In vitro Analysis of XLAsp-P2 Peptide Loaded Cellulose Acetate Nanofiber for Wound Healing.

IF 3.7 3区 医学 Q2 CHEMISTRY, MEDICINAL
Saranya Selvaraj, Monali Perera, Piumika Yapa, Imalka Munaweera, Inoka C Perera, Tharindu Senapathi, Laksiri Weerasinghe
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Abstract

Recently, nanofiber-based wound dressings are currently a viable strategy to expedite the healing of wounds by providing a suitable microenvironment for tissue growth with active ingredients. This research study subjects the development of electrospun cellulose acetate (CA) nanofibers loaded with the XLAsp-P2, an antimicrobial peptide (AMP) that holds great potential for enhanced wound healing as a therapeutic agent. The synthesized XLAsp-P2-loaded CA nanofibers were fabricated via three loading percentages, 0.1 %, 0.2 %, and 0.3 % w/w, and characterized and evaluated their antimicrobial potential with MTT assay and Agar overlay methods as an alternative strategy. FT-IR analysis confirmed the compatibility of the peptide loaded CA nanocomposite, showing distinct peaks corresponding to the constituent materials. Scanning electron microscopy (SEM) analysis was employed to characterize the morphology of electrospun peptide CA nanocomposites and illustrate the fiber's size at the nanoscale. The in vitro release study during the 24 hrs, 87 % of the peptide was released which was approximately 5.2 mg; which was closer matched to the square root model of Higuchi at room temperature. MTT assay presented sensitive results towards Gram-positive bacteria compared to Gram Negative bacteria; which corresponded to the inhibition zones of the Agar overlay method proving that Escherichia coli (ATCC 25922) 17.66 ± 0.38 mm and Pseudomonas aeruginosa (ATCC 27853) 17.44 ± 0.38 mm exhibited moderate susceptibility, while Staphylococcus aureus (ATCC 25923)19.89 ± 0.69 mm and Bacillus cereus (ATCC 11778) 23.00 ± 0.33 mm showed promising responses. Collectively, The study's findings indicate that the XLAsp-P2 incorporated CA mat possesses an opportunity to function as an efficient platform for delivering therapeutic peptides.

用于伤口愈合的 XLAsp-P2 肽负载醋酸纤维素纳米纤维的体外分析
最近,以纳米纤维为基础的伤口敷料是一种可行的策略,它能为含有活性成分的组织生长提供合适的微环境,从而加快伤口愈合。本研究的主题是开发负载了 XLAsp-P2 的电纺醋酸纤维素(CA)纳米纤维,XLAsp-P2 是一种抗菌肽(AMP),作为一种治疗剂,它在促进伤口愈合方面具有巨大潜力。通过 0.1%、0.2% 和 0.3% w/w 三种负载百分比合成了负载 XLAsp-P2 的醋酸纤维,并采用 MTT 检测法和琼脂覆盖法作为一种替代策略对其抗菌潜力进行了表征和评估。傅立叶变换红外分析证实了多肽负载 CA 纳米复合材料的相容性,显示出与组成材料相对应的明显峰值。扫描电子显微镜(SEM)分析表明了电纺多肽 CA 纳米复合材料的形态特征,并显示了纤维的纳米级尺寸。在 24 小时的体外释放研究中,87% 的肽被释放出来,约为 5.2 毫克;这与室温下的樋口平方根模型比较接近。与革兰氏阴性菌相比,MTT 法对革兰氏阳性菌更敏感;这与琼脂覆盖法的抑菌区一致,证明大肠杆菌(ATCC 25922)17.66 ± 0.38 毫米和铜绿假单胞菌(ATCC 27853)17.44 ± 0.38 毫米表现出中等敏感性,而金黄色葡萄球菌(ATCC 25923)19.89 ± 0.69 毫米和蜡样芽孢杆菌(ATCC 11778)23.00 ± 0.33 毫米表现出良好的反应。总之,研究结果表明,含有 XLAsp-P2 的 CA 垫有机会成为递送治疗肽的有效平台。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.30
自引率
13.20%
发文量
367
审稿时长
33 days
期刊介绍: The Journal of Pharmaceutical Sciences will publish original research papers, original research notes, invited topical reviews (including Minireviews), and editorial commentary and news. The area of focus shall be concepts in basic pharmaceutical science and such topics as chemical processing of pharmaceuticals, including crystallization, lyophilization, chemical stability of drugs, pharmacokinetics, biopharmaceutics, pharmacodynamics, pro-drug developments, metabolic disposition of bioactive agents, dosage form design, protein-peptide chemistry and biotechnology specifically as these relate to pharmaceutical technology, and targeted drug delivery.
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