Polymeric micelles as new drug carriers

被引:809
作者
Kwon, GS
Okano, T
机构
[1] TOKYO WOMENS MED COLL,INST BIOMED ENGN,SHINJUKU KU,TOKYO 162,JAPAN
[2] UNIV ALBERTA,FAC PHARM & PHARMACEUT SCI,EDMONTON,AB T6G 2N8,CANADA
关键词
nanoscopic drug carriers; drug targeting; polymeric micelles; poly(ethylene oxide); poly(beta-benzyl-L-aspartate); poly(L-lactic acid); doxorubicin;
D O I
10.1016/S0169-409X(96)00401-2
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
Advances in block copolymer syntheses have led to polymeric micelles that may serve as nanoscopic drug carriers. For drug delivery, micelles were prepared from biocompatible and biodegradable block copolymers. The polymeric micelles display functional groups on their surfaces for attachment of pilot molecules. Researchers are establishing chemical as well as physical routes of loading drugs into polymeric micelles. Notably, polymeric micelles solubilize hydrophobic drugs suffering from poor water solubility. Recent studies suggest that polymeric micelles may have solid-like cores. Thus, they may remain intact for long durations under sink conditions and may also slowly release drugs. Mechanistically, polymeric micelles may act as drug carriers by circumventing host defenses, circulating for prolonged periods and extravasating from the vascular system, preferentially delivering drug to solid tumors.
引用
收藏
页码:107 / 116
页数:10
相关论文
共 43 条
[1]
BERGIN C, 1995, AM J HLTH SYS PHARM, V52, P201
[2]
VASCULAR TARGETING - A NEW APPROACH TO THE THERAPY OF SOLID TUMORS [J].
BURROWS, FJ ;
THORPE, PE .
PHARMACOLOGY & THERAPEUTICS, 1994, 64 (01) :155-174
[3]
FUNCTIONAL POLY[(ETHYLENE OXIDE)-CO-(BETA-BENZYL-L-ASPARTATE)] POLYMERIC MICELLES - BLOCK-COPOLYMER SYNTHESIS AND MICELLES FORMATION [J].
CAMMAS, S ;
KATAOKA, K .
MACROMOLECULAR CHEMISTRY AND PHYSICS, 1995, 196 (06) :1899-1905
[4]
FLUORESCENCE STUDIES OF AMPHIPHILIC POLY(METHACRYLIC ACID)-BLOCK-POLYSTYRENE-BLOCK-POLY(METHACRYLIC ACID) MICELLES [J].
CAO, T ;
MUNK, P ;
RAMIREDDY, C ;
TUZAR, Z ;
WEBBER, SE .
MACROMOLECULES, 1991, 24 (23) :6300-6305
[5]
STRUCTURE AND DYNAMICS OF BLOCK-COPOLYMER COLLOIDS [J].
CHU, B .
LANGMUIR, 1995, 11 (02) :414-421
[6]
GABIZON A, 1994, CANCER RES, V54, P987
[7]
THERAPY OF MYCOBACTERIUM-AVIUM COMPLEX INFECTIONS IN BEIGE MICE WITH STREPTOMYCIN ENCAPSULATED IN STERICALLY STABILIZED LIPOSOMES [J].
GANGADHARAM, PRJ ;
ASHTEKAR, DR ;
FLASHER, DL ;
DUZGUNES, N .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (03) :725-730
[8]
THE CONTROLLED INTRAVENOUS DELIVERY OF DRUGS USING PEG-COATED STERICALLY STABILIZED NANOSPHERES [J].
GREF, R ;
DOMB, A ;
QUELLEC, P ;
BLUNK, T ;
MULLER, RH ;
VERBAVATZ, JM ;
LANGER, R .
ADVANCED DRUG DELIVERY REVIEWS, 1995, 16 (2-3) :215-233
[9]
GREGORIADIS G, 1993, TIBTECH, V11
[10]
THE NEUROLEPTIC ACTIVITY OF HALOPERIDOL INCREASES AFTER ITS SOLUBILIZATION IN SURFACTANT MICELLES - MICELLES AS MICROCONTAINERS FOR DRUG TARGETING [J].
KABANOV, AV ;
CHEKHONIN, VP ;
ALAKHOV, VY ;
BATRAKOVA, EV ;
LEBEDEV, AS ;
MELIKNUBAROV, NS ;
ARZHAKOV, SA ;
LEVASHOV, AV ;
MOROZOV, GV ;
SEVERIN, ES ;
KABANOV, VA .
FEBS LETTERS, 1989, 258 (02) :343-345