Study on in situ intestinal absorption of baicalin contained in Tiangou Jiangya capsules / 中国中药杂志
Zhongguo Zhong Yao Za Zhi
; (24): 894-898, 2013.
Article
em Zh
| WPRIM
| ID: wpr-318621
Biblioteca responsável:
WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To study in situ intestinal absorption kinetics of baicalin contained in Tiangou Jiangya capsules, and the effect of different intestinal segments, pH value, drug concentration and P-gp inhibitor on the absorption.</p><p><b>METHOD</b>The in situ intestinal perfusion test was adopted, and HPLC method was used to determine the content of baicalin in samples at different time points. Ultra-violet (UV) spectrophotometry was used to determine the content of phenol red in samples at different time points.</p><p><b>RESULT</b>When pH value was at 5. 0, 6. 5, 7. 4, the absorption of baicalin was not impacted. P-gp inhibitor verapamil could enhance the absorption of baicalin. When the quality concentration of the test solution ranged between 5-20 g L -1 , the linearity of the absorption amount of baicalin increased. The absorption kinetic equation of baicalin was Y = -0. 073 7X +0. 118 7 (r = 0. 994 8) , K. 0. 073 7 h -1 , t1/2 9. 40 h.</p><p><b>CONCLUSION</b>Baicalin is mainly absorbed in colon. The absorption of baicalin shows the first-order kinetics process, with the absorption mechanism of passive diffusion. Baicalin is a substrate for P-gp.</p>
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Índice:
WPRIM
Assunto principal:
Farmacologia
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Controle de Qualidade
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Padrões de Referência
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Álcoois Benzílicos
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Flavonoides
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Cinética
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Verapamil
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Química
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Ratos Wistar
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Lignanas
Limite:
Animals
Idioma:
Zh
Revista:
Zhongguo Zhong Yao Za Zhi
Ano de publicação:
2013
Tipo de documento:
Article