Synthesis and characterization of retrograded starch nanoparticles through homogenization and miniemulsion cross-linking

被引:13
作者
Ding, Yongbo [1 ,2 ]
Zheng, Jiong [1 ,2 ]
Zhang, Fusheng [1 ,2 ]
Kan, Jianquan [1 ,2 ]
机构
[1] Southwest Univ, Coll Food Sci, Tiansheng Rd 1, Chongqing 400715, Peoples R China
[2] Minist Agr, Lab Qual & Safety Risk Assessment Agroprod Storag, Chongqing 400715, Peoples R China
关键词
Box-Behnken design; Homogenization; RS3NPs; Physicochemical properties; AQUEOUS-SOLUTION; REMOVAL; DIGESTIBILITY; ADSORPTION; GRANULES; KINETICS; CHITOSAN;
D O I
10.1016/j.carbpol.2016.06.007
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Anew and convenient route to synthesizing retrograded starch nanoparticles (RS3NPs) through homogenization combined with a water-in-oil miniemulsion cross-linking technique was developed. The RS3NPs were optimized using Box-Behnken experimental design. Homogenization pressure (X-1), oil/water ratio (X-2), and surfactant (X-3) were selected as independent variables, whereas particle size was considered as a dependent variable. Results indicated that homogenization pressure was the main contributing variable for particle size. The optimum values for homogenization pressure, oil/water ratio, and surfactant were 30 MPa, 9.34:1, and 2.54 g, respectively, whereas the particle size was predicted to be 288.2 nm. Morphological, physical, chemical, and functional properties of the RS3NPs were the assessed. Scanning electron microscopy and dynamic light scattering images showed that RS3NP granules were broken down to size of about 222.2 nm. X-ray diffraction results revealed a disruption in crystallinity. The RS3NPs exhibited a slight decrease in To, but Tp and Tc increased and narrowest Tc-To. The solubility and swelling power were also increased. New peaks at 1594.84 and 1403.65 cm(-1) were observed in the FTIR graph. However, homogenization minimally influenced the antidigestibility of RS3NPs. The absorption properties improved, and the adsorption kinetic described the contact time on the adsorption of captopril onto RS3NPs. In vitro release experiment indicated that the drug was released as follows: 21% after 2 h in SGF, 42.78% at the end of 8 h (2 h in SGF and 6 h in SIF), and 92.55% after 12 h in SCF. These findings may help better utilize RS3NP in biomedical applications as a drug delivery material. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:656 / 665
页数:10
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