Continuous-flow encapsulation of ketoprofen in copolymer microbeads via co-axial microfluidic device: Influence of operating and material parameters on drug carrier properties

被引:44
作者
Khan, Ikram Ullah [1 ,2 ,3 ]
Serra, Christophe A. [2 ]
Anton, Nicolas [1 ]
Vandamme, Thierry [1 ]
机构
[1] Univ Strasbourg, Fac Pharm, Equipe Pharm Biogalen, Lab Concept & Applicat Mol Bioact,CNRS 7199, F-67400 Illkirch Graffenstaden, France
[2] Univ Strasbourg, ECPM, LIPHT, EAc CNRS 4379,G2IP, F-67087 Strasbourg, France
[3] Govt Coll Univ, Coll Pharm, Faisalabad, Pakistan
关键词
Microfluidics; Ketoprofen; Microbeads; Ethyl acrylate; Drug delivery; CHITOSAN MICROPARTICLES; MICROSPHERE SIZE; IN-VITRO; RELEASE; POLYMER; UV; MICROENCAPSULATION; KINETICS;
D O I
10.1016/j.ijpharm.2012.12.024
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Microchannels based microfluidic systems are able to obtain monodispersed microparticles but are limited by cost, time and channel clogging. We succeeded in on the fly encapsulation of high ketoprofen contents in acrylate-based copolymer microbeads by environment friendly UV induced free radical polymerization in off-the-shelf co-axial microfluidic device. FTIR shows complete polymerization of acrylate monomers and interaction between carboxylic group of ketoprofen and ester group of monomers. DSC and XRD confirm amorphous nature of drug in microbeads. Different comonomer content formulations show limited drug release at low pH, a helpful properties to avoid gastric irritating effect of ketoprofen associated with conventional dosage forms. At pH 6.8 microbeads release higher content of drug by a non-Fickian diffusion mechanism. Their drug release rate depends upon the weight content of ethyl acrylate in the formulation as well as their size, increasing by increasing the former and decreasing the later. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:809 / 817
页数:9
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