{"title":"一种可注射、可生物降解的聚乙二醇共聚酯作为内皮细胞的载体","authors":"L. Suggs, C. Garcia, A. Mikos","doi":"10.1109/SBEC.1998.666672","DOIUrl":null,"url":null,"abstract":"INTRODUCTION We have developed a block copolymer of poly(propy1ene fumarate-co-ethylene glycol), P(PFCO-EG)’, in order to adprobIems with currcntIy used cardiovascular stenting materials. P(PF-co-EG) is crosslinkable through the fumarate double bonds forming a mechanicaUy stable hydrogel which degrades into fumaric acid, propylene glycol, and PEG. Because of these properties, P(F‘F-co-EG) has potential for use as an injectable, biodegradable implant. We propose to embed endotheIial cells during the crosslinking process and have assessed the feasibility of using this material as a carrier for endothelial cells. The cytotoxicity of preformed copolymer disks was examined as well as cell viabiLity upon embedding.","PeriodicalId":122159,"journal":{"name":"Proceedings of the 17th Southern Biomedical Engineering Conference","volume":"121 ","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1998-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"An Injectable, Biodegradable PEG Copolyester As A Carrier For Endothelial Cells\",\"authors\":\"L. Suggs, C. Garcia, A. Mikos\",\"doi\":\"10.1109/SBEC.1998.666672\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"INTRODUCTION We have developed a block copolymer of poly(propy1ene fumarate-co-ethylene glycol), P(PFCO-EG)’, in order to adprobIems with currcntIy used cardiovascular stenting materials. P(PF-co-EG) is crosslinkable through the fumarate double bonds forming a mechanicaUy stable hydrogel which degrades into fumaric acid, propylene glycol, and PEG. Because of these properties, P(F‘F-co-EG) has potential for use as an injectable, biodegradable implant. We propose to embed endotheIial cells during the crosslinking process and have assessed the feasibility of using this material as a carrier for endothelial cells. The cytotoxicity of preformed copolymer disks was examined as well as cell viabiLity upon embedding.\",\"PeriodicalId\":122159,\"journal\":{\"name\":\"Proceedings of the 17th Southern Biomedical Engineering Conference\",\"volume\":\"121 \",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1998-02-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Proceedings of the 17th Southern Biomedical Engineering Conference\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/SBEC.1998.666672\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Proceedings of the 17th Southern Biomedical Engineering Conference","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/SBEC.1998.666672","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
An Injectable, Biodegradable PEG Copolyester As A Carrier For Endothelial Cells
INTRODUCTION We have developed a block copolymer of poly(propy1ene fumarate-co-ethylene glycol), P(PFCO-EG)’, in order to adprobIems with currcntIy used cardiovascular stenting materials. P(PF-co-EG) is crosslinkable through the fumarate double bonds forming a mechanicaUy stable hydrogel which degrades into fumaric acid, propylene glycol, and PEG. Because of these properties, P(F‘F-co-EG) has potential for use as an injectable, biodegradable implant. We propose to embed endotheIial cells during the crosslinking process and have assessed the feasibility of using this material as a carrier for endothelial cells. The cytotoxicity of preformed copolymer disks was examined as well as cell viabiLity upon embedding.