Design of chemical valve system based on the concept of molecular-specific synchronization

基于分子特异性同步概念的化工阀门系统设计

基本信息

  • 批准号:
    11167210
  • 负责人:
  • 金额:
    $ 31.68万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for Scientific Research on Priority Areas
  • 财政年份:
    1998
  • 资助国家:
    日本
  • 起止时间:
    1998 至 2002
  • 项目状态:
    已结题

项目摘要

The objective of this study is to construct chemical-valve system based on the concept of molecular synchronization. For this purpose, two-types of materials systems were examined here : (1)Networked structure of polymers (polymeric gels) and (2)nano-associates of block copolymers (polymeric micelles). The former system was focused on the development of materials undergoing abrupt change in their volume at physiological condition responding to external glucose concentration. A basis of the system studied here is the shift in the equilibrium between the uncharged and charged form of phenylboronic acid moieties in the polymer chain thorough complex formation with glucose. An increased glucose-concentration shifts the equilibrium in the direction of increasing fraction of borate anions and decreasing the fraction of the uncharged form. Charged borates are certainly more hydrophilic than the uncharged form. Thus, a glucose-dependent change in the ratio between uncharged and charged borates in the polymer chain should crucially affect the polymer solubility, if the polymer chain has an amphiphilic character. Apparently, this materials system should be useful to construct self-regulating insulin-releasing device for the treatment of diabetes. The latter system was designed to dissociate upon its internalization into the intracellular compartment so as to release cargo compounds selectively inside of target cells. These stimuli-sensitive polymeric micelles should be useful as nanocanrriers for gene and drug delivery.
本研究的目的是基于分子同步化的概念构建化学阀系统。为此,本文研究了两类材料体系:(1)聚合物的网络结构(聚合物凝胶)和(2)嵌段共聚物的纳米缔合物(聚合物胶束)。前一个系统的重点是在生理条件下响应于外部葡萄糖浓度而发生体积突变的材料的开发。在这里研究的系统的基础是移动之间的平衡的不带电和带电的形式的苯基硼酸部分的聚合物链中通过与葡萄糖形成复合物。增加的葡萄糖浓度在增加硼酸根阴离子的分数和减少不带电形式的分数的方向上移动平衡。带电荷的硼酸盐当然比不带电荷的硼酸盐更亲水。因此,如果聚合物链具有两亲特性,则聚合物链中不带电和带电硼酸盐之间的比率的葡萄糖依赖性变化应该对聚合物溶解度产生关键影响。该材料体系有望用于构建治疗糖尿病的自调节胰岛素释放装置。后一种系统被设计成在其内化到细胞内隔室中时解离,以便在靶细胞内选择性地释放货物化合物。这些刺激敏感的聚合物胶束应该可用作基因和药物递送的纳米载体。

项目成果

期刊论文数量(57)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
A.Harada, K.Kataoka: "Macromolecular Symposia, Vol.172 (Polymers in Medicine)"Wiley-VCH, Weinheim. 1-10 (2001)
A.Harada、K.Kataoka:“高分子研讨会,第 172 卷(医学中的聚合物)”Wiley-VCH,Weinheim。
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    0
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N.Nishiyama, K.Kataoka: "Polymeric Drugs in the Clinical Stage : Advantages and Prospects"Eds., H.Maeda, A.V.Kabanov, K.Kataoka, T.Okano, Kluwer, New York(in press).
N.Nishiyama、K.Kataoka:“临床阶段的高分子药物:优势和前景”Eds.、H.Maeda、A.V.Kabanov、K.Kataoka、T.Okano、Kluwer,纽约(正在出版)。
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    0
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H.R.Stapert,N.Nishiyama,D.L.Jiang,T.Aida,K.Kataoka: "Polyion complex micelles encapsulating light-harvesting ionic dendrimer zinc porphyrins"Langmuir. 16(21). 8182-8188 (2000)
H.R.Stapert、N.Nishiyama、D.L.Jiang、T.Aida、K.Kataoka:“封装光捕获离子树枝状聚合物锌卟啉的聚离子复合胶束”Langmuir。
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    0
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Y.Akiyama,A.Harada,Y.Nagasaki,K.Kataoka: "Synthesis of poly (ethylene glycol)-block-poly (ethyleneimine) possessing an acetal group at the PEC end"Macromolecules. 33(16). 5841-5845 (2000)
Y.Akiyama,A.Harada,Y.Nagasaki,K.Kataoka:“在PEC末端具有缩醛基团的聚(乙二醇)-嵌段-聚(乙撑亚胺)的合成”大分子。
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    0
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A.Harada, K.Kataoka: "Pronounced Activity of Enzymes through the Incorporation into the Core of Polyion Complex Micelles Made from Charged Block Copolymers"J. Controlled Release. 72(1-3). 85-91 (2001)
A.Harada、K.Kataoka:“通过掺入由带电嵌段共聚物制成的聚离子复合胶束的核心,酶具有明显的活性”J。
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KATAOKA Kazunori其他文献

