Abstract
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.
Original language | English |
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Pages (from-to) | 122-130 |
Number of pages | 9 |
Journal | International Journal of Pharmaceutics |
Volume | 485 |
Issue number | 1-2 |
Early online date | 25 Feb 2015 |
DOIs | |
Publication status | Published (in print/issue) - 15 May 2015 |
Keywords
- Liposomes
- Microfluidics
- Poorly soluble drugs
- Bilayer loading
- High throughput