until now, do not explain the overwhelming hazardous effects of smoking, this invention describes the isolation, identification and procedures for determination of the structure, properties and assay of a relatively stable major harmful oxidant (cs-oxidant) present in the cigarette smoke, the content of which is about 190±10 µg per cigarette, the cs-oxidant alone almost quantitatively accounts for the oxidative damage of proteins produced by the aqueous extract of whole cigarette smoke, the cs-oxidant is also responsible for the oxidative damage of DNA, since the cs-oxidant is relatively stable, it further explains the deleterious effects of the sidestream smoke and passive smoking, a number of chemical compounds / agents including vitamin C have been found to prevent the cs-oxidant induced protein oxidation in vitro.

Full Text

A PROCESS FOR THE ISOLATION OF A MAJOR HARMFUL OXIDANT FROM CIGARETTE SMOKE AND ITS INACTIVATION Field of invention The present invention relates to a process for the isolation of p-benzosemiquinone of formula 1, (Formula Removed) a major harmful oxidant from cigarette smoke. More particularly the present invention provides a process for the isolation of p-benzosemiquinone, a major harmful oxidant from cigarette smoke which is responsible for the oxidative damage of proteins and DNA Background of the invention Exposure to cigarette smoke is a major cause of life-threatening diseases like bronchitis, emphysema, other diseases of the respiratory tract, coronary heart diseases, lung cancer and other malignancies [1-5]. In fact, cigarette smoke is the overwhelming cause of lung cancer, now the most common cancer globally. Since approaches to cessation of smoking by public health campaigns and anti-smoking laws passed by local Governments have had limited success, the most practicable approach is the prevention of the hazardous effects caused by cigarette smoke. Cigarette smoke in known to contain about 4000 components, out of which about 3000 components are present in the gas phase and about 1000 components in the tar phase [6]. The oxidants in the gas phase, such as O-2, H2O2, NO, peroxyl radical are extremely unstable [7]. If the gas phase is passed into phosphate buffer and the resultant solution is added to albumin solution, no protein oxidation occurs (7). Apparently, any damage caused by the gas phase is expected to be restricted to the buccal cavity and upper respiratory tract [8]. On the other hand, the oxidant (s) present in the tar are quite stable and these are apparently responsible for producing oxidative damage in the lung, heart and other organs [7,9]. About 48 per cent of the tar components are water soluble [10] and the aqueous extract of tar is known to produce oxidative damage of biological macromolecules including proteins and DNA [7,11,12]. However, it is perplexing to conceive how many of the components present in the aqueous extract of tar are responsible for producing oxidative damage in the biological system. Uptil now, among the many components of cigarette smoke, three classes of compounds have been suggested to be implicated as causative agents in the development of cancer and degenerative diseases, namely, (i) polycyclic aromatic hydrocarbons (ii) nitrosamines and (iii) free radicals. Among the polycyclic hydrocarbons, benzo [a] pyrene is by far the best studied. But it is not a carcinogen and requires metabolic activation through cytochrome P450 system to become the ultimate carcinogen, benzo [a] pyrene diol epoxide. Moreover, the concentration of benzo [a] pyrene in cigarette smoke is meagre, about 20 to 40 ng per cigarette [13] and benzo [a] pyrene cannot explain oxidative damage of protein produced by cigarette smoke. Among the tobacco specific nitrosamines (TSNA), the most studied ones are N1-nitrosonornicotine (NNN) and 4- (methylnitrasamino) -1- (3-pyridyl) -1- butanone (NNK). Again TSNA are not direct carcinogens and also their concentrations in tobacco smoke vary widely. The observed range for NNN is 0.004µg to 1.35µg and for NNK, Another aspect of the hazardous component of cigarette smoke is free radical. Pryor and his associates made considerable studies on free radical chemistry of cigarette smoke and its toxicological implications. These authors suggest that the principal relatively stable free radical in cigarette tar may be a quinone / hydroquinone complex which is an active redox system and that this redox system is capable of reducing molecular oxygen to produce superoxide, leading to hydrogen peroxide and hydroxyl radicals [15], that may eventually lead to oxidative damage of biological macromolecules but we have observed that oxidative damage of proteins produced by the stable tar radicals is not inhibited by SOD or catalyst indicating that the oxidative damage is not mediated by superoxide radical or hydrogen peroxide. We have further observed that the tar radicals oxidize proteins in nitrogen atmosphere and in the absence of molecular oxygen, indicating a direct interaction of the tar radicals with biological macromolecules. However, these authors admit that the principal radical they have identified in tar is actually not a monoradical and probably is not a single species (16). They also admit that cigarette tar is an incredibly complex mixture and since the tar radicals have not been isolated and unambiguously identified, any conclusion concerning the chemistry or biochemistry of the tar radicals must be regarded as tentative [15]. It is noteworthy to mention that by the 1960s, the tobacco industry in general had proven in its own laboratory that cigarette tar causes cancer in animals [17]. Throughout 1960s the companies' researchers tried to discover the toxic elements in cigarette smoke with the conviction that if the toxic components could be identified, these agents could be removed or eliminated and a "safe" cigarette could be created, which would deliver nicotine without delivering the toxic substances [17]. But by the late 1970s, the tobacco industry had largely abandoned this particular research, because the objective proved to be unattainable. It was a problem technically difficult to solve and proved untractable [17]. Very recently, we have observed that aqueous extract; of whole cigarette smoke / tar contains a major harmful oxidant in relatively high amount, approximately 190±10µg per cigarette. We have isolated the oxidant, determined the structure and found it to be p-benzosemiquinone. The oxidant almost quantitatively accounts for the oxidative damage of proteins produced by the aqueous extract of whole cigarette smoke / tar. The oxidant is also responsible for DNA oxidation. Nagata et al. (18) have shown that semiquinone radicals bind to DNA and damage it. It is also known that oxidative damage of DNA is implicated with mutation and cancer. The oxidant is relatively stable. Its half-life in the solid state at the room temperature is approximately 48 hours. The presence of the stable oxidant in cigarette smoke would explain the deleterious effects of side stream smoke and passive smoking (7). The oxidant is absent in nonsmoking tobacco and is produced during burning of the cigarette (7). We have identified a number of chemical compounds /agents those inactivate the oxidant and may be used as antidotes. Objects of the invention (i) Isolation and characterization of a major harmful oxidant from aqueous extract of whole cigarette smoke / tar, which is mainly responsible for the oxidative damage of biological macromolecules including proteins and DNA. (ii) To provide a method for the quantitative assay of cs oxidant present in the whole cigarette solution (iii) Identification of chemical compounds / agents those will inactivate the oxidant and act as antidotes for combating the harmful effect of the oxidant. Summary of the invention A relatively stable major harmful oxidant has been isolated from aqueous extract of whole N. cigarette smoke / tar and purified to the extent of >99% by differential solvent extraction, thin layer chromatography and preparative HPLC. The yield is about 16µg per cigarette, which is about 8.4% of the amount (200 ±10µg) present in the smoke of one cigarette. Comparable results were obtained from twelve different brands of commercial cigarettes. The purified oxidant crystallizes in fine needle shaped very pale yellow crystals from a solution in acetone. The structure of the oxidant has been found to be p-benzosemiquinone as evidenced by elemental analysis, mass spectrum, UV, fluorescence, IR, H-NMR, C-NMR and ESR spectroscopy as well as by chemical properties. The oxidant can be measured quantitatively by either UV absorption spectroscopy or HPLC. In p-benzosemiquinone, the unpaired electron is delocalised over an aromatic framework containing heteroatoms leading to different mesomeric forms, namely, anionic, neutral and cationic forms (Fig.l, see ref.19). This resonance would explain the stability of the semiquinone. The half-life of the oxidant stored in the solid state at the room temperature in air and under darkness is about 48 hours as determined by its capacity to oxidize ascorbic acid. In aqueous solution at pH 7.4, the half-life is about 1.5 hours. Using oxidation of BSA or oxidative degradation of guinea pig lung microsomal proteins as model systems, the oxidant quantitatively accounts for the oxidative damage produced by the aqueous extract of whole cigarette smoke. The cs-oxidant is also responsible for DNA oxidation. A number of chemical compounds/agents have been identified those inactivate the oxidant and act as antidotes. Detailed description of the invention Accordingly the present invention provides a process for the isolation of p-benzosemiquinone of formula 1 (Formula Removed) major harmful oxidant from cigarette smoke responsible for the oxidative damage of proteins and DNA, the said process comprising the steps of: a) collecting tar or cs (cigarette smoke) solution from lighted conventional filtered tipped cigarette, b)collecting tar by lighting conventional filter-tipped cigarettes having a tar content of 20 -30 mg per cigarette in a glass flask dipped in a mixture of ice and salt and allowing the tar to condense and settle at