Nanoparticles in cancer therapy and diagnosis

被引:380
作者
Brigger, Irene [1 ]
Dubernet, Catherine [1 ]
Couvreur, Patrick [1 ]
机构
[1] Univ Paris 11, Fac Pharm, UMR CNRS 8612, F-92296 Chatenay Malabry, France
关键词
Nanoparticles; Nanospheres; Nanocapsules; Conventional or long-circulating carriers; Passive or active tumor targeting; EPR effect; Multidrug resistance (MDR); Oligonucleotide delivery; Tumor imaging; DOXORUBICIN-LOADED NANOPARTICLES; PROTEIN SURFACE INTERACTIONS; POLYALKYLCYANOACRYLATE NANOPARTICLES; MULTIDRUG-RESISTANCE; TISSUE DISTRIBUTION; DRUG-DELIVERY; LYMPH-NODES; POLYCYANOACRYLATE NANOPARTICLES; ANTISENSE OLIGONUCLEOTIDES; VASCULAR-PERMEABILITY;
D O I
10.1016/j.addr.2012.09.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Numerous investigations have shown that both tissue and cell distribution profiles of anticancer drugs can be controlled by their entrapment in submicronic colloidal systems (nanoparticles). The rationale behind this approach is to increase antitumor efficacy, while reducing systemic side-effects. This review provides an update of tumor targeting with conventional or long-circulating nanoparticles. The in vivo fate of these systems, after intravascular or tumoral administration, is discussed, as well as the mechanism involved in tumor regression. Nanoparticles are also of benefit for the selective delivery of oligonucleotides to tumor cells. Moreover, certain types of nanoparticles showed some interesting capacity to reverse MDR resistance, which is a major problem in chemotherapy. The first experiments, aiming to decorate nanoparticles with molecular ligand for 'active' targeting of cancerous cells, are also discussed here. The last part of this review focus on the application of nanoparticles in imaging for cancer diagnosis. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:24 / 36
页数:13
相关论文
共 103 条
[1]  
Allemann E, 1996, INT J CANCER, V66, P821, DOI 10.1002/(SICI)1097-0215(19960611)66:6<821::AID-IJC19>3.0.CO
[2]  
2-5
[3]  
ASTIER A, 1988, CANCER RES, V48, P1835
[4]   Spongelike alginate nanoparticles as a new potential system for the delivery of antisense oligonucleotides [J].
Aynié, I ;
Vauthier, C ;
Chacun, H ;
Fattal, E ;
Couvreur, P .
ANTISENSE & NUCLEIC ACID DRUG DEVELOPMENT, 1999, 9 (03) :301-312
[5]   Control of tumour vascular permeability [J].
Baban, DF ;
Seymour, LW .
ADVANCED DRUG DELIVERY REVIEWS, 1998, 34 (01) :109-119
[6]   STEALTH ME.PEG-PLA NANOPARTICLES AVOID UPTAKE BY THE MONONUCLEAR PHAGOCYTES SYSTEM [J].
BAZILE, D ;
PRUDHOMME, C ;
BASSOULLET, MT ;
MARLARD, M ;
SPENLEHAUER, G ;
VEILLARD, M .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1995, 84 (04) :493-498
[7]   ENHANCED CYTOTOXICITY OF DOXORUBICIN ENCAPSULATED IN POLYISOHEXYLCYANOACRYLATE NANOSPHERES AGAINST MULTIDRUG-RESISTANT TUMOR-CELLS IN CULTURE [J].
BENNIS, S ;
CHAPEY, C ;
COUVREUR, P ;
ROBERT, J .
EUROPEAN JOURNAL OF CANCER, 1994, 30A (01) :89-93
[8]   Green- and red-fluorescent nanospheres for the detection of cell surface receptors by flow cytometry [J].
Bhalgat, MK ;
Haugland, RP ;
Pollack, JS ;
Swan, S ;
Haugland, RP .
JOURNAL OF IMMUNOLOGICAL METHODS, 1998, 219 (1-2) :57-68
[9]   DIMINISHED GENOTOXICITY OF MITOMYCIN-C AND FARMORUBICIN INCLUDED IN POLYBUTYLCYANOACRYLATE NANOPARTICLES [J].
BLAGOEVA, PM ;
BALANSKY, RM ;
MIRCHEVA, TJ ;
SIMEONOVA, MI .
MUTATION RESEARCH, 1992, 268 (01) :77-82
[10]   Superparamagnetic agents in magnetic resonance imaging: Physicochemical characteristics and clinical applications - A review [J].
Bonnemain, B .
JOURNAL OF DRUG TARGETING, 1998, 6 (03) :167-174