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黄芩苷多功能生物医学应用的温敏凝胶给药平台。

Thermogelling Platform for Baicalin Delivery for Versatile Biomedical Applications.

机构信息

Department of Pharmaceutics & Pharmaceutical Technology, College of Pharmacy , University of Sharjah , Sharjah 27272 , United Arab Emirates.

Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy , Cairo University , Cairo 11562 , Egypt.

出版信息

Mol Pharm. 2018 Aug 6;15(8):3478-3488. doi: 10.1021/acs.molpharmaceut.8b00480. Epub 2018 Jul 12.

Abstract

Baicalin (BG) is a natural glycoside with several promising therapeutic and preventive applications. However, its pharmaceutical potential is compromised by its poor water solubility, complex oral absorption kinetics, and low bioavailability. In this work, BG was incorporated in a series of chitosan (Ch)/glycerophosphate (GP)-based thermosensitive hydrogel formulations to improve its water solubility and control its release profile. Molecular interactions between BG and GP were investigated using Fourier transform infrared spectroscopy (FT-IR), and the ability of GP to enhance the water solubility of BG was studied in different release media. Drug-loaded Ch/GP hydrogels were prepared and characterized for their gelation time, swelling ratio, and rheological properties in addition to surface and internal microstructure. Polyethylene glycol (PEG) 6000 and hydroxypropyl methyl cellulose (HPMC) were incorporated in the formulations at different ratios to study their effect on modulating the sol-gel behavior and the in vitro drug release. In vivo pharmacokinetic (PK) studies were carried out using a rabbit model to study the ability of drug-loaded Ch/GP thermosensitive hydrogels to control the absorption rate and improve the bioavailability of BG. Results showed that the solubility of BG was enhanced in the presence of GP, while the incorporation of PEG and/or HPMC had an impact on gelation time, rheological behavior, and rate of drug release in vitro. PK results obtained following buccal application of drug-loaded Ch/GP thermosensitive hydrogels to rabbits showed that the rate of BG absorption was controlled and the in vivo bioavailability was increased by 330% relative to BG aqueous oral suspension. The proposed Ch/GP thermosensitive hydrogel is an easily modifiable delivery platform that is not only capable of improving the solubility and bioavailability of BG following buccal administration but also can be suited for various local and injectable therapeutic applications.

摘要

黄芩苷(BG)是一种具有多种有前途的治疗和预防应用的天然糖苷。然而,其较差的水溶性、复杂的口服吸收动力学和低生物利用度限制了其药物潜力。在这项工作中,将 BG 掺入一系列壳聚糖(Ch)/甘油磷酸酯(GP)基温敏水凝胶制剂中,以提高其水溶性并控制其释放曲线。使用傅里叶变换红外光谱(FT-IR)研究了 BG 与 GP 之间的分子相互作用,并研究了 GP 在不同释放介质中提高 BG 水溶性的能力。制备了载药 Ch/GP 水凝胶,并对其胶凝时间、溶胀比、流变学性能以及表面和内部微观结构进行了表征。还以不同比例将聚乙二醇(PEG)6000 和羟丙基甲基纤维素(HPMC)掺入配方中,以研究它们对调节溶胶-凝胶行为和体外药物释放的影响。使用兔模型进行体内药代动力学(PK)研究,以研究载药 Ch/GP 温敏水凝胶控制 BG 吸收速率和提高 BG 生物利用度的能力。结果表明,GP 的存在增强了 BG 的溶解度,而 PEG 和/或 HPMC 的掺入对凝胶时间、流变行为和体外药物释放速率有影响。兔口腔应用载药 Ch/GP 温敏水凝胶后的 PK 结果表明,BG 的吸收速率得到控制,BG 水溶液口服混悬剂的体内生物利用度提高了 330%。所提出的 Ch/GP 温敏水凝胶是一种易于修饰的给药平台,不仅能够提高 BG 经口腔给药后的溶解度和生物利用度,而且还适用于各种局部和注射治疗应用。

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