涂有药物载体脂肪间充质干细胞的创新型伤口敷料可促进糖尿病患者的伤口愈合

Yinglin Bao, Feng Liu, Qing Xia, Qingxia Luan, Albandri Bin Ammar, Nessar Ahmed, M. Slevin, Kamela Ali, Donghui Liu
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引用次数: 0

摘要

伤口愈合受损与糖尿病患者的高血糖有关。高血糖会诱导蛋白质糖化并形成高级糖化终产物(AGEs),AGEs 在体内的积累会导致组织蛋白质的结构和功能发生改变。本研究对具有抗糖化活性的化合物(S-Ally1 半胱氨酸(SAC)、N-乙酰半胱氨酸(NAC)和模拟化合物 A)进行了评估。通过荧光法、十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)-银染色法、Western 印迹法和酶联免疫吸附试验(ELISA)等几种方法评估了几种抑制剂存在和不存在时的糖化程度。此外,这项研究还旨在评估和量化人脂肪间充质干细胞(hADMSCs)吸收和释放这些药物作为潜在疗法的潜力。为此,研究人员用 SAC/NAC 和模拟化合物 A 的组合来激发 hADMSCs,并使用高效液相色谱法(HPLC)分析其浓度。SAC/NAC和模拟化合物A能阻止AGEs的形成,而SAC/NAC和化合物A负载的hADMSCs的条件培养基(CM)能诱导BAECs的细胞迁移和管形成。hADMSCs为开发创新的靶向和药物输送系统提供了独特的机会,该系统能有效地将治疗药物输送到伤口或其他受损组织的特定区域。所提供的数据证明了 hADMSCs 作为一种药物输送方法具有改善伤口愈合的潜力,并可能为糖尿病并发症的发展提供潜在的靶向治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Innovative Wound Dressing Coated with Drug-Loaded Adipose Mesenchymal Stem Cells to Promote Wound Healing in Diabetes
Impaired wound healing is associated with hyperglycaemia in patients with diabetes. Hyperglycaemia induces protein glycation and the formation of Advanced Glycation End-Products (AGEs). The accumulation of AGEs in the body results in the structural and functional modification of tissue proteins. This study was conducted to evaluate compounds with antiglycation activities (S-Ally1 Cysteine (SAC), N-Acetylcysteine (NAC) and the mimic compound A). The extent of glycation in the presence and absence of several inhibitors was assessed via several methods including fluorescence, Sodium Dodecyl Sulphate-Polyacrylamide Gel Electrophoresis (SDS-PAGE)- silver stain, Western blotting, and Enzyme-Linked Immunosorbent Assays (ELISA). Additionally, this research aimed to evaluate and quantify the potential of Human Adipose Mesenchymal Stem Cells (hADMSCs) to uptake and release these drugs as potential therapeutics. To achieve this, hADMSCs were primed with a combination of SAC/NAC and mimic compound A and their concentrations were analysed using High-Performance Liquid Chromatography (HPLC). The SAC/NAC and mimic compound A prohibit the formation of AGEs while the Conditioned Medium (CM) from SAC/NACand compound A-loaded hADMSCs induced cell migration and tube formation in BAECs. hADMSCs provide a unique opportunity for the development of an innovative targeting and drug-delivery system which could effectively deliver therapeutics to specific regions of wounds or other damaged tissues. The data provided demonstrate the potential of hADMSCs as a drug delivery method with the potential to improve wound healing, and it may offer potential therapeutic targeting for the development of diabetic complications.
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