Title of Invention

A METHOD OF PREPARING HYDROXYPROPYL METHYL CELLULOSE PHTHALATE NANOPARTICLE"

Abstract

The present invention relates to a preparation method of solvent-free water-dispersible hydroxypropyl methyl cellulose phthalate nonoparticle, and more particularly, to a preparation method of solvent-free water-dispersible hydroxypropyl methyl cellulose phthalate nanoparticle, which is environment-friendly and advantageous in disintegration and dissolution when sued as an enteric coating material, which is prepared by obtaining suitable hydroxypropyl methyl cellulose phthalate (HPMCP) particle through aqueous emulsification process and regulating content of remaining electrolyte through ion exchange process.

Full Text

Field of the Invention The present invention relates to a method of preparing solvent-free water-dispersible hydroxypropyl methyl cellulose phthalate nanoparticle. Background of the Invention The present invention relates to a preparation method of solvent-free water-dispersible hydroxypropyl methyl cellulose phthalate nanoparticle, and more particularly, to a preparation method of solvent-free water-dispersible hydroxypropyl methyl cellulose phthalate nanoparticle, which is environment-friendly and advantageous in disintegration and dissolution when used as an enteric coating material, which is prepared by obtaining suitable hydroxypropyl methyl cellulose phthalate (HPMCP) particle through aqueous emulsification process and regulating content of remaining electrolyte through ion exchange process. Until now, mainly hydroxypropyl methyl cellulose phthalate and acrylate have been used as enteric coating materials. However, for hydroxypropyl methyl cellulose phthalate, organic solvent is used during coating process, which may cause environmental problem. And, for acrylate, although the water-dispersible product is available, it is a synthetic polymer rather than a natural material and it has poor film properties compared to those of hydroxypropyl methyl cellulose phthalate. Therefore, need of a new type of environment-friendly material has been increased. In this regard, water-dispersible hydroxypropyl methyl cellulose phthalate has been prepared. The conventional method of preparing this water-dispersible hydroxypropyl methyl cellulose phthalate comprises: completely dissolving hydroxypropyl methyl cellulose phthalate with organic solvent and dispersing it in water; removing organic solvent in tne solution to obtain water-dispersible type of hydroxypropyl methyl cellulose phthalate. However, the product obtained by this method has poor stability in water-dispersible phase. Further, the use of an organic solvent incurs an increase in manufacturing cost, and it also has a drawback that the organic solvent is hardly removed from the final product thereby causing an environmental problem. USP No. 5,560,930 discloses a method of preparing particle of about 0.2pm, by emulsifying hydroxypropyl methyl cellulose phthalate in water after dissolving it in acetone and removing the organic solvent through distillation under reduced pressure. It discloses examples of using a solvent mixture, such as ethanol/water and methanol/ water. USP No. 5,512,092 discloses a method of dissolving hydroxypropyl methyl cellulose phthalate in ethanol and emulsifying it; and USP No. 5,346,542 discloses a method of dissolving carboxymethyl ethyl cellulose in methyl acetate and emulsifying it in water. Although these methods do not have problems of latex particle size or dispersion, product stability after emulsification is poor and leaves the organic solvent in the final product because it is difficult to remove organic solvent remaining in the solution. We prepared water-dispersible hydroxypropyl methyl cellulose phthalate according to the above method in lcmXlcm film. When it was placed in aqueous solution of pH 1.2 for 2hr, the film was dissolved. And, we diluted this water-dispersible hydroxypropyl methyl cellulose phthalate to 7wt% with distilled water and coated it on the tablet using Hi-Coater (HCT Labo, Freund Co.). The disintegration test (pharmatest P1Z hi) showed that disintegration took place m 2hr under pH 1.2. Because of this, commercialization of water-dispersible hydroxypropyl methyl cellulose phthalate has not been achieved as yet. SUMMARY OF THE INVENTION In order to solve these problems, we prepared stable particles by introducing aqueous emulsification process of hydroxypropyl methyl cellulose phthalate (HPMCP) without using an organic solvent. And, we regulated the amount of remaining electrolytes through ion exchange process in order to obtain hydroxypropyl methyl cellulose phthalate. Accordingly, an object of the present