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基于阳离子可德兰衍生物的用于生物医学应用的抗菌水凝胶

Antimicrobial Hydrogels Based on Cationic Curdlan Derivatives for Biomedical Applications.

作者信息

Suflet Dana M, Popescu Irina, Stanciu Magdalena-Cristina, Rimbu Cristina Mihaela

机构信息

Petru Poni Institute of Macromolecular Chemistry, Aleea Grigore Ghica Voda 41A, 700487 Iasi, Romania.

Faculty of Veterinary Medicine, "Ion Ionescu de la Brad" University of Life Sciences, Mihail Sadoveanu Alley 8, 707027 Iasi, Romania.

出版信息

Gels. 2024 Jun 27;10(7):424. doi: 10.3390/gels10070424.

Abstract

Hydrogels based on biocompatible polysaccharides with biological activity that can slowly release an active principle at the wound site represent promising alternatives to traditional wound dressing materials. In this respect, new hydrogels based on curdlan derivative with 2-hydroxypropyl dimethyl octyl ammonium groups (QCurd) and native curdlan (Curd) were obtained at room temperature by covalent cross-linking using a diepoxy cross-linking agent. The chemical structure of the QCurd/Curd hydrogels was investigated by Fourier transform infrared spectroscopy (FTIR) spectroscopy. Scanning electron microscopy (SEM) revealed well-defined regulated pores with an average diameter between 50 and 75 μm, and hydrophobic micro-domains of about 5 μm on the pore walls. The high swelling rate (21-24 g/g) and low elastic modulus values (7-14 kPa) make them ideal for medical applications as wound dressings. To evaluate the possible use of the curdlan-based hydrogels as active dressings, the loading capacity and release kinetics of diclofenac, taken as a model drug, were studied under simulated physiological skin conditions. Several mathematical models have been applied to evaluate drug transport processes and to calculate the diffusion coefficients. The prepared QCurd/Curd hydrogels were found to have good antibacterial properties, showing a bacteriostatic effect after 48 h against , , , and . The retarded drug delivery and antimicrobial properties of the new hydrogels support our hypothesis that they are candidates for the manufacture of wound dressings.

摘要

基于具有生物活性的生物相容性多糖的水凝胶,能够在伤口部位缓慢释放活性成分,是传统伤口敷料材料的有前景的替代品。在这方面,通过使用双环氧交联剂进行共价交联,在室温下获得了基于具有2-羟丙基二甲基辛基铵基团的凝胶多糖衍生物(QCurd)和天然凝胶多糖(Curd)的新型水凝胶。通过傅里叶变换红外光谱(FTIR)对QCurd/Curd水凝胶的化学结构进行了研究。扫描电子显微镜(SEM)显示出孔径明确且规则,平均直径在50至75μm之间,并且孔壁上有大约5μm的疏水微区。高溶胀率(21 - 24 g/g)和低弹性模量值(7 - 14 kPa)使其成为作为伤口敷料的医疗应用的理想选择。为了评估基于凝胶多糖的水凝胶作为活性敷料的可能用途,在模拟生理皮肤条件下研究了作为模型药物的双氯芬酸的负载能力和释放动力学。应用了几种数学模型来评估药物传输过程并计算扩散系数。发现制备的QCurd/Curd水凝胶具有良好的抗菌性能,对金黄色葡萄球菌、大肠杆菌、铜绿假单胞菌和白色念珠菌在48小时后显示出抑菌作用。新型水凝胶的缓释药物和抗菌性能支持了我们的假设,即它们是制造伤口敷料的候选材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de00/11276469/511af651a923/gels-10-00424-g001.jpg

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