Gliadin-based nanoparticles: Fabrication and stability of food-grade colloidal delivery systems

被引:99
作者
Joye, Iris J. [1 ,2 ]
Nelis, Veronique A. [1 ]
McClements, D. Julian [2 ]
机构
[1] Katholieke Univ Leuven, Dept Microbial & Mol Syst, Lab Food Chem & Biochem, B-3001 Louvain, Belgium
[2] Univ Massachusetts, Dept Food Sci, Biopolymers & Colloids Res Lab, Amherst, MA 01003 USA
基金
美国农业部;
关键词
Gliadin; Liquid antisolvent precipitation; Glutaraldehyde; Stability; WHEAT GLUTEN; GLUTARALDEHYDE; PRECIPITATION; SOLUBILITY; ULTRASOUND; FRACTIONS; SOLVENT; DRUGS; ACID;
D O I
10.1016/j.foodhyd.2014.09.008
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
There is great interest in converting gluten, a by-product from wheat starch isolation, into a value added functional food ingredient. The insolubility of monomeric gluten, i.e. gliadin, in water makes these proteins interesting materials to produce nanoparticles using liquid antisolvent precipitation. The effect of different production parameters (such as mixing speed, time, sonication parameters, gliadin concentration) on the properties of gliadin particles formed by liquid antisolvent precipitation was investigated. The produced particles were also hardened using glutaraldehyde (0-0.25%). The stability of the produced gliadin particles was investigated in different pH and salt conditions relevant for food processing and upon short term temperature treatments and isothermal long-term storage. Gliadin nanoparticles (diameter <200 nm) could be produced, however, they had poor stability in different conditions relevant to food processing: they redissolved below pH 4.0 and flocculated near their isoelectric point (pH approximate to 6.5), at elevated salt levels, and after heat treatment (T > 40 degrees C for 30 min). A slight improvement in particle stability was obtained by chemical hardening (0.25% glutaraldehyde). Gliadin nanoparticles may be useful in the development of delivery systems to encapsulate, protect, target and release active ingredients during food processing or after ingestion. However, additional strategies to stabilize the particles should be explored. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:86 / 93
页数:8
相关论文
共 33 条
[1]  
AACC, 2000, APPR METH AM ASS CER
[2]  
AOAC, 1995, 99003 AOAC OFF METH
[3]   Electrophoretic separation and characterisation of gliadin fractions from isolates and nanoparticulate drug delivery systems [J].
Arangoa, MA ;
Campanero, MA ;
Popineau, Y ;
Irache, JM .
CHROMATOGRAPHIA, 1999, 50 (3-4) :243-246
[4]   Gliadin nanoparticles as carriers for the oral administration of lipophilic drugs. Relationships between bioadhesion and pharmacokinetics [J].
Arangoa, MA ;
Campanero, MA ;
Renedo, MJ ;
Ponchel, G ;
Irache, JM .
PHARMACEUTICAL RESEARCH, 2001, 18 (11) :1521-1527
[5]  
Belitz H.-D., 2009, Food Chemistry, V4th, P374
[6]   Controlling Particle Size of a Poorly Water-Soluble Drug Using Ultrasound and Stabilizers in Antisolvent Precipitation [J].
Dalvi, Sameer V. ;
Dave, Rajesh N. .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2009, 48 (16) :7581-7593
[7]   Wheat Gluten Functionality as a Quality Determinant in Cereal-Based Food Products [J].
Delcour, Jan A. ;
Joye, Iris J. ;
Pareyt, Bram ;
Wilderjans, Edith ;
Brijs, Kristof ;
Lagrain, Bert .
ANNUAL REVIEW OF FOOD SCIENCE AND TECHNOLOGY, VOL 3, 2012, 3 :469-492
[8]   The pathogenesis of coeliac disease [J].
Dewar, D ;
Pereira, SP ;
Ciclitira, PJ .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2004, 36 (01) :17-24
[9]   Evaluation of gliadins nanoparticles as drug delivery systems: a study of three different drugs [J].
Duclairoir, C ;
Orecchioni, AM ;
Depraetere, P ;
Osterstock, F ;
Nakache, E .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2003, 253 (1-2) :133-144
[10]   Formation of gliadin nanoparticles: Influence of the solubility parameter of the protein solvent [J].
Duclairoir, C ;
Nakache, E ;
Marchais, H ;
Orecchioni, AM .
COLLOID AND POLYMER SCIENCE, 1998, 276 (04) :321-327