pH-responsive release of proteins from biocompatible and biodegradable reverse polymer micelles

被引:51
作者
Koyamatsu, Yuichi [1 ,2 ]
Hirano, Taisuke [1 ]
Kakizawa, Yoshinori [1 ]
Okano, Fumiyoshi [1 ]
Takarada, Tohru [2 ]
Maeda, Mizuo [2 ]
机构
[1] Toray Industries Ltd, New Frontiers Res Labs, Kamakura, Kanagawa 2488555, Japan
[2] RIKEN, Bioengn Lab, Wako, Saitama 3510198, Japan
关键词
Reverse polymer micelle; Biopharmaceutical; Biodegradable; Biocompatible; pH; Erythropoietin; BLOCK-COPOLYMER VESICLES; DRUG-DELIVERY; BIOMEDICAL APPLICATIONS; COMPLEX MICELLES; NANOPARTICLES; LIPOSOMES; VEHICLES; CARRIERS; NANOCONTAINERS; CYTOPLASM;
D O I
10.1016/j.jconrel.2013.10.035
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A reverse polymer micelle with a diameter of 100 nm was prepared for a protein carrier releasing payloads in a pH-dependent manner. The reverse polymer micelle was made from an amphiphilic diblock copolymer of biodegradable poly(D,L-lactic-co-glycolic acid) (PLGA) and biocompatible poly(ethylene glycol) (PEG). PLGA having a terminal carboxyl group was additionally embedded in the micelle's PLGA layer via hydrophobic interaction. The micelles encapsulating bovine serum albumin and streptavidin released the proteins under neutral and basic conditions, whereas the proteins remained in the interior at acidic pH. Using erythropoietin as a protein drug, it was also exemplified that the released protein retained its cell proliferation activity even after rigorous formulation processes, including water-in-oil emulsion. The present reverse polymer micelle could potentially find application as an oral protein drug delivery carrier. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:89 / 95
页数:7
相关论文
共 50 条
[1]   Solid lipid nanoparticles as a drug delivery system for peptides and proteins [J].
Almeida, Antonio J. ;
Souto, Eliana .
ADVANCED DRUG DELIVERY REVIEWS, 2007, 59 (06) :478-490
[2]   Stimuli-responsive polypeptide vesicles by conformation-specific assembly [J].
Bellomo, EG ;
Wyrsta, MD ;
Pakstis, L ;
Pochan, DJ ;
Deming, TJ .
NATURE MATERIALS, 2004, 3 (04) :244-248
[3]   pH-induced release from P2VP-PEO block copolymer vesicles [J].
Borchert, Uwe ;
Lipprandt, Ute ;
Bilang, Matthias ;
Kimpfler, Andrea ;
Rank, Anja ;
Peschka-Suess, Regine ;
Schubert, Rolf ;
Lindner, Peter ;
Forster, Stephan .
LANGMUIR, 2006, 22 (13) :5843-5847
[4]   Microgels and microcapsules in peptide and protein drug delivery [J].
Bysell, Helena ;
Mansson, Ronja ;
Hansson, Per ;
Malmsten, Martin .
ADVANCED DRUG DELIVERY REVIEWS, 2011, 63 (13) :1172-1185
[5]   PEG-SS-PPS: Reduction-sensitive disulfide block copolymer vesicles for intracellular drug delivery [J].
Cerritelli, Simona ;
Velluto, Diana ;
Hubbell, Jeffrey A. .
BIOMACROMOLECULES, 2007, 8 (06) :1966-1972
[6]   Thermosensitive cross-linked polymer vesicles for controlled release system [J].
Chen, XR ;
Ding, XB ;
Zheng, ZH ;
Peng, YX .
NEW JOURNAL OF CHEMISTRY, 2006, 30 (04) :577-582
[7]   Polymer vesicles containing small vesicles within interior aqueous compartments and pH-Responsive transmembrane channels [J].
Chiu, Hsin-Cheng ;
Lin, Yue-Wen ;
Huang, Yi-Fong ;
Chuang, Chih-Kai ;
Chern, Chorng-Shyan .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2008, 47 (10) :1875-1878
[8]   Polymersome carriers: From self-assembly to siRNA and protein therapeutics [J].
Christian, David A. ;
Cai, Shenshen ;
Bowen, Diana M. ;
Kim, Younghoon ;
Pajerowski, J. David ;
Discher, Dennis E. .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2009, 71 (03) :463-474
[9]   Liposomes: Vehicles for the targeted and controlled delivery of peptides and proteins [J].
Crommelin, DJA ;
Daemen, T ;
Scherphof, GL ;
Vingerhoeds, MH ;
Heeremans, JLM ;
Kluft, C ;
Storm, G .
JOURNAL OF CONTROLLED RELEASE, 1997, 46 (1-2) :165-175
[10]   Protein drug stability: A formulation challenge [J].
Frokjaer, S ;
Otzen, DE .
NATURE REVIEWS DRUG DISCOVERY, 2005, 4 (04) :298-306