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亲水性和功能化纳米氧化石墨烯增强了醋酸甲地孕酮的快速溶解。

Hydrophilic and Functionalized Nanographene Oxide Incorporated Faster Dissolving Megestrol Acetate.

机构信息

Department of Chemistry and Environmental Science, New Jersey Institute of Technology, Newark, NJ 07102, USA.

Bristol Myers Squibb Research and Early Development, Princeton, NJ 08543, USA.

出版信息

Molecules. 2021 Mar 31;26(7):1972. doi: 10.3390/molecules26071972.

Abstract

The aim of this work is to present an approach to enhance the dissolution of progestin medication, megestrol acetate (also known as MEGACE), for improving the dissolution rate and kinetic solubility by incorporating nano graphene oxide (nGO). An antisolvent precipitation process was investigated for nGO-drug composite preparation, where prepared composites showed crystalline properties that were similar to the pure drug but enhanced aqueous dispersibility and colloidal stability. To validate the efficient release profile of composite, in vitro dissolution testing was carried out using United States Pharmacopeia, USP-42 paddle method, with gastric pH (1.4) and intestinal pH (6.5) solutions to mimic in vivo conditions. Pure MA is practically insoluble (2 µg/mL at 37 °C). With the incorporation of nGO, it was possible to dissolve nearly 100% in the assay. With the incorporation of 1.0% of nGO, the time required to dissolve 50% and 80% of drug, namely T and T, decreased from 138.0 min to 27.0 min, and the drug did not dissolve for 97.0 min in gastric media, respectively. Additionally, studies done in intestinal media have revealed T did not dissolve for 92.0 min. This work shows promise in incorporating functionalized nanoparticles into the crystal lattice of poorly soluble drugs to improve dissolution rate.

摘要

本工作旨在提出一种方法,通过掺入纳米氧化石墨烯(nGO)来提高孕激素药物醋酸甲地孕酮(也称为 MEGACE)的溶解度,以提高其溶解速率和动力学溶解度。研究了反溶剂沉淀法制备 nGO-药物复合材料,所制备的复合材料表现出类似于纯药物的结晶性质,但增强了水相分散性和胶体稳定性。为了验证复合药物的有效释放特性,采用美国药典(USP-42 桨法)进行了体外溶解试验,使用胃 pH(1.4)和肠 pH(6.5)溶液模拟体内条件。纯 MA 在 37°C 时几乎不溶(2μg/mL)。通过掺入 nGO,可以实现近 100%的溶解。当掺入 1.0%的 nGO 时,溶解 50%和 80%药物所需的时间(即 T 和 T)分别从 138.0 分钟缩短至 27.0 分钟,且药物在胃介质中 97.0 分钟不溶解。此外,在肠介质中的研究表明,药物在 92.0 分钟内不溶解。本工作表明,将功能化纳米粒子掺入难溶性药物的晶格中以提高溶解速率具有广阔的前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cc1/8036621/bf4db8972a90/molecules-26-01972-g001.jpg

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