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Hydrophilic and hydrophobic amino acid copolymers for nano-comminution of poorly soluble drugs

Authors
Lee, M. K.Kim, S.Ahn, C. -H.Lee, J.
Issue Date
Jan-2010
Publisher
ELSEVIER SCIENCE BV
Keywords
Nanoparticles; Nanocrystals; Particle size; Poorly water-soluble drug; Dispersion; Particle engineering
Citation
INTERNATIONAL JOURNAL OF PHARMACEUTICS, v.384, no.1-2, pp 173 - 180
Pages
8
Journal Title
INTERNATIONAL JOURNAL OF PHARMACEUTICS
Volume
384
Number
1-2
Start Page
173
End Page
180
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/22672
DOI
10.1016/j.ijpharm.2009.09.041
ISSN
0378-5173
1873-3476
Abstract
Nano-comminution has successfully brought nanoparticle formulations of poorly soluble drugs to our daily life. The key for the successful nano-comminution of a drug is the choice of a proper polymeric steric stabilizer. To systematically elucidate the rationale of stabilizer selection, two types of helical amino acid copolymers, relatively hydrophilic and hydrophobic copolymers, were used in nano-comminution. The hydrophilic copolymers had lysine as their major component. The addition of relatively hydrophobic leucine and phenylalanine to them could not make significant changes in particle size. However, when a small amount of hydrophilic glutamic acid or lysine was added into elastin-like hydrophobic copolymers of valine, glycine, and proline, significant composition dependence was found. Therefore, specific interactions between the functional groups of polymers and drug surfaces seem to be important for successful nano-comminution. The stimuli responsive behavior of the hydrophobic copolymer induced the temperature dependence of particle size. (C) 2009 Elsevier B.V. All rights reserved.
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공과대학 (화학공학과)
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