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Supramolecular Formation, Complexation and Dynamics in Colloidal Polyelectrolyte-Surfactant Complexes

Supramolecular Formation, Complexation and Dynamics in Colloidal Polyelectrolyte-Surfactant Complexes
胶体聚电解质-表面活性剂复合物中的超分子形成、络合和动力学
批准号:
0454887
负责人:
Benjamin Chu
金额:
$34.5万
依托单位:
依托单位国家:
美国
项目类别:
Continuing Grant
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-03-15 至 2009-10-31

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中文摘要
翻译
本项目的重点将是可溶性胶体聚电解质-表面活性剂络合物(CPSCs)。胶体粒子与凝聚和包裹的聚电解质(如DNA片段)形成络合物和超分子组装,需要引入更具挑战性的表面活性剂性质和表面活性剂分子拓扑设计。星形三臂表面活性剂由亲水嵌段、带电可溶嵌段和附加的可生物降解的柔性疏水嵌段(B)组成,在疏水和亲水环境中都有可能成为具有胶束形成性质的通用表面活性剂。由于强烈的静电相互作用,动力学处理是操纵复杂地层的基本要素。对结合过程的时间分辨观察对于更好地理解C-PSC的超分子形成机制具有重要作用。表面活性剂中可生物降解的疏水嵌段(B)将被设计成具有几种有用的功能。它可以修饰PSC链段的疏水表面。因此,CPSC可以设计为在水和疏水环境中均可溶解。PSC表面疏水链和亲水链的双重存在可以增加对CPSC中聚电解质(如DNA)的保护作用。此外,生物可降解块的设计将破坏CPSCs的稳定性,从而最终释放聚电解质。合成了星形三臂表面活性剂。基础研究将侧重于(I)这种新型表面活性剂在选择性溶剂中的胶束化,(Ii)它们在水和疏水环境中与聚电解质的定向络合物的形成,以及(Iii)CPSCs的分解,根据(A)表面活性剂的形态和结构,包括三个嵌段的化学组成、总嵌段长度和嵌段比,(B)pH,(C)离子强度,(D)反离子的性质,以及溶剂质量、浓度和温度。智力价值拟议中的研究涉及使用可以发生疏水和静电相互作用的表面活性剂,对聚电解质缩合和封装的微相行为进行科学研究。这一发现将为设计更好的聚电解质载体,特别是DNA片段提供新的途径。这可能会对嵌段共聚物作为基因和药物输送载体的使用产生影响,这是基于线团到球形的转变以及更复杂的具有相反电荷的聚电解质的嵌段共聚物的自组装。从聚合物科学的角度来看,它在体外非病毒基因治疗应用中的生物学意义可能特别富有成效。广泛影响该方法在药物和基因输送以及组织工程方面具有实际应用的潜力。这些都是重要的主题,可以利用我们在材料科学方面的知识将其应用于生物学和医学。此外,该项目在聚合物合成(化学)、聚合物加工(工程)和表征(物理)以及聚合物理论与具体的及时目标之间有着独特而自然的联系。对于从高中到博士后的下一代科学家和工程师来说,肥沃的土壤是吸引人的主题。
英文摘要
The emphasis in this project will be on soluble colloidal polyelectrolyte-surfactant complexes (CPSCs). The complex formation and supra-molecular assembly of colloidal particles with condensed and encapsulated polyelectrolytes, e.g., DNA fragments, require the introduction of more challenging designs on the nature of the surfactant and the surfactant molecular topology. Star tri-arm surfactants are proposed which consist of a hydrophilic block , a charged soluble block, and an additional biodegradable and flexible hydrophobic bloc (B), and which have the potential of being universal surfactants having micelle formation properties in both hydrophobic and hydrophilic environments. Kinetic processing is an essential element to manipulate the complex formation due to strong electrostatic interactions. Time-resolved observation of the binding process should play an important role in reaching a better understanding of the mechanism of C-PSC supra-molecular formation. The biodegradable hydrophobic block (B) in the surfactant will be designed to serve several useful functions. It can modify the hydrophobic surface of the PSC segments. The CPSC can thus be designed to be soluble in both the aqueous and hydrophobic environments. The presence of a duality of hydrophobic and hydrophilic chains on the PSC surface could increase the protection for the polyelectrolyte (e.g., DNA) in the CPSC. Furthermore the biodegradable block will be designed to destabilize the CPSCs for eventual release of the polyelectrolyte. Star tri-armed surfactants have synthesized . Fundamental studies will be carried out with emphasis on (i) the micellization of this new type of surfactants in selective solvents, (ii) their directed complex formation with polyelectrolytes in aqueous and hydrophobic environments, and (iii) the disassembly of CPSCs, in terms of (a) surfactant morphology and architecture, including chemical composition of the three blocks, total block length, and block ratio, (b) pH, (c) ionic strength, (d) the nature of counter ions, as well as solvent quality, concentration and temperature. Intellectual MeritThe proposed study deals with scientific investigations on the micro-phase behavior of polyelectrolyte condensation and encapsulation, using surfactants that can undergo hydrophobic and electrostatic interactions. The findings should provide new pathways on the design of better carriers for polyelectrolytes in general and for DNA fragments in particular. It could have an impact on the use of block copolymers as vehicles for gene and drug delivery, based on the coil-to-globule transition and the self-assembly of more complex block copolymers with oppositely charged polyelectrolyte. Its biological implication for in-vitro non-viral gene therapy applications could be especially fruitful from the polymer science viewpoint.Broader ImpactsThe proposed approach has potential for practical applications to drug and gene delivery, as well as tissue engineering. These are important topics that can take advantage of our knowledge in materials science for applications to biology and medicine. Furthermore, the project has unique and natural connections among the disciplines of polymer synthesis (chemistry), polymer processing (engineering) and characterization (physics), as well as polymer theory with specific timely objectives. The fertile grounds are appealing subject matters for the next generation of scientists and engineers, from high school to post-doctoral students.
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会议论文
2004 Gordon Research Conference on Colloidal, Macromolecular, and Polyelectric Solutions to be held in Ventura, California February 1-6, 2004
  • 批准号:
    0338386
  • 项目类别:
    Standard Grant
  • 资助金额:
    $2.3万
  • 财政年份:
    2004
  • 负责人:
    Benjamin Chu
  • 依托单位:
Nanostructures and Activity of Polyelectrolyte/Surfactant Complexes
  • 批准号:
    9984102
  • 项目类别:
    Standard Grant
  • 资助金额:
    $28.5万
  • 财政年份:
    2000
  • 负责人:
    Benjamin Chu
  • 依托单位:
Formation of Nanostructures in Hydrogels
  • 批准号:
    9612386
  • 项目类别:
    Continuing Grant
  • 资助金额:
    $24.0万
  • 财政年份:
    1996
  • 负责人:
    Benjamin Chu
  • 依托单位:
Self-Assembly of Block Copolymers in Supercritical Fluids, U.S.-Turkey Cooperative Research
  • 批准号:
    9515361
  • 项目类别:
    Continuing Grant
  • 资助金额:
    $1.92万
  • 财政年份:
    1996
  • 负责人:
    Benjamin Chu
  • 依托单位:
国内基金
海外基金
The formation and evolution of planetary systems in dense star clusters
  • 批准号:
    11043007
  • 项目类别:
    专项基金项目
  • 资助金额:
    10.0万元
  • 批准年份:
    2010
  • 负责人:
    柯文采
  • 依托单位: