Design of Biodegradable Adhesion Prevention

可生物降解的防粘连设计

基本信息

  • 批准号:
    06453221
  • 负责人:
  • 金额:
    $ 3.71万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
  • 财政年份:
    1994
  • 资助国家:
    日本
  • 起止时间:
    1994 至 1996
  • 项目状态:
    已结题

项目摘要

The development of tissue adhesion prevention material has been long awaited in surgery. Tissue adhesion after surgery occasionally causes serious complications. Various studies have been undertaken to develop materials that prevent tissue adhesion. These function as a barrier to enable traumatized tissue to be separated from adjacent tissues during the healing process. These materials should be free from cellular adhesion, should be flexible and tough enough to provide for a tight cover over the traumatized soft tissues, and should be biodegradable and resorbable after the injured tissue is completely regenerated. To fully realize these requirements, natural polymers such as fiberous proteins or polysaccharides, which exist as highly water-adsorbable biomaterials filling interstices of tissues, have been considered to be best suited as basic materials. Synthetic polypeptides and their copolymers which carry hydrophilic components offer potential for enzymatic degradable medical applic … More ations.We have prepared many types of hydrophilic polypeptide membranes which are composed of hydrophilic and hydrophobic amino acid components as models of natural fibrous proteins. These includes ; A-B-A type block copolymers consisting of a hydrophilic polypeptide as the A component and polyisoprene as the B component, copoly (N-hydroxyalkyl-D,L-glutamaine)s, two-component random copolypeptides consisting of N-hydroxyalkyl-L-glutamine and L-alanine, L-leucine, or L-valine, and three-component random copolypeptides consisting of N-hydroxyalkyl-L-glutamine, L-glutamic acid, and L-lysine. Hydrophilic membranes or hydrogels were prepared by using a crosslinking reaction with diamine on the starting membranes. It was commonly shown that the effective crosslink density was proportional to the molar % of diamine in the reaction mixture. The relation between their bulk structure and properties was investigated with regard to the swelling ratio in water, tensile properties, and enzymatic degradation behavior in a pseudo-extracellular fluid (PECF). The tensile properties of the hydrophilic membranes were highly dependent on the swelling ratio in PECF,and on the hydrophobic portions in molecular chains, whose behavior was typical of an elastomer. Biodegradations of these membranes in viro by a protease indicated that the degradation took place in bulk rather than on a surface, and that the rate of degradation was also highly dependent on the swelling ratio of membranes, the hydrophobicity, effective charge density, as well as D,L-comonomer composition, of the side chains of samples. Less
组织防粘连材料的开发一直是外科界期待已久的课题。手术后组织粘连偶尔会引起严重的并发症。已经进行了各种研究来开发防止组织粘连的材料。这些功能作为屏障,使创伤组织在愈合过程中与相邻组织分离。这些材料应不含细胞粘附,应具有足够的柔韧性和坚韧以在创伤软组织上提供紧密的覆盖,并且在损伤组织完全再生后应是可生物降解和可再吸收的。为了充分实现这些要求,天然聚合物如纤维状蛋白质或多糖,其作为填充组织间隙的高度吸水性生物材料存在,被认为最适合作为基础材料。合成多肽及其共聚物携带亲水性组分,为酶降解医疗应用提供了潜力 ...更多信息 我们已经制备了许多类型的亲水性多肽膜,其由亲水性和疏水性氨基酸组分组成,作为天然纤维蛋白的模型。其中包括:由作为A组分的亲水性多肽和作为B组分的聚异戊二烯组成的A-B-A型嵌段共聚物,共聚(N-羟烷基-D,L-丙氨酸),由N-羟烷基-L-谷氨酰胺和L-丙氨酸、L-亮氨酸或L-缬氨酸组成的双组分无规共聚肽,和由N-羟烷基-L-谷氨酰胺、L-谷氨酸和L-赖氨酸组成的三组分无规共聚肽。亲水性膜或水凝胶通过使用与起始膜上的二胺的交联反应来制备。通常表明,有效交联密度与反应混合物中二胺的摩尔%成比例。研究了它们的体相结构与性能之间的关系,包括在水中的溶胀率、拉伸性能和在假细胞外液(PECF)中的酶降解行为。亲水性膜的拉伸性能高度依赖于在PECF中的溶胀比,以及分子链中的疏水部分,其行为是典型的弹性体。这些膜在体内的蛋白酶的生物降解表明,降解发生在散装,而不是在表面上,降解速率也高度依赖于膜的溶胀比,疏水性,有效电荷密度,以及D,L-共聚单体组合物,样品的侧链。少