invention is to provide a preparation method of solvent-free water-dispersible hydroxypropyl methyl cellulose phthalate nanoparticle, which is environment-friendly and advantageous in disintegration and dissolution without having the problem of leaving the organic solvent in the final product. Detailed Description of the Invention The present invention is characterized by a preparation method of solvent-free water-dispersible hydroxypropyl methyl cellulose phthalate nanoparticles, which comprises: 1) a step of emulsifying hydroxypropyl methyl cellulose phthalate at 20-70 °C for 4-6hr using emulsifying agent and NH4OH; and 2) an ion exchange step of reducing content of electrolyte remaining in hydroxypropyl methyl cellulose phthalate obtained by the step 1) to 0-50 mS using ion exchange resin or membrane. Hereunder is given a detailed description of the present invention. The present invention is characterized by a preparation method of water-dispersible hydroxypropyl methyl cellulose phtiialate iianoparticle stable in water, by neutralizing a phthalate group of hydroxypropyl methyl cellulose phthalate with NH4OH and controlling electrolyte content remaining in the solution through ion exchange process. Hereunder is given a more detailed description of the present invention. Firstly, the step 1 is a step of forming water-stable particle by emulsifying hydroxypropyl methyl cellulose phthalate at 20-70°C for 4-6hr using an emulsifying agent and NH4OH. For hydroxypropyl methyl cellulose phthalate, the one with 40,000-60,000 of mean molecular weight can be used. And as an emulsifying agent, Pluronic F-68, Triton X-405, Tween-80, Polystep B-1 or Polystep F-9 can be used. The emulsifying agent is preferred to be used in 0.05-1.0wt% against hydroxypropyl methyl cellulose phthalate. If its content is below 0.05wt%, stability of water-stable HPMCP is deteriorated; and if it exceeds 1.0wt%, film property is lowered when it is coated on tablet. For neutralizer, NH4OH can be used. Its content is preferred to be 1.6-4.0wt% against hydroxypropyl methyl cellulose phthalate. If it is below 1.6wt%, there can arise a stability problem because particle size is enlarged; and if it exceeds 4.0wt%, the tablet may give off ammonia-like odor due to excess use of NH4OH. In particular, it is preferred to use 28% NH4OH solution. The step 2 is an ion exchange step to regulate remaining electrolyte content to 0-50mS by using ion exchange resin or membrane. If the remaining electrolyte content is above this range, excess amount of ion exchange resin has to be used to remove the remaining electrolyte. For ion exchange resin, cation exchange resin, e.g., Dowex MR-3 (Sigma-Aldrich, US) can be used. For membrane, it is recommended to use the one with pores of 100-300nm in size. If the pore size is below l00nm, a considerable amount of time is required to remove remaining electrolyte; and if it exceeds 300nm, the HPMCP particle may penetrate the membrane, which may cause reduction of solid content. Here, the remaining electrolyte means the ammonium ion which forms salt, and it affects physical properties of hydroxypropyl methyl cellulose phthalate. The present invention includes water-dispersible hydroxypropyl methyl cellulose hthalate prepared by said steps 1 and 2. The obtained water-dispersible hydroxypropyl methyl cellulose phthalate has 100-1000nm of particle size and contains 7-30wt% of solid contents. The hydroxypropyl methyl cellulose phthalate prepared by the present invention shows no particle sedimentation when stored for long time in water and does not dissolve in pH 1.2 when it is coated on tablet. Therefore, it can be used as environment-friendly enteric coating material. Statement of Invention Accordingly, the present invention relates to a method of preparing solvent-free water-dispersible hydroxypropyl methyl cellulose phthalate nanoparticle comprising steps of: (i) emulsifying hydroxypropyl methyl cellulose phthalate at 20-70°C for 4 - 6 hr using an emulsifying agent such as herein described in the range of 0.05 to 1.0wt% against said hydroxypropyl methyl cellulose phthalate and NH4OH in the range of 1.6 to 4.0 wt%, against said hydroxypropyl methyl cellulose phthalate ; and (ii) regulating the remaining electrolyte content to 0-50 mS using cation exchange resin or membrane, wherein pore size of said membrane is 100-300 nm. The following examples are intended to be illustrative of the present invention, and they should not be construed as limiting the scope of this invention. Example 1 400g of distilled water, l.0g of Pluronic F-68 and l00g of hydroxypropyl methyl cellulose phthalate (Mw 40,000-60,000, Samsung Fine Chemicals Co., Ltd.) were placed in 1L reactor