Rashid Saman, Ijaz Munaza, Rafique Sana, Yasin Haya, Mushtaq Mahnoor, Khan Abida Kalsoom, Khan Madiha, Nasir Bushra, Murtaza Ghulam
Faculty of Pharmacy, Bahauddin Zakariya University, Multan, Pakistan.
Department of Microbiology, University of Central Punjab, Lahore, Pakistan.
Curr Drug Deliv. 2025 Jun 18. doi: 10.2174/0115672018374558250607134659.
This study aims to fabricate dual drug-loaded nanofibrous films made from polyvinyl alcohol (PVA) and chitosan, incorporating cefadroxil and mupirocin to meet the critical needs of burn wound care.
Electrospinning was utilized to fabricate cefadroxil- and mupirocin-loaded polyvinyl alcohol PVA/Chitosan nanofibers. Characterization of structural and morphological properties of these nanofibers was done through Fourier Transform IR Spectroscopy, Scanning Electron Microscopy, Thermal analysis by TGA, and XRD spectroscopy. The kinetic profiles of the drug release mechanisms were considered to determine the release of cefadroxil and mupirocin. Antibacterial activity was determined against the bacteria Staphylococcus aureus and Pseudomonas aeruginosa, while the wound healing efficacy was tested in a rabbit model using full-thickness wounds.
SEM analysis demonstrated the formation of uniform and smooth nanofibers possessing a well-defined morphology. FTIR spectroscopy confirmed the successful incorporation of cefadroxil and mupirocin into the PVA/Chitosan matrix. TGA analysis indicated the thermal stability of the nanofibers, while XRD results suggested that the drugs were either molecularly dispersed or in an amorphous state within the biopolymeric blend. Drug release studies showed distinct profiles, with an initial burst release followed by sustained drug release. Over 80% of mupirocin was released within the first 2 hours, while cefadroxil exhibited a cumulative release exceeding 60%. Antibacterial assays showed significant inhibition zones, with the largest being 20 mm against Staphylococcus aureus. In vivo studies utilizing a full-thickness rabbit wound model revealed that the drug-loaded nanofibers accelerated wound contraction, achieving approximately 90% closure by day 17, compared to less than 70% for the control.
The study demonstrates that cefadroxil-mupirocin nanofiber films provide superior antibacterial activity and faster wound healing rates, highlighting their potential in advanced burn wound management.
本研究旨在制备由聚乙烯醇(PVA)和壳聚糖制成的载双药纳米纤维膜,其中包含头孢羟氨苄和莫匹罗星,以满足烧伤创面护理的关键需求。
采用静电纺丝法制备载头孢羟氨苄和莫匹罗星的聚乙烯醇PVA/壳聚糖纳米纤维。通过傅里叶变换红外光谱、扫描电子显微镜、热重分析(TGA)和X射线衍射光谱对这些纳米纤维的结构和形态特性进行表征。考虑药物释放机制的动力学曲线来确定头孢羟氨苄和莫匹罗星的释放情况。测定对金黄色葡萄球菌和铜绿假单胞菌的抗菌活性,同时在兔全层伤口模型中测试伤口愈合效果。
扫描电子显微镜分析表明形成了形态明确、均匀光滑的纳米纤维。傅里叶变换红外光谱证实头孢羟氨苄和莫匹罗星成功掺入PVA/壳聚糖基质中。热重分析表明纳米纤维具有热稳定性,而X射线衍射结果表明药物在生物聚合物共混物中要么是分子分散状态,要么是无定形状态。药物释放研究显示出不同的曲线,先是初始突释,然后是持续药物释放。超过80%的莫匹罗星在最初2小时内释放,而头孢羟氨苄的累积释放超过60%。抗菌试验显示出明显的抑菌圈,对金黄色葡萄球菌的最大抑菌圈为20毫米。利用兔全层伤口模型进行的体内研究表明,载药纳米纤维加速了伤口收缩,在第17天时伤口闭合率达到约90%,而对照组不到70%。
该研究表明头孢羟氨苄-莫匹罗星纳米纤维膜具有卓越的抗菌活性和更快的伤口愈合速度,突显了其在烧伤创面高级管理中的潜力。