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1.
Int J Biol Macromol ; 247: 125504, 2023 Aug 30.
Article in English | MEDLINE | ID: mdl-37356692

ABSTRACT

Preventing wound infection is a major challenge in biomedicine. Conventional wound dressings often have poor moisturizing and antimicrobial properties unfavorable for wound healing. In this study, we prepared a multifunctional electrospun nanofiber dressing (PCQX-M) containing xyloglucan, quaternized chitosan, Polyvinyl alcohol, and collagen. By applying the concept of wet healing, xyloglucan and quaternized chitosan polysaccharides with excellent water solubility were employed to improve the absorption and moisturizing properties and maintain a moist microenvironment for the wound healing process. PCQX-M demonstrated high mechanical, thermodynamic, and biocompatible properties, providing suitable healing conditions for wounds. In addition, PCQX-M showed exceptional antibacterial properties and a potential inhibitory effect on the growth of microorganisms in infected wounds. More intriguingly, the restorative healing effect was investigated on a mouse model of whole skin injury infected with Staphylococcus aureus. Wound healing, collagen deposition, and immunofluorescence results showed that PCQX-M significantly promoted cell proliferation and angiogenesis at the injury site and facilitated the healing of the infected wound. Our study suggests that PCQX-M has excellent potential for clinical application in infected wound healing.


Subject(s)
Chitosan , Nanofibers , Wound Infection , Mice , Animals , Chitosan/pharmacology , Wound Healing , Anti-Bacterial Agents/pharmacology , Anti-Bacterial Agents/therapeutic use , Bandages/microbiology , Collagen/pharmacology , Wound Infection/drug therapy
2.
Chem Biol Drug Des ; 90(5): 943-952, 2017 Nov.
Article in English | MEDLINE | ID: mdl-28498641

ABSTRACT

Twenty-one novel 5-phenyl-1,3,4-oxadiazole-2-thiol (POT) substituted N-hydroxyethyl quaternary ammonium salts (6a-g, 7a-g, 8a-g) were prepared and characterized by FTIR, NMR, and elemental analysis. Compounds 6a, 6c, and 8a were confirmed by X-ray single-crystal diffraction. They display the unsurpassed antibacterial activity against Staphylococcus aureus, α-H-tococcus, Escherichia coli, P. aeruginosa, Proteus vulgaris, Canidia Albicans, especially 6g, 7g, 8g with dodecyl group. Compounds 8a-d with N,N-dihydroxyethyl and POT groups display unsurpassed antibacterial activity and non-toxicity. The structure-activity relationships indicate that POT and flexible dihydroxyethyl group in QAS are necessary for antibacterial activity and cytotoxicity. SEM and TEM images of E. coli morphologies of 8d show the antibacterial agents can adhere to membrane surfaces to inhibit bacterial growth by disrupting peptidoglycan formation and releasing bacterial cytoplasm from cell membranes.


Subject(s)
Anti-Bacterial Agents/pharmacology , Bacteria/drug effects , Oxadiazoles/pharmacology , Quaternary Ammonium Compounds/pharmacology , Anti-Bacterial Agents/chemistry , Bacterial Infections/drug therapy , Escherichia coli/drug effects , Humans , Microbial Sensitivity Tests , Models, Molecular , Oxadiazoles/chemistry , Proteus vulgaris/drug effects , Quaternary Ammonium Compounds/chemistry , Staphylococcus aureus/drug effects , Structure-Activity Relationship
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