Polymer therapeutics: Concepts and applications

被引:962
作者
Haag, R
Kratz, F
机构
[1] Free Univ Berlin, Dept Chem & Biochem, D-14195 Berlin, Germany
[2] Tumor Biol Ctr, D-79106 Freiburg, Germany
关键词
cancer therapy; dendrimers; functional polymers; gene transfection; multivalent interactions;
D O I
10.1002/anie.200502113
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Polymer therapeutics encompass polymer-protein conjugates, drug-polymer conjugates, and supramolecular drug-delivery systems. Numerous polymer-protein conjugates with improved stability and pharmacokinetic properties have been developed, for example, by anchoring enzymes or biologically relevant proteins to polyethylene glycol components (PEGylation). Several polymer-protein conjugates have received market approval, for example the PEGylated form of adenosine deaminase. Coupling low-molecular-weight anticancer drugs to high-molecular-weight polymers through a cleavable linker is an effective method for improving the therapeutic index of clinically established agents, and the first candidates have been evaluated in clinical trials, including, N-(2-hydroxypropyl)methacrylamide conjugates of doxorubicin, camptothecin, paclitaxel, and platinum(II) complexes. Another class of polymer therapeutics are drug-delivery systems based on well-defined multivalent and dendritic polymers. These include polyanionic polymers for the inhibition of virus attachment, polycationic complexes with DNA or RNA (polyplexes), and dendritic core-shell architectures for the encapsulation of drugs. In this Review an overview of polymer therapeutics is presented with a focus on concepts and examples that characterize the salient features of the drug-delivery systems. © 2006 Wiley-VCH Verlag GmbH & Co. KGaA.
引用
收藏
页码:1198 / 1215
页数:18
相关论文
共 173 条
[1]   Partial synthetic glucan sulfates as potential new antithrombotics: A review [J].
Alban, S ;
Franz, G .
BIOMACROMOLECULES, 2001, 2 (02) :354-361
[2]  
Amir R., 2003, Angew. Chem., V115, P4632
[3]   Self-immolative dendrimers [J].
Amir, RJ ;
Pessah, N ;
Shamis, M ;
Shabat, D .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (37) :4494-4499
[4]  
[Anonymous], ENCY MOL CELL BIOL M
[5]  
ARFORS KE, 1993, J LAB CLIN MED, V121, P201
[6]  
Auzenne E, 2002, CLIN CANCER RES, V8, P573
[7]  
Baars M. W. P. L., 2000, ANGEW CHEM, V112, P1341
[8]  
Baars MWPL, 2000, TOP CURR CHEM, V210, P131
[9]  
Baars MWPL, 2000, ANGEW CHEM INT EDIT, V39, P1285, DOI 10.1002/(SICI)1521-3773(20000403)39:7<1285::AID-ANIE1285>3.0.CO
[10]  
2-F