Towards the development of a supercritical carbon dioxide spray process to coat solid protein particles

被引:3
|
作者
Yu, Miao [1 ]
Sediq, Ahmad S. [2 ]
Zhang, Shiduo [1 ]
Nejadnik, M. Reza [2 ]
Every, Hayley A. [3 ]
Jiskoot, Wim [2 ]
Witkamp, Geert-Jan [1 ]
机构
[1] Delft Univ Technol, Dept Biotechnol, Maasweg 9, NL-2629 HZ Delft, Netherlands
[2] Leiden Univ, LACDR, Cluster BioTherapeut, Div Drug Delivery Technol, Einsteinweg 55, NL-2333 CC Leiden, Netherlands
[3] FeyeCon Dev & Implementat BV, Rijnkade I7-A, NL-1382 GS Weesp, Netherlands
关键词
Supercritical carbon dioxide; Lysozyme; Dextran sulphate; Drug delivery systems; Proteins; CONTROLLED-RELEASE; DELIVERY; ENCAPSULATION; MICROSPHERES; LIQUID; MICRO; MICROENCAPSULATION; LYSOZYME; POLYMERS; CHITOSAN;
D O I
10.1016/j.supflu.2017.12.014
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The aim of this study was to develop a supercritical carbon dioxide (scCO(2)) spray process to coat solid protein particles with a hydrophilic polymer. The final purpose is to manufacture drug particles exhibiting controlled release behaviour in patients. Lysozyme microparticles (about 20 mu m) were suspended in a vessel into which a dextran sulphate (DS) solution was dispersed by scCO(2) via a nozzle. Upon interaction with the droplets, DS was deposited onto or mixed with suspended lysozyme particles. Particles of about 100 mu m were obtained. The zeta potential analysis and elemental analysis indicated that the top layer of the particles consisted of both lysozyme and DS. Some of the produced particulate materials showed retarded lysozyme release when exposed to water or phosphate buffered saline, holding promise for future production of controlled drug delivery systems for therapeutic proteins.
引用
收藏
页码:49 / 59
页数:11
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