equipped with a stirrer and stirred at 300-350 rpm. 28%-NH40H (8g) was slowly added to this solution and the temperature was raised to 60 °C. After stirring for another 4-5hr while maintaining the temperature, the remaining ammonium ion concentration was adjusted to 0.0-7ms using ion exchange resin [Dowex MR-3, Sigma-Aldrich, US]. The prepared water-dispersible hydroxypropyl methyl cellulose phthalate had 4.6+1.0 of pH, 25±5 % of solid content, 140±5 of acid value and 300±50nm of particle size. The pH was measured with a pH meter of Orion research, Inc.. and the solid content was measured by gravimetric determination. The acid value represents distribution of a carboxyl group per unit surface area. 0.1N KOH was used to determine the acid value; and THF and methanol were used to dissolve dry sample. The particle size was measured by dynamic light scattering (DLS; Zetaplus, Brookhaven Instruments). The obtained water-dispersible hydroxypropyl methyl cellulose phthalate was made into 1cm x 1cm film and placed in pH 1.2 of an aqueous solution. When it was taken out arter 2hr, it remained in shape without being dissolved. The water-dispersibie hydroxypropyl methyl cellulose phthalate was diluted to 7wt% with distilled water and coated on tablet using Hi-Coater (HCT Labo) The disintegration test (Pharmatest PTZ E) showed that no disintegration took place for 2hr under pH 1.2. Example 2 400g of distilled water, 0.53g of Triton X-405 and 106g of hydroxypropyl methyl cellulose phthalate (Mw 40,000-60,000, Samsung Fine Chemicals Co., Ltd.) were put in 1L reactor equipped with a stirrer and stirred at 300-350 rpm at room temperature. 28%-NH4OH (lOg) was slowly added to this solution and it was stirred for another 4-5hr. The remaining ammonium ion concentration was regulated to 0.0-7mS using ion exchange resin [Dowex MR-3, Sigma-Aldrich, US]. The prepared water-dispersible hydroxypropyl methyl cellulose phthalate had 4.8±1.0 of pH, 19.9% of solid content, 145 of acid value and 700±50nm of particle size. The obtained water-dispersible hydroxypropyl methyl cellulose phthalate was made into IcmXlcm film and put in pH 1.2 of an aqueous solution. When it was taken out after 2hr, it remained in shape without being dissolved. The water-dispersible hydroxypropyl methyl cellulose phthalate was diluted to 7wt% with distilled water and coated on a tablet using Hi-Coater (HCT Labo). The disintegration test (Pharmatest PTZ E) showed that no disintegration took place in 2hr under pH 1.2. Example 3 400g of distilled water, 0.7 g of Polystep B-l and lOOg of hydroxypropyl methyl cellulose phthalate (Mw 40,000-60,000, Samsung Fine Chemicals Co., Ltd.) were placed in a 1L reactor equipped with a stirrer and stirred at 300-350 rpm at room temperature. 28%-NH4OH (11.5g) was slowly added to this solution and it was stirred for another 4-5hr. The remaining ammonium ion concentration was adjusted to 0.0-7mS using membrane (pore size: 200nm). Because emulsifying agent is removed together with the remaining ammonium ion, the emulsifying agent was replenished continuously so as not to alter the emulsifying agent concentration. The prepared water-dispersible hydroxypropyl methyl cellulose phthalate had 8 ±0.5 of pH, 20.0% of solid content, 140 of acid value and 100±50nm of particle size. The obtained water-dispersible hydroxypropyl methyl cellulose phthalate was made into lcmXlcm film and placed in pH 1.2 of an aqueous solution. When it was taken out after 2hr, it remained in shape without being dissolved. The water-dispersible hydroxypropyl methyl cellulose phthalate was diluted to 7wt% with distilled water and coated on tablet using Hi-Coater (HCT Labo). The disintegration test (Pharmatest PTZ E) showed that no disintegration took place in Zhr under pH 1.2. Example 4 400g of distilled water, 0.5 g of Tween-80 and lOOg of hydroxypropyl methyl cellulose phthalate (Mw 40,000-60,000, Samsung Fine Chemicals Co., Ltd.) were placed in a 1L reactor equipped with a stirrer and stirred at 300-350 rpm. 28%-NH4OH (8g) was slowly added to this solution and the temperature was raised to 60 °C. After stirring for another 4-5hr while maintaining the temperature, the remaining ammonium ion concentration was adjusted to 0.0-7mS using ion exchange resin (Dowex MR-3, Sigma-Aldrich, US). The prepared water-dispersible hydroxypropyl methyl cellulose phthalate had 4.6±1.0 of pH, 25±5% of solid content, 140±5 of acid value and 500±50nm of particle size. The obtained water-dispersible hydroxypropyl methyl cellulose phthalate was made into lcmXlcm film and placed in pH 1.2 of an aqueous solution. When it was taken out after 2hr, it remained in shape without being dissolved. The water-dispersible hydroxypropyl methyl cellulose phthalate was diluted to 7wt% with distilled water and coated on a tablet using Hi-Coater (HCT Labo). The disintegration test (Pharmatest PTZ E) showed that no disintegration took place in 2hr under pH 1.2. Example 5 400g of distilled water, 0.65g of Polystep F-9 and 106g of hydroxypropyl methyl cellulose phthalate (Mw 40,000-60,000, Samsung Fine Chemicals Co., Ltd.) were placed in a 1L reactor equipped with a stirrer and stirred at 300-350 rpm at room temperature. 