Targeted delivery of antibiotics using liposomes and nanoparticles: research and applications

被引:296
作者
Pinto-Alphandary, H [1 ]
Andremont, A
Couvreur, P
机构
[1] Univ Paris 11, Fac Pharm, UMR CNRS 8612, F-92296 Chatenay Malabry, France
[2] Univ Paris 07, CHU Xavier Bichat, F-75018 Paris, France
关键词
liposome; nanoparticle; antibiotic; carrier; targeting; intracellular infection;
D O I
10.1016/S0924-8579(99)00121-1
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
This review examines current technologies for increasing the bioavailability of antibiotics by means of liposomes or nanoparticles. The main focus is on liposomes. These carriers were preferentially developed because their composition is compatible with biological constituents. Biodegradable polymers in the form of colloidal particles have also been used and show promise for future applications in antimicrobial chemotherapy. The in vivo behaviour of both types of carriers and consequently their therapeutic potential, are determined by their route of administration. Conventional carrier strategies permit the mononuclear phagocyte system to be targeted by intravenous injection of antibiotics. Stealthy strategies avoid major uptake by these cells and extend the systemic presence of these carriers. The purpose of this review is to provide background information in antibiotic targeting gathered from papers published over the last twenty years. It seems clear that such drug carriers (liposomes, nanoparticles) allow increased drug concentration at infected sites but reduce drug toxicity. (C) 2000 Elsevier Science B.V. and International Society of Chemotherapy. All rights reserved.
引用
收藏
页码:155 / 168
页数:14
相关论文
共 139 条
  • [1] Al Khouri F, 1986, INT J PHARMACEUT, V28, P125
  • [2] ALLEMANN E, 1993, EUR J PHARM BIOPHARM, V39, P173
  • [3] Allen T.M., 2008, J LIPOSOME RES, V2, P289, DOI [10.3109/08982109209010210, DOI 10.3109/08982109209010210]
  • [4] ALVING C R, 1988, Advanced Drug Delivery Reviews, V2, P107, DOI 10.1016/0169-409X(88)90007-5
  • [5] TESTING THE SUSCEPTIBILITY OF BACTERIA IN BIOFILMS TO ANTIBACTERIAL AGENTS
    ANWAR, H
    DASGUPTA, MK
    COSTERTON, JW
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1990, 34 (11) : 2043 - 2046
  • [6] ASSIL KK, 1991, INVEST OPHTH VIS SCI, V32, P3216
  • [7] EFFECT OF LIPID-COMPOSITION ON ACTIVITY OF LIPOSOME-ENTRAPPED AMPICILLIN AGAINST INTRACELLULAR LISTERIA-MONOCYTOGENES
    BAKKERWOUDENBERG, IAJM
    LOKERSE, AF
    ROERDINK, FH
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1988, 32 (10) : 1560 - 1564
  • [8] EFFECT OF LIPOSOME-ENTRAPPED AMPICILLIN ON SURVIVAL OF LISTERIA-MONOCYTOGENES IN MURINE PERITONEAL-MACROPHAGES
    BAKKERWOUDENBERG, IAJM
    LOKERSE, AF
    VINKVANDENBERG, JC
    ROERDINK, FH
    MICHEL, MF
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1986, 30 (02) : 295 - 300
  • [9] FREE VERSUS LIPOSOME-ENTRAPPED AMPICILLIN IN TREATMENT OF INFECTION DUE TO LISTERIA-MONOCYTOGENES IN NORMAL AND ATHYMIC (NUDE) MICE
    BAKKERWOUDENBERG, IAJM
    LOKERSE, AF
    ROERDINK, FH
    REGTS, D
    MICHEL, MF
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1985, 151 (05) : 917 - 924
  • [10] LIPOSOMES IN THE TREATMENT OF INFECTIONS
    BAKKERWOUDENBERG, IAJM
    STORM, G
    WOODLE, MC
    [J]. JOURNAL OF DRUG TARGETING, 1994, 2 (05) : 363 - 371