Lysozyme encapsulation within PLGA and CaCO3 microparticles using supercritical CO2 medium

被引:22
|
作者
Tran, M. -K. [1 ,2 ]
Hassani, L. N. [1 ,2 ]
Calvignac, B. [1 ,2 ]
Beuvier, T. [3 ]
Hindre, F. [1 ,2 ]
Boury, F. [1 ,2 ]
机构
[1] LUNAM Univ, Angers, France
[2] INSERM, U1006, IBS, F-49933 Angers 9, France
[3] Univ Maine, CNRS, UMR 6087, Lab Phys Etat Condense, F-72085 Le Mans 9, France
来源
JOURNAL OF SUPERCRITICAL FLUIDS | 2013年 / 79卷
关键词
Supercritical CO2; Emulsification; Non-toxic solvents; Protein encapsulation; Microparticles; WATER-MISCIBLE SOLVENTS; CALCIUM-CARBONATE; PROTEIN MICROENCAPSULATION; EMBOLIC LIQUIDS; HIGH-PRESSURE; IN-VITRO; PRECIPITATION; MICROSPHERES; STABILITY; RELEASE;
D O I
10.1016/j.supflu.2013.02.024
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
This study is part of a global project which aims at conceiving and characterizing implantable synthetic extracellular matrices seeded with multifunctional particles for bone and cartilage tissue engineering. To date, protein encapsulation remains a challenge in the field of microencapsulation. The aim of this work is to use supercritical CO2 to generate polymeric and inorganic particles for protein encapsulation. Poly(lactic-co-glycolic) (PLGA) and calcium carbonate (CaCO3) microparticles were chosen to be investigated. In both cases, spherical particles were successfully obtained based on the formation of an emulsion in CO2 media. Most importantly, only non-toxic solvents or aqueous solution were used for the formulation of microparticles. Encapsulation experiments were carried out to provide a proof of concept. Lysozyme was chosen as a model protein and experimental designs were made in order to better understand the system and to better predict the encapsulation yield. The encapsulation yield can reach about 60% in both cases. The mechanism of particle formation and lysozyme encapsulation will also be discussed in detail. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:159 / 169
页数:11
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