Environmentally responsive peptides as anticancer drug carriers

被引:108
作者
Aluri, Suhaas [1 ]
Janib, Siti M. [1 ]
Mackay, J. Andrew [1 ]
机构
[1] Univ So Calif, Dept Pharmacol & Pharmaceut Sci, Los Angeles, CA 90033 USA
关键词
EPR; Tumor; Hyperthermia; Peptides; Drug delivery; Redox; Cancer; pH; Chemotherapy; RECEPTOR-MEDIATED ENDOCYTOSIS; ELASTIN-LIKE POLYPEPTIDE; PH-SENSITIVE LIPOSOMES; HUMAN TUMOR XENOGRAFT; IN-VIVO; TARGETED DELIVERY; CARBOXYMETHYL POLY(L-HISTIDINE); INTRACELLULAR DELIVERY; DOXORUBICIN CONJUGATE; GELATIN NANOPARTICLES;
D O I
10.1016/j.addr.2009.07.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The tumor microenvironment provides multiple cues that may be exploited to improve the efficacy of established chemotherapeutics; furthermore, polypeptides are uniquely situated to capitalize on these signals. Peptides provide: 1) a rich repertoire of biologically specific interactions to draw upon: 2) environmentally responsive phase behaviors, which may be tuned to respond to signatures of disease; 3) opportunities to direct self-assembly: 4) control over routes of biodegradation; 5) the option to seamlessly combine functionalities into a single polymer via a one-step biosynthesis. As development of cancer-targeted nanocarriers expands, peptides provide a unique source of functional units that may target disease. This review explores potential microenvironmental physiology indicative of tumors and peptides that have demonstrated an ability to target and deliver to these signals. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:940 / 952
页数:13
相关论文
共 154 条
[1]   Combined radiofrequency ablation and adjuvant liposomal chemotherapy: Effect of chemotherapeutic agent, nanoparticle size, and circulation time [J].
Ahmed, M ;
Lukyanov, AN ;
Torchilin, V ;
Tournier, H ;
Schneider, AN ;
Goldberg, SN .
JOURNAL OF VASCULAR AND INTERVENTIONAL RADIOLOGY, 2005, 16 (10) :1365-1371
[2]   Drug delivery systems: Entering the mainstream [J].
Allen, TM ;
Cullis, PR .
SCIENCE, 2004, 303 (5665) :1818-1822
[3]  
[Anonymous], 2008, Cancer facts and figures
[4]   Cancer treatment by targeted drug delivery to tumor vasculature in a mouse model [J].
Arap, W ;
Pasqualini, R ;
Ruoslahti, E .
SCIENCE, 1998, 279 (5349) :377-380
[5]   Carboxymethyl poly(L-histidine) as a new pH-sensitive polypeptide to enhance polyplex gene delivery [J].
Asayama, Shoichiro ;
Sudo, Miyuki ;
Nagaoka, Shoji ;
Kawakami, Hiroyoshi .
MOLECULAR PHARMACEUTICS, 2008, 5 (05) :898-901
[6]   Carboxymethyl poly(L-histidine) as a new pH-sensitive polypeptide at endosomal/lysosomal pH [J].
Asayama, Shoichiro ;
Kato, Hiroyuki ;
Kawakami, Hiroyoshi ;
Nagaoka, Shoji .
POLYMERS FOR ADVANCED TECHNOLOGIES, 2007, 18 (04) :329-333
[7]   The role of glutathione in cancer [J].
Balendiran, GK ;
Dabur, R ;
Fraser, D .
CELL BIOCHEMISTRY AND FUNCTION, 2004, 22 (06) :343-352
[8]  
BARONZIO GF, 2006, LANDES BIOSCI
[9]   A thermally targeted elastin-like polypeptide-doxorubicin conjugate overcomes drug resistance [J].
Bidwell, Gene L., III ;
Davis, Aisha N. ;
Fokt, Izabela ;
Priebe, Waldemar ;
Raucher, Drazen .
INVESTIGATIONAL NEW DRUGS, 2007, 25 (04) :313-326
[10]   Development of elastin-like polypeptide for thermally targeted delivery of doxorubicin [J].
Bidwell, Gene L., III ;
Fokt, Izabela ;
Priebe, Waldemar ;
Raucher, Drazen .
BIOCHEMICAL PHARMACOLOGY, 2007, 73 (05) :620-631