An edible kanamycin sulfate cross-linked cellulose active against multiple pathogenic bacteria.
Antibacterial
Carrier
Cellulose
Cross-link
Kanamycin sulfate
Journal
International journal of biological macromolecules
ISSN: 1879-0003
Titre abrégé: Int J Biol Macromol
Pays: Netherlands
ID NLM: 7909578
Informations de publication
Date de publication:
01 Jan 2022
01 Jan 2022
Historique:
received:
24
09
2021
revised:
06
11
2021
accepted:
14
11
2021
pubmed:
22
11
2021
medline:
4
1
2022
entrez:
21
11
2021
Statut:
ppublish
Résumé
In this work, an edible cellulose-based antibacterial material was prepared by cross-linking α-cellulose and kanamycin sulfate via glutaraldehyde to form kanamycin sulfate-glutaraldehyde-cellulose. Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy and X-ray diffraction results indicated that the kanamycin sulfate molecule was cross-linked with the molecular chain of cellulose. The optimal mass ratio of kanamycin sulfate to α-cellulose was 1:100 and the degree of substitution reached 1.11%. The optimal kanamycin sulfate-glutaraldehyde-cellulose material showed an excellent inhabitation against both Gram-positive and Gram-negative bacteria. Meantime, the optimal kanamycin sulfate-glutaraldehyde-cellulose had a marked resistance to gastric acid and had low cell cytotoxicity. To promote the application of the kanamycin sulfate-glutaraldehyde-cellulose material, the porous microspheres were prepared via the sol-gel method. The particle size of the homogeneous porous microspheres is mainly distributed between 1.5 and 2.0 μm. Therefore, the kanamycin sulfate-glutaraldehyde-cellulose described herein is a potential edible, eco-friendly, potent, stable, inexpensive, and antibacterial carrier material for delivering drugs, proteins, or vaccines.
Identifiants
pubmed: 34801585
pii: S0141-8130(21)02490-9
doi: 10.1016/j.ijbiomac.2021.11.085
pii:
doi:
Substances chimiques
Anti-Bacterial Agents
0
Kanamycin
59-01-8
Cellulose
9004-34-6
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
435-444Informations de copyright
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