the bottom of the flask, c) taking the above said flask to room temperature and extracting the said tar with 30-60 mM potassium phosphate buffer at a pH ranging between 7.4 to 7.8, filtering the above solution through 0.45µm Millipore filter, adjusting the pH of the filtrate ranging between 7.4 to7.6 by adding NaOH solution to obtain the desired tar solution, d) extracting the above said tar solution thrice with equal volume of methylene chloride, discarding the lower methylene chloride layer and collecting the upper yellow coloured aqueous layer termed as aqueous extract of cigarette smoke. e) extracting the above said aqueous extract of cigarette smoke twice with equal volume of of water saturated n-butanol, lyophilizing the pooled yellow butanol extract in a lyophilizer at a temperature ranging between -50 °C to -60°C under vacuum followed by extraction of the lyophilized material twice with HPLC grade acetone and drying the acetone solution under vacuum and dissolving the said acetone extract with HPLC grade methanol, f) subjecting the above said methanol solution to band TLC using non-fluorescent silica plates, developing the said silica plates using a mixture of toluene and ethyl acetate in a ratio of 80:20, taking out the plate and drying at about 25-30 ° C using a drier, cutting small strips containing the developed material from both sides of the plates and keeping them in an iodine chamber for the location of the band corresponding to Rf 0.26 , scraping the band and extracting the band material with HPLC grade acetone followed by collection of the acetone layer and drying it under vacuum, g) dissolving the above said acetone extract which appeared as pale yellow needles by adding equal volume of milli Q water, extracting the aqueous solution with equal volume of HPLC grade water saturated n-butanol followed by drying upper n-butanol layer in small glass tubes under vacuum to obtain the major cigarette smoke (cs) oxidant with a purity of 98-99% and yield of 18-22 µg per cigarette, h) purifying the above said cs oxidant as obtained in step (g) by dissolving it in a mobile solvent comprising a mixture of methylene chloride and methanol in a ratio of 90:10 (v/v) and injecting it in a HPLC instrument with a normal phase 25 cm silica column using a uv detector at 294 nm at a flow rate of o.5 ml/min, at a temperature of about 25°C , at a pressure of about 29 kgf/cm2 and collecting the effluent which appears as a single peak at a retention time of 8.808 min with a purity of 100 % and yield of 8.4% of the total cs oxidant present in the parent tar solution. In an another embodiment the present invention provides a process for the isolation of p-berizosemiquinone of formula 1, a major harmful oxidant from cigarette smoke responsible for the oxidative damage of proteins and DNA, the said process further comprising a) passing the whole cigarette smoke collected from conventional filter tipped cigarette having a tar content of 20 -30 mg per cigarette into 30-60 mM potassium buffer at pH 7.4 - 7.8, filtering the above solution through 0.45µm Millipore filter, adjusting the pH of the filtrate ranging between 7.4 to7.6 by adding NaOH solution to obtain the desired cigarette smoke solution (cs solution) b) extracting the above said cs solution thrice with equal volume of methylene chloride, discarding the lower methylene chloride layer and collecting the upper yellow coloured aqueous layer termed as aqueous extract of cigarette smoke. c) extracting the above said aqueous layer of cigarette smoke twice with equal volume of water saturated n-butanol , lyophilizing the pooled yellow butanol extract in a Lyolab lyophilizer at a temperature ranging between -50 °C to -60°C under vacuum followed by extraction of the lyophilized material twice with HPLC grade acetone and drying the acetone solution under vacuum and dissolving the said acetone extract with HPLC grade methanol, d) subjecting the above said methanol solution to band TLC using non-fluorescent silica plates, developing the said silica plates using a mixture of toluene and ethyl acetate in a ratio of 80:20, taking out the plate and drying at about 25 ° C to 30 ° C using a drier, cutting small strips containing the developed material from both sides of the plates and keeping them in an iodine chamber for the location of the band corresponding to Rf 0.26 , scraping the band and extracting the band material with HPLC grade acetone followed by collection of the acetone layer and drying it under vacuum, e) dissolving the above said acetone extract which appeared as pale yellow needles by adding equal volume of milli Q water , extracting the aqueous solution with equal volume of HPLC grade water saturated n-butanol followed by drying the upper n-butanol layer in small glass tubes under vacuum to obtain the major cs oxidant with a purity of 98-99% and yield of 18-22 |Jg per cigarette, f) purifying the above said cs oxidant as obtained in step e by dissolving it in a mobile solvent comprising a mixture of methylene chloride and methanol in a ratio of 90:10(v/v) and injecting it in a HPLC instrument with a normal phase 25 cm silica column using a uv detector at 294 nm at a flow rate of 0.5 ml/min, at a temperature of about 25°C , at a pressure of about 29 kgf/cm2 and collecting the effluent which appears as a single peak at a retention time of 8.808 min with a purity of 100 % and yield of 8.4% of the total cs oxidant present in the parent cs solution. In yet another embodiment of the present invention the said isolated pure cigarette smoke (cs) oxidant has the following properties a) when crystallized from acetone solution appears as small needle shaped faint yellow coloured crystals having pungent smell, similar to that of rancid butterfat, b) UV absorption maxima in methanol solution are at 293.4 nm and 223.0 nm and in aqueous solution are in 288nm and 221nm respectively, c) on excitation at 293 nm in methanol solution the observed emission maxima are at 329.6 nm and 651.4 nm and on excitation at 224 nm, the observed emission maxima are at 329.6 nm and 652.6 nm respectively, d) when excitation scanning is monitored keeping the emission at 330 nm, the observed excitation maxima are at 228.2 nm and 293.8 nm and when the emission is kept at 651 nm and excitation scanning is monitored, the observed excitation maxima are at 229.2 nm and 294.8 nm respectively, e) highly soluble in methanol, ethanol, acetone, n-butanol, fairly soluble in water, sparingly soluble in methylene chloride, di-ethyl ether, chloroform and insoluble in benzene and petroleum ether, f) the compound looses its oxidizing potency in acidic pH ranging between 4 to 5 and on keeping the solution at alkaline pH ranging between 9 to 10, the compound gradually turns brown, at pH 10 and above there is instantaneous darkening with loss of both activity and aromaticity as evidenced by UV spectroscopy. g) the half-life of the oxidant, when stored in the solid state at a temperature ranging between 25 °C to 30 °C under darkness is about 48 hours as determined by its oxidative potency, but in solution of 50 mM potassium phosphate buffer, pH 7.4 at 25°C to 30°C the half life is about Ihour 30 min, h) reduces ferricytochrome c and ferric chloride, i) oxidizes ascorbic acid, proteins and DNA, j) the melting point is 162°C, In yet another embodiment the present invention provides a process for the quantitative determination of p-benzosemiquinone of formula 1, a major harmful oxidant isolated from cigarette smoke responsible for the oxidative damage of proteins and DNA, the said process comprising the steps of a) collecting tar or cs solution from lighted conventional filtered tipped cigarette, b)collecting tar by lighting conventional filter-tipped cigarettes having a tar content of 20 -30 mg per cigarette in a glass flask dipped in a mixture of ice and salt and allowing the tar to condense and settle at the bottom of the flask, c) taking the above said flask to room temperature and extracting the said tar with 30-60 mM potassium phosphate buffer at a pH ranging between 7.4 to 7.8, filtering the above solution through 0.45 µm Millipore filter, adjusting the pH of the filtrate ranging between 7.4 to7.6 by adding NaOH solution to obtain the desired tar solution, d) extracting the above said tar solution thrice with equal volume of methylene chloride, discarding the lower methylene chloride layer and collecting the upper yellow coloured aqueous layer termed as aqueous extract of cigarette smoke. e) extracting the above said aqueous extract of cigarette smoke twice with equal volume of water saturated n-butanol, lyophilizing the pooled yellow butanol extract in a lyophilizer at a temperature ranging between -50 °C to -60°C under vacuum followed by extraction of the lyophilized material twice with HPLC grade acetone and drying the acetone solution under vacuum and dissolving the said acetone extract with HPLC grade methanol, f) subjecting the above said methanol solution to band TLC using non-fluorescent silica plates, developing the said silica plates using a mixture of toluene and ethyl acetate in a ratio of 80:20, taking out the plate and drying at about 25-30 ° C using a drier, cutting small strips containing the developed material from both sides of the plates and keeping them in an iodine chamber for the location of the band corresponding to Rf 0.26 , scraping the band and extracting the band material with HPLC grade acetone followed by collection of the acetone layer and drying it under vacuum, g) dissolving the above said acetone extract which appeared as pale yellow needles by adding equal volume of milli Q water, extracting the aqueous solution with equal volume of HPLC grade water saturated n-butanol followed by drying upper n-butanol layer in small glass tubes under vacuum to obtain the major cigarette smoke (cs) oxidant with a purity of 98-99% and yield of 18-22 µg per cigarette, h) purifying the above said cs oxidant as obtained in step (g) by dissolving it in a mobile solvent comprising a mixture of methylene chloride and methanol in a ratio of 90:10 (v/v) and injecting it in a HPLC instrument with a normal phase 25 cm silica column using a uv detector at 294 