28%-NH4OH (lOg) was slowly added to this solution and it was stirred for another 4-5hr. The remaining ammonium ion concentration was adjusted to 0.0-7mS using ion exchange resin (Dowex MR-3; Sigma-Aldrich, US). The prepared water-dispersible hydroxypropyi methyl cellulose phthalate had 4.8±1.0 of pH, 19.9% of solid content, 145 of acid value and 200±50nm of particle size. The obtained water-dispersible hydroxypropyi methyl cellulose phthalate was made into lcmXlcm film and put in pH 1.2 aqueous solution. When it was taken out after 2hr, it remained in shape without being dissolved. The water-dispersible hydroxypropyi methyl cellulose phthalate was diluted to 7wt% with distilled water and coated on a tablet using Hi-Coater (HCT Labo). The disintegration test (Pharmatest PTZ E) showed that no disintegration took place for 2hr under pH 1.2. Comparative Example 1 USP No. 5,560,930 discloses the following method. 0.3kg of hydroxypropyi methyl cellulose phthalate dissolved in 9.7kg of acetone is emulsified in 10kg of distilled water while stirring at 100 rpm. The prepared emulsion is distilled under reduced pressure under the condition of 50 °C/-590mm to remove an organic solvent. However, when we followed this procedure, although there was no problem of latex particle size or dispersion, there was a problem of product stability after emulsification and it was difficult to remove the organic solvent. Especially, the organic solvent remained in the final product. We also made 1cm x 1cm film with the obtained water-dispersible hydroxypropyi methyl cellulose phthalate and put in pH 1.2 of an aqueous solution. When it was taken out after 2hr, the film had been dissolved. Also, we diluted the water-dispersible hydroxypropyi methyl cellulose phthalate to 7wt% with distilled water and coated it on a tablet using Hi-Coater (HCT Labo). The disintegration test (Pharmatest PTZ E) showed that disintegration took place for 2hr under pH 1.2. As explained above, the present invention provides a new type of preparation method of water-dispersible hydroxypropyl methyl cellulose phthalate nanoparticle by preparing stable particle through introduction of aqueous emulsification process and regulating remaining electrolyte content through ion exchange process. As a result, the present invention resolves the environmental problem of the conventional method using organic solvent while maintaining basic properties of hydroxypropyl methyl cellulose phthalate. Therefore, it can be used as a new concept for environment-friendly enteric coating material. We claim: 1. A method of preparing solvent-free water-dispersible hydroxypropyl methyl cellulose phthalate nanoparticle comprising steps of: (i) emulsifying hydroxypropyl methyl cellulose phthalate at 20-70°C for 4-6 hr using an emulsifying agent such as herein described in the range of 0.05 to 1.0wt% against said hydroxypropyl methyl cellulose phthalate and NH4OH in the range of 1.6 to 4.0 wt%, against said hydroxypropyl methyl cellulose phthalate ; and (ii) regulating the remaining electrolyte content to 0-50 mS using cation exchange resin or membrane, wherein pore size of said membrane is 100-300 nm. 2. Water-dispersible hydroxypropyl methyl cellulose phthalate prepared by the preparation method as claimed in claim 1. 3. Water-dispersible hydroxypropyl methyl cellulose phthalate as claimed in claim 2, which has 100-1000 nm of particle size and 7-30 wt% of solid content.

Documents:

1430-delnp-2004-abstract.pdf

1430-delnp-2004-claims.pdf

1430-delnp-2004-complete specification(as files).pdf

1430-delnp-2004-complete specification(granted).pdf

1430-delnp-2004-correspondence-others.pdf

1430-delnp-2004-correspondence-po.pdf

1430-delnp-2004-description (complete).pdf

1430-delnp-2004-form-1.pdf

1430-delnp-2004-form-18.pdf

1430-delnp-2004-form-2.pdf

1430-delnp-2004-form-26.pdf

1430-delnp-2004-form-3.pdf

1430-delnp-2004-form-5.pdf

1430-delnp-2004-pct-210.pdf

1430-delnp-2004-pct-301.pdf

1430-delnp-2004-pct-304.pdf

1430-delnp-2004-pct-306.pdf

1430-delnp-2004-pct-308.pdf

1430-delnp-2004-pct-332.pdf

1430-delnp-2004-pct-409.pdf

1430-delnp-2004-pct-416.pdf

1430-delnp-2004-petition-137.pdf

1430-delnp-2004-petition-138.pdf