Department of Chemical Engineering, Indian Institute of Technology, Guwahati, Assam 781039, India.
Centre of Polymer Systems, University Institute, Tomas Bata University in Zlín, Tř. T. Bati 5678, 760 01 Zlín, Czech Republic.
ACS Appl Bio Mater. 2022 Aug 15;5(8):3722-3733. doi: 10.1021/acsabm.2c00226. Epub 2022 Jul 19.
Wound dressing materials fabricated using biocompatible polymers have become quite relevant in medical applications, and one such material is bacterial cellulose (BC) with exceptional properties in terms of biocompatibility, high purity, crystallinity (∼88%), and high water holding capacity. However, the lack of antibacterial activity slightly restricts its application as a wound dressing material. In this work, polycaprolactone (PCL) was first impregnated into the BC matrix to fabricate flexible bacterial cellulose-based PCL membranes (BCP), which was further functionalized with antibiotics gentamicin (GEN) and streptomycin (SM) separately, to form wound dressing composite scaffolds to aid infectious wound healing. Fourier transform infrared spectroscopy (FT-IR) results confirmed the presence of characteristic PCL and cellulose peaks in the composite scaffolds at 1720 cm, 3400 cm, and 2895 cm, respectively, explaining the successful interaction of PCL with the BC matrix, which is further corroborated by scanning electron microscopy (SEM) images. X-ray diffraction (XRD) studies revealed the formation of highly crystalline BCP films (∼86%). In vitro studies of the BC and BCP scaffolds against baby hamster kidney (BHK-21) cells revealed their cytocompatible nature; also the wettability studies indicated the hydrophilicity of the developed scaffolds, qualifying the main criterion in wound dressing applications. Energy dispersive X-ray analysis (EDX) of the drug loaded scaffolds showed the presence of sulfur in the composites. The prepared scaffolds also exhibited excellent antimicrobial activity against and . The release profiles initially indicated a burst release (6 h) followed by controlled release of GEN (∼42%) and SM (∼58%) from the prepared scaffolds within 48 h. Hence, these results interpret that the prepared drug-functionalized cellulosic scaffolds have great potential as a wound dressing material in biomedical applications.
基于生物相容性聚合物制备的创伤敷料材料在医学应用中变得非常重要,其中一种材料是具有出色生物相容性、高纯度、结晶度(约 88%)和高持水能力的细菌纤维素(BC)。然而,缺乏抗菌活性略微限制了其作为创伤敷料材料的应用。在这项工作中,首先将聚己内酯(PCL)浸渍到 BC 基质中,制备出具有柔韧性的细菌纤维素基 PCL 膜(BCP),然后分别用抗生素庆大霉素(GEN)和链霉素(SM)对其进行功能化,形成用于感染性伤口愈合的创伤敷料复合支架。傅里叶变换红外光谱(FT-IR)结果证实,复合支架在 1720 cm、3400 cm 和 2895 cm 处分别存在特征性的 PCL 和纤维素峰,分别解释了 PCL 与 BC 基质的成功相互作用,这进一步得到扫描电子显微镜(SEM)图像的证实。X 射线衍射(XRD)研究表明,形成了高结晶度的 BCP 薄膜(约 86%)。BC 和 BCP 支架对仓鼠肾细胞(BHK-21)的体外研究表明其具有细胞相容性;还表明了支架的润湿性研究,表明了所开发支架的亲水性,这是伤口敷料应用的主要标准。载药支架的能量色散 X 射线分析(EDX)表明复合材料中存在硫。制备的支架还表现出对 和 的优异抗菌活性。释放曲线最初表明存在突释(6 h),随后在 48 h 内从制备的支架中控制释放 GEN(约 42%)和 SM(约 58%)。因此,这些结果表明,制备的药物功能化纤维素支架作为生物医学应用中的伤口敷料材料具有很大的潜力。