nm at a flow rate of o.5 ml/min, at a temperature of about 25°C , at a pressure of about 29 kgf/cm2 and collecting the effluent which appears as a single peak at a retention time of 8.808 min with a purity of 100 % and yield of 8.4% of the total cs oxidant present in the parent tar solution. In yet another embodiment the present invention provides a process for the quantitative determination of p-benzosemiquinone of formula 1, a major harmful oxidant isolated from cigarette smoke responsible for the oxidative damage of proteins and DNA, the said process further comprising a) passing the whole cigarette smoke collected from conventional filter tipped cigarette having a tar content of 20 -30 mg per cigarette into 30-60 mM potassium buffer at pH 7.4 -7.8, filtering the above solution through 0.45µm Millipore filter, adjusting the pH of the filtrate ranging between 7.4 to7.6 by adding NaOH solution to obtain the desired cigarette smoke solution (cs solution) b) extracting the above said cs solution thrice with equal volume of methylene chloride, discarding the lower methylene chloride layer and collecting the upper yellow coloured aqueous layer termed as aqueous extract of cigarette smoke. c) extracting the above said aqueous layer of cigarette smoke twice with equal volume of water saturated n-butanol , lyophilizing the pooled yellow butanol extract in a Lyolab lyophilizer at a temperature ranging between -50 °C to -60°C under vacuum followed by extraction of the lyophilized material twice with HPLC grade acetone and drying the acetone solution under vacuum and dissolving the said acetone extract with HPLC grade methanol, d) subjecting the above said methanol solution to band TLC using non-fluorescent silica plates, developing the said silica plates using a mixture of toluene and ethyl acetate in a ratio of 80:20, taking out the plate and drying at about 25 ° C to 30 ° C using a drier, cutting small strips containing the developed material from both sides of the plates and keeping them in an iodine chamber for the location of the band corresponding to Rf 0.26 , scraping the band and extracting the band material with HPLC grade acetone followed by collection of the acetone layer and drying it under vacuum, e) dissolving the above said acetone extract which appeared as pale yellow needles by adding equal volume of milli Q water , extracting the aqueous solution with equal volume of HPLC grade water saturated n-butanol followed by drying the upper n-butanol layer in small glass tubes under vacuum to obtain the major cs oxidant with a purity of 98-99% and yield of 18-22 |Jg per cigarette, f) purifying the above said cs oxidant as obtained in step e by dissolving it in a mobile solvent comprising a mixture of methylene chloride and methanol in a ratio of 90:10(v/v) and injecting it in a HPLC instrument with a normal phase 25 cm silica column using a uv detector at 294 nm at a flow rate of o.5 ml/min, at a temperature of about 25°C , at a pressure of about 29 kgf/cm2 and collecting the effluent which appears as a single peak at a retention time of 8.808 min with a purity of 100 % and yield of 8.4% of the total cs oxidant present in the parent cs solution. In yet another embodiment the said p-benzosemiquinone present in cs solution is also quantitatively assayed by HPLC attached with a UV detector using a 25 cm reverse phase ODS column and a mixture of water and methanol in a ratio of 95: 5 (v/v) as a mobile solvent, at an absorbance of 288nm, at a flow rate of 0.8 ml/min, at a temperature of about 25°C, at a pressure of about 147 Kgf/cm2 and at a retention time of 13.46 min In yet another embodiment the said p-benzosemiquinone is the major cause of oxidative damage of proteins produced by the whole cs solution, In yet another embodiment the cs oxidant is also responsible for the oxidative damage of DNA, In yet another embodiment the present further provides a process for the quantitative assay of oxidative damage of proteins by p-benzosemiquinone present in cs solution which comprises measuring protein carbonyl formation by reacting the protein with p- benzosemiquinone obtained from the cs solution followed by reaction with 2,4 dinitriphenyl hydrazine (DNPH) and finally measuring the absorbance at 390nm wherein the formation of said carbonyl is indicative of oxidative damage of protein, In yet another embodiment the present further provides a process for the quantitative assay of oxidative damage of proteins by p-benzosemiquinone present in cs solution further comprises measuring oxidative degradation of guinea pig tissue microsomal proteins by reacting the said protein with p-benzosemiquinone present in cs solution followed by SDS- PAGE and densitometric scanning, In yet another embodiment the protein used for the assay of oxidative damages of protein is selected from the group consisting of BSA and guinea pig lung microsomal proteins In yet another embodiment the BSA oxidation produced by the whole cs solution is done only by the p-benzosemiquinone present in the cs solution and not by the components of cs solution other than p-benzosemiquinone , In yet another embodiment the BSA oxidation produced by the cs oxidant as evidenced by nmoles of carbonyl formed/ mg BSA is 9.56 ± 0.14 in comparison to 7.53 ± 0.34 produces by the whole cs solution, In yet another embodiment the BSA oxidation produced by the cs oxidant as evidenced by nmoles of carbonyl formed/ mg BSA is 9.56 ± 0.14 in comparison to 8.16 ± 0.24 produces by the aqueous extract of cigarette smoke, In yet another embodiment the BSA oxidation produced by the cs oxidant as evidenced by nmoles of carbonyl formed/ mg BSA is 9.56 ± 0.14 in comparison to 9.23 ± 0.14 produces by the TLC purified aqueous extract of cigarette smoke, In yet another embodiment the oxidative degradation of guinea pig tissue microsomal proteins produced by the p-benzosemiquinone solution as evidenced by SDS-PAGE is comparable to that produced by the whole cs solution, In still another embodiment of the present invention provides a method for the prevention of cigarette smoke induced protein oxidation in vitro, the said method comprises inhibiting the BSA oxidation by using a chemical compound or agent selected from the group consisting of ascorbic acid, sodium dithionite, tartaric acid, citric acid, oxalic acid, succinic acid, histidine, lysine, thiouria, glutathione, black tea extract, green tea extract, catechine, epigallocatechin and epicatechin, the said inhibition of BSA oxidation is shown below in a tabular form Protection of cs-oxidant-induced albumin oxidation by different chemical agents. Ser. No. Agents used Concentration / amount % Protection 1. Ascorbic acid 100µM 76 2. Sodium dithionite 2mM 97 3. Tartaric acid 1 mM 75 Tartaric acid 500 µM 67 4. Citric acid 1 mM 75 Citric acid 500 µM 67 5. Oxalic acid 500µM 53 6. Succinic acid I mM 60 7. Histidine 1 mM 67 8. Black tea extract 2.5 mg 50 9. Catechin 750 µg 54 10. Epigallocatechin 140 µg 95 11. Epicatechin 50 µg 50 12. Green tea extract 2.5 mg 50 13. Lysine 1 mM 35 14. Thiourea 10 mM 52 15. Glutathione 1 mM 37 In yet another embodiment the compound p-benzosemiquinone is useful to study the mechanism of oxidative damage-induced degenerative diseases and cancer caused by cigarette smoke producing oxidative damage to an isolated protein, DNA, cultured cells or to an experimental model under laboratory conditions. In yet another embodiment the quantitative determination of said cs oxidant p-benzosemiquinone in cigarettes is based on the tar content of the particular commercial brand of the cigarettes. In yet another embodiment the amount p-benzosemiquinone isolated from smoke of different commercial brands of burning cigarettes is used to determine the toxicity index of a particular brand of cigarette based on the quantity of p-benzosemiquinone present. In still another embodiment, a smoking material formulated based on the amount of p-benzosemiquinone generated by the smoke of said smoking material when used in a cigarette, cigar or any other similar means using the method as claimed in claims 1-5 for the quantitative estimation of the said compound p-benzosemiquinone . Brief description of the accompanying drawings Fig.l shows Mesomeric forms of p-benzosemiquinone, a.anionic, b) and c) neutral and d)cationic; Fig.2 Band thin layer chromatography of the methanol solution after lyophilization - indicates the band of the cs-oxidant Fig. 3 HPLC profile of the butanol extract after TLC. The cs-oxidant (step 6) eluted as a major peak at the retention time of 8.808 min The amount of cs-oxidant eluted was ~ 12µg. Fig.4 HPLC profile of the pure cs-oxidant, eluted at the retention time of 8.808 mon. Fig.5 Thin layer chromatography of the pure cs-oxidant (Rf = 0.26) Fig.6a Fluorescence spectroscopic profile of the cs-oxidant in methanol. The excitation was at 293 nm and emission scanning was measured from 300 nm to 800 nm. The emission maxima were at 329.6 nm and at 651.4 nm. Fig.6b Fluorescence spectroscopic profile of the cs-oxidant in methanol. The excitation was at 224 nm and emission scanning was measured from 225 nm to 800 nm. The emission maxima were at 329.6 nm and at 652.6 nm. Fig.7a Fluorescence spectroscopic profile of the cs-oxidant in methanol. The emission was at 330 nm and excitation scanning was measured from 220 nm to 325 nm. The excitation maxima were at 228.2 nm and 293.8 nm. Fig.7b Fluorescence spectroscopic profile of the cs-oxidant in methanol. The emission was at 651 nm and excitation scanning was measured from 220 nm to 650 nm. The excitation maxima were at 229.2 nm and at 294.8 nm. Fig. 8 Crystal structure of the pure cs-oxidant. Fig.9 UV-specytrophotometric profile of the cs-oxidant in methanol. It has two absorption maxima, one at 293.4 nm and another at 223.0 nm. Fig. 10 Stability of the solid oxidant kept at 25"C under darkness. The stability was determined by its capacity to oxidize ascorbic acid. Ascorbic acid was measured by HPLC analysis at 254 nm. Fig. 11 Standard curve of ascorbic acid based on HPLC analysis at 254 nm. Fig. 12 Stability of the cs-oxidant in 50 mM potassium phosphate buffer at 25°C measured by its potency to oxidize ascorbate as evidenced by