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阿苯达唑混悬液及含羟丙基-β-环糊精溶液在绵羊体内的口服生物利用度。

Oral bioavailability in sheep of albendazole from a suspension and from a solution containing hydroxypropyl-beta-cyclodextrin.

作者信息

Evrard B, Chiap P, DeTullio P, Ghalmi F, Piel G, Van Hees T, Crommen J, Losson B, Delattre L

机构信息

Lab of Pharmaceutical Technology, Institute of Pharmacy, University of Liège, CHU-Tour 4, Bât B36, Avenue de l'Hôpital 1, 4000 1, Liège, Belgium.

出版信息

J Control Release. 2002 Dec 13;85(1-3):45-50. doi: 10.1016/s0168-3659(02)00270-5.

Abstract

Albendazole (ABZ) is a benzimidazole derivative with a broad spectrum of activity against human and animal helminthe parasites. ABZ has a very poor aqueous solubility. This study shows that hydroxypropyl-beta-cyclodextrin (HP-beta-CD) is able to form inclusion complexes with ABZ and that is able to increase its aqueous solubility. A synergistic effect exists between HP-beta-CD and citric acid. The combination of HP-beta-CD (200 mM) and citric acid (50 mM) allows dissolution of more than 1.5 mg of ABZ per ml. The aim of this study is the in vivo evaluation in sheep of a solution of the inclusion complex of ABZ with HP-beta-CD in comparison with a suspension of the same drug. A significant (P<0.05) increase in the relative bioavailability is obtained with the solution containing the ABZ-HP-beta-CD complex as measured by ABZSO plasma levels. The area under the curve (AUC(0--> proportional, variant )) of the solution is 37% higher than that obtained with the suspension. Likewise the peak plasma concentration (C(max)) is twice that of the solution while the time to reach C(max) (T(max)) is reduced.

摘要

阿苯达唑(ABZ)是一种苯并咪唑衍生物,对人和动物体内的蠕虫寄生虫具有广泛的活性。阿苯达唑的水溶性很差。本研究表明,羟丙基-β-环糊精(HP-β-CD)能够与阿苯达唑形成包合物,并能增加其水溶性。HP-β-CD与柠檬酸之间存在协同作用。HP-β-CD(200 mM)和柠檬酸(50 mM)的组合可使每毫升溶解超过1.5毫克的阿苯达唑。本研究的目的是在绵羊体内评估阿苯达唑与HP-β-CD包合物溶液与相同药物悬浮液的比较。通过阿苯达唑亚砜血浆水平测定,含阿苯达唑-HP-β-CD复合物的溶液相对生物利用度显著(P<0.05)提高。该溶液的曲线下面积(AUC(0-->∞))比悬浮液高37%。同样,血浆峰浓度(C(max))是悬浮液的两倍,而达到C(max)的时间(T(max))缩短。

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