A new process for drug loaded nanocapsules preparation using a membrane contactor

被引:13
作者
Charcosset, C [1 ]
Fessi, H [1 ]
机构
[1] Univ Lyon 1, ESCPE Lyon, CNRS,UMR 5007, Lab Automat & Genie Proc, F-69622 Villeurbanne, France
关键词
membrane reactor; membrane contactor; drug loaded nanocapsule; nanoparticle;
D O I
10.1080/03639040500306237
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In this paper, we describe a new process for the preparation of drug loaded nanocapsules using a membrane contactor which may be scaled up for industrial applications. Nanocapsules are prepared according to the nanoprecipitation method. The organic phase (solvent, polymer, oil, and drug) is pressed through the pores of an ultrafiltration membrane via the filtrate side. The aqueous phase (water and surfactant) circulates inside the membrane module, and sweeps away the nanocaspules forming at the pore outlets. Two model drugs are selected for the preparation of drug loaded nanocapsules: indomethacin and vitamin E. It is shown that indomethacin loaded nanocapsules with a mean diameter of 240 nm and vitamin E loaded nanocapsules with a mean diameter of 230 nm are obtained with a 150,000 daltons ultrafiltration membrane, a transmembrane pressure of 3 bar, and a crossflow rate of 1.7 m.s(-1) . High fluxes are also obtained (around 0.6 m(3)/h.m(2) ), leading to the preparation of 1.8 10(-3) m(3) drug loaded nanocapsules in 8 min. The advantage of this membrane contactor compared to other processes for drug loaded nanocapsules preparation is shown to be its scale-up ability.
引用
收藏
页码:987 / 992
页数:6
相关论文
共 16 条
[1]   IN-VITRO EXTENDED-RELEASE PROPERTIES OF DRUG-LOADED POLY(DL-LACTIC ACID) NANOPARTICLES PRODUCED BY A SALTING-OUT PROCEDURE [J].
ALLEMANN, E ;
LEROUX, JC ;
GURNY, R ;
DOELKER, E .
PHARMACEUTICAL RESEARCH, 1993, 10 (12) :1732-1737
[2]  
ALLEMANN E, 1993, EUR J PHARM BIOPHARM, V39, P173
[3]   INVITRO RELEASE KINETIC PATTERN OF INDOMETHACIN FROM POLY(D,L-LACTIDE) NANOCAPSULES [J].
AMMOURY, N ;
FESSI, H ;
DEVISSAGUET, JP ;
PUISIEUX, F ;
BENITA, S .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1990, 79 (09) :763-767
[4]   Synthesis and characterization of polyurethane and poly(ether urethane) nanocapsules using a new technique of interfacial polycondensation combined to spontaneous emulsification [J].
Bouchemal, K ;
Briançon, S ;
Perrier, E ;
Fessi, H ;
Bonnet, I ;
Zydowicz, N .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2004, 269 (01) :89-100
[5]   The membrane emulsification process - a review [J].
Charcosset, C ;
Limayem, I ;
Fessi, H .
JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY, 2004, 79 (03) :209-218
[6]  
CHARCOSSET C, 2005, IN PRESS J MEMBRANE
[7]   Membrane dispersion precipitation method to prepare nanopartials [J].
Chen, GG ;
Luo, GS ;
Xu, JH ;
Wang, JD .
POWDER TECHNOLOGY, 2004, 139 (02) :180-185
[8]   Nanocapsule technology: A review [J].
Couvreur, P ;
Barratt, G ;
Fattal, E ;
Legrand, P ;
Vauthier, C .
CRITICAL REVIEWS IN THERAPEUTIC DRUG CARRIER SYSTEMS, 2002, 19 (02) :99-134
[9]   Membrane contactors and catalytic membrane reactors in process intensification [J].
Drioli, E ;
Criscuoli, A ;
Curcio, E .
CHEMICAL ENGINEERING & TECHNOLOGY, 2003, 26 (09) :975-981
[10]   NANOCAPSULE FORMATION BY INTERFACIAL POLYMER DEPOSITION FOLLOWING SOLVENT DISPLACEMENT [J].
FESSI, H ;
PUISIEUX, F ;
DEVISSAGUET, JP ;
AMMOURY, N ;
BENITA, S .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1989, 55 (01) :R1-R4