Intracellular targeting of polymer-bound drugs for cancer chemotherapy

被引:261
作者
Nori, A
Kopecek, J
机构
[1] Univ Utah, Dept Pharmaceut & Pharmacuet Chem, CCCD, Salt Lake City, UT 84112 USA
[2] Univ Utah, Dept Bioengn, Salt Lake City, UT 84112 USA
关键词
polymers; HPMA; molecular signaling; cell-penetrating peptides; subcellular trafficking; nuclear localization sequences;
D O I
10.1016/j.addr.2004.10.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Macromolecules have been traditionally employed as drug carriers due to their ability to selectively accumulate in malignant tissues compared to healthy tissues by either passive or active targeting, thus precluding undesirable side effects generated by free drug. The therapeutic activity proffered by such conjugates requires that the drug concentrate at its specific subcellular target such as the nucleus. Thus, the suitability of macromolecules as carriers also extends to their propensity to deliver the drug to a predetermined intracellular location. As binding a macromolecule to a drug facilitates cellular uptake by endocytosis, various approaches have been employed to either guide the drug to targets different from endosomal/lysosomal compartments by mediating vesicular escape, or to directly accomplish intracellular (cytoplasmic and nuclear) localization. This review discusses the utility of macromolecules in drug delivery and describes the numerous modalities (with a focus on cell-Penetrating peptides) currently available for achieving effective intracellular drug delivery. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:609 / 636
页数:28
相关论文
共 149 条
[1]   Nuclear targeting of chlorin e(6) enhances its photosensitizing activity [J].
Akhlynina, TV ;
Jans, DA ;
Rosenkranz, AA ;
Statsyuk, NV ;
Balashova, IY ;
Toth, G ;
Pavo, I ;
Rubin, AB ;
Sobolev, AS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (33) :20328-20331
[2]  
Akhlynina TV, 1999, INT J CANCER, V81, P734, DOI 10.1002/(SICI)1097-0215(19990531)81:5<734::AID-IJC12>3.0.CO
[3]  
2-J
[4]   Hypersensitization of multidrug resistant human ovarian carcinoma cells by pluronic P85 block copolymer [J].
Alakhov, VY ;
Moskaleva, EY ;
Batrakova, EV ;
Kabanov, AV .
BIOCONJUGATE CHEMISTRY, 1996, 7 (02) :209-216
[5]   Ligand-targeted therapeutics in anticancer therapy [J].
Allen, TM .
NATURE REVIEWS CANCER, 2002, 2 (10) :750-763
[6]   DOWN-REGULATION OF AMYLOID PRECURSOR PROTEIN INHIBITS NEURITE OUTGROWTH IN-VITRO [J].
ALLINQUANT, B ;
HANTRAYE, P ;
MAILLEUX, P ;
MOYA, K ;
BOUILLOT, C ;
PROCHIANTZ, A .
JOURNAL OF CELL BIOLOGY, 1995, 128 (05) :919-927
[7]  
[Anonymous], 1986, Journal of Bioactive and Compatible Polymers
[8]  
Anthoney DA, 1999, METH MOLEC MED, V28, P1, DOI 10.1385/1-59259-687-8:1
[9]   Conjugates of antisense oligonucleotides with the Tat and antennapedia cell-penetrating peptides: Effects on cellular uptake, binding to target sequences, and biologic actions [J].
Astriab-Fisher, A ;
Sergueev, D ;
Fisher, M ;
Shaw, BR ;
Juliano, RL .
PHARMACEUTICAL RESEARCH, 2002, 19 (06) :744-754
[10]   Sensitization of cells overexpressing multidrug-resistant proteins by Pluronic P85 [J].
Batrakova, EV ;
Li, S ;
Alakhov, VY ;
Elmquist, WF ;
Miller, DW ;
Kabanov, AV .
PHARMACEUTICAL RESEARCH, 2003, 20 (10) :1581-1590