项目成果

期刊论文数量(32)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Toshio Hayashi: "Biodegradable Polymers for Biomedical Uses in 「Progress in Polymer Science」" Pergamon Pub., 40 (1994)
Toshio Hayashi:““高分子科学进展”中用于生物医学用途的生物可降解聚合物”Pergamon Pub.,40 (1994)
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    0
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林 壽郎: "生体分解吸収性材料の最近の進歩(分担執筆)「人工臓器 1994-1995」" 中山書店, 6 (1994)
Hisao Hayashi:“生物可降解和可吸收材料的最新进展(合著者)‘人造器官 1994-1995’” 中山书店,6 (1994)
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    0
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T.Hayashi,E.Nakanishi,Y.Iizuka,M.Oya,and M.Iwatsuki,: "^・Preparation and Properties of Copoly(N-hydroxyalkyl-D,L-glutamine)Membranes^・" European Polymer Journal. 31(5). 453-458 (1995)
T. Hayashi、E. Nakanishi、Y. Iizuka、M. Oya 和 M. Iwatsuki,:“^·共聚(N-羟烷基-D,L-谷氨酰胺)膜的制备和性能^·”《欧洲聚合物杂志》31。 (5)。453-458(1995)。
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    0
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I.Fuke,T.Hayashi,Y.Tabata,and Y.Ikada: "Synthesis of Poly(ethylene glycol)Derivatives with Different Branching and Their Use for Protein Modification" J.Control Release. 30. 27-34 (1994)
I.Fuke、T.Hayashi、Y.Tabata 和 Y.Ikada:“具有不同支化的聚乙二醇衍生物的合成及其在蛋白质修饰中的用途”J.Control Release。
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  • 期刊:
  • 影响因子:
    0
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  • 通讯作者:
Y. Miyachi, K. Jokei, M. Oka, and T. Hayashi: ""Enzymatic Hydrolysis of Copoly (N-hydroxypropyl L-glutamine/L-leucine) Hydrogels in vitro"" J. Biomaterial Science-Polymer Ed.7・9. 805-816 (1996)
Y. Miyachi、K. Jokei、M. Oka、T. Hayashi:“共聚(N-羟丙基L-谷氨酰胺/L-亮氨酸)水凝胶的体外酶水解”J. Biomaterial Science-Polymer Ed.7・9.805-816(1996)
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  • 影响因子:
    0
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HAYASHI Toshio其他文献

HAYASHI Toshio的其他文献

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{{ truncateString('HAYASHI Toshio', 18)}}的其他基金

