Amphiphilic hydrogel nanoparticles. Preparation, characterization, and preliminary assessment as new colloidal drug carriers

被引:99
作者
Missirlis, D
Tirelli, N
Hubbell, JA
机构
[1] Univ Manchester, Sch Pharm, Manchester M13 9PL, Lancs, England
[2] Univ Manchester, Mat Mol Ctr, Manchester M13 9PL, Lancs, England
[3] Ecole Polytech Fed Lausanne, Lab Regenerat Med & Pharmacobiol LMRP, Swiss Fed Inst Technol, Inst Biomed Engn, CH-1015 Lausanne, Switzerland
[4] Ecole Polytech Fed Lausanne, Lab Regenerat Med & Pharmacobiol LMRP, Integrat Biosci Inst, CH-1015 Lausanne, Switzerland
关键词
D O I
10.1021/la047367s
中图分类号
O6 [化学];
学科分类号
0703 [化学];
摘要
Inverse emulsion photopolymerization of acrylated poly(ethylene glycol)-bl-poly(propylene glycol)-bl-poly(ethylene glycol) and poly(ethylene glycol) was successfully employed to prepare stable, cross-linked, amphiphilic nanoparticles. Even at low emulsifier concentrations (2%) and high water-to-hexane weight ratios (35/65), the stability of the inverse emulsion allowed for the formation of well-defined colloidal material. Inverse emulsion characteristics and polymerization conditions could be controlled to vary the size of the nanoparticles between 50 and 500 nm. The presence of hydrophobic nanodomains within these otherwise hydrophilic nanoparticles was verified by using pyrene as a microenvironmentally sensitive probe. The hydrophobic poly(propylene glycol)-rich domains appear to be suitable for incorporation of hydrophobic drugs, encapsulating Doxorubicin up to 9.8% (w/w). We believe that the complex nano-architecture of these materials makes them a potentially interesting colloidal drug delivery carrier system and that the method should be useful for a number of amphiphilic macromolecular precursors.
引用
收藏
页码:2605 / 2613
页数:9
相关论文
共 38 条
[1]
Block copolymer-based formulation of doxorubicin. From cell screen to clinical trials [J].
Alakhov, V ;
Klinski, E ;
Li, SM ;
Pietrzynski, G ;
Venne, A ;
Batrakova, E ;
Bronitch, T ;
Kabanov, A .
COLLOIDS AND SURFACES B-BIOINTERFACES, 1999, 16 (1-4) :113-134
[2]
Intratumoral administration of paclitaxel in an in situ gelling poloxamer 407 formulation [J].
Amiji, MM ;
Lai, PK ;
Shenoy, DB ;
Rao, M .
PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY, 2002, 7 (02) :195-202
[3]
Free-radical polymerization in inverse microemulsions [J].
Barton, J .
PROGRESS IN POLYMER SCIENCE, 1996, 21 (03) :399-438
[4]
Cross-linked polyvinylpyrrolidone nanoparticles: a potential carrier for hydrophilic drugs [J].
Bharali, DJ ;
Sahoo, SK ;
Mozumdar, S ;
Maitra, A .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2003, 258 (02) :415-423
[5]
CANDAU F, 1997, EMULSION POLYM EMULS
[6]
Gelatin nanoparticles produced by a simple W/O emulsion as delivery system for methotrexate [J].
Cascone, MG ;
Lazzeri, L ;
Carmignani, C ;
Zhu, ZH .
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 2002, 13 (05) :523-526
[7]
Cellesi F, 2002, MACROMOL CHEM PHYSIC, V203, P1466, DOI 10.1002/1521-3935(200207)203:10/11<1466::AID-MACP1466>3.0.CO
[8]
2-P
[9]
Cruise GM, 1998, BIOTECHNOL BIOENG, V57, P655, DOI 10.1002/(SICI)1097-0290(19980320)57:6<655::AID-BIT3>3.0.CO
[10]
2-K