HPLC area. Fig. 13 Quantitative reduction of ferricytochrome c by the oxidant as measured by the ormation of ferrocytochrome c with time at 550 nm. The reaction was carried out in 50 mM potassium phosphate buffer, pH 7.4, keeping the final concentration of ferricytochrome c at lOOµM. One nmole of the oxidant reduced 0.71 nmoles of ferricytochrome c. Fig. 14 Standard curve of the oxidant on the basis of HPLC area at 294 nm. Different amounts of the cs-oxidant were used ranging from 10 ng to 100 ng in 20µl of mobile solvent. Fig. 15 Standard curve of the oxidant on the basis of reduction of cytochrome c by using different amount of the oxidant ranging from lµg to 5µg Fig. 16 Mass spectrum of the pure cs-oxidant. Fig. 17 UV-spectrophotometric profile of hydroquinone in methanol. It has two absorption maxima, one at 293.8 nm and another at 224.2 nm. Fig. 18 UV-spectrophotometric profile of the cs-oxidant stored at room temperature in dark for 8 days. The two absorption maxima are at 293.6 nm and at 224.4 nm. Fig. 19 UV-spectrophotometric profile of equimolar mixture of p-benzoquinone and hydroquinone in methanol. There is a shoulder near 242 nm (the λmax of p- benzoquinone). Fig.20 Fluorescence spectroscopic profile of hydroquinone in methanol. The excitation was at 294 nm and emission scanning was measured from 300 nm to 800 nm. The emission maxima were at 329.4 nm and at 651.6 nm. Fig.21 FTIR spectroscopic profile of the cs-oxidant. Fig.22 FTIR spectroscopic profile of hydroquinone. Fig.23 H-NMR spectroscopic profile of the cs-oxidant in CD3COCD3. Fig.24 H-NMR spectroscopic profile of hydroquinone in CD3COCD3. Fig.25 Comparative H-NMR spectroscopic profiles of (a) cs-oxidant and (b) hydroquinone, Fig.26 H-NMR spectroscopic profile of the cs-oxidant after reduction with sodium dithionite. Fig.27 C-NMR spectroscopic profile of the cs-oxidarit in CD3COCD3. Fig.28 C- NMR spectroscopic profile of the hydroquinone in CD3COCD3. Fig.29 Room temperature ESR spectrum of cs-oxidant, freshly prepared from 100 cigarettes. The spectrum was recorded on a JES-REIX ESR spectrometer (Tokyo, Japan). The spectral parameters were as follows: microwave frequency, 9.4356 GHz; power, 2mW; field modulation width, 0.4mT; modulated frequency, 100kHz; time constant, 0.3 sec; scant rate, 2.5 mT/sec. Fig.30 Room temperature ESR spectrum of aged (10 days) cs-oxidant, prepared from 400 cigarettes. Fig.31 HPLC profile of the whole cs solution analyzed in the silica column (LiChrospherR Si 60,Merck) - indicates the retention time, area and the concentration (13.6682%) of the cs-oxidant. Fig.32 HPLC profile of the aqueous extract cs solution analyzed in the silica column (LiChrospherR Si 60,Merck) - indicates the retention time, area and the concentration (13.6682%) of the cs-oxidant. Fig.33 HPLC profile of the whole cs solution analyzed in the ODS column (Shim-pack CLC-ODS, Shimadzu). The cs-oxidant eluted at 13.467 min. Fig. 34 HPLC profile of the pure-cs-oxidant analyzed in the CLC-ODS column (Shim-pack CLC-ODS, Shimadzu)eluted at the retention time of 13.458 min. Fig.35a SDS-PAGE of the quinea pig lung microscomal proteins treated with whole cs solution and the cs-oxidant. Lane 1, untreated microsomes; lane 2, microsomes treated with 50µl cs solution; lane 3, microsomes treated with 100 µl cs solution; lane 4, microsomes treated with lOµg cs-oxidant; lane 5, microsomes treated with 20µg cs-oxidant. Fig.35b Densitometric scanning of the protein bands of different lanes as in Fig.35a. Example 1 Isolation and purification of a major hazardous component (cs-oxidant) from cigarette tar or whole cigarette smoke solution (i) Five Indian commercial filter-tipped cigarette (74 mm) with a tar content of 25 mg each was mounted in glass tubes that penetrated the hole in the glass stopper of a one litre glass Erlenmeyer flask with a side arm and ended about 2 cm away from the bottom of the flask. The flask was dipped in a mixture of ice and salt and the side arm connected to a water pump. The cigarettes were lit and the tar was allowed to condense and settle at the bottom of the flask. Altogether tar from twenty cigarettes was collected. The jar was taken out to room temperature and the tar was extracted with 20 ml of 50 mM potassium phosphate buffer pH 7.4. The solution was filtered through 0.45 µm Millipore filter. The pH of the filtrate was adjusted to 7.4 with addition of 20 µlof 2N NaOH solution. The colour of the solution was brownish yellow. This solution has been termed tar solution. Instead of isolating the cs-oxidant from cigarette tar, it can also be isolated from whole cigarette smoke. In that case, smoke from 20 cigarettes in batches of 5 is passed directly into 20 ml of 50 mM potassium phosphate buffer, pH 7.4, and the rest of the procedure is similar to that used in tar. The solution obtained after passing the whole cs into the buffer has been termed whole cs solution. The yield of the cs-oxidant was similar irrespective of whether the tar solution or whole cs solution was used as the starting material. (ii) The filtered tar solution obtained in step 1 was extracted thrice with 15-ml methylene chloride. The lower methylene chloride layer was discarded and the upper yellow coloured aqueous layer was collected and called the aqueous extract of cigarette smoke, (iii) The aqueous layer from step 2 was extracted twice with 10 ml of water saturated n-butanol and the pooled yellow butanol extract was then lyophilized in the Lyolab lyophilizer at -55°C under vacuum. The lyophilized material was extracted twice with 1 ml of HPLC grade acetone and the acetone solution was dried in a Speed Vac (Savant, SC 100) and dissolved in 120µl of HPLC grade methanol. (iv) The methanol solution obtained in step 3 was then subjected to band TLC using 10 cm x lO cm non-fluorescent 0.2-mm thick silica plates (TLC aluminium sheets, Silica gel 60, MERCK, No 1.05553). Material from 5 cigarettes (~ 30µl methanol solution) was spotted along a line about 1.5 cm above the bottom. The plate was developed using toluene: ethyl acetate (80:20) for 15 min. When the developing solvent front was 0.5 cm away from the top, the plate was taken out and dried at room temperature using a drier. After drying, 0.5 cm strips from both the right and the left side of the plate was cut out and kept in a iodine chamber for 3 minutes for location of the bands. The band corresponding to Rf 0.26 (Fig.2) was scraped from each plate, taken in 1.5 ml eppendorf tube and extracted for 30 min with 600 µl HPLC grade acetone with occasional vortexing. The tubes were then centrifuged for 10 min at room temperature at 12000 rpm. The supernatant acetone layer was carefully taken in another eppendorf tube. The pooled acetone extract was finally dried in one eppendorf tube in a speed vac. (v) To the dried material obtained in step 4, which appeared as pale yellow needles, was added 200µl milli Q water and to this 200µl water saturated n-butanol was added and vortexed for 5 min followed by centriragation for 5 min at 12000 rpm at room temperature. The upper n-butanol layer was carefully taken out and dried in a small glass tube in a speed vac. Yield ~ 400 µg from 20 cigarettes. At this stage, the cs-oxidant is 98.5% pure as evidenced by HPLC analysis. (vi) The total sample obtained after step 5 was dissolved in 400µl of the mobile solvent and 20 µl of this solution (~ 20 µg oxidant) was injected in a Shimadzu 10AVP HPLC instrument with a normal phase Merck 25 cm silica column (LiChrospher® Si 60) using the UV detector and an attached chromatopac C-R6A. Altogether 20 injections were made in different batches. The other conditions maintained were as follows. Absorbance : 294 nm (The λmax of the oxidant in methanol was 293.4 nm as evidence by UV-spectrophotometric scanning, see Fig. 9) Mobile solvent: methylene chloride: methanol (90:10) Flow rate : 0.5 ml/min Pressure : 29 kgf/cm2 Temperature : 25°C Retention time of the oxidant : 8.808 min The oxidant eluted as a major peak at retention time of 8.808 min (Fig.3). The pooled HPLC eluant obtained from different batches of injection was collected in a 25-ml glass beaker and dried in the speed vac. The oxidant appeared as very-faint yellow tiny needle-shaped crystals. The HPLC-purified oxidant, when reinjected under identical conditions, appeared as a single peak in the HPLC profile at a retention time of 8.808-min (Fig.4), indicating 100% purity. Yield ~300µg from 20 cigarettes. (vii) On the basis of the amount of sample loaded and the corresponding peak area (arbitrary) of the cs-oxidant obtained in HPLC analysis, the percentage recovery of the active oxidant from the whole cs solution was calculated as follows. Four µl of the filtered whole cs solution (see step 1) was diluted to 80 µl with mobile solvent and 20µl was injected in the HPLC column. The arbitrary area of the oxidant in 20 ul, corresponding to retention time 8.808 min, was 340583 Therefore, area in 80µl = 1362332 = 4 µl of whole cs solution So, arbitrary area of the oxidant in one ml of whole cs solution = 3.4 x 108 Since one ml of the whole cs solution is equivalent to one cigarette (see step 1), the area of the cs-oxidant per cigarette = 3.4 x 108 The yield of pure oxidant after HPLC purification from 20 cigarettes = 300µg So, yield from one cigarette = 15 µg = 15OOOng From the standard curve (see Fig. 14), HPLC peak area of 100 ng of pure cs-oxidant = 190000 Therefore, peak area of 15000 ng, equivalent to one cigarette = 2.85 x 107 Thus the recovery of the pure cs-oxidant from whole cs solution is (2.85 x 107 x 100) / 3.4 x 108 = 8.4% (viii) The oxidative potency of the cs-oxidant at different stages of purification was determined by measuring the oxidation of bovine serum albumin (BSA). The results are presented as nmoles of protein carbonyl formed per rng BSA (Table 1). At different stages of purification, as stated under 'Isolation and purification procedure1 above, an amount of material equivalent to one twentieth of a cigarette (50 µl solution) was used in the cases of tar solution (step 1), aqueous extract (step 2) and butanol extract (step 3). In the case of butanol extract, 50µl of the butanol solution was taken, butanol evaporated off