Seo Young Kim, Karthika Muthuramalingam, Hyun Jong Lee
{"title":"Effects of fragmented polycaprolactone electrospun nanofiber in a hyaluronic acid hydrogel on fibroblasts","authors":"Seo Young Kim, Karthika Muthuramalingam, Hyun Jong Lee","doi":"10.1016/j.tice.2024.102582","DOIUrl":null,"url":null,"abstract":"<div><div>Hyaluronic acid (HA) hydrogels have shown promise as biomaterials for soft tissue engineering applications due to their biocompatibility and ability to mimic the extracellular matrix (ECM). However, their limited cell adhesion properties and the need for improved crosslinking methods have hindered their widespread use. In this study, we developed an ECM-mimicking HA hydrogel reinforced with alkaline hydrolyzed (1 M NaOH) fragmented (1.5 cm×1.5 cm) electrospun polycaprolactone (PCL) fibers to enhance cell adhesion and mechanical properties of HA hydrogel. Formation of HA hydrogel was achieved through a thiol-ene click reaction, which is initiated by exposure to visible blue light-activated biocompatible photoinitiator, riboflavin phosphate. The incorporation of alkaline hydrolyzed PCL fiber fragments (PFF) (0 %, 0.1 %, and 1 % w/v) into HA hydrogel precursor solution significantly increased the mechanical stiffness of the HA hydrogel, with the storage modulus ranging from 18.6 ± 0.7 Pa to 216.0 ± 38.2 Pa. The cytocompatibility of the PCL fiber-reinforced HA hydrogel was evaluated using NIH/3T3 fibroblasts. The results demonstrated improved cell adhesion, proliferation, and enhanced cellular functions, including increased production of glycosaminoglycans (GAGs) and collagen, in the PCL fiber-reinforced HA hydrogel compared to the control HA hydrogel. These findings suggest that the developed PCL fiber-reinforced HA hydrogel system, with tunable mechanical properties and excellent cytocompatibility, has potential applications in soft tissue engineering and regenerative medicine.</div></div>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0040816624002830","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0
Abstract
Hyaluronic acid (HA) hydrogels have shown promise as biomaterials for soft tissue engineering applications due to their biocompatibility and ability to mimic the extracellular matrix (ECM). However, their limited cell adhesion properties and the need for improved crosslinking methods have hindered their widespread use. In this study, we developed an ECM-mimicking HA hydrogel reinforced with alkaline hydrolyzed (1 M NaOH) fragmented (1.5 cm×1.5 cm) electrospun polycaprolactone (PCL) fibers to enhance cell adhesion and mechanical properties of HA hydrogel. Formation of HA hydrogel was achieved through a thiol-ene click reaction, which is initiated by exposure to visible blue light-activated biocompatible photoinitiator, riboflavin phosphate. The incorporation of alkaline hydrolyzed PCL fiber fragments (PFF) (0 %, 0.1 %, and 1 % w/v) into HA hydrogel precursor solution significantly increased the mechanical stiffness of the HA hydrogel, with the storage modulus ranging from 18.6 ± 0.7 Pa to 216.0 ± 38.2 Pa. The cytocompatibility of the PCL fiber-reinforced HA hydrogel was evaluated using NIH/3T3 fibroblasts. The results demonstrated improved cell adhesion, proliferation, and enhanced cellular functions, including increased production of glycosaminoglycans (GAGs) and collagen, in the PCL fiber-reinforced HA hydrogel compared to the control HA hydrogel. These findings suggest that the developed PCL fiber-reinforced HA hydrogel system, with tunable mechanical properties and excellent cytocompatibility, has potential applications in soft tissue engineering and regenerative medicine.
透明质酸(HA)水凝胶因其生物相容性和模拟细胞外基质(ECM)的能力而有望成为软组织工程应用的生物材料。然而,它们有限的细胞粘附特性和对改进交联方法的需求阻碍了它们的广泛应用。在本研究中,我们开发了一种仿细胞外基质的 HA 水凝胶,用碱性水解(1 M NaOH)的片段(1.5 cm×1.5 cm)电纺聚己内酯(PCL)纤维进行增强,以提高 HA 水凝胶的细胞粘附性和机械性能。HA 水凝胶的形成是通过硫醇-烯点击反应实现的,该反应是在可见蓝光激活的生物相容性光引发剂--核黄素磷酸酯的照射下启动的。将碱性水解 PCL 纤维片段(PFF)(0 %、0.1 % 和 1 % w/v)加入 HA 水凝胶前体溶液中可显著提高 HA 水凝胶的机械刚度,储存模量从 18.6 ± 0.7 Pa 增加到 216.0 ± 38.2 Pa。使用 NIH/3T3 成纤维细胞评估了 PCL 纤维增强 HA 水凝胶的细胞相容性。结果表明,与对照 HA 水凝胶相比,PCL 纤维增强 HA 水凝胶的细胞粘附性、增殖性和细胞功能均有所改善,包括糖胺聚糖(GAG)和胶原蛋白的生成增加。这些研究结果表明,所开发的 PCL 纤维增强 HA 水凝胶系统具有可调的机械性能和良好的细胞相容性,有望应用于软组织工程和再生医学领域。