Polyurethane-based drug delivery systems

被引:224
作者
Cherng, Jong Yuh [1 ]
Hou, Ting Yi [1 ]
Shih, Mei Fen [2 ]
Talsma, Herre [3 ]
Hennink, Wim E. [3 ]
机构
[1] Natl Chung Cheng Univ, Dept Chem & Biochem, Chiayi, Taiwan
[2] Chia Nan Univ Pharm & Sci, Dept Pharm, Tainan, Taiwan
[3] Univ Utrecht, Dept Pharmaceut, Utrecht Inst Pharmaceut Sci, NL-3508 TB Utrecht, Netherlands
关键词
Polyurethane; Isocyanate; Biodegradability; Biocompatibility; Controlled release; Drug delivery; ENZYME-INDUCED BIODEGRADATION; CONTROLLED-RELEASE; TRANSFECTION EFFICIENCY; MECHANICAL-PROPERTIES; POLYCARBONATE-POLYURETHANES; HYDROLYTIC STABILITY; SUSTAINED-RELEASE; MOLECULAR-WEIGHT; IN-VITRO; DEGRADATION;
D O I
10.1016/j.ijpharm.2013.04.063
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Polyurethanes (PUs) are formed by a reaction between isocyanates and diols to yield polymers with urethane bonds (-NH-COO-) in their main chain. A great variety of building blocks is commercially available that allows the chemical and physical properties of PUs to be tailored to their target applications, particularly for the biomedical and pharmaceutical fields. This article reviews the synthesis and characterization of PUs and PU-copolymers, as well as their in vitro and in vivo biodegradability and biocompatibility. Particular emphasis is placed on the use of PUs for the controlled release of drugs and for the (targeted) delivery of biotherapeutics. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:145 / 162
页数:18
相关论文
共 125 条
[1]   Immobilization of a nonsteroidal antiinflammatory drug onto commercial segmented polyurethane surface to improve haemocompatibility properties [J].
Abraham, GA ;
de Queiroz, AAA ;
San Román, J .
BIOMATERIALS, 2002, 23 (07) :1625-1638
[2]   Biodegradable injectable polyurethanes: Synthesis and evaluation for orthopaedic applications [J].
Adhikari, Raju ;
Gunatillake, Pathiraja A. ;
Griffiths, Ian ;
Tatai, Lisa ;
Wickramaratna, Malsha ;
Houshyar, Shadi ;
Moore, Tim ;
Mayadunne, Roshan T. M. ;
Field, John ;
McGee, Margaret ;
Carbone, Tania .
BIOMATERIALS, 2008, 29 (28) :3762-3770
[3]   *DAS DI-ISOCYANAT-POLYADDITIONSVERFAHREN (POLYURETHANE) [J].
BAYER, O .
ANGEWANDTE CHEMIE, 1947, 59 (09) :257-272
[4]   Bioactivity of polyurethane-based scaffolds coated with Bioglass® [J].
Bil, M. ;
Ryszkowska, J. ;
Roether, J. A. ;
Bretcanu, O. ;
Boccaccini, A. R. .
BIOMEDICAL MATERIALS, 2007, 2 (02) :93-101
[5]   Physical properties of poly(ester-urethanes) prepared from different molar mass polycaprolactone-diols [J].
Bogdanov, B ;
Toncheva, V ;
Schacht, E ;
Finelli, L ;
Sarti, B ;
Scandola, M .
POLYMER, 1999, 40 (11) :3171-3182
[6]   Design and characterization of bi-soft segmented polyurethane microparticles for biomedical application [J].
Campos, Elisa ;
Cordeiro, Rosemeyre ;
Santos, Ana Cristina ;
Matos, Claudia ;
Gil, M. H. .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2011, 88 (01) :477-482
[7]   Study on the Liquefied-MDI-Based shape memory polyurethanes [J].
Cao, Qi ;
Chen, Shaojun ;
Hu, Jinlian ;
Liu, Pengsheng .
JOURNAL OF APPLIED POLYMER SCIENCE, 2007, 106 (02) :993-1000
[8]   Effect of the hard segment chemistry and structure on the thermal and mechanical properties of novel biomedical segmented poly(esterurethanes) [J].
Caracciolo, P. C. ;
Buffa, F. ;
Abraham, G. A. .
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 2009, 20 (01) :145-155
[9]   Structural engineering of polyurethane coatings for high performance applications [J].
Chattopadhyay, D. K. ;
Raju, K. V. S. N. .
PROGRESS IN POLYMER SCIENCE, 2007, 32 (03) :352-418
[10]   Preparation and characterization of PEG-modified polyurethane pressure-sensitive adhesives for transdermal drug delivery [J].
Chen, Xuemei ;
Liu, Wei ;
Zhao, Yanbing ;
Jiang, Lingyu ;
Xu, Huibi ;
Yang, Xiangliang .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2009, 35 (06) :704-711