Stability and structure of protein-polysaccharide coacervates in the presence of protein aggregates

被引:34
作者
Sanchez, C
Renard, D
机构
[1] INRA, Unite Physicochim Macromol, F-71627 Nantes 3, France
[2] INPL, ENSAIA, Lab Physicochim & Genie Alimentaires, F-54505 Vandoeuvre Les Nancy, France
关键词
complex coacervation; beta-lactoglobulin; acacia gum; microencapsulation; light scattering; confocal scanning laser microscopy;
D O I
10.1016/S0378-5173(02)00174-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We have studied at pH 4.2 and three protein (Pr):polysaccharide (Pol) weight ratios (8:1, 2:1 and 1:1) the structure and stability of beta-lactoglobulin/acacia gum/water dispersions containing protein aggregates (BLG/AG/W) or free from aggregates (AF-BLG/AG/W). Phase diagrams were characteristic of complex coacervation. BLG/AG/W dispersions displayed a larger biphasic area than AF-BLG/AG/W dispersions, that moved towards the protein axis. It was concluded that protein aggregates affected complex coacervation both by entropic (size and molecular masses of aggregates) and enthalpic (surface properties of aggregates) effects. Laser light scattering measurements revealed that the particles diameter (d(43)) induced by demixing was controlled by protein aggregates in AF-BLG/AG/W dispersions. At 1 wt.% biopolymer concentration, particles were 15-20 times larger in AF-BLG/AG/W dispersions than in BLG/AG/W dispersions at (Pr:Pol) ratios of 2:1 or 1:1. Confocal scanning laser microscopy showed that AF-BLG/AG/W dispersions only contained spherical coacervates. BLG/AG/W dispersions contained both coacervates and aggregates coated with AG or/and BLG/AG coacervates. At a (Pr:Pol) ratio of 2:1 and 1:1, coacervates were vesicular or multivesicular. Coacervates were smaller in BLG/AG/W dispersions than in AF-BLG/AG/W dispersions. It was concluded that protein aggregates have the intrinsic ability to stabilize complex coacervates and could be used to design multifunctional delivery systems. This study showed that composite dispersions containing both protein aggregates embedded in protein-polysaccharide coacervates and free coacervates may be performed. In this respect, the design of protein aggregates with controlled size distribution and surface properties could open new possibilities both in the non-chemical control of coacervates stability and in the development of multifunctional delivery systems. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:319 / 324
页数:6
相关论文
共 21 条
[11]   CHARACTERISTICS OF MEDICATED AND UNMEDICATED MICROGLOBULES RECOVERED FROM COMPLEX COACERVATES OF GELATIN-ACACIA [J].
NEWTON, DW ;
MCMULLEN, JN ;
BECKER, CH .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1977, 66 (09) :1327-1330
[12]   Effect of formulation and process variables on the formation of chitosan-gelatin coacervates [J].
RemunanLopez, C ;
Bodmeier, R .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1996, 135 (1-2) :63-72
[13]  
SANCHEZ C, FOFOOD HYDROCOLL, V16, P257
[14]   Complex coacervation between β-lactoglobulin and acacia gum in aqueous medium [J].
Schmitt, C ;
Sanchez, C ;
Thomas, F ;
Hardy, J .
FOOD HYDROCOLLOIDS, 1999, 13 (06) :483-496
[15]   Structure and technofunctional properties of protein-polysaccharide complexes: A review [J].
Schmitt, C ;
Sanchez, C ;
Desobry-Banon, S ;
Hardy, J .
CRITICAL REVIEWS IN FOOD SCIENCE AND NUTRITION, 1998, 38 (08) :689-753
[16]   Study of β-lactoglobulin/acacia gum complex coacervation by diffusing-wave spectroscopy and confocal scanning laser microscopy [J].
Schmitt, C ;
Sanchez, C ;
Lamprecht, A ;
Renard, D ;
Lehr, CM ;
de Kruif, CG ;
Hardy, J .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2001, 20 (03) :267-280
[17]   Effect of protein aggregates on the complex coacervation between β-lactoglobulin and acacia gum at pH 4.2 [J].
Schmitt, C ;
Sanchez, C ;
Despond, S ;
Renard, D ;
Thomas, F ;
Hardy, J .
FOOD HYDROCOLLOIDS, 2000, 14 (04) :403-413
[18]  
SCHMITT C, 2000, THESIS INPL VANDOEUV
[19]   Determination of protein surface concentration for emulsions containing a partially crystalline dispersed phase [J].
Segall, KI ;
Goff, HD .
FOOD HYDROCOLLOIDS, 1999, 13 (04) :291-297
[20]  
THIES C, 1982, CRIT REV BIOMED ENG, V8, P335