Preparation of self-microemulsifying soft capsule and investigation of dissolution for pueraria lobata isoflavone
- VernacularTitle:葛根黄酮自微乳化软胶囊的制备和溶出度的考察
- Author:
Shengmiao CUI
;
Chunshun ZHAO
;
Zhonggui HE
- Publication Type:Journal Article
- Keywords:
pueraria lobata isoflavone;
selfmicroemulsifying;
soft capsule;
dissolution.
- From:
Chinese Traditional Patent Medicine
1992;0(07):-
- CountryChina
- Language:Chinese
-
Abstract:
AIM: In order to prepare the self-microemulsifying soft capsule(SMESC)of pueraria lobata isoflavone and investigate its dissolution property. METHODS: Through solubility experiment,self-microemulsification in vitro,phase diagram and the stability of solution,the optimum formulation was selected for pueraria lobata isoflavone.The dissolution of SMESC was measured taking the commercial tablet as reference. RESULTS: In the selected formulation,Tween-80,1,2-Propanediol and ethyl oleate were screened as emulsifier,co-emulsifier and oil phase,respectively.The optimized proportion was 65∶20∶15 .The dissolution of SMESC in the condition of distilled water,pH6.8 phosphate buffer and 0.1 mol/L HCl were more than 90% in 10 min,while those of the commercial tablet were less than 40% in 90 min. CONCLUSION:In comparison with the commercial tablet,the dissolution of pueraria lobata isoflavone is sufficiently improved at various conditions.
