Construction of sodium alginate/konjac glucomannan/chitosan oligosaccharide/Zeolite P hydrogel microspheres loaded with potassium diformate for sustained intestinal bacterial inhibition. (5th June 2022)
- Record Type:
- Journal Article
- Title:
- Construction of sodium alginate/konjac glucomannan/chitosan oligosaccharide/Zeolite P hydrogel microspheres loaded with potassium diformate for sustained intestinal bacterial inhibition. (5th June 2022)
- Main Title:
- Construction of sodium alginate/konjac glucomannan/chitosan oligosaccharide/Zeolite P hydrogel microspheres loaded with potassium diformate for sustained intestinal bacterial inhibition
- Authors:
- Yang, ZhongXin
Yang, YuHang
Zhang, XiaoNan
Fu, Bei
Xu, WenQin
Xue, DengPing
Chen, NanChun
Wang, XiuLi
Xie, QingLin - Abstract:
- Graphical abstract: Highlights: Optimization of preparation of hydrogel microspheres by using response surface methodology. ALG/KGM/COS/Zeolite P hydrogel microspheres with pH sensitivity. Zeolite P as a key factor to control release of hydrogel microspheres. The great potential of ALG/KGM/COS/Zeolite P hydrogel microspheres in intestinal bacterial inhibition. Abstract: Owing to their non-toxicity and non-resistance to bacteria, potassium diformate (KDF) bacterial inhibitors may act as antibacterials in the intestinal tract and are good alternatives to antibiotics; however, KDF has low intestinal utilization rate when used directly. We prepared pH-sensitive sodium alginate (ALG)/konjac glucomannan (KGM)/chitosan oligosaccharide (COS)/Zeolite P hydrogel microspheres for the slow release of KDF using a complex coalescence method to ensure better bacterial inhibition and balance of the gut flora in the intestine. We found that the hydrogen bonding interaction between ALG and KGM, chelating interaction between ALG and Ca 2+, and electrostatic interaction of COS together build a three-dimensional porous network structure. Notably, Zeolite P contributes to the formation of a dense three-dimensional network structure to avoid premature release of KDF in the stomach, improve the stability of KDF and prolong its release in the intestine. In vitro bacterial inhibition experiments showed that the maximum antibacterial rates of the hydrogel microspheres were 92 ± 3%, 86 ± 4%, andGraphical abstract: Highlights: Optimization of preparation of hydrogel microspheres by using response surface methodology. ALG/KGM/COS/Zeolite P hydrogel microspheres with pH sensitivity. Zeolite P as a key factor to control release of hydrogel microspheres. The great potential of ALG/KGM/COS/Zeolite P hydrogel microspheres in intestinal bacterial inhibition. Abstract: Owing to their non-toxicity and non-resistance to bacteria, potassium diformate (KDF) bacterial inhibitors may act as antibacterials in the intestinal tract and are good alternatives to antibiotics; however, KDF has low intestinal utilization rate when used directly. We prepared pH-sensitive sodium alginate (ALG)/konjac glucomannan (KGM)/chitosan oligosaccharide (COS)/Zeolite P hydrogel microspheres for the slow release of KDF using a complex coalescence method to ensure better bacterial inhibition and balance of the gut flora in the intestine. We found that the hydrogen bonding interaction between ALG and KGM, chelating interaction between ALG and Ca 2+, and electrostatic interaction of COS together build a three-dimensional porous network structure. Notably, Zeolite P contributes to the formation of a dense three-dimensional network structure to avoid premature release of KDF in the stomach, improve the stability of KDF and prolong its release in the intestine. In vitro bacterial inhibition experiments showed that the maximum antibacterial rates of the hydrogel microspheres were 92 ± 3%, 86 ± 4%, and 88 ± 4% against Escherichia coli, Staphylococcus aureus, and Bacillus subtilis, respectively, indicating that they can effectively inhibit bacterial growth and balance the bacterial flora. In addition, hydrogel antibacterial microspheres are biodegradable and non-cytotoxic. Thus, ALG/KGM/COS/Zeolite P hydrogel microspheres may be used for colon-targeted delivery of drugs. … (more)
- Is Part Of:
- European polymer journal. Volume 172(2022)
- Journal:
- European polymer journal
- Issue:
- Volume 172(2022)
- Issue Display:
- Volume 172, Issue 2022 (2022)
- Year:
- 2022
- Volume:
- 172
- Issue:
- 2022
- Issue Sort Value:
- 2022-0172-2022-0000
- Page Start:
- Page End:
- Publication Date:
- 2022-06-05
- Subjects:
- Hydrogel microspheres -- Bacterial inhibition -- Response surface methodology
Polymers -- Periodicals
Polymerization -- Periodicals
Polymères -- Périodiques
Polymérisation -- Périodiques
Polymerization
Polymers
Periodicals
Electronic journals
547.705 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00143057 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.eurpolymj.2022.111233 ↗
- Languages:
- English
- ISSNs:
- 0014-3057
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3829.791000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 21503.xml