Self-biomineralized in situ injectable CaSO4 nanorods-enriched collagen-hyaluronic acid composite hydrogels for biomimetic bone reconstruction in a minimally invasive manner
{"title":"Self-biomineralized in situ injectable CaSO4 nanorods-enriched collagen-hyaluronic acid composite hydrogels for biomimetic bone reconstruction in a minimally invasive manner","authors":"Xingzhu Liu, Yajie Zhang, Zahid Hussain, Penghui Zheng, Mingsheng Xu, Hongbo Zhao, Yuanshan Liu, Yi Cao, Ismat Ullah, Akiyoshi Osaka, Renjun Pei","doi":"10.1016/j.apmt.2022.101693","DOIUrl":null,"url":null,"abstract":"In situ injectable natural polymer-based hydrogels can be utilized to fill irregular defects and promote tissue regeneration. However, most hydrogels showed limited ability for self-biomineralization and can not guide the formation of new bone. Herein, according to the challenges encountered in advancing materials to clinical research, an injectable collagen-hyaluronic acid (Col-HA) hydrogel embedded with calcium sulfate nanorods (CSN) was developed via a bio-orthogonal reaction between norbornene (Nb) and tetrazine (Tz). The formulated [email protected] composite hydrogels not only have the potential to enhance cell adhesion and proliferation, but also serve as the system to control Ca2+ release. This composite hydrogel displayed impressive injectability, allowing straightforward in situ injection and subsequent adaption of composite hydrogels to irregularly shaped bone defects. CSN-incorporated composite hydrogels facilitate self-biomineralization, thereby fast-forming bone-like hydroxyapatite (HAp) within the hydrogel. Furthermore, Ca2+ released in a steady and sustained way from the composite hydrogels stimulated the differentiation of preosteoblasts, and promoted in situ bone growth. Our findings suggested that [email protected] composite hydrogels can successfully mediate the optimized CSN degradation, effectively accelerate HAp formation, and boost in situ bone development via the minimally invasive application.","PeriodicalId":94299,"journal":{"name":"Applied materials today","volume":"204 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied materials today","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.apmt.2022.101693","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
In situ injectable natural polymer-based hydrogels can be utilized to fill irregular defects and promote tissue regeneration. However, most hydrogels showed limited ability for self-biomineralization and can not guide the formation of new bone. Herein, according to the challenges encountered in advancing materials to clinical research, an injectable collagen-hyaluronic acid (Col-HA) hydrogel embedded with calcium sulfate nanorods (CSN) was developed via a bio-orthogonal reaction between norbornene (Nb) and tetrazine (Tz). The formulated [email protected] composite hydrogels not only have the potential to enhance cell adhesion and proliferation, but also serve as the system to control Ca2+ release. This composite hydrogel displayed impressive injectability, allowing straightforward in situ injection and subsequent adaption of composite hydrogels to irregularly shaped bone defects. CSN-incorporated composite hydrogels facilitate self-biomineralization, thereby fast-forming bone-like hydroxyapatite (HAp) within the hydrogel. Furthermore, Ca2+ released in a steady and sustained way from the composite hydrogels stimulated the differentiation of preosteoblasts, and promoted in situ bone growth. Our findings suggested that [email protected] composite hydrogels can successfully mediate the optimized CSN degradation, effectively accelerate HAp formation, and boost in situ bone development via the minimally invasive application.