Preparation and evaluation of silibinin solid dispersions in vitro / 第二军医大学学报
Academic Journal of Second Military Medical University
;
(12)2000.
Article
Dans Chinois
| WPRIM
| ID: wpr-677190
ABSTRACT
Objective:
To prepare silibinin solid dispersion and measure its dissolution in vitro .Methods:
Silibinin solid dispersions were obtained with urea, PVP and poloxamer188 as carriers by melting and coevaporation methods. Differential thermal analysis and powder X ray diffraction were used to determine the status of drug in carriers, and the dissolution characteristics in vitro were studied in simulated gastric juice.Results:
In PVP silibinin solid dispersions drug was amorphous; in poloxamer188 silibinin solid dispersions, drug existed as fine crystal, while in urea silibinin solid dispersions most of silibinin existed as crystal, only a little as molecule. Poloxamer188 was the better carrier in improving the solution and dissolution rate of the drug.Conclusion:
Poloxamer188 is a very useful carrier in improving the solubility and dissolution of silibinin. [
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
langue:
Chinois
Texte intégral:
Academic Journal of Second Military Medical University
Année:
2000
Type:
Article
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