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Study on Formulations and in Vitro Drug Release of Sustained-release Bioadhesive Danazol Suppository / 中国药房
China Pharmacy ; (12)1991.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-520764
Responsible library: WPRO
ABSTRACT

OBJECTIVE:

To screen the formulations of bioadhesive danazol suppository,and to study its drug release in vitro.

METHODS:

Hydroxypropyl methylcellulse(HPMC),polyethylene glycol(PEG)6000and PEG600were employed in the bioadhesive sustained-release formulation.Suppositories were prepared and the correlation between drug release rate from suppositories and the ratio of HPMC to PEGs used in the formulae was studied.

RESULTS:

HPMC retarded drug release,and drug gradually released in the12-hours period when the ratio of HPMC to PEGs was1∶6.5;the law of drug release was conformed to weibull models and mono-exponential models.

CONCLUSION:

HPMC,PEG6000and PEG600were suitable to the formulation of bioadhesive danazol suppositories,and HPMC could slow down the drug release from the this preparation;the best ratio of HPMC to PEGs was1∶6.5.

Full text: Available Database: WPRIM (Western Pacific) Language: Chinese Journal: China Pharmacy Year: 1991 Document type: Article
Full text: Available Database: WPRIM (Western Pacific) Language: Chinese Journal: China Pharmacy Year: 1991 Document type: Article
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