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학술논문

시클로덱스트린류와의 복합체 형성에 의한 벤즈이미다졸계 구충 약물의 용해성 및 용출 증가

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영문명
Solubilization and Dissolution Enhancement of Benzimidazole Antnelmintic Drugs by Cyclodextrin Complexation
발행기관
대한약학회
저자명
전인구(In Koo Chun) 박인숙(In Sook Park)
간행물 정보
『약학회지』제37권 제3호 (1993년), 216~227쪽, 전체 12쪽
주제분류
의약학 > 기타의약학
파일형태
PDF
발행일자
1993.06.30
4,240

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국문 초록

영문 초록

Complex formations of practically insoluble antelmintic drugs such as mebendazole (MBZ), albendazole (ABZ) and flubendazole (FBZ) with dimethyl-beta-cyclodextrin (DM-beta-CyD) and 2-hydroxypropyl-beta-cyclodextrin (HP-beta-CyD) together with alpha-, beta- and gammar-cyclodextrins (CyDs) in buffered solutions were investigated by solubility method. AL type phase solubility diagrams were obtained in all cases except for the complexation (BS type) of FBZ with gammar-CyD. The highest stability constants were obtained with DM-P-CyD, followed by allpha-CyD > beta-CYD > HP-beta-CyD > gammar-CyD for ABZ, and HP-beta-CyD > gammar-CyD > beta-CyD > alpha-CyD for FBZ at pH 1.2. On the other hand, solid dispersion systems of ABZ and FBZ with beta- and DM-beta-CyDs were prepared by solvent evaporation method and evaluated by dissolution, differential thermal analysis and powder x-ray diffractometry. The dissolution rates of ABZ- and FBZ-DM-P-CyD solid dispersions were much faster than those of drugs alone, corresponding physical mixtures and tablets on market both at pH 1.2 and 6.8. Although dissolution rates of all samples at pH 6.8 were by far lower than those obtained at pH 1.2, as explained by pH-solubility profiles for ABZ and FBZ, the dissolution rates at pH 6.8 of ABZ from beta- and DM-beta-CyD solid dispersions exceeded the respective equilibrium solubility (23.9mcg/ml). Fast dissolution of ABZ from solid dispersions with CyDs was attributed to the reduction of drug crystallinity and particle size which was supported by DTA and powder x-ray diffractometry. Consequently these results suggest that solid dispersion systems with CyDs may provide useful means to markedly enhance the solubility and dissolution of benzimidazole antelmintic drugs.

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APA

전인구(In Koo Chun),박인숙(In Sook Park). (1993).시클로덱스트린류와의 복합체 형성에 의한 벤즈이미다졸계 구충 약물의 용해성 및 용출 증가. 약학회지, 37 (3), 216-227

MLA

전인구(In Koo Chun),박인숙(In Sook Park). "시클로덱스트린류와의 복합체 형성에 의한 벤즈이미다졸계 구충 약물의 용해성 및 용출 증가." 약학회지, 37.3(1993): 216-227

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