Superclear, Porous Cellulose Membranes with Chitosan-Coated Nanofibers for Visualized Cutaneous Wound Healing Dressing

Easy and rapid continuous large-scale industrial production of transparent visualized cutaneous wound healing dressing from natural polymers is very worth studying in medical natural polymer materials and multifunction gauze dressing design fields. In this work, superclear, porous cellulose membrane...

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Veröffentlicht in:ACS applied materials & interfaces 2020-05, Vol.12 (21), p.24370-24379
Hauptverfasser: Xia, Jian, Zhang, Hao, Yu, Faquan, Pei, Ying, Luo, Xiaogang
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container_end_page 24379
container_issue 21
container_start_page 24370
container_title ACS applied materials & interfaces
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creator Xia, Jian
Zhang, Hao
Yu, Faquan
Pei, Ying
Luo, Xiaogang
description Easy and rapid continuous large-scale industrial production of transparent visualized cutaneous wound healing dressing from natural polymers is very worth studying in medical natural polymer materials and multifunction gauze dressing design fields. In this work, superclear, porous cellulose membranes (CMs) with chitosan-coated nanofibers were fabricated using a simple, one-step electrostatic spinning technology and evaluated as potential wound dressings. First, the pure CMs were dissolved by a simple physical method, and then, the membranes were regenerated in an acidic coagulation bath by the casting method. The chitosan solution was polarized into nanofibers and formed a continuous fiber mat on CMs because of the charge repulsion between molecules. The prepared chitosan-coated CMs (CM-CS) were characterized by scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, differential scanning calorimetry, tensile tests, and so forth. The results indicated that CM-CS showed high wettability, hydrophilicity, and gas permeability, in addition to excellent light transmittance and mechanical compliance. Cell cytotoxicity and morphology assay and antibacterial activity against Escherichia coli and Staphylococcus aureus were also studied. They exhibited good biocompatibility and antibacterial activity of CM-CS. Moreover, evaluation of an in vivo wound healing model in mice revealed that CM-CS had a good effect in promoting wound healing. This work provided an easy and rapid continuous large-scale industrial design strategy for natural bioresource-based wound dressing materials, which could act as potential wound dressings for clinical use.
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Cell cytotoxicity and morphology assay and antibacterial activity against Escherichia coli and Staphylococcus aureus were also studied. They exhibited good biocompatibility and antibacterial activity of CM-CS. Moreover, evaluation of an in vivo wound healing model in mice revealed that CM-CS had a good effect in promoting wound healing. 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The prepared chitosan-coated CMs (CM-CS) were characterized by scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, differential scanning calorimetry, tensile tests, and so forth. The results indicated that CM-CS showed high wettability, hydrophilicity, and gas permeability, in addition to excellent light transmittance and mechanical compliance. Cell cytotoxicity and morphology assay and antibacterial activity against Escherichia coli and Staphylococcus aureus were also studied. They exhibited good biocompatibility and antibacterial activity of CM-CS. Moreover, evaluation of an in vivo wound healing model in mice revealed that CM-CS had a good effect in promoting wound healing. 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subjects Animals
Anti-Bacterial Agents - chemistry
Anti-Bacterial Agents - pharmacology
Bandages
Cell Survival - drug effects
Cellulose - chemistry
Chitosan - chemistry
Chitosan - pharmacology
Escherichia coli - drug effects
Hydrophobic and Hydrophilic Interactions
Membranes, Artificial
Mice, Inbred BALB C
Nanofibers - chemistry
Permeability
Porosity
Staphylococcus aureus - drug effects
Wettability
Wound Healing - drug effects
title Superclear, Porous Cellulose Membranes with Chitosan-Coated Nanofibers for Visualized Cutaneous Wound Healing Dressing
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