Bas van Bochove*, Lieke H.A. van Dommelen, Anne-Constance Macarez, Marc Ankoné, Elly M.M. Versteeg, Toin H. van Kuppevelt, Willeke F. Daamen, André A. Poot and Dirk W. Grijpma,
{"title":"基于不溶性胶原蛋白和聚碳酸三甲酯的光交联多孔杂化网络。","authors":"Bas van Bochove*, Lieke H.A. van Dommelen, Anne-Constance Macarez, Marc Ankoné, Elly M.M. Versteeg, Toin H. van Kuppevelt, Willeke F. Daamen, André A. Poot and Dirk W. Grijpma, ","doi":"10.1021/acs.biomac.5c00971","DOIUrl":null,"url":null,"abstract":"<p >Porous hybrid networks were formed from methacrylated collagen (ICol-MA) fibrils and methacrylated PTMC (PTMC-tMA). Dispersing ICol-MA and dissolving PTMC-tMA in DMSO acidified with HCl (DMSO/HCl), followed by mixing, casting, freezing, photo-cross-linking, and solvent extraction, resulted in networks with high porosities and gel contents. ATR-FTIR showed that hybrid networks had compositions similar to the mixture compositions prior to photo-cross-linking. Mechanical testing of porous hybrid networks, in particular the ICol-MA:PTMC-tMA 17:83 wt % network, showed improved mechanical properties compared to non-cross-linked ICol and ICol-MA networks prepared in DMSO/HCl. Additionally, cross-linking alone already improves the properties of porous collagen structures. Interestingly, photo-cross-linking ICol-MA in acetic acid solution resulted in the best mechanical properties, suggesting that the solvent affects collagen fibril structure and thus network mechanical properties. Indeed, acetic acid does not alter the collagen banding structure, whereas DMSO/HCl does. Thus, further investigation into the effect of the solvent on the network properties is needed.</p>","PeriodicalId":30,"journal":{"name":"Biomacromolecules","volume":"26 8","pages":"5399–5408"},"PeriodicalIF":5.4000,"publicationDate":"2025-07-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/pdf/10.1021/acs.biomac.5c00971","citationCount":"0","resultStr":"{\"title\":\"Photo-Cross-Linked Porous Hybrid Networks Based on Insoluble Collagen and Poly(trimethylene carbonate)\",\"authors\":\"Bas van Bochove*, Lieke H.A. van Dommelen, Anne-Constance Macarez, Marc Ankoné, Elly M.M. Versteeg, Toin H. van Kuppevelt, Willeke F. Daamen, André A. Poot and Dirk W. Grijpma, \",\"doi\":\"10.1021/acs.biomac.5c00971\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Porous hybrid networks were formed from methacrylated collagen (ICol-MA) fibrils and methacrylated PTMC (PTMC-tMA). Dispersing ICol-MA and dissolving PTMC-tMA in DMSO acidified with HCl (DMSO/HCl), followed by mixing, casting, freezing, photo-cross-linking, and solvent extraction, resulted in networks with high porosities and gel contents. ATR-FTIR showed that hybrid networks had compositions similar to the mixture compositions prior to photo-cross-linking. Mechanical testing of porous hybrid networks, in particular the ICol-MA:PTMC-tMA 17:83 wt % network, showed improved mechanical properties compared to non-cross-linked ICol and ICol-MA networks prepared in DMSO/HCl. Additionally, cross-linking alone already improves the properties of porous collagen structures. Interestingly, photo-cross-linking ICol-MA in acetic acid solution resulted in the best mechanical properties, suggesting that the solvent affects collagen fibril structure and thus network mechanical properties. Indeed, acetic acid does not alter the collagen banding structure, whereas DMSO/HCl does. Thus, further investigation into the effect of the solvent on the network properties is needed.</p>\",\"PeriodicalId\":30,\"journal\":{\"name\":\"Biomacromolecules\",\"volume\":\"26 8\",\"pages\":\"5399–5408\"},\"PeriodicalIF\":5.4000,\"publicationDate\":\"2025-07-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.acs.org/doi/pdf/10.1021/acs.biomac.5c00971\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biomacromolecules\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.biomac.5c00971\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomacromolecules","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.biomac.5c00971","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Photo-Cross-Linked Porous Hybrid Networks Based on Insoluble Collagen and Poly(trimethylene carbonate)
Porous hybrid networks were formed from methacrylated collagen (ICol-MA) fibrils and methacrylated PTMC (PTMC-tMA). Dispersing ICol-MA and dissolving PTMC-tMA in DMSO acidified with HCl (DMSO/HCl), followed by mixing, casting, freezing, photo-cross-linking, and solvent extraction, resulted in networks with high porosities and gel contents. ATR-FTIR showed that hybrid networks had compositions similar to the mixture compositions prior to photo-cross-linking. Mechanical testing of porous hybrid networks, in particular the ICol-MA:PTMC-tMA 17:83 wt % network, showed improved mechanical properties compared to non-cross-linked ICol and ICol-MA networks prepared in DMSO/HCl. Additionally, cross-linking alone already improves the properties of porous collagen structures. Interestingly, photo-cross-linking ICol-MA in acetic acid solution resulted in the best mechanical properties, suggesting that the solvent affects collagen fibril structure and thus network mechanical properties. Indeed, acetic acid does not alter the collagen banding structure, whereas DMSO/HCl does. Thus, further investigation into the effect of the solvent on the network properties is needed.
期刊介绍:
Biomacromolecules is a leading forum for the dissemination of cutting-edge research at the interface of polymer science and biology. Submissions to Biomacromolecules should contain strong elements of innovation in terms of macromolecular design, synthesis and characterization, or in the application of polymer materials to biology and medicine.
Topics covered by Biomacromolecules include, but are not exclusively limited to: sustainable polymers, polymers based on natural and renewable resources, degradable polymers, polymer conjugates, polymeric drugs, polymers in biocatalysis, biomacromolecular assembly, biomimetic polymers, polymer-biomineral hybrids, biomimetic-polymer processing, polymer recycling, bioactive polymer surfaces, original polymer design for biomedical applications such as immunotherapy, drug delivery, gene delivery, antimicrobial applications, diagnostic imaging and biosensing, polymers in tissue engineering and regenerative medicine, polymeric scaffolds and hydrogels for cell culture and delivery.