Polymeric Modification and Its Implication in Drug Delivery: Poly-ε-caprolactone (PCL) as a Model Polymer

被引:170
作者
Dash, Tapan K. [1 ]
Konkimalla, V. Badireenath [1 ]
机构
[1] NISER, Sch Biol Sci, Sainik Sch, Bhubaneswar 751005, Orissa, India
关键词
copolymers; polymeric modification; polymer selection; amphiphilization; counterbalancing properties; polymeric prodrugs; responsive polymers; multidrug resistance; RING-OPENING POLYMERIZATION; OVERCOMING MULTIDRUG-RESISTANCE; METHOXY POLY(ETHYLENE GLYCOL); IN-VITRO; BLOCK-COPOLYMER; ETHYLENE-GLYCOL; TRIBLOCK COPOLYMER; RELEASE BEHAVIOR; MECHANICAL-PROPERTIES; DIBLOCK COPOLYMERS;
D O I
10.1021/mp3001952
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Biodegradable polymers provided the opportunity to explore beyond conventional drug delivery and turned out to be the focus of current drug delivery. In spite of availability of diverse class of polymers, several of these polymers lack important physicochemical and biological properties, limiting their widespread application in pharmaceutical drug delivery. However, most polymers in the form of blends, copolymers and functionally modified polymers have exhibited their applicability to overcome specific limitations and to produce novel and/or fiinctionalized formulations for drug delivery as well as tissue engineering. This review aims to provide the need of polymeric modification, approaches adopted to modify and their scope. Special emphasis has been given to synthetic polyester PCL, as it is widely demonstrated in its modified form to overcome its problem of hydrophobicity and much slower degradation over the past decade. Past studies show a significantly higher utility of modified form of PCL in comparison to its native form. From the statistical analysis of these modifications and the formulations prepared, we present a basic understanding of the impact of selective modifications on the formulation design. In conclusion, we remark that a thorough understanding of the polymer and its modification has a huge potential to be the future trend for drug delivery and tissue engineering applications.
引用
收藏
页码:2365 / 2379
页数:15
相关论文
共 119 条
[1]   Polyurethane/polycaprolactane blend with shape memory effect as a proposed material for cardiovascular implants [J].
Ajili, Shadi Hassan ;
Ebrahimi, Nadereh Golshan ;
Soleimani, Masoud .
ACTA BIOMATERIALIA, 2009, 5 (05) :1519-1530
[2]   A biodegradable poly(ester amine) based on polycaprolactone and polyethylenimine as a gene carrier [J].
Arote, Rohidas ;
Kim, Tae-Hee ;
Kim, You-Kyoung ;
Hwang, Soon-Kyung ;
Jiang, Hu-Lin ;
Song, Ho-Hyun ;
Nah, Jae-Woon ;
Cho, Myung-Haing ;
Cho, Chong-Su .
BIOMATERIALS, 2007, 28 (04) :735-744
[3]   Multifunctional Nano-Micelles Formed by Amphiphilic Gold-Polycaprolactone-Methoxy Poly(ethylene glycol) (Au-PCL-MPEG) Nanoparticles for Potential Drug Delivery Applications [J].
Aryal, Santosh ;
Pilla, Srikanth ;
Gong, Shaoqin .
JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY, 2009, 9 (10) :5701-5708
[4]   Polymeric endoaortic paving: Mechanical, thermoforming, and degradation properties of polycaprolactone/polyurethane blends for cardiovascular applications [J].
Ashton, J. H. ;
Mertz, J. A. M. ;
Harper, J. L. ;
Slepian, M. J. ;
Mills, J. L. ;
McGrath, D. V. ;
Vande Geest, J. P. .
ACTA BIOMATERIALIA, 2011, 7 (01) :287-294
[5]   Degradable Poly(2-hydroxyethyl methacrylate)-co-polycaprolactone Hydrogels for Tissue Engineering Scaffolds [J].
Atzet, Sarah ;
Curtin, Scott ;
Trinh, Phalen ;
Bryant, Stephanie ;
Ratner, Buddy .
BIOMACROMOLECULES, 2008, 9 (12) :3370-3377
[6]   Preparation and characterization of starch-poly-ε-caprolactone microparticles incorporating bioactive agents for drug delivery and tissue engineering applications [J].
Balmayor, E. R. ;
Tuzlakoglu, K. ;
Azevedo, H. S. ;
Reis, R. L. .
ACTA BIOMATERIALIA, 2009, 5 (04) :1035-1045
[7]   Biodegradable polycaprolactone-polyanhydrides blends [J].
Ben-Shabat, S ;
Abuganima, E ;
Raziel, A ;
Domb, AJ .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2003, 41 (23) :3781-3787
[8]   Development of a polymeric micellar formulation for valspodar and assessment of its pharmacokinetics in rat [J].
Binichathlan, Ziyad ;
Hamdy, Dalia A. ;
Brocks, Dion R. ;
Lavasanifar, Afsaneh .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2010, 75 (02) :90-95
[9]   Ring-opening polymerization of ε-caprolactone initiated by the antitumor agent doxifluridine [J].
Chang, Kuo-Yung ;
Lee, Yu-Der .
ACTA BIOMATERIALIA, 2009, 5 (04) :1075-1081
[10]   Chitosan-poly(ε-caprolactone)-poly(ethylene glycol) graft copolymers: Synthesis, self-assembly, and drug release behavior [J].
Chen, Chen ;
Cai, Guoqiang ;
Zhang, Haiwen ;
Jiang, Hongliang ;
Wang, Liqun .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2011, 96A (01) :116-124