Core-crosslinked pH-sensitive degradable micelles: A promising approach to resolve the extracellular stability versus intracellular drug release dilemma

被引:153
作者
Wu, Yali [1 ,2 ]
Chen, Wei [1 ,2 ]
Meng, Fenghua [1 ,2 ]
Wang, Zhongjuan [3 ]
Cheng, Ru [1 ,2 ]
Deng, Chao [1 ,2 ]
Liu, Haiyan [3 ]
Zhong, Zhiyuan [1 ,2 ]
机构
[1] Soochow Univ, Biomed Polymers Lab, Dept Polymer Sci & Engn, Coll Chem Chem Engn & Mat Sci, Suzhou 215123, Peoples R China
[2] Soochow Univ, Jiangsu Key Lab Adv Funct Polymer Design & Applic, Dept Polymer Sci & Engn, Coll Chem Chem Engn & Mat Sci, Suzhou 215123, Peoples R China
[3] Soochow Univ, Inst Biol & Med Sci, Lab Cellular & Mol Tumor Immunol, Suzhou 215123, Peoples R China
基金
中国国家自然科学基金;
关键词
Micelles; pH-sensitive; Degradable; core-crosslinking; Drug delivery; Anticancer drugs; BLOCK-COPOLYMER MICELLES; POLYMERIC MICELLES; SUPRAMOLECULAR ASSEMBLIES; BIODEGRADABLE MICELLES; TRIGGERED RELEASE; ANTICANCER DRUGS; GENE DELIVERY; PHASE-I; DOXORUBICIN; CANCER;
D O I
10.1016/j.jconrel.2012.07.011
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The extracellular stability versus intracellular drug release dilemma has been a long challenge for micellar drug delivery systems. Here, core-crosslinked pH-sensitive degradable micelles were developed based on poly(ethylene glycol)-b-poly(mono-2,4,6-trimethoxy benzylidene-pentaerythritol carbonate-co-acryloyl carbonate) (PEG-b-P(TMBPEC-co-AC)) diblock copolymer that contains acid-labile acetal and photo-crossslinkable acryloyl groups in the hydrophobic polycarbonate block for intracellular paclitaxel (PTX) release. The micelles following photo-crosslinking while displaying high stability at pH 7.4 were prone to rapid hydrolysis at mildly acidic pHs of 4.0 and 5.0, with half lives of ca. 12.5 and 38.5 h, respectively. Notably, these micelles showed high drug loading efficiencies of 76.0-93.2% at theoretical PTX loading contents of 5-15 wt.%. Depending on drug loading contents, PTX-loaded micelles had average sizes varying from 132.2 to 171.6 nm, which were decreased by 17-22 nm upon photo-crosslinking. The in vitro release studies showed that PTX release at pH 7.4 was greatly inhibited by crosslinking of micelles. Notably, rapid drug release was obtained under mildly acidic conditions, in which 90.0% and 78.1% PTX was released in 23 h at pH 4.0 and 5.0, respectively. MTT assays showed that PTX-loaded crosslinked micelles retained high anti-tumor activity with a cell viability of 9.2% observed for RAW 264.7 cells following 72 h incubation, which was comparable to PTX-loaded non-crosslinked counterparts (cell viability 7.5%) under otherwise the same conditions, supporting efficient drug release from PTX-loaded crosslinked micelles inside the tumor cells. These core-crosslinked pH-responsive biodegradable micelles with superior extracellular stability and rapid intracellular drug release provide a novel platform for tumor-targeting drug delivery. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:338 / 345
页数:8
相关论文
共 43 条
[31]   Biodegradable micelles with sheddable poly(ethylene glycol) shells for triggered intracellular release of doxorubicin [J].
Sun, Huanli ;
Guo, Bingnan ;
Cheng, Ru ;
Meng, Fenghua ;
Liu, Haiyan ;
Zhong, Zhiyuan .
BIOMATERIALS, 2009, 30 (31) :6358-6366
[32]   Functionalized micellar systems for cancer targeted drug delivery [J].
Sutton, Damon ;
Nasongkla, Norased ;
Blanco, Elvin ;
Gao, Jinming .
PHARMACEUTICAL RESEARCH, 2007, 24 (06) :1029-1046
[33]   Nanobody - Shell functionalized thermosensitive core-crosslinked polymeric micelles for active drug targeting [J].
Talelli, Marina ;
Rijcken, Cristianne J. F. ;
Oliveira, Sabrina ;
van der Meel, Roy ;
Henegouwen, Paul M. P. van Bergen En ;
Lammers, Twan ;
van Nostrum, Cornelus F. ;
Storm, Gert ;
Hennink, Wim E. .
JOURNAL OF CONTROLLED RELEASE, 2011, 151 (02) :183-192
[34]   Core-crosslinked polymeric micelles with controlled release of covalently entrapped doxorubicin [J].
Talelli, Marina ;
Iman, Maryam ;
Varkouhi, Amir K. ;
Rijcken, Cristianne J. F. ;
Schiffelers, Raymond M. ;
Etrych, Tomas ;
Ulbrich, Karel ;
van Nostrum, Cornelus F. ;
Lammers, Twan ;
Storm, Gert ;
Hennink, Wim E. .
BIOMATERIALS, 2010, 31 (30) :7797-7804
[35]   Use of block copolymers of poly(ortho esters) and poly (ethylene glycol) micellar carriers as potential tumour targeting systems [J].
Toncheva, V ;
Schacht, E ;
Ng, SY ;
Barr, J ;
Heller, J .
JOURNAL OF DRUG TARGETING, 2003, 11 (06) :345-353
[36]   Micellar nanocarriers: Pharmaceutical perspectives [J].
Torchilin, V. P. .
PHARMACEUTICAL RESEARCH, 2007, 24 (01) :1-16
[37]   Polymeric anticancer drugs with pH-controlled activation [J].
Ulbrich, K ;
Subr, V .
ADVANCED DRUG DELIVERY REVIEWS, 2004, 56 (07) :1023-1050
[38]   Covalently cross-linked amphiphilic block copolymer micelles [J].
van Nostrum, Cornelus F. .
SOFT MATTER, 2011, 7 (07) :3246-3259
[39]   A new, crystalline high melting bis(hydroxymethyl)polycarbonate and its acetone ketal for biomaterial applications [J].
Vandenberg, EJ ;
Tian, D .
MACROMOLECULES, 1999, 32 (11) :3613-3619
[40]   Folate-conjugated crosslinked biodegradable micelles for receptor-mediated delivery of paclitaxel [J].
Xiong, Juan ;
Meng, Fenghua ;
Wang, Chao ;
Cheng, Ru ;
Liu, Zhuang ;
Zhong, Zhiyuan .
JOURNAL OF MATERIALS CHEMISTRY, 2011, 21 (15) :5786-5794