in a speed vac, the dried residue weighed and used directly for the oxidation of BSA. For materials obtained at step 4 (TLC) and step 6 (HPLC), the amounts used were 15 µg and 10 µ.g respectively, (ix) Criteria of purity of the cs-oxidant (a) TLC: A single spot was obtained in TLC, Rf 0.26, using toluene: ethyl acetate (80:20) as the developing solvent (Fig.5). (b) HPLC: A single peak was obtained by HPLC analysis. The retention time was 8.808 min using the mobile solvent, methylene chloride: methanol (90:10) (Fig.4). (c) Melting point: The compound melts sharply at 162°C. (d) Fluorescence spectroscopy: The UV spectrophotometric scanning of the cs-oxidant (5mg in 1ml of methanol) produced two absorption maxima at 293.4 nm and at 223.0 nm (see fig.9). Fluorescence spectroscopy was performed in methanol solution as used for UV spectrophotometric scanning. When excited at 293 nm, the emission scanning was monitored from 300 nm to 800 nm and when excited at 224 nm, the emission scanning was monitored from 225 nm to 800 nm. When excited at 293 nm, the observed emission maxima were at 329.6 nm and 651.4 nm (Fig.6a). When excited at 224 nm, the observed emission maxima were at 329.6 nm and at 652.6 nm (Fig.6b). When excitation scanning was monitored keeping the emission at 330 nm, the observed excitation maxima were at 228.2 nm and at 293.8 nm (fig.7a). Again, when the emission was kept at 651 nm and excitation scanning was monitored, the observed excitation maxima were at 229.2 nm and at 294.8 nm (Fig.7b). The observed spectral profiles indicate that the two absorption maxima are coming from the same compound and attributes to the purity of the isolated cs-oxidant. Example 2 Quantitative assay of protein damage by measuring carbonyl content. The incubation system contained 1 mg BSA and 50 µl of cs solution or its equivalent amounts obtained at different stages of purification in a final volume of 200µl of 50 mM potassium phosphate buffer, pH 7.4. The incubation was carried out at 37°C for 1 hour. Protein carbonyl was measured by reaction with 2, 4 - dinitrophenyl hydrazine (DNPH) following the method of Levine et al (Methods Enzymol. 186: 464-478, 1990) similar to that done before in our laboratory (Panda et al., Free Radic. Biol. & Med. 27: 1064-1079, 1999). After incubation of BSA with whole phase cs solution, the aqueous extract of cs or the cs-oxidant (final volume 200 ul), the proteins were precipitated with 200 ul of 20 % trichloroacetic acid solution followed by a wash with 200 ul of 10 % trichloroacetic acid solution to free the pellet of cs components. To this washed pellet was then added 500 ul of 10 mM DNPH solution in 2M HC1 and incubated at 37 °C for 1 h with occasional vortexing. Thereafter, the protein was again precipitated with 500µ1 of cold 20% trichloroacetic acid solution and the pellet was first washed with 500 ul of 10% trichloroacetic acid solution followed by three successive washes with 1ml of a mixture of ethanol: ethyl acetate (1:1, v/v). Finally, the washed precipitate was dissolved in 1ml of 6M guanidium hydrochloride (pH 2.3) and the absorbance was measured at 390 nm using a double beam Hitachi spectrophotometer model U 3020 against a reagent blank of 2M HC1. The results were expressed as n moles of phenylhydrazones formed per milligram protein using a molar extinction coefficient of 22,000. From the gross phenylhydrazone values obtained after incubation of BSA with the cs-oxidant, the phenylhydrazone values of that obtained with untreated BSA were deducted to get the values of net protein carbonyl formed. The results are given in table 1. Example 3 Physico-chemical properties of the cs-oxidant (a) Appearance: When crystallized from acetone solution, the oxidant appeared as small needle shaped faint yellow coloured crystals (Fig.8). In the dry condition or in solution, the compound gradually turns brown in air under light. (b) Odour: Pungent smell, similar to that of rancid butterfat. (c) UV absorption: The oxidant has two absorption maxima in methanol solution, one at 293.4 nm and another at 223.0 nm (Fig.9). In aqueous solution, the absorption maxima are at 288 nm and 221 nm. There was no absorption in the visible region of 400 nm to 700 nm indicating that the oxidant lacks chromophoric group. Example 4 Chemical properties of the cs-oxidant (a) Solubility: Highly soluble in methanol, ethanol, acetone, n-butanol, fairly soluble in water, sparingly soluble in methylene chloride, di-ethyl ether, chloroform and insoluble in benzene, petroleum ether. (b) Effect of pH: In acidic pH (4-5), the compound does not turn brown but looses its oxidizing potency. On keeping the solution at alkaline pH (pH 9), the compound gradually turns brown. At pH near 10 and above, there is instantaneous darkening with loss of both activity and aromaticity as evidenced by UV spectroscopy. (c) Stability of the solid oxidant: The half-life of the oxidant, when stored in the solid state at the room temperature under darkness, has been found to be 48 hours as deteimined by its ability to oxidize ascorbic acid (Fig. 10). The oxidation of ascorbic acid was measured by HPLC analysis. A standard curve of ascorbic acid, prepared using different concentrations of ascorbic acid, is shown in Fig.ll. To determine the stability of the cs-oxidant, freshly prepared oxidant was distributed in five separate sample tubes. Each tube contained 5 µg of cs-oxidant. One tube was immediately examined (dayO, Fig. 10) to determine its capacity to oxidize ascorbic acid. Other tubes were examined subsequently on day 1,2,3 and 5 respectively (Fig. 10). To each tube, 5 µg of ascorbate in 200 µl of 50-mM potassium phosphate buffer was added and incubated for 45 min at the room temperature. After that, 16µl of the assay mixture was withdrawn at different time intervals and added to 24 µl of the mobile solvent to make the final volume to 40 µl. Twentyµl of this diluted solution, initially equivalent to 200 ng of ascorbic acid, was injected. A parallel control was kept without the oxidant to monitor the autoxidation of ascorbate. Ascorbic acid was detected at 254 nm. Under the conditions, retention time of ascorbic acid was 6.1 min. The minimum amount of ascorbate that could be determined by HPLC under the condition was 500 pg. The conditions of HPLC analysis were Instrument: Shimadzu 10A Column : Lichro CART 250-4 NH2 column (Merck) Mobile solvent: Acetonitrile : 50 mM KH2PO4 (75:25) Flow rate : 1.5 ml/min Pressure : 132 kgf/cm2 Temperature : 25 °C (d) Stability of the oxidant in solution In contrast to the half-life of 48 hours when stored in the solid condition, the half-life of the oxidant was about Ihour 30 min when stored in solution of 50 mM potassium phosphate buffer, pH 7.4 at 25°C (Fig. 12). The assay condition was same as described above under 'stability of the solid oxidant'. (e) Reaction with ferric chloride solution To 200 µl methanol solution containing 500µg of the cs-oxidant, 20 µl of aqueous solution of ferric chloride (1 mg) was added. An instant transient green colour appeared. This indicates that the oxidant contains phenolic - OH group. (f) Reduction of ferricytochrome c The oxidant not only oxidizes proteins and ascorbic acid (as shown later), but also reduces ferricytochrome c quantitatively as measured by the formation of ferrocytochrome c with time (Fig. 13). To 890 µl of 50-mM potassium phosphate buffer, pH 7.4, 100 µl of ImM ferricytochrome c solution was added to obtain a final concentration of 100 µM. To this was added a solution of 4.5 µg cs-oxidant in 10 µl of 50-mM potassium phosphate buffer, pH 7.4 and the absorbance was recorded at 550 nm at 30-second intervals. The results (Fig. 13) indicate that Inmole of the oxidant (taking M.W=110 as shown later) reduce 0.71 n mole of ferreicytochrome c, which approximates the molar ratio of 1:1. Or in other words, it appears that the oxidant contains one reducing group per molecule. Molar extinction coefficient of ferrocytochrome c at 550 nm was taken as 25xl03 cm-1. It was also observed that the reduction of ferricytochrome c by hydroquinone was approximately in the molar ratio of 1:0.71, indicating that the reducing component of the cs-oxidant is similar to that of hydroquinone. (g) Oxidation of ascorbic acid Oxidation of ascorbic acid by freshly prepared solution of the cs-oxidant was measured by HPLC analysis of ascorbic acid as described before under stability of the solid oxidant (item c under chemical properties of the cs-oxidant). Ascorbate oxidation was measured using both limiting amount of ascorbate (28.41 nmoles) and excess of ascorbate (85.23 nmoles) with respect to a fixed amount of the oxidant (45.45 nmoles) in a final volume of 200 |Jl of 50 mM potassium buffer, pH 7.4. Aliquots were withdrawn at different time intervals as discussed in item c under chemical properties of the cs-oxidant and ascorbate was assayed by HPLC analysis. A similar result of ascorbate oxidation was obtained irrespective of using high amount (85.23 nmoles) or limiting amount (28.41 nmoles) of ascorbate. After 45 min of incubation, the ratio of nmoles of ascorbate oxidized to nmoles of the cs-oxidant was 0.55 (Table 2). This ratio is actually 1:1, because oxidation of ascorbate is one electron transfer reaction and the product, ascorbate radical (AH ' ), is chemically inert and decays by disproportionation reaction as shown below. 