Colloidal drug carriers: achievements and perspectives

被引:235
作者
Barratt, G [1 ]
机构
[1] Univ Paris 11, UMR CNRS 8612, Fac Pharm, Lab Physicochim & Biopharm, F-92296 Chatenay Malabry, France
关键词
drug delivery; liposome; nanocapsule; nanoparticle; nanosphere; poly(ethylene glycol); polymer; targeting;
D O I
10.1007/s000180300002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Colloidal drug carriers such as liposomes and nanoparticles are able to modify the distribution of an associated substance. They can therefore be used to improve the therapeutic index of drugs by increasing their efficacy and/or reducing their toxicity. If these delivery systems are carefully designed with respect to the target and route of administration, they may provide one solution to some of the delivery problems posed by new classes of active molecules such as peptides, proteins, genes, and oligonucleotides. They may also extend the therapeutic potential of established drugs such as doxorubicin and amphotericin B. This article discusses the use of colloidal, particulate carrier systems (25 nm to 1 mum in diameter) in such applications. In particular, systems which show diminished uptake by mononuclear phagocytes are described. Specific targeting of carriers to particular tissues or cells is also considered.
引用
收藏
页码:21 / 37
页数:17
相关论文
共 171 条
  • [1] Aboubakar M, 2000, DRUG DEVELOP RES, V49, P109, DOI 10.1002/(SICI)1098-2299(200002)49:2<109::AID-DDR4>3.0.CO
  • [2] 2-#
  • [3] Superior chemotherapeutic efficacy of amphotericin B in tuftsin-bearing liposomes against Leishmania donovani infection in hamsters
    Agrawal, AK
    Agrawal, A
    Pal, A
    Guru, PY
    Gupta, CM
    [J]. JOURNAL OF DRUG TARGETING, 2002, 10 (01) : 41 - 45
  • [4] Mucosal immunogenicity elicited in mice by oral vaccination with phosphorylcholine encapsulated in poly (D,L-lactide-co-glycolide) microspheres
    Allaoui-Attarki, K
    Fattal, E
    Pecquet, S
    Trollé, S
    Chachaty, E
    Couvreur, P
    Andremont, A
    [J]. VACCINE, 1998, 16 (07) : 685 - 691
  • [5] Therapeutic opportunities for targeted liposomal drug delivery
    Allen, TM
    Moase, EH
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 1996, 21 (02) : 117 - 133
  • [6] LARGE UNILAMELLAR LIPOSOMES WITH LOW UPTAKE INTO THE RETICULOENDOTHELIAL SYSTEM
    ALLEN, TM
    CHONN, A
    [J]. FEBS LETTERS, 1987, 223 (01) : 42 - 46
  • [7] Allen TM, 1998, NATO ADV SCI I A-LIF, V300, P61
  • [8] JEJUNAL-ABSORPTION, PHARMACOLOGICAL ACTIVITY, AND PHARMACOKINETIC EVALUATION OF INDOMETHACIN-LOADED POLY(D,L-LACTIDE) AND POLY(ISOBUTYL-CYANOACRYLATE) NANOCAPSULES IN RATS
    AMMOURY, N
    FESSI, H
    DEVISSAGUET, JP
    DUBRASQUET, M
    BENITA, S
    [J]. PHARMACEUTICAL RESEARCH, 1991, 8 (01) : 101 - 105
  • [9] EFFECT ON CEREBRAL BLOOD-FLOW OF ORALLY-ADMINISTERED INDOMETHACIN-LOADED POLY(ISOBUTYLCYANOACRYLATE) AND POLY(DL-LACTIDE) NANOCAPSULES
    AMMOURY, N
    FESSI, H
    DEVISSAGUET, JP
    ALLIX, M
    PLOTKINE, M
    BOULU, RG
    [J]. JOURNAL OF PHARMACY AND PHARMACOLOGY, 1990, 42 (08) : 558 - 561
  • [10] [Anonymous], LIPOSOME TECHNOL