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Enhanced sealing strength of a hydrophobically-modified Alaska pollock gelatin-based sealant

机译:增强了疏水性改性的阿拉斯加波特洛素的胶凝素的密封剂的密封强度

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摘要

The aim of this study was the development of an innovative biocompatible sealant composed of Alaska pollock-derived gelatin partially modified with a dodecyl group (C12-ApGltn) and a poly(ethylene glycol)based crosslinker, pentaerythritol poly(ethylene glycol) ether tetrasuccinimidyl glutarate. The burst strength of the developed sealants was measured using porcine aorta and rat lungs. The maximum burst strength of a C12-ApGltnbased sealant against the porcine aorta was 4-fold higher than that of an original ApGltn (Org-ApGltn)-based sealant. No significant increase in the burst strength was observed between C12-ApGltnbased sealants with 4.2 and 8.9 mol% modification ratios. From histological observation after burst strength measurement, tissue tearing was observed when a C12-ApGltnbased sealant was applied. In contrast, the Org-ApGltnbased sealant was peeled away from the aorta surface due to cohesion failure. Similar to the porcine aorta, the burst strength of C12-ApGltnbased sealants applied on a rat lung defect was 3-fold higher than that of an Org-ApGltnbased sealant. The curing time of the C12-ApGltnbased sealant measured by a simple mixing method was shorter (2.6 +/- 0.1 s) than that of the Org-ApGltnbased sealant (4.1 +/- 0.3 s). The swelling ratio of the C12-ApGltnbased sealant (23.7 +/- 3.1) was significantly lower than that of the Org-ApGltnbased sealant (32.3 +/- 1.1). The C12-ApGltnbased sealant was completely degraded within 28 days after implantation in the backs of rats without a severe inflammation reaction. However, the Org-ApGltnbased sealant disappeared within 14 days. These results indicated that hydrophobically-modified ApGltn has an effective sealing effect on moist tissues and bio-compatibility in vivo.
机译:本研究的目的是开发由一甲基甲基(C12-APGLTN)和聚(乙二醇)的交联剂,季戊四醇聚醚四琥珀酰亚胺氨基乙烯基氨基丙氨酸戊二酸戊二酸戊二酸戊二酸戊二酸戊二氨基氨基乙烯基氨基丙氨酸戊二酰戊二酸戊二酸戊丙基氨基酰亚胺基(Collack)和聚(乙二醇)的交联剂组成的创新生物相容性密封剂。 。使用猪主动脉和大鼠肺部测量发育密封剂的突发强度。 C12-APGLTNABASED密封剂对猪主动脉的最大突发强度比原始APGLTN(ORG-APGLTN)的密封剂高4倍。在C12-APGLTNASED密封剂之间没有显着增加突发强度,其中4.2和8.9mol%改性比率。根据突发强度测量后的组织学观察,当施加C12-APGLTNACED密封剂时,观察到组织撕裂。相反,由于内聚力衰竭,ORG-APGLTNABASED密封剂从主动脉表面剥离。类似于猪主动脉,在大鼠肺缺陷上施加的C12-APGLTNABASED密封剂的突发强度比磁体 - APGLTNABASED密封剂高出3倍。通过简单的混合方法测量的C12-APGLTNABASED密封剂的固化时间较短(2.6 +/- 0.1 s),比org-apgltnbased密封剂(4.1 +/- 0.3s)更短(2.6 +/- 0.1 s)。 C12-APGLTNABASED密封剂(23.7 +/- 3.1)的溶胀比显着低于ORG-APGLTNABASED密封剂(32.3 +/- 1.1)。 C12-APGLTnbased密封剂在植入大鼠背面后28天内完全降解,没有严重的炎症反应。然而,ORG-APGLTNBASED密封剂在14天内消失。这些结果表明,疏水性修饰的APGLTN对体内湿润组织和生物相容性具有有效的密封效果。

著录项

  • 来源
    《Biomaterials Science》 |2017年第5期|共8页
  • 作者单位

    Univ Tsukuba Grad Sch Pure &

    Appl Sci 1-1-1 Tennodai Tsukuba Ibaraki 3058577 Japan;

    Univ Tsukuba Grad Sch Pure &

    Appl Sci 1-1-1 Tennodai Tsukuba Ibaraki 3058577 Japan;

    Tokyo Univ Sci Fac Engn Shinjuku Ku 1-3 Kagurazaka Tokyo 1628601 Japan;

    Univ Tsukuba Grad Sch Pure &

    Appl Sci 1-1-1 Tennodai Tsukuba Ibaraki 3058577 Japan;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分子生物学;
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