Colloidal drug carriers: achievements and perspectives
被引:235
作者:
Barratt, G
论文数: 0引用数: 0
h-index: 0
机构:
Univ Paris 11, UMR CNRS 8612, Fac Pharm, Lab Physicochim & Biopharm, F-92296 Chatenay Malabry, FranceUniv Paris 11, UMR CNRS 8612, Fac Pharm, Lab Physicochim & Biopharm, F-92296 Chatenay Malabry, France
Barratt, G
[1
]
机构:
[1] Univ Paris 11, UMR CNRS 8612, Fac Pharm, Lab Physicochim & Biopharm, F-92296 Chatenay Malabry, France
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