Self-crosslinked chitosan/dialdehyde xanthan gum blended hypromellose hydrogel for the controlled delivery of ampicillin, minocycline and rifampicin
Language English Country Netherlands Media print-electronic
Document type Journal Article
PubMed
33212108
DOI
10.1016/j.ijbiomac.2020.11.100
PII: S0141-8130(20)35025-X
Knihovny.cz E-resources
- Keywords
- Antibacterial activity, Antibiotic drug delivery, Biopolymers, Hydrogel,
- MeSH
- Ampicillin pharmacology MeSH
- Anti-Bacterial Agents pharmacology MeSH
- Polysaccharides, Bacterial chemistry MeSH
- Biocompatible Materials chemistry MeSH
- Cell Line MeSH
- Chitosan chemistry MeSH
- Hypromellose Derivatives chemistry MeSH
- Escherichia coli drug effects MeSH
- Fibroblasts MeSH
- Hydrogels chemical synthesis chemistry pharmacokinetics toxicity MeSH
- Hydrogen-Ion Concentration MeSH
- Microbial Sensitivity Tests MeSH
- Microscopy, Electron, Scanning MeSH
- Minocycline pharmacology MeSH
- Mice MeSH
- Drug Carriers chemistry MeSH
- Rheology MeSH
- Rifampin pharmacology MeSH
- Spectroscopy, Fourier Transform Infrared MeSH
- Staphylococcus aureus drug effects MeSH
- Thermogravimetry MeSH
- Drug Liberation MeSH
- Cell Survival drug effects MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Ampicillin MeSH
- Anti-Bacterial Agents MeSH
- Polysaccharides, Bacterial MeSH
- Biocompatible Materials MeSH
- Chitosan MeSH
- Hypromellose Derivatives MeSH
- Hydrogels MeSH
- Minocycline MeSH
- Drug Carriers MeSH
- Rifampin MeSH
- xanthan gum MeSH Browser
The design of improved biopolymeric based hydrogel materials with high load-capacity to serve as biocompatible drug carriers is a challenging task with vital implications in health sciences. In this work, chitosan crosslinked dialdehyde xanthan gum interpenetrated hydroxypropyl methylcellulose gels were developed for the controlled delivery of different antibiotic drugs including ampicillin, minocycline and rifampicin. The prepared hydrogel scaffolds were characterized by rheology method, FTIR, SEM, TGA and compression analysis. In addition, gelation kinetics, swelling, in vitro degradation and drug release rate were studied under simulated gastrointestinal fluid conditions of pH 2.0 and 7.4 at 37 °C. Results demonstrated the gel composition and structure affected drug release kinetics. The release study showed more than 50% cumulative release within 24 h for all investigated antibiotic drugs. In vitro cell cytocompatibility using mouse embryonic fibroblast cell lines depicted ≥80% cell viability, indicating the gels are non-toxic. Finally, the antibacterial activity of loaded gels was evaluated against Gram-negative and positive bacteria (Escherichia coli, Staphylococcus aureus and Klebsiella pneumonia), which correlated well with swelling and drug release results. Overall, the present study demonstrated that the produced hydrogel scaffolds serves as promising material for controlled antibiotic delivery towards microbial growth inhibition.
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