Microfluidic-controlled manufacture of liposomes for the solubilisation of a poorly water soluble drug

被引:120
作者
Kastner, Elisabeth [1 ]
Verma, Varun [1 ]
Lowry, Deborah [1 ]
Perrie, Yvonne [1 ]
机构
[1] Aston Univ, Sch Life & Hlth Sci, Aston Pharm Sch, Birmingham B4 7ET, W Midlands, England
基金
英国工程与自然科学研究理事会;
关键词
Liposomes; Microfluidics; Poorly soluble drugs; Bilayer loading; High throughput; ON-A-CHIP; GENE DELIVERY; FORMULATION; CHOLESTEROL; PROPOFOL; DEVICES;
D O I
10.1016/j.ijpharm.2015.02.063
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Besides their well-described use as delivery systems for water-soluble drugs, liposomes have the ability to act as a solubilizing agent for drugs with low aqueous solubility. However, a key limitation in exploiting liposome technology is the availability of scalable, low-cost production methods for the preparation of liposomes. Here we describe a new method, using microfluidics, to prepare liposomal solubilising systems which can incorporate low solubility drugs (in this case propofol). The setup, based on a chaotic advection micromixer, showed high drug loading (41 mol%) of propofol as well as the ability to manufacture vesicles with at prescribed sizes (between 50 and 450 nm) in a high-throughput setting. Our results demonstrate the ability of merging liposome manufacturing and drug encapsulation in a single process step, leading to an overall reduced process time. These studies emphasise the flexibility and ease of applying lab-on-a-chip microfluidics for the solubilisation of poorly water-soluble drugs. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:122 / 130
页数:9
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