Fabrication of KDF-loaded chitosan-oligosaccharide-encapsulated konjac glucomannan/sodium alginate/zeolite P microspheres with sustained-release antimicrobial activity

被引:16
|
作者
Yang, Zhongxin [1 ]
Zhang, Xiaonan [1 ]
Li, Yuyan [1 ]
Fu, Bei [1 ]
Yang, Yuhang [1 ]
Chen, Nanchun [1 ]
Wang, Xiuli [4 ]
Xie, Qinglin [2 ,3 ]
机构
[1] Guilin Univ Technol, Coll Mat Sci & Engn, Guilin 541004, Peoples R China
[2] Guilin Univ Technol, Coll Environm Sci & Engn, Guilin 541006, Peoples R China
[3] Guilin Univ Technol, Collaborat Innovat Ctr Water Pollut Control & Wat, Guilin 541006, Peoples R China
[4] Guilin Univ Technol, Coll Chem & Biomed Engn, Guilin 541006, Peoples R China
基金
中国国家自然科学基金;
关键词
Potassium diformate; pH-sensitive; Bacteriostatic microspheres; Sustained release; POTASSIUM DIFORMATE; NANOPARTICLES; DELIVERY; OXIDE;
D O I
10.1016/j.molstruc.2021.131682
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
Potassium diformate(KDF) is a non-antibiotic growth promoter. To improve the utilization of KDF in the intestinal tract, P-type zeolite molecular sieve (zeolite P) was used as the drug-binding effector of KDF and was encapsulated in sodium alginate (ALG)/konjac glucomannan (KGM)/chitosan oligosaccharide (COS) composite hydrogel microspheres to prepare environment friendly, intelligent and pH-sensitive composite hydrogel microspheres for controlling the release of KDF. The composite hydrogel microspheres were characterized using XRD, FT-IR, TGA, and SEM. In addition, the swelling behavior of the composite hydrogel microspheres in three buffered media was determined. Thus, the phase composition, structural characteristics, thermal stability, apparent morphology and swelling properties were determined. Results indicated that the composite hydrogel microspheres possessed pH sensitivity, compatibility and porous 3D network structure. Furthermore, ALG formed polyelectrolyte complexes with COS, providing the composite hydrogel microspheres a complete three-dimensional network structure. The embedded network structure of zeolite P, which limited the size of the inner capsule, assisted in improving the thermal stability, and allowed expansion and controlled release of KDF. Under a simulated gastrointestinal environment, the in vitro release conformed to a good pH-sensitive drug release pattern and prevented premature release of KDF in the gastric juice. In the in vitro antibacterial test, the maximum inhibition rate of the antibacterial agent against Escherichia coli, Staphylococcus aureus and Bacillus subtilis were 96.63%, 93.81% and 93.31%, respectively, indicating its considerable potential as an intestinal antibacterial. (c) 2021 Elsevier B.V. All rights reserved.
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页数:9
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