School of Chemical, Materials and Biomedical Engineering, College of Engineering, University of Georgia, 220 Riverbend Road, Athens, Georgia 30602, United States.
ACS Biomater Sci Eng. 2020 Apr 13;6(4):2062-2071. doi: 10.1021/acsbiomaterials.0c00146. Epub 2020 Mar 25.
Hydrogen sulfide (HS) is an endogenous gasotransmitter in the human body involved in various physiological functions including cytoprotection, maintaining homeostasis, and regulation of organ development. Therefore, HS-releasing polymers that can imitate endogenous HS release can offer great therapeutic potential. Despite decades of research, the use of HS donors in medical device applications is mostly unexplored largely due to the challenge of the steady HS release from a suitable polymeric platform that does not compromise the normal cellular functions of the host. In this work, an exogenous HS release system was developed by integrating sodium sulfide (NaS), a common HS donor, into a medical-grade thermoplastic silicone-polycarbonate-urethane polymer, Carbosil 20 80A (hereon as Carbosil), via a facile solvent evaporation technique. The spatial distribution and nature of NaS in Carbosil were characterized through X-ray diffraction (XRD) spectroscopy and field emission scanning electron microscopy (FESEM) with energy-dispersive spectroscopy (EDS), indicating an amorphous phase shift upon incorporating NaS in Carbosil. The composite, NaS-Carbosil, is responsive in physiological conditions, resulting in sustained HS release measured for 3 h. cellular responses of 3T3 mouse fibroblasts, human lung epithelial (HLE), and primary human umbilical vein endothelial cells (HUVEC) were investigated. Fibroblast cells showed cell proliferation in 24 h and complete cell migration in 42 h . The NaS-Carbosil composites were cytocompatible toward HUVEC and HLE cells. This study provided important proof of concept that warrants potential use of these HS-releasing platforms in engineering biomedical devices, tissue engineering, and drug delivery applications.
硫化氢(HS)是人体内的一种内源性气体递质,参与多种生理功能,包括细胞保护、维持内稳态和调节器官发育。因此,能够模拟内源性 HS 释放的 HS 释放聚合物具有巨大的治疗潜力。尽管经过几十年的研究,但由于从合适的聚合物平台稳定释放 HS 而不损害宿主正常细胞功能的挑战,HS 供体在医疗器械应用中的使用大多仍未得到探索。在这项工作中,通过简便的溶剂蒸发技术,将常见的 HS 供体硫化钠(NaS)整合到医用级热塑性硅酮-聚碳酸酯-聚氨酯聚合物 Carbosil 20 80A(以下简称 Carbosil)中,开发了一种外源性 HS 释放系统。通过 X 射线衍射(XRD)光谱和场发射扫描电子显微镜(FESEM)与能量色散光谱(EDS)对 Carbosil 中 NaS 的空间分布和性质进行了表征,表明在 Carbosil 中掺入 NaS 后发生非晶相转变。该复合材料 NaS-Carbosil 在生理条件下具有响应性,可测量到 3 小时的持续 HS 释放。研究了 3T3 小鼠成纤维细胞、人肺上皮(HLE)和原代人脐静脉内皮细胞(HUVEC)的细胞反应。成纤维细胞在 24 小时内表现出细胞增殖,在 42 小时内完全迁移。NaS-Carbosil 复合材料对 HUVEC 和 HLE 细胞均具有细胞相容性。这项研究提供了重要的概念验证,证明了这些 HS 释放平台在工程生物医学设备、组织工程和药物输送应用中具有潜在用途。