2 AH2 + 2OX = 2AH' + 2OXH 2AH' =AH2 +A 2AH2 + 2OX = AH2 + A +2OXH (AH2 = ascorbate, A= dehydroascorbate, OX= oxidant) [(Bielski, B.H.Jr. and Richter, H.W. (1975), Some properties of the ascorbate free radical. Ann. N.Y. Acad. Sci, 258. pp. 231-237)]. The results obtained on ascorbate oxidation and ferricytochrome c reduction (item f above) indicate that the cs-oxidant contains one oxidizing group and one reducing group in the molecule in stoichiometric proportion. Example 5 Quantitative measurement of the cs-oxidant The oxidant can be quantitatively measured by (a)UV spectroscopy (b) HPLC analysis and (c) reduction of ferricytochrome c. (a) UV absorption 5 µg of the oxidant was dissolved in 1 ml of HPLC grade methanol and UV absorption of the solution was recorded at 200-500 nm against methanol in a Hitachi double beam spectrophotometer (model U3020). Fig.9 shows that the oxidant has two absorption maxima (λ max). λ max absorption 293.4 nm 0.3192 223.0 nm 0.6994 The absorption at 293.4 nm was proportional to the concentration of the oxidant. The molar extinction coefficient of the oxidant based on its absorption maximum at 293.4 nm was calculated from Fig.9 and found to be E293.4 = 7018 cm-1 (b) HPLC analysis Different concentrations of the oxidant ranging from 10 ng to 100 ng in 20 µl of the mobile solvent were injected in the HPLC and the oxidant was detected at 294 nm. A standard curve was prepared (Fig. 14) based on the peak area (arbitrary) of the oxidant. The minimum amount of the oxidant that could be detected by the HPLC analysis under the condition was 500 pg. The parameters used were: Instrument : Shimadzu 10A Column 25 cm silica column (LiChrospher® Si 60,Merck) Mobile solvent Methylene chloride : methanol (90:10 , v/v ) Flow rate 0.5 ml/min Pressure 29 Kgf/cm2 Temperature 25°C Retention time 8.808 min (c) Reduction of ferricytochrome c Different amounts of the cs-oxidant ranging from 1 µg to 5 µg were used to reduce ferricytochrome c according to the method described under item (f) under chemical properties of the oxidant. A standard curve was drawn based on the results obtained (Fig.15). Example 6 Determination of the structure of the cs-oxidant The structure of the oxidant was determined by the following parameters: Elemental analysis, mass spectroscopy, melting point determination, UV spectroscopy, fluorescence spectroscopy, FTIR, H-NMR, C-NMR, ESR and XRF analysis. (a) Elemental analysis Using 1 mg of the oxidant, elemental analysis was performed in PERKIN ELMER 2400 Series 11 CHNS/O Analyser. Results Carbon % Hydrogen % Nitrogen % 64.06 5.33 1.16 The ratio of C, H and O from this percentage analysis was: Carbon : 5.34 Hydrogen : 5.33 Oxygen (by difference) : 1.84 So the empirical formula is C6H6O2 (b) Mass spectroscopy Molecular weight of the oxidant was determined by VG 7070 H mass spectrometer using El technique at 70 eV. The observed molecular weight was 110 with two subsequent fragments of m/e 81 and 53 respectively (Fig. 16). Although the molecular weight of the compound appears to be that of hydroquinone (CeHeC^), the compound is actually a strong oxidant. Comparative H-NMR spectroscopic studies (shown later) indicate that the oxidant has less amount of heteroatom-linked proton than that of hydroquinone and the g factor calculated from ESR spectroscopy (shown later) indicate that the compound is p-benzosemiquinone (MW 109). The observed molecular weight of 110 of the compound may be explained by the fact that the mass spectra was done with a sample stored for 7 days at the room temperature. It is possible that on storage in the solid state at the room temperature, p-benzosemiquinone is converted to its cationic form. It has been observed that cr. storage for 5-7 days in the solid state, the compound gives a UV absorption spectrum similar to that of hydroquinone (MW 110), accompanied by loss of oxidant activity (shown later). (c) Melting point determination The melting point of the cs-oxidant was found to be 162°C.Initially the oxidant appeared as a bunch of dark blackish rod like crystals under the microscope. With increase in temperature from about 140°C, the brightness at the edge of the crystals increased and there was separation of one crystal from another. The blackish shade from the edge of the crystals started disappearing and the distinctness and shine of the crystals increased as the temperature approached near the melting point. After just melting of most of the major portion of the crystals at 162°C, a few tiny rod like crystals appeared in the melted pool that subsequently melted at 172°C, which is known to be the melting point of hydroquinone. It is possible that at the high melting temperature, a portion of the oxidant was converted to hydroquinone. Under similar conditions, the melting point of hydroquinone was found to be 172°C. The characteristic change in the pattern of the crystals of the oxidant before melting as described above was less distinct in the case of hydroquinone. Mixed melting point studies Equal amounts of hydroquinone and the cs- oxidant were dissolved in acetone and dried to get the mixed crystals. The melting point of the mixed crystals was found to be 165°C. From the melting point experiment it is evident that the compound is not hydroquinone. (c) UV spectrophotometric analysis Five fig of the oxidant was dissolved in 1 ml methanol and the wave length scanning was monitored from 500 nm to 200 nm against methanol as the blank in a Hitachi double beam spectrophotometer, model U3020. The absorption maxima as indicated in Fig.9 are as follows: λ max absorption 293.4 mm 0.3192 223.0 nm 0.6994 Ratio of the absorption at λmax 223 nm: λmax 293.4 nm = 2.19 The UV spectrophotometric analysis of hydroquinone under similar condition produced a ratio of 1.98 (Fig. 17), which was different from that of the oxidant. It is interesting to note that on storage at room temperature in the dark for upto eight days, the UV-spectra of the stored oxidant was more similar to that of hydroquinone giving a ratio of 1.99 (Fig. 18). This would indicate that on storage the cs-oxidant is converted slowly to hydroquinone. On storage there was no indication of the formation of p-benzoquinone. When p- benzoquinone is mixed with hydroquinone in equimolar proportion, the absorption spectrum shows a shoulder near 242 nm (Fig. 19). Such shoulder is completely absent in the stored oxidant (Fig 18). (e) Fluorescence spectroscopy Using excitation wavelength at 294 nm, fig.20 shows that the fluorescent emission pattern of the oxidant is similar to that of hydroquinone under identical conditions (cf.Fig.6a). (f) FTIR spectroscopy FTIR spectroscopic analysis of the oxidant was carried out in the FTIR-8300 spectrophotometer, Shimadzu, Japan. With 1 mg of dry oxidant, a KBr pellet was prepared and used for FTIR spectroscopy. Fig.21 indicates peaks corresponding to • O-H stretching at 3234.4 cm-1 • C-H stretching for aromatic ring at 3030.0 cm-1 • C-C- stretching at 1514.0 cm-1 • O-H bending at 1355.9 cm-1 • C-O stretching at 1193.9 cm-1 • C-H bending at 756.0 cm-1 The FTIR spectrum of hydrcquinonc was carried out under similar conditions and it gave a comparable pattern of peaks (Fig.22) with some subtle difference. (g) NMR spectroscopy NMR spectroscopy was done using the Bruker 500 MHz spectrometer. Analysis and interpretation: 1H-NMR: 200-µg oxidant was dissolved in 500µl CD3COCD3 and analyzed. The NMR profile shows one sharp peak at 6.56 ppm corresponding to the four aromatic protons of hydroquinone structure and another peak at 7.55 ppm corresponding to the heteroatom linked proton, the proton(s) linked to the oxygen atom in hydroquinone (Fig.23). The H-NMR profile of hydroquinone in CD3COCD3 is given in (Fig.24). There is no difference in the chemical shift of the two peaks between hydroquinone and the oxidant. In deutereated acetone, the ratio of the aromatic protons to the heteroatom-linked protons for hydroquinone was found to be 1:0.4143. For the oxidant, this particular ratio was 1:0.2589. This shows that the oxidant contains less amount of heteroatom linked proton than that of hydroquinone. Fig.25 shows that there is a distinct difference between the nature of the peaks of the oxidant and that of hydroquinone at 7.55 ppm. When a pinch of sodium dithionite was added to the oxidant solution in CD3COCD3, the ratio of the aromatic protons to the heteroatom linked protons became 1:0.36. This indicates that the oxidant is reduced to hydroquinone by dithionite (Fig.26). C-NMR: The C-NMR profile of the oxidant (Fig. 27) indicates that this is identical to that of hydroquinone (Fig. 28). In both the cases, with protons completely decoupled and using CD3COCD3 as the solvent, peaks have been obtained at 116.101 ppm and 150.695 ppm respectively. The peak at 150.695 ppm represents heteroatom (>C = O) linked carbon. (h) XRF analysis All analyses, described so far, lead to the idea that the structure of the cs-oxidant is similar to that of hydroquinone except that it contains less amount of heteroatom linked proton. Moreover, in contrast to hydroquinone, the cs-oxidant is a strong oxidant. Using 1 mg BSA in 200-µl-incubation mixture containing 50mM potassium phosphate buffer, pll 7.4, 10 µg of the oxidant produced 9 mmoles of carbonyl in 1 hour. Under similar conditions, 10 µg of hydroquinone produced negligible amount of protein carbonyl. Also in contrast to hydroquinone, the oxidant oxidizes ascorbate stoichiometrically. It would thus appear that the cs-oxidant might be either a transition metal complex of hydroquinone or a free radical, namely, p-benzosemiquinone containing an unpaired electron. For detecting the presence of metal, if any, the compound was subjected to X-ray fluorescence spectroscopy. The oxidant was analyzed in the form of a pressed pellet after mixing with milled soil sample with boric acid backup. The major and trace elements were determined using Philips PW 2404 wavelength dispersive x-ray fluorescence spectrometer (WDXRF) with a Rhodium x-ray tube. Operating conditions were 50 KV and 40 mA. XRF analysis did not indicate the presence of any transition metal in the compound. Thus the strong oxidizing property of the compound was not due to the presence of any transition metal. (i) ESR analysis Since the compound does not contain any transition metal as evidenced by XRF analysis, the other alternative remains that the oxidant is a free radical, most likely p- benzosemiquinone. To detect the presence of an unpaired electron, the oxidant was subjected to ESR spectroscopic analysis using two different approaches. Approach # 1. Since on storage, the activity of the cs-oxidant undergoes decay, ESR spectroscopy was studied with freshly prepared oxidant. Tar from 100 cigarettes was pooled and the oxidant purified on the same day and subjected to ESR spectroscopy. The instrument used was JES-REIX ESR spectrometer (Tokyo, Japan). The parameters used were: Field modulation width = 0.4 mT Temperature = 25°C Power = 2 mW Scan field =(335±10)mT