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以月桂酸蔗糖酯为稳定剂制备完全可再分散的干燥纳米晶体以增加难溶性药物的表面积和溶解速率

Development of Fully Redispersible Dried Nanocrystals by Using Sucrose Laurate as Stabilizer for Increasing Surface Area and Dissolution Rate of Poorly Water-Soluble Drugs.

作者信息

Prajapati Hetal, Serajuddin Abu T M

机构信息

College of Pharmacy and Health Sciences, Department of Pharmaceutical Sciences, St. John's University, 8000 Utopia Parkway, Queens, NY 11439, USA.

College of Pharmacy and Health Sciences, Department of Pharmaceutical Sciences, St. John's University, 8000 Utopia Parkway, Queens, NY 11439, USA.

出版信息

J Pharm Sci. 2022 Mar;111(3):780-793. doi: 10.1016/j.xphs.2021.10.004. Epub 2021 Oct 18.

Abstract

There is much interest in converting poorly water-soluble drugs into nanocrystals as they provide extremely high surface area that increases dissolution rate and oral bioavailability. However, nanocrystals are prepared as aqueous suspensions, and once the suspensions are dried for development of solid dosage forms, the nanocrystals agglomerate as large particles to reduce the excess surface energy. For successful development of drug products, it is essential that any agglomeration is reversible, and the dried nanocrystals regain original particle sizes after redispersion in aqueous media. We have established that sucrose laurate serves as a superb stabilizer to ensure complete redispersion of dried nanocrystals in aqueous media with mild agitation. Nanocrystals (150-300 nm) of three neutral drugs (fenofibrate, danazol and probucol) were produced with sucrose laurate by media milling, and suspensions were dried by tray drying under vacuum, spray drying, and lyophilization. Dried solids and their tablets redispersed into original particle sizes spontaneously. Preliminary studies showed that sucrose laurate can also redisperse acidic and basic drugs, indicating its versatile application. Fatty acid ester of another disaccharide, lactose laurate, also performed like sucrose laurate. Thus, we have developed a method of retaining high dissolution rate and, by implication, high bioavailability of nanocrystals from solid formulations.

摘要

将难溶性药物转化为纳米晶体引起了人们的广泛关注,因为纳米晶体具有极高的比表面积,能够提高药物的溶解速率和口服生物利用度。然而,纳米晶体通常制成水悬浮液,一旦将悬浮液干燥以开发固体剂型,纳米晶体会聚集成大颗粒,以降低过高的表面能。为了成功开发药品,至关重要的是任何团聚都应是可逆的,并且干燥后的纳米晶体在重新分散于水性介质中后能够恢复到原始粒径。我们已经证实,月桂酸蔗糖酯是一种出色的稳定剂,能够确保干燥后的纳米晶体在温和搅拌下于水性介质中完全重新分散。通过介质研磨法,使用月桂酸蔗糖酯制备了三种中性药物(非诺贝特、达那唑和普罗布考)的纳米晶体(150 - 300纳米),并通过真空托盘干燥、喷雾干燥和冷冻干燥对悬浮液进行干燥。干燥后的固体及其片剂能自发地重新分散为原始粒径。初步研究表明,月桂酸蔗糖酯也能使酸性和碱性药物重新分散,这表明其具有广泛的应用前景。另一种二糖的脂肪酸酯,月桂酸乳糖酯,也表现出与月桂酸蔗糖酯类似的性能。因此,我们开发了一种方法,能够保持纳米晶体在固体剂型中的高溶解速率,进而保持高生物利用度。

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