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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Ex-vivo intestinal absorption study of boswellic acid, cyclodextrin complexes and poloxamer solid dispersions using everted gut sac technique
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Ex-vivo intestinal absorption study of boswellic acid, cyclodextrin complexes and poloxamer solid dispersions using everted gut sac technique

机译:使用永久性肠囊技术的叶属酸,环糊精配合物和泊洛沙姆固体分散体的ex-Vivo肠道吸收研究

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摘要

Acetyl-Keto-beta-boswellic acid (AKBA) is a pentacyclic triterpenic acid found in gum resin of Boswellia serrata. Even though it is shown to have anti-inflammatory activity, its bioavailability gets limited due to its poor aqueous solubility and permeability. The present study, hence, deals in enhancement of the intestinal absorption of AKBA from total boswellic acid fraction (TA fraction) using cyclodextrin (CD) and poloxamer solid dispersion (PXM SDs) formulations. Absorption studies were performed using the everted gut sac model prepared from rat jejunum. The glucose uptake assay was performed to show viability of gut sac tissue. The apparent permeability (P-app) value of AKBA from TA fraction was 1.08 +/- 0.17 x 10(-6) which was found to be increased by 10-14 fold with CD complex and SD formulations. The intestinal absorption studies showed highest absorption of AKBA from HP-beta-CD complex and PXM 407 SD as compared to that from TA fraction. From this study, it can be concluded that HP-beta-CD and PXM 407 effectively enhanced intestinal absorption through improved solubility, highlighting their role as efficient drug delivery agents and bioavailability enhancers. (C) 2018 Published by Elsevier B.V.
机译:乙酰基 - β-β-蕨菜(AKBA)是在Boswellia Serrata的胶树脂中发现的五胞苷三萜酸。尽管它显示出具有抗炎活动,但其生物利用度由于其差的水溶性和渗透性而受到限制。因此,本研究涉及使用环糊精(CD)和泊洛沙姆固体分散体(PXM SDS)制剂从总末骨酸馏分(TA级分)增强AKBA的肠道吸收。使用由大鼠Jejunum制备的Everted Gut SAC模型进行吸收研究。进行葡萄糖摄取测定以显示肠囊组织的活力。来自TA级分的AkBa的表观渗透率(P-APP)值为1.08 +/- 0.17×10(-6),该含量增加了10-14倍,CD复合物和SD制剂。与TA级分相比,肠道吸收研究表明,来自HP-Beta-Cd复合物的AkBa和PXM 407SD的吸收最高。从本研究中,可以得出结论,HP-Beta-CD和PXM 407通过改进的溶解度有效地增强了肠道吸收,突出了它们作为有效的药物递送剂和生物利用度增强剂的作用。 (c)2018由elestvier b.v出版。

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