Sweep time = 8 min or 2.5 mT per min Time constant = 0.3 sec Receiver gain =32x1000 The ESR profile (Fig.29) shows the presence of a single symmetrical Lorentzian line. This is indicative of a single type of radical consisting of an unpaired electron delocalised over an aromatic framework. The spectroscopic splitting factor or the g-factor was calculated with reference to a standard solid DPPH (di-phenyl picryl hydrazyl) radical. The difference in positions of the exact centers (where the 1st derivative signals crossed zero) of the cs-oxidant and the DPPH is 13 mm, corresponding to 1.8 G. Since both spectra were recorded at the same fixed frequency, the frequency (v) at which resonance occurs (hv = gBH) is the same for both spectra: h. VDPPH - g DPPH- B. H DPPH and h. V CS-oxidant = g cs-oxidant . B . H cs-oxidant Since VDPPH and v cs-oxidant are the same g DPPH- B. H DPPH = g cs-oxidant - B . H cs-oxidant B is a constant, therefore g DPPH • H DPPH = g cs-oxidant • H cs-oxidant H DPPH is about 3353.15 G and therefore H cs-oxidant would be (3353.15G-1.8G) = 3351.35G. Rearranging gives: gcs-oxidant = 2.0036 x 3353.15 / 3351.35 = 2.00468 This g- value of the cs-oxidant is almost identical to the g-value of p-benzosemiquinone (2.004679 ± 0.000006) reported before (Wertz, J.E. and Bolton, J.R. Electron spin resonance, theory and practical applications, McGraw-Hill Book Company, New York, 1972, p. 465). The spin density of the cs-oxidant was calculated using standard picein as a reference and found to be 1.82 x 1013 mg"1 for 100 cigarettes or, the spin density = 1.82 X 1011 /cigarette Approach # 2. Tar from 400 cigarettes, collected in batches each day, was pooled together during 7 days and stored at -72°C. Purification of the cs-oxidant from pooled tar was carried out during the next two days. ESR spectroscopy of the purified oxidant (8mg) was carried out on the 10th day. Fig. 30 shows the ESR spectrum of the aged cs-oxidant collected from 400 cigarettes. The spin density of the molecule was calculated using standard picein as before and found to be 1.0713 x 1013 rng'-1(From 400 cigarettes) or, 0.2678 x 1011/cigarette It should be noted that the spin density of the aged cs-oxidant (0.2678 X 101'/cigarette), purified during 10 days as stated in approach # 2, is only about 15% of the spin density (1.82 X 1011 / cigarette) of the freshly prepared cs-oxidant (approach # 1). This loss of paramagnetism was accompanied by about 85% loss of the oxidant activity of the aged cs-oxidant, as evidenced by the capacity to oxidize ascorbic acid. The result is corroborative of the fact that the paramagnetism accompanied by the oxidizing activity of the cs-oxidant decays on storage. Molecular structure of the cs-oxidant Based on the results obtained with HPLC analysis as well as chemical and spectroscopic studies, the molecular structure of the cs-oxidant can be derived as follows. (i). The cs-oxidant contains an unpaired electron and its g-value is identical to that of p-benzosemiquinone. (ii). The structure is similar to that of hydroquinone with the exception that its M.P. is low (162°C) & it contains less amount of heteroatom linked proton than that of hydroquinone. On reduction with Na2S2O4, the oxidant is converted to hydroquinone. (iii) In contrast to hydroquinone, the cs-oxidant is a strong oxidizing agent. It oxidizes protein as well as ascorbic acid. (iv) The oxidant also contains a reducing group as evidenced by the reduction of ferricytochrome c. (v) The reduction of ferricytochrome c and oxidation of ascorbic acid are stoichiometric; that is the molecule contains one reducing group and one oxidizing group in stoichiometric proportion. The phenolic OH attributed the reducing property and the oxygen with unpaired electron attributes the oxidizing property. It would thus appear that the molecular structure of the cs-oxidant is p-benzosemiquinone, as shown below (Formula Removed) p-Benzosemiquinone may exist in different mesomeric forms, namely, anionic, neutral or cationic forms, as depicted in Fig.l, indicating delocalization of an unpaired electron over an aromatic framework containing heteroatoms. This is why p-benzosemiquinone is a relatively stable free radical, which could be isolated from cigarette smoke solution in the solid crystalline state. Nevertheless, on storage the isolated pure oxidant loses the paramagnetism accompanied by loss of the oxidant activity as shown above under ESR studies. The half-life of the oxidant is 48 hours when stored at the room temparature in the solid state under darkness and about 1.5 hours when stored in solution of 50mM potassium phosphate buffer, pH 7.4. Example 7 The purified cs-oxidant alone quantitatively accounts for the protein oxidation produced by the whole cigarette smoke solution Using BSA oxidation as a model system, the aforesaid statement has been substantiated by the following observations. (i) BSA oxidation produced by the whole cs solution as evidenced by cabbonyl formation, is retained in the purified cs oxidant ( stable one). The components of the whole cs solution discarded in the various steps of isolation and purification of the oxidant such as solvent extraction, TLC and HPLC did not produce BSA oxidation. For example, at the stage of solvent extraction, BSA oxidation was practically nil by the methylene chloride extract (Step 2, under Isolation and purification) (ii) TLC of the lyophilized material (Step 4, under Isolation and purification) produced six bands including the band of the cs- oxidant at Rt = 0.26 as shown in Fig.2. Extracts of all the bands were collected separately as described before and used for BSA oxidation. BSA uAJdatioji WA» j.ioduced only by the extract of the band corresponding to Rt-= 0.26 containing the cs- oxidant. Extracts of all other bands having Rf = 0.12, 0.14, 0.16, 0.30, 0.80 as well as that from the base line, when used separately or conjointly, did not produced BSA oxidation, (iii) During HPLC of the butanol extract at the penultimate stage of purification procedure (Step 6, under Isolation and purification), only the eluant from the major peak (retention time 8.808 min, Fig.3b) corresponding to the cs-oxidant produced BSA oxidation. Other minor peaks having retention times ranging from 4.55 min to 7.25 min did not produce BSA oxidation. (iv) HPLC analysis of the whole cs solution using the silica column indicated the presence of several peaks having retention times ranging from 5.717 min to 17.782 min including a major peak of the cs oxidant having retention time 8.813 min (Fig.31). When instead of the whole cs solution, aqueous extract of cs was used, the oxidant eluted out at a retention time of 8.808 min (Fig.32), which is identical to the peak of the cs-oxidant having retention time of 8.808 min as revealed by HPLC analysis of the pure cs-oxidant (Fig.4). Only the effluent from the peak corresponding to the cs-oxidant (retention time 8.813 min) produced BSA oxidation. Effluents from all other peaks separately or conjointly did not oxidize BSA. (v) HPLC analysis of the whole cs solution was also carried out using ODS column. The parameters used were: Column: Shim-pack CLC-ODS (M) Mobile solvent: water: methanol (95:5) Flow rate: 0.8 ml/min Pressure: 147 kgf7cm2 Temperature: 25°C Absorbance: 288 nm (A max of the cs-oxidant in water) HPLC analysis of the whole cs solution using the ODS column produced about 13 peaks including a major peak at 13.467 min (Fig. 33), which is the peak of the cs-oxidant as evidenced by the HPLC analysis of the pure cs-oxidant (retention time 13.46 min, Fig. 34). Under this condition also, as observed using the silica column as stated before, only the effluent from the peak corresponding to the cs-oxidant (retention time 13.46 min) produced BSA oxidation. Effluents from the other peaks , separately or conjointly did not oxidize BSA. It should be mentioned that although the resolution obtained using the ODS column was better than that of the silica column, the ODS column could not be routinely used for analyzing cigarette smoke solution or the cs-oxidant. After a few run with whole cs solution, aqueous extract of cs or the cs-oxidant, the ODS column underwent degeneration as evidenced by increased backpressure and loss of capacity of resolution. The aforesaid results indicate that only the cs-oxidant is responsible for the oxidation of BSA. No other component of the whole cs solution can oxidize BSA. This is further confirmed by the results presented in Table 3. The table shows that when the whole cs solution is used, a peak area of 17030 X 103 corresponding to the cs-oxidant (retention time, 8.813 min) produces 7.53nmoles of carbonyl, which is equivalent to 4.42 X 10"7 nmole of carbonyl per unit area. The table (Table 3) further shows that when instead of the whole cs solution, the HPLC-purified cs-oxidant is used, a peak area of 19010 x 1013 having retention time 8.808 min produces 9.56 nmoles of carbonyl, which is equivalent to 5.03 X 10-7 nmole of carbonyl per unit area. The results indicate that the oxidation of BSA produced by the whole cs solution is almost quantitatively reproduced separately by the pure oxidant alone when the latter is used in amount corresponding to that present in the whole cs solution. The cs-oxidant not only quantitatively accounts for the oxidative damage of proteins caused by the whole cs solution, but also it is a major hazardous component of the cigarette smoke as evidenced by its content. From HPLC analysis (p.8, under recovery of the cs-oxidant), it is observed that the cs-oxidant present in one ml of the whole cs solution (equivalent to one cigarette) gives an arbitrary area of 3.4 x 108. From the standard HPLC curve, 100 ng of pure cs-oxidant gives an area of 190000. So the content of the cs-oxidant in the whole cs solution from one cigarette is about 190±10 µg. Comparable yields were obtained from 12 different brands of commercial cigarette with or without standard filters. It should be mentioned that the cs-oxidant is not present in nonsmoking tobacco but formed during burning of the cigarette. That the purified cs-oxidant quantitatively accounts for the oxidative damage of proteins produced by the