Preparing amorphous hydrophobic drug nanoparticles by nanoporous membrane extrusion

Author:

Guo Peng123,Hsu Tammy M1,Zhao Yaping14,Martin Charles R2,Zare Richard N5

Affiliation:

1. Department of Chemistry, Stanford University, Stanford, CA 94305-5080, USA

2. Department of Chemistry, University of Florida, Gainesville, FL 32611-7200, USA

3. School of Engineering & Applied Sciences, Harvard University, Cambridge, MA 02138, USA

4. School of Chemistry & Chemical Engineering, Shanghai Jiao Tong University, Shanghai, 200240, China

5. Department of Chemistry, Stanford University, Stanford, CA 94305-5080, USA. .

Abstract

Aim: The aim of the present study was to develop a simple and straightforward method for formulating hydrophobic drugs into nanoparticulate form in a scalable and inexpensive manner. Materials & methods: The nanoporous membrane extrusion (NME) method was used to prepare hydrophobic drug nanoparticles. NME is based on the induced precipitation of drug-loaded nanoparticles at the exits of nanopores. Three common hydrophobic drug models (silymarin, β-carotene and butylated hydroxytoluene) were tested. The authors carefully investigated the morphology, crystallinity and dissolution profile of the resulting nanoparticles. Results: Using NME, the authors successfully prepared rather uniform drug nanoparticles (∼100 nm in diameter). These nanoparticles were amorphous and show an improved dissolution profile compared with untreated drug powders. Conclusion: These studies suggest that NME could be used as a general method to produce nanoparticles of hydrophobic drugs.Original submitted 8 June 2011; Revised submitted 7 May 2012; Published online 3 September 2012

Publisher

Future Medicine Ltd

Subject

Development,General Materials Science,Biomedical Engineering,Medicine (miscellaneous),Bioengineering

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