The regression of atherosclerosis through the regulation of cellular senescence: the possible new therapy for Japanese lifestyle related diseases
通过调节细胞衰老来消退动脉粥样硬化:日本生活方式相关疾病的可能新疗法
  • 批准号:
    24590881
  • 财政年份:
    2012
  • 资助金额:
    $ 3.71万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Investigation of the regression of advanced atherosclerosis through the regulation of cellular senescence-custom-made therapy to Japanese elderly-
通过细胞衰老调节来消退晚期动脉粥样硬化的研究——日本老年人的定制疗法
  • 批准号:
    21590762
  • 财政年份:
    2009
  • 资助金额:
    $ 3.71万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Geriatric and gerontological approach for asian elderly to prevent their atherosclerotic disease and get successful aging.
针对亚洲老年人的老年病学和老年学方法,以预防动脉粥样硬化疾病并实现成功老龄化。
  • 批准号:
    20406004
  • 财政年份:
    2008
  • 资助金额:
    $ 3.71万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Regression of Atherosclerosis by the regulation of nitric oxide and superoxide on vascular endocrinology and vascular aging
通过一氧化氮和超氧化物调节血管内分泌和血管老化来消退动脉粥样硬化
  • 批准号:
    19591043
  • 财政年份:
    2007
  • 资助金额:
    $ 3.71万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
A Study on Mechanisms of Regional Differences of Side Effects of Hormone Replacement Treatment (HRT)
激素替代治疗(HRT)副作用区域差异机制研究
  • 批准号:
    16406001
  • 财政年份:
    2004
  • 资助金额:
    $ 3.71万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Gene Therapy of Combined Nitric Oxide Synthases and Related Enzymes to Achieve Complete Regression of Advanced Atherosclerosis-Combined Regulation of Substrate of the Enzymes, Co-factors, Transcriptional Factors and Intracellular Enzymes-
一氧化氮合成酶及相关酶联合基因治疗,实现晚期动脉粥样硬化的彻底消退-酶底物、辅因子、转录因子和细胞内酶的联合调控-
  • 批准号:
    13670704
  • 财政年份:
    2001
  • 资助金额:
    $ 3.71万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Conformational Analysis of Periodic Polypeptides Containing Pro Residue
含Pro残基的周期性多肽的构象分析
  • 批准号:
    11450373
  • 财政年份:
    1999
  • 资助金额:
    $ 3.71万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Therapy for Advanced Atherosclerosis by Using Vascular Endocrinological System
血管内分泌系统治疗晚期动脉粥样硬化
  • 批准号:
    11670672
  • 财政年份:
    1999
  • 资助金额:
    $ 3.71万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Radiation Effects on Hybrid-Type Medical Materials
放射线对混合型医用材料的影响
  • 批准号:
    08558100
  • 财政年份:
    1996
  • 资助金额:
    $ 3.71万
  • 项目类别:
    Grant-in-Aid for Scientific Research (A)

相似海外基金

Evaluation of extracellular matrix gel for adhesion prevention and tissue healing intendon surgery
细胞外基质凝胶预防粘连和组织愈合意向手术的评价
  • 批准号:
    10482261
  • 财政年份:
    2022
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    $ 3.71万
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Improving the safety and effectiveness of adhesion prevention following colorectal procedures with high risk of cancer or infection
提高癌症或感染高风险结直肠手术后预防粘连的安全性和有效性
  • 批准号:
    10603903
  • 财政年份:
    2022
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    $ 3.71万
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Development of pericardial adhesion prevention sheet using biodegradable copolymers and Mesothelial cell-selective adhesive peptides
使用可生物降解的共聚物和间皮细胞选择性粘附肽开发心包粘连预防片
  • 批准号:
    19K18175
  • 财政年份:
    2019
  • 资助金额:
    $ 3.71万
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    Grant-in-Aid for Early-Career Scientists
Basement Membrane Targeted Nanoparticles for Post-Surgical Adhesion Prevention
用于预防术后粘连的基底膜靶向纳米颗粒
  • 批准号:
    10538489
  • 财政年份:
    2019
  • 资助金额:
    $ 3.71万
  • 项目类别:
Basement Membrane Targeted Nanoparticles for Post-Surgical Adhesion Prevention
用于预防术后粘连的基底膜靶向纳米颗粒
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    10297844
  • 财政年份:
    2019
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    $ 3.71万
  • 项目类别:
A novel adhesion prevention strategy using PAI-1 inhibitor
使用 PAI-1 抑制剂的新型粘连预防策略
  • 批准号:
    18K08724
  • 财政年份:
    2018
  • 资助金额:
    $ 3.71万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Adhesion prevention of micromechanisms using quantum electromagnetic forces
利用量子电磁力防止微机构粘附
  • 批准号:
    25390117
  • 财政年份:
    2013
  • 资助金额:
    $ 3.71万
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    Grant-in-Aid for Scientific Research (C)
Device for Surgical Adhesion Prevention
预防手术粘连装置
  • 批准号:
    7909040
  • 财政年份:
    2010
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    $ 3.71万
  • 项目类别:
Application of hydrogels for adhesion prevention after thoracotomy
水凝胶在开胸术后防粘连中的应用
  • 批准号:
    19591645
  • 财政年份:
    2007
  • 资助金额:
    $ 3.71万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Experimental study of tendon adhesion prevention by a biocompatible polymer hydrogel.
生物相容性聚合物水凝胶预防肌腱粘连的实验研究。
  • 批准号:
    17591548
  • 财政年份:
    2005
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    $ 3.71万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
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