• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Degradation of polyetherurethane by subcutaneous implantation into rats. II. Changes of contact angles, infrared spectra, and nuclear magnetic resonance spectra.

作者信息

Sato M, Xi T, Nakamura A, Kawasaki Y, Umemura T, Tsuda M, Kurokawa Y

机构信息

National Institute of Health Sciences, Tokyo, Japan.

出版信息

J Biomed Mater Res. 1995 Oct;29(10):1201-13. doi: 10.1002/jbm.820291007.

DOI:10.1002/jbm.820291007
PMID:8557722
Abstract

In vivo degradation of polyetherurethanes (PEUs) was studied using two kinds of PEUs, U-3 and U-8, coated on a base film of ethylene/vinyl alcohol copolymer (EVAL). U-3 is a nonsegmented PEU prepared from 4,4'-diisocyanatodiphenylmethane (MDI) and poly(tetramethylene oxide) (PTMO 1000). U-8 is a segmented PEU prepared from MDI, PTMO 1000, and 1,4-butanediol. Previous studies of PEUs were conducted using gel permeation chromatography and scanning electron microscopy. In this study, the explanted materials were examined with contact angle measurement, ATR-FTIR, and nuclear magnetic resonance (NMR) spectroscopies. All data obtained by these methodologies indicate that the PTMO/MDI oligomers diffused to the material surface in the early stage of implantation. Then, the low-molecular-weight fraction of the oligomers leached out from the surface to the exudate. Degradation became dominant after 2-4 weeks. In the case of PU-8, the PTMO fraction decreased approximately 35-40% from the surface at 24 weeks postimplantation. In the case of PU-3, the loss of coating material (U-3) on the base film (EVAL) was observed after 10 weeks. The PTMO fraction of the surface U-3 remained on EVAL at 6 weeks postimplantation, however, it was 64% of the initial material. The molecular weight of the U-3 remaining on EVAL also decreased. Degradation of U-3 occurred more rapidly than that of U-8. The data obtained with our materials were insufficient in determining evidence of oxidative degradation with IR or NMR spectra.

摘要

相似文献

1
Degradation of polyetherurethane by subcutaneous implantation into rats. II. Changes of contact angles, infrared spectra, and nuclear magnetic resonance spectra.
J Biomed Mater Res. 1995 Oct;29(10):1201-13. doi: 10.1002/jbm.820291007.
2
Degradation of polyetherurethane by subcutaneous implantation into rats. I. Molecular weight change and surface morphology.
J Biomed Mater Res. 1994 Apr;28(4):483-90. doi: 10.1002/jbm.820280411.
3
Hydrogels based on poly(ethylene oxide) and poly(tetramethylene oxide) or poly(dimethyl siloxane). III. In vivo biocompatibility and biostability.基于聚环氧乙烷、聚四亚甲基醚二醇或聚二甲基硅氧烷的水凝胶。III. 体内生物相容性和生物稳定性。
J Biomed Mater Res A. 2003 Feb 1;64(2):309-19. doi: 10.1002/jbm.a.10424.
4
Long term in vitro biostability of segmented polyisobutylene-based thermoplastic polyurethanes.分段聚异丁烯基热塑性聚氨酯的长期体外生物稳定性。
J Biomed Mater Res A. 2010 Dec 1;95(3):774-82. doi: 10.1002/jbm.a.32897.
5
Difference in tumor incidence and other tissue responses to polyetherurethanes and polydimethylsiloxane in long-term subcutaneous implantation into rats.
J Biomed Mater Res. 1992 May;26(5):631-50. doi: 10.1002/jbm.820260506.
6
Studies on the tumor-promoting activity of polyurethanes: depletion of inhibitory action of metabolic cooperation on the surface of a polyalkyleneurethane but not a polyetherurethane.聚氨酯促肿瘤活性的研究:聚亚烷基聚氨酯而非聚醚聚氨酯表面代谢协同抑制作用的耗竭。
J Biomed Mater Res. 1995 Jul;29(7):835-41. doi: 10.1002/jbm.820290708.
7
Long-term in vivo biostability of poly(dimethylsiloxane)/poly(hexamethylene oxide) mixed macrodiol-based polyurethane elastomers.基于聚(二甲基硅氧烷)/聚(氧化六亚甲基)混合大分子二醇的聚氨酯弹性体的长期体内生物稳定性
Biomaterials. 2004 Sep;25(20):4887-900. doi: 10.1016/j.biomaterials.2004.01.004.
8
Nonfouling biomaterials based on polyethylene oxide-containing amphiphilic triblock copolymers as surface modifying additives: solid state structure of PEO-copolymer/polyurethane blends.基于含聚环氧乙烷两亲性三嵌段共聚物作为表面改性添加剂的非污损生物材料:PEO共聚物/聚氨酯共混物的固态结构
J Biomed Mater Res A. 2008 Jun 15;85(4):862-72. doi: 10.1002/jbm.a.31548.
9
Biological stability of polyurethane modified with covalent attachment of di-tert-butyl-phenol.通过共价连接二叔丁基苯酚改性的聚氨酯的生物稳定性。
J Biomed Mater Res A. 2007 Sep 15;82(4):1004-11. doi: 10.1002/jbm.a.31215.
10
Degradation of biomaterials by phagocyte-derived oxidants.吞噬细胞衍生的氧化剂对生物材料的降解作用。
J Clin Invest. 1993 Nov;92(5):2360-7. doi: 10.1172/JCI116841.