Multifunctional nanomicellar systems for delivering anticancer drugs

被引:33
作者
Chen, Yi-Chun [1 ,2 ,3 ]
Lo, Chun-Liang [4 ]
Hsiue, Ging-Ho [1 ,2 ,3 ]
机构
[1] Natl Tsing Hua Univ, Dept Chem Engn, Hsinchu 300, Taiwan
[2] Chung Yuan Christian Univ, Dept Chem Engn, Chungli 320, Taiwan
[3] Chung Yuan Christian Univ, R&D Ctr Membrane Technol, Chungli 320, Taiwan
[4] Natl Yang Ming Univ, Dept Biomed Engn, Taipei 112, Taiwan
关键词
micelles; stimuli responsive; controlled drug delivery; cancer therapy; tumor targeting; BIODEGRADABLE POLYMERIC MICELLES; BLOCK-COPOLYMER MICELLES; IN-VIVO EVALUATION; DIBLOCK COPOLYMERS; CANCER-THERAPY; N-ISOPROPYLACRYLAMIDE; PHOTODYNAMIC THERAPY; MULTIDRUG-RESISTANCE; PIRARUBICIN MICELLES; RESPONSIVE MICELLES;
D O I
10.1002/jbm.a.34850
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Most anticancer drugs cause severe side effect due to the lack of selectivity for cancer cells. In recent years, new strategies of micellar systems, which design for specifically target anticancer drugs to tumors, are developed at the forefront of polymeric science. To improve efficiency of delivery and cancer specificity, considerable emphasis has been placed on the development of micellar systems with passive and active targeting. In this review article, we summarized various strategies of designing multifunctional micellar systems in the purpose of improving delivery efficiency. Micellar systems compose of a multifunctional copolymer or a mixture of two or more copolymers with different properties is a plausible approach to tuning the resulting properties and satisfied various requirements for anticancer drug delivery. It appears that multifunctional micellar systems hold great potential in cancer therapy. (c) 2013 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 102A: 2024-2038, 2014.
引用
收藏
页码:2024 / 2038
页数:15
相关论文
共 127 条
[1]
Agrawal CM, 2001, J BIOMED MATER RES, V55, P141, DOI 10.1002/1097-4636(200105)55:2<141::AID-JBM1000>3.3.CO
[2]
2-A
[3]
Biodegradable polymersomes loaded with both paclitaxel and doxorubicin permeate and shrink tumors, inducing apoptosis in proportion to accumulated drug [J].
Ahmed, Fariyal ;
Pakunlu, Refika I. ;
Brannan, Aaron ;
Bates, Frank ;
Minko, Tamara ;
Discher, Dennis E. .
JOURNAL OF CONTROLLED RELEASE, 2006, 116 (02) :150-158
[4]
Polymeric micelles for the pH-dependent controlled, continuous low dose release of paclitaxel [J].
Alani, Adam W. G. ;
Bae, Younsoo ;
Rao, Deepa A. ;
Kwon, Glen S. .
BIOMATERIALS, 2010, 31 (07) :1765-1772
[5]
Ligand-targeted therapeutics in anticancer therapy [J].
Allen, TM .
NATURE REVIEWS CANCER, 2002, 2 (10) :750-763
[6]
Preparation and biological characterization of polymeric micelle drug carriers with intracellular pH-triggered drug release property: Tumor permeability, controlled subcellular drug distribution, and enhanced in vivo antitumor efficacy [J].
Bae, Y ;
Nishiyama, N ;
Fukushima, S ;
Koyama, H ;
Yasuhiro, M ;
Kataoka, K .
BIOCONJUGATE CHEMISTRY, 2005, 16 (01) :122-130
[7]
In vivo antitumor activity of the folate-conjugated pH-Sensitive polymeric micelle selectively releasing adriamycin in the intracellular acidic compartments [J].
Bae, Younsoo ;
Nishiyama, Nobuhiro ;
Kataoka, Kazunori .
BIOCONJUGATE CHEMISTRY, 2007, 18 (04) :1131-1139
[8]
pH-Triggered Release of Platinum Drugs Conjugated to Micelles via an Acid-Cleavable Linker [J].
Binauld, Sandra ;
Scarano, Wei ;
Stenzel, Martina H. .
MACROMOLECULES, 2012, 45 (17) :6989-6999
[9]
Nanoparticle and targeted systems for cancer therapy [J].
Brannon-Peppas, L ;
Blanchette, JO .
ADVANCED DRUG DELIVERY REVIEWS, 2004, 56 (11) :1649-1659
[10]
Small oligomeric micelles based on end group modified mPEG-oligocaprolactone with monodisperse hydrophobic blocks [J].
Carstens, Myrra G. ;
Bevernage, Jan J. L. ;
van Nostrum, Cornelus F. ;
van Steenbergen, Mies J. ;
Flesch, Frits M. ;
Verrijk, Ruud ;
de Leede, Leo G. J. ;
Crommelin, Daan J. A. ;
Hennink, Wim E. .
MACROMOLECULES, 2007, 40 (01) :116-122