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初级未结合胆汁酸对亲水性药物纳米囊泡药物制剂的影响:药理学意义。

The Effects of Primary Unconjugated Bile Acids on Nanoencapsulated Pharmaceutical Formulation of Hydrophilic Drugs: Pharmacological Implications.

机构信息

The Biotechnology and Drug Development Research Laboratory, Curtin Medical School & Curtin Health Innovation Research Institute, Curtin University, Bentley, Perth, 6102, WA, Australia.

Hearing Therapeutics, Ear Science Institute Australia, Queen Elizabeth II Medical Centre, Nedlands, Perth, 6009, WA, Australia.

出版信息

Drug Des Devel Ther. 2021 Oct 23;15:4423-4434. doi: 10.2147/DDDT.S328526. eCollection 2021.

Abstract

INTRODUCTION

In a recent study, in our laboratory, primary unconjugated bile acids, commonly found in humans, chenodeoxycholic acid (CDCA), have been shown to improve stability of nanoencapsulated lipophilic drugs and improve their release profile after oral administration likely via electrokinetic stabilisation. Hence, this study aimed to examine the effects of CDCA on exerting similar effects on hydrophilic drugs.

METHODS

Various CDCA-based formulations were produced for the orally administered hydrophilic drug, metformin. Analyses of these formulations included electrokinetic potentials, topography, drug and CDCA formulation contents, nano size distribution, heat-induced deformation and outer-core expansion indices, release profiles, shell-resistance ratio, and thermal and chemical indices. With the drug's main target being pancreatic beta-cells, the formulations' effects on cell viability, functions and inflammatory profiles were also investigated.

RESULTS AND CONCLUSIONS

CDCA-based metformin formulations exhibited improved stability and release profiles via thermal, chemical and electrokinetic effects, which were formulation-dependent suggesting potential applications of CDCA in the oral targeted delivery of hydrophilic drugs.

摘要

简介

在最近的一项研究中,我们实验室发现,常见于人体内的初级非结合胆酸——鹅去氧胆酸(CDCA)能够提高亲脂性纳米药物的稳定性,并改善其口服后的释放特性,这可能是通过电动稳定作用实现的。因此,本研究旨在探讨 CDCA 对亲水性药物是否具有类似的作用。

方法

为口服亲水性药物二甲双胍制备了各种基于 CDCA 的制剂。对这些制剂进行了电动电位、形貌、药物和 CDCA 制剂含量、纳米粒径分布、热诱导变形和外核膨胀指数、释放特性、壳阻力比以及热化学指数等分析。由于该药物的主要靶标是胰岛β细胞,因此还研究了这些制剂对细胞活力、功能和炎症特征的影响。

结果与结论

基于 CDCA 的二甲双胍制剂通过热、化学和电动效应表现出更好的稳定性和释放特性,这些特性与制剂有关,这表明 CDCA 在亲水性药物的口服靶向递送上具有潜在的应用前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97d5/8550211/767e6fb09ca3/DDDT-15-4423-g0001.jpg

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