梨形番茄β- d-葡聚糖的分离、表征及创面愈合潜力研究

IF 3.1 4区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Elif Yavuz-Dokgöz, Meltem Güleç, Burçin İzbudak, Onur Şahin, Ayça Bal-Öztürk
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引用次数: 0

摘要

蘑菇已经成为替代医学的一个突出焦点,现在是越来越详细的科学研究的主题。本研究探讨了从梨形番茄中分离、纯化和表征β- d-葡聚糖,特别强调了其伤口愈合潜力。本研究的目的是从蘑菇的自然栖息地中分离、纯化和表征β-葡聚糖化合物。采用凝胶渗透色谱(GPC)、傅里叶变换红外光谱(FTIR)和核磁共振(NMR)光谱对化合物进行了表征。使用NIH 3T3细胞评估体外细胞毒性,并通过电子显微镜评估表面形态。光谱分析(GPC, FTIR和NMR)证实了β-(1→3)和β-(1→6)键的存在,并表明分离的β- d -葡聚糖具有多分散性。细胞毒性试验显示,即使浓度为1000 μg/mL,对NIH 3T3细胞也无毒性作用。较低浓度(20、100和500 μg/mL)可促进细胞迁移和伤口愈合。溶血活性维持在5%以下。研究结果表明,从梨形番茄中提取的β- d -葡聚糖可能因其无毒、血液相容性和促凝特性而促进伤口愈合。未来的研究将集中在阐明其作用机制和评估临床疗效上。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Isolation, Characterization, and Wound-Healing Potential of β-D-Glucan from Lycoperdon pyriforme Schaeff.

Mushrooms have become a prominent focus in alternative medicine and are now the subject of increasingly detailed scientific investigation. This study explores the isolation, purification, and characterization of β-D-glucan from Lycoperdon pyriforme, with particular emphasis on its wound-healing potential. The aim of this research is to isolate, purify, and characterize β-glucan compounds from mushrooms collected in their natural habitat. Gel permeation chromatography (GPC), Fourier transform infrared spectroscopy (FTIR), and nuclear magnetic resonance (NMR) spectroscopy are employed to characterize the compound. In vitro cytotoxicity is assessed using NIH 3T3 cells, and surface morphology is evaluated via electron microscopy. Spectroscopic analyses (GPC, FTIR, and NMR) confirmed the presence of β-(1 → 3) and β-(1 → 6) linkages and indicated polydispersity in the isolated β-D-glucan. Cytotoxicity assays show no toxic effect on NIH 3T3 cells, even at 1000 μg/mL. Lower concentrations (20, 100, and 500 μg/mL) promoted cell migration and wound closure in scratch assays. Hemolytic activity remained below 5%. The findings suggest that β-D-glucan from Lycoperdon pyriforme may support wound healing due to its non-toxic, hemocompatible, and coagulation-promoting properties. Future studies will focus on elucidating its mechanisms of action and evaluating clinical efficacy.

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来源期刊
ChemistryOpen
ChemistryOpen CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
4.80
自引率
4.30%
发文量
143
审稿时长
1 months
期刊介绍: ChemistryOpen is a multidisciplinary, gold-road open-access, international forum for the publication of outstanding Reviews, Full Papers, and Communications from all areas of chemistry and related fields. It is co-owned by 16 continental European Chemical Societies, who have banded together in the alliance called ChemPubSoc Europe for the purpose of publishing high-quality journals in the field of chemistry and its border disciplines. As some of the governments of the countries represented in ChemPubSoc Europe have strongly recommended that the research conducted with their funding is freely accessible for all readers (Open Access), ChemPubSoc Europe was concerned that no journal for which the ethical standards were monitored by a chemical society was available for such papers. ChemistryOpen fills this gap.
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