Determination of borneol in Fufang Danshen intestinal adhesion pellets and study its in vitro dissolution in different dosage form.
- Author:
Zhen WANG
;
Shou-ying DU
;
Yang LU
;
Zhuang ZHAO
;
Jie BAI
;
Peng-yue LI
;
Bo-yu DONG
;
Qin DU
;
Lin ZHANG
- Publication Type:Journal Article
- MeSH:
Bornanes;
adverse effects;
chemistry;
pharmacology;
Chemistry, Pharmaceutical;
methods;
Dosage Forms;
Drugs, Chinese Herbal;
adverse effects;
chemistry;
pharmacology;
Humans;
Intestinal Mucosa;
drug effects;
metabolism;
Models, Biological;
Solubility
- From:
China Journal of Chinese Materia Medica
2015;40(16):3194-3199
- CountryChina
- Language:Chinese
-
Abstract:
The borneol was included with β-CD and prepared Fufang Danshen intestinal adhesion pellets. GC method for determination of borneol in Fufang Danshen intestinal adhesion pellets was established to study its in vitro dissolution and make a comparison with the Fufang Danshen tablet, in this way, the rationality of dosage form was evaluated. The first method of dissolution determination was used for determining the in vitro dissolution of borneol in Fufang Danshen intestinal adhesion pellets in artificial intestinal juice, and Fufang Danshen tablet in artificial gastric juice and intestinal juice, respectively. Result shows: the concentration of borneol in Fufang Danshen intestinal adhesion pellets and Fufang Danshen tablet was 0.79% and 0.80%, respectively. Its in vitro dissolution was nearly 70% within 12 h in Fufang Danshen intestinal adhesion pellets, and in Fufang Danshen tablet, the dissolution was about 60% within 20 min and more than 90% within 40 min, and in artificial gastric juice, was less than 20% within 40 min but more than 80% till 150 min. Research suggests that in comparison with Fufang Danshen tablet, in vitro dissolution of borneol in the Fufang Danshen intestinal adhesion pellets showed an obvious sustained release behavior. The borneol in Fufang Danshen intestinal adhesion pellets was included with β-CD and prepared enteric preparations. To some extent, the stimulation on stomach and intestinal mucosa can be reduced and safety can be improved.
