A smart flower-like polymeric micelle for pH-triggered anticancer drug release

Authors
Oh, Kyung TaekOh, Young TaikOh, Nam-MukKim, KwangmyungLee, Don HaengLee, Eun Seong
Issue Date
2009-06-22
Publisher
ELSEVIER SCIENCE BV
Citation
INTERNATIONAL JOURNAL OF PHARMACEUTICS, v.375, no.1-2, pp.163 - 169
Abstract
Novel pH-responsive flower-like micelles were developed to provide the mechanism for pH-triggered drug release from drug carriers. The micelles (particle size: similar to 165 nm; critical micelle concentration (CMC): similar to 4 mu g/ml), constructed from poly(N-epsilon-(3-diethylamino)propyl isothiocyanatO-L-lysine)-b-poly(ethylene glycol)-b-poly(L-lactide) [poly(DEAP-Lys)-b-PEG-b-PLLA], were designed to have a self-assembled flower-like arrangement consisting of two hydrophobic blocks [deprotonated poly(DEAP-Lys) block and PLLA block] and a petal-like hydrophilic PEG block at physiological pH. As the pH decreases to slightly acidic pH (<pH 7.0), as in tumor extracellular pH (pH(e)), the flower-like micelles undergo a change in the hydrophobicity of the micellar core. The protonation of poly(DEAP-Lys) changed the physical property of the polymer from hydrophobic to hydrophilic, resulting in disintegration of the micellar core. The co-presence of a pH-insensitive PLLA block in the micellar core affected the protonation of poly(DEAP-Lys), allowing the micelle to be stable at pH 7.0-7.4. In this study using doxorubicin (DOX) as the model drug, DOX release from the micelles accelerated in response to tumor pH(e). (C) 2009 Elsevier B.V. All rights reserved.
Keywords
TUMOR EXTRACELLULAR PH; MACROMOLECULAR THERAPEUTICS; MULTIDRUG-RESISTANCE; CANCER; DELIVERY; NANOTECHNOLOGY; PERMEABILITY; DOXORUBICIN; GLYCOL); OPPORTUNITIES; TUMOR EXTRACELLULAR PH; MACROMOLECULAR THERAPEUTICS; MULTIDRUG-RESISTANCE; CANCER; DELIVERY; NANOTECHNOLOGY; PERMEABILITY; DOXORUBICIN; GLYCOL); OPPORTUNITIES; pH-sensitive flower-like micelle; 3-Diethylamino propyl; isothiocyanato-L-lysine; pH-dependent drug release; Tumor targeting
ISSN
0378-5173
URI
https://pubs.kist.re.kr/handle/201004/132384
DOI
10.1016/j.ijpharm.2009.04.005
Appears in Collections:
KIST Article > 2009
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