KATAOKA Kazunori的其他文献

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{{ truncateString('KATAOKA Kazunori', 18)}}的其他基金

Development of Polymeric Micelles for Brain-Targeted Delivery of Nucleic Acid Drugs to Treat Intractable Neurological Diseases
开发用于脑靶向递送核酸药物以治疗难治性神经系统疾病的聚合物胶束
  • 批准号:
    25000006
  • 财政年份:
    2013
  • 资助金额:
    $ 31.68万
  • 项目类别:
    Grant-in-Aid for Specially Promoted Research
Development of multifunctional polymeric micelles for systemic siRNA delivery
开发用于系统性 siRNA 递送的多功能聚合物胶束
  • 批准号:
    20240046
  • 财政年份:
    2008
  • 资助金额:
    $ 31.68万
  • 项目类别:
    Grant-in-Aid for Scientific Research (A)
Polymeric micelle nanocarrier for drug and gene delivery
用于药物和基因递送的聚合物胶束纳米载体
  • 批准号:
    17016017
  • 财政年份:
    2005
  • 资助金额:
    $ 31.68万
  • 项目类别:
    Grant-in-Aid for Scientific Research on Priority Areas
Development of functional polymeirc micelles responding to intracellular microenvironments for cancer chemotherapy
开发响应细胞内微环境的功能性聚合物胶束用于癌症化疗
  • 批准号:
    17200031
  • 财政年份:
    2005
  • 资助金额:
    $ 31.68万
  • 项目类别:
    Grant-in-Aid for Scientific Research (A)
Creation of intelligent polymeric micelle nanocapsuls for gene delivery
创建用于基因传递的智能聚合物胶束纳米胶囊
  • 批准号:
    14380391
  • 财政年份:
    2002
  • 资助金额:
    $ 31.68万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Biomedical approach of new materials with well-organized interfaces
具有组织良好的界面的新材料的生物医学方法
  • 批准号:
    11694129
  • 财政年份:
    1999
  • 资助金额:
    $ 31.68万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Development of self-regulated insulin delivery system based on novel glucose-responsive gel
基于新型葡萄糖反应凝胶的自我调节胰岛素输送系统的开发
  • 批准号:
    10559019
  • 财政年份:
    1998
  • 资助金额:
    $ 31.68万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Design and characterization of polymeric micelles with entrapped peptides
包载肽的聚合物胶束的设计和表征
  • 批准号:
    07558130
  • 财政年份:
    1995
  • 资助金额:
    $ 31.68万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Molecular design of polymer with lymphocyte-activating ability
具有淋巴细胞激活能力的聚合物的分子设计
  • 批准号:
    07458239
  • 财政年份:
    1995
  • 资助金额:
    $ 31.68万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Development of contimous cell separation system using polymeric adsorbent with surface micro-structures
使用具有表面微结构的聚合物吸附剂开发连续细胞分离系统
  • 批准号:
    05558118
  • 财政年份:
    1993
  • 资助金额:
    $ 31.68万
  • 项目类别:
    Grant-in-Aid for Developmental Scientific Research (B)
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