Nanoparticle drug delivery system for restenosis

被引:138
作者
Labhasetwar, V [1 ]
Song, CX [1 ]
Levy, RJ [1 ]
机构
[1] UNIV MICHIGAN,CTR MED,DIV PEDIAT CARDIOL,ANN ARBOR,MI 48109
关键词
local drug delivery; intra-arterial localization; angioplasty; smooth muscle cell proliferation; reocclusion; polymers; thrombosis;
D O I
10.1016/S0169-409X(96)00483-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Restenosis, an arterial reobstruction occurring in thirty to fifty percent of patients undergoing coronary angioplasty, because of its localized nature can possibly be best treated by local drug therapy. In recent years, several local drug delivery strategies have been investigated for the prevention of restenosis. In this review we discuss the therapeutic potential of nanoparticles as a drug delivery system for restenosis. Nanoparticles, for the purpose of this review, are 30-500 nm diameter polymeric spherical particles. Nanoparticles possess several advantages as a carrier system for the intra-arterial localization of therapeutic agents. These advantages include their subcellular size, targeted surfaces, good suspensibility, and uniform dispersity for a catheter-based delivery, and an easy penetration into the arterial wall without causing trauma. In various studies we have demonstrated an efficient intra-arterial localization of nanoparticles, biocompatibility in the arterial wall, and effectiveness for the inhibition of experimental restenosis. Thus, nanoparticles could prove to be an effective dosage form for an intra-arterial localization of therapeutic agents for preventing restenosis in a clinical setting.
引用
收藏
页码:63 / 85
页数:23
相关论文
共 191 条
[1]   IN-VITRO EXTENDED-RELEASE PROPERTIES OF DRUG-LOADED POLY(DL-LACTIC ACID) NANOPARTICLES PRODUCED BY A SALTING-OUT PROCEDURE [J].
ALLEMANN, E ;
LEROUX, JC ;
GURNY, R ;
DOELKER, E .
PHARMACEUTICAL RESEARCH, 1993, 10 (12) :1732-1737
[2]  
Arai K, 1987, Drug Des Deliv, V2, P109
[3]   LOCAL-DELIVERY OF VASCULAR ENDOTHELIAL GROWTH-FACTOR ACCELERATES REENDOTHELIALIZATION AND ATTENUATES INTIMAL HYPERPLASIA IN BALLOON-INJURED RAT CAROTID-ARTERY [J].
ASAHARA, T ;
BAUTERS, C ;
PASTORE, C ;
KEARNEY, M ;
ROSSOW, S ;
BUNTING, S ;
FERRARA, N ;
SYMES, JF ;
ISNER, JM .
CIRCULATION, 1995, 91 (11) :2793-2801
[4]  
ASTIER A, 1988, CANCER RES, V48, P1835
[5]   DECREASED PLATELET DEPOSITION AND SMOOTH-MUSCLE CELL-PROLIFERATION AFTER INTRAMURAL HEPARIN DELIVERY WITH HYDROGEL-COATED BALLOONS [J].
AZRIN, MA ;
MITCHEL, JF ;
FRAM, DB ;
PEDERSEN, CA ;
CARTUN, RW ;
BARRY, JJ ;
BOW, LM ;
WATERS, DD ;
MCKAY, RG .
CIRCULATION, 1994, 90 (01) :433-441
[6]   THE UPTAKE OF AMPICILLIN-LOADED NANOPARTICLES BY MURINE MACROPHAGES INFECTED WITH SALMONELLA-TYPHIMURIUM [J].
BALLAND, O ;
PINTOALPHANDARY, H ;
PECQUET, S ;
ANDREMONT, A ;
COUVREUR, P .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1994, 33 (03) :509-522
[7]   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
[8]   INFLUENCE OF POLYBUTYLCYANOACRYLATE NANOPARTICLES AND LIPOSOMES ON THE EFFICACY AND TOXICITY OF THE ANTICANCER DRUG MITOXANTRONE IN MURINE TUMOR-MODELS [J].
BECK, P ;
KREUTER, J ;
RESZKA, R ;
FICHTNER, I .
JOURNAL OF MICROENCAPSULATION, 1993, 10 (01) :101-114
[9]   INHIBITION OF HIV IN-VITRO BY ANTIVIRAL DRUG-TARGETING USING NANOPARTICLES [J].
BENDER, A ;
SCHAFER, V ;
STEFFAN, AM ;
ROYER, C ;
KREUTER, J ;
RUBSAMENWAIGMANN, H ;
VONBRIESEN, H .
RESEARCH IN VIROLOGY, 1994, 145 (3-4) :215-220
[10]   INHIBITION OF VASCULAR SMOOTH-MUSCLE CELL-PROLIFERATION IN-VITRO AND IN-VIVO BY C-MYC ANTISENSE OLIGODEOXYNUCLEOTIDES [J].
BENNETT, MR ;
ANGLIN, S ;
MCEWAN, JR ;
JAGOE, R ;
NEWBY, AC ;
EVAN, GI .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (02) :820-828