whole cs solution is further evidenced by SDS-PAGE of the guinea pig lung microsomal proteins treated with whole cs solution as well as the cs-oxidant (Fig. 35a). The figure shows that compared to untreated microsomes (lane 1), substantial damage is produced by 50µl cs solution (lane 2) andlOOµl cs solution (lane 3) respectively. When the cs solution is replaced by pure cs-oxidant in amounts present in the cs solution, the damage is even more as depicted in lane 4 (lOµg cs-oxidant) and lane 5 (20µg cs-oxidant). Fig.35b shows densitometric scanning of the protein bands of different lanes (lane 1-5), indicating graphical representation of the comparative extent of damage produced by cs solution and the cs-oxidant in amounts present in the cs solution. Example 8 cs-oxidant induced oxidative damage of DNA It has been reported that cigarette smoke solution produces DNA damage as evidenced by single strand break and formation of 8-hydroxyguanosine. It is also known that DNA damage is implicated with mutation and cancer. About 80% of the lung cancer in the world is caused by cigarette smoke. We produce data to indicate that cigarette smoke- induced oxidative damage of DNA is caused by the cs- oxidant. Two mg of plasmid DNA was incubated with 15 µg of cs-oxidant in 50 mM potassium phosphate buffer, pH 7.4 at 37°C for one hour in a final volume of 200µ1. A control incubation system was kept without cs-oxidant. After incubation, the DNA was precipitated with 500(4.1 of ethanol, centrifiiged, washed free of salt with 70% ethanol, lyophilized, stored at -70°C and subsequently analyzed for oxidative damage. The DNA damage was measured by the production of 8-hydroxyguanosine and 5-hydroxy-6-methyl hydantoin using GC-mass. The results show that cs-oxidant induces the formation of 24 nmoles of 8-hydroxyguanosine and 121 nmoles of 5-hydroxy-6-methyl hydantoin per 106 DNA bases. Example 9 Prevention of cs-oxidant induced protein oxidation by different chemical compounds / agents A number of chemical compounds / agents have been identified those prevent oxidation of BSA in vitro to the extent of 35 to 97%. The chemical compounds / agents include, besides ascorbic acid, tartaric acid, citric acid, oxalic cid, glutathione, tea extract and individual components of tea (Table. 4). Example 10 The content of the cs-oxidant depends on the tar content of the particular commercial brand of cigarette . We have used 12 different brands of cigarettes having tar content varying between 15mg to 25mg per cigarette. The content of the cs oxidant of different brands of cigarette by HPLC analysis is given below Brand No. tar content Content of cs-oxidant (µg) 1 25 200± 10 2 20 150±10 3 15 120110 In all these cases, the yield of the pure cs- oxidant at the final stage was 8-9% References l)Bartecchi, C.E.; Mackenzie, T.D. and Schier, R.W. The human costs of tobacco use. N.Engl. J. Med. 530:907-912; 1994 2)Frank, E. Benefits of stopping smoking. West J. Med. 759:83-87; 1993 3)U.S. Surgen General's Report. Department of Health, Education and Welfare; Deparment of Health and Human Services, USA; 1985 4)Shah, P.K.; Helfant, R.H. Smoking and coronary artery disease. Chest 94:449-452; 1988 5)Sherman, C.B. Health effect of cigarette smoking. Clin. Chest Med. 72:643; 1991, J.N.; Green, C.R.; Best, F.W. and Newell, M.P. Smoke composition: an extensive investigation of the water-soluble portion of cigarette smoke. J. Agric. Food Chem. 25:310-320; 1977 6) Cross, C.E. Moderator. Oxygen radicals and human disease. Ann. Intern. Med. 107:526- 545; 1987 7) Panda, K.; Chattopadhyay, R.; Ghosh, M.K.; Chattopadhyay, D.J.; and Chatterjee, I.B. Vitamin C prevents cigarette smoke-induced oxidative damage of proteins and increased proteolysis. Free Radio Bio) Med 27-1064-1079: 1999 8)Eiserich, J.P., Vossen, V.; O'Neill, C.A., Ilalliwcl, B.; Cross, C.E.; and Van der Vliet. A molecular mechanism of damage by excess nitrogen oxides : nitration of tyrosine by gas phase cigarette smoke. FEBS Lett. 553:53-56; 1994 9) Panda, K.; Chattopadhyay, R.; Chattopadhyay, D.J.; and Chatterjee, I.B. Vitamin C prevents cigarette smoke-induced oxidative damage in vivo. Free Radic. Biol. Med. 29,115- 124, 2000 10) SchumacherNakayama, T.; Kaneko, M,; Kodama, M. and Nagata, C. Cigarette smoke induces DNA single strand breaks in human cells. Nature 374:462-464; 1985 ll)Nakayama, T.; Kaneko, M,; Kodama, M. and Nagata, C. Cigarette smoke induces DNA single strand breaks in human cells. Nature 374:462-464; 1985 12) Borish, E.T.; Cosgrove, J.P.; Chirch, D.F.; Deutesch, W.A. and Pryor, W.A. Cigarette tar causes single-strand breaks in DNA. Biochem. Biophys. Res. Commun. 733:780-786; 1985 13) Denissoenko, M.F.; Pao, A.; Targ, M-S. and Pfeifer, G.P. Preferential formation of benzo [a] pyrene adducts at lung cancer mutational hotspots in P53. Science, 274:430-432; 1996 14) Fischer, S.; Spiegelhalder, B. and Preussmann, R. Tobacco specific nitrosamines in European and USA cigarettes. Arch. Geschwulstforsch, 60:169-177; 1990 15) Church, D.F. and Pryor, W.A. Free radical chemistry of cigarette smoke and its toxicological implications. Environ. Health Perspect. 64:111-126; 1985 16) Pryor, W.A., Hales, B.J., Premovic, P.I. and Church, D.F. The radical in cigarette tar : Their nature and suggested physiological implication. Science 220 : 425-427, 1983. 17) Glantz, S.A.; Slade, J.; Bero, L.A.; Hanauer, P. and Barnes, D.E. The cigarette papers. University of California Press, Berkely, USA, 1996. 18) Nagata, C.; Kodama, M. and loki, Y. In Polycyclic Hydrocarbons and Cancer, Gelboin, H.V. and P.O.P. Ts'o, Eds. (Academic Press, New York), J: 247; 1978. 19) Wertz, J.E. and Bolton, J.R. Electron spin resonance, elementary theory and practical applications. McGrow-Hill Book company, New York, 1972, p- 213. Table I. Estimation of oxidativc potency at different stages of purification of the cs-oxidant (Table Removed) * Actual weight after deducting the dry weight of the salt present in 50 j.il of potassium phosphate buffer solution. ** Mean values are given, S.D Table.2 Oxidation of ascorbic acid by the cs-oxidant as measured by HPLC analysis (Table Removed) Table.3 BSA oxidation by fractions of CS-solution at different stages of purification (Table Removed) *Similarr results were obtained when whole cs solution was replaced by equal amount of tar solution. Table 4. Protection of cs-oxidant-induced albumin oxidation by different chemical agents. (Table Removed) The incubation system and carbonyl estimation are described in the text. We Claim: 1. A process for the isolation of a major harmful oxidant from cigarette smoke , p-benzosemiquinone of formula 1 as shown below , having characteristics such as described herein and responsible for the oxidative damage of proteins and DNA (Formula Removed) the said process comprising the steps of (a) collecting tar or cs (cigarette smoke) solution from lighted conventional filtered tipped cigarettes, (b) collecting tar by lighting conventional filter-tipped cigarettes having a tar content of 20-30 mg per cigarette in a glass flask clipped in a mixture of ice and salt and allowing the tar to condense and settle at the bottom of the flask, (c) keeping the above said flask at room temperature and extracting the said tar with 30-60 mM potassium phosphate buffer at a pH ranging between 7.4 to 7.8, filtering the above solution through 0.45 urn Millipore filter and adjusting the pH of the filtrate ranging between 7.4 to 7.6 by adding NaOH solution to obtain the desired tar solution, (d) extracting the above said tar solution thrice with equal volume of methylene chloride, discarding the lower methylene chloride layer and collecting the upper yellow coloured aqueous layer termed as aqueous extract of cigarette smoke, (e) extracting the above said aqueous extract of cigarette smoke twice with equal volume of water saturated n-butanol, lyophilizing the pooled yellow butanol extract in a lyophilizer at a temperature ranging between -50 °C. to -60 °C. under vacuum followed by extraction of the lyophilized material twice with HPLC grade acetone and drying the acetone solution under vacuum and dissolving the said acetone extract with HPLC grade methanol, (f) subjecting the above said methanol solution to band TLC using non-fluorescent silica plates, developing the said silica plates using a mixture of toluene and ethyl acetate in a ratio of 80:20, taking out the said plate and drying it at about 25-30° C using a drier, cutting small strips containing the developed material from both sides of the plates and keeping them in an iodine chamber for the location of the band corresponding to Rf 0.26, scraping the band and extracting the band material with HPLC grade acetone followed by collection of the acetone layer and drying it under vacuum, (g) dissolving the above said acetone extract which appeared as pale yellow needles by adding equal volume of milli Q water, extracting the resultant aqueous solution with equal volume of HPLC grade water saturated n-butanol followed by drying upper n-butanol layer in small glass tubes under vacuum to obtain the major cigarette smoke (cs) oxidant with a purity .of 98-99% and yield of about 18-22µg per cigarette, (h) purifying the above said cs oxidant as obtained in step (g) by dissolving it in a mobile solvent comprising a mixture of methylene chloride and methanol in a ratio of 90:10 (v/v) and injecting it in a HPLC instrument with a normal phase 25 cm silica column using a uv detector at 294 nm at a flow rate of 0.5 ml/min, at a temperature of about 25° C and at a pressure of about 29 kgf/cm.sup.2 followed by collecting the effluent which appears as a single peak at a retention time of 8.808 min with a purity of 100% and yield of 8.4% of the total cs oxidant present in the parent tar solution. 2. A process as claimed in claim 1 wherein protein used for assay of oxidative damages of protein is selected from the group consisting bovine serum albumin (BSA) and guinea pig lung microsomal protein. 3. A process for the isolation of a major harmful oxidant from cigarette smoke , p- benzosemiquinone substantially as herein described with reference to examples.

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