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受自然启发制备明确聚合物纳米颗粒的策略:化学与多功能性

Strategies Toward Well-Defined Polymer Nanoparticles Inspired by Nature: Chemistry versus Versatility.

作者信息

Elsabahy Mahmoud, Wooley Karen L

机构信息

Department of Chemistry, Texas A&M University, P.O. Box 30012, 3255 TAMU, College Station, Texas 77842-3012 ; Department of Chemistry, Laboratory for Synthetic-Biologic Interactions, Texas A&M University, P.O. Box 30012, 3255 TAMU, College Station, Texas 77842-3012 ; Department of Pharmaceutics, Faculty of Pharmacy, Assiut University, Assiut, Egypt.

Department of Chemistry, Texas A&M University, P.O. Box 30012, 3255 TAMU, College Station, Texas 77842-3012 ; Department of Chemistry, Laboratory for Synthetic-Biologic Interactions, Texas A&M University, P.O. Box 30012, 3255 TAMU, College Station, Texas 77842-3012 ; Department of Chemical Engineering, Texas A&M University, P.O. Box 30012, 3255 TAMU, College Station, Texas 77842-3012.

出版信息

J Polym Sci A Polym Chem. 2012 May 15;50(10):1869-1880. doi: 10.1002/pola.25955.

Abstract

Polymeric nanoparticles are promising delivery platforms for various biomedical applications. One of the main challenges toward the development of therapeutic nanoparticles is the premature disassembly and release of the encapsulated drug. Among the different strategies to enhance the kinetic stability of polymeric nanoparticles, shell- and core-crosslinking have been shown to provide robust character, while creating a suitable environment for encapsulation of a wide range of therapeutics, including hydrophilic, hydrophobic, metallic, and small and large biomolecules, with gating of their release as well. The versatility of shell- and core-crosslinked nanoparticles is driven from the ease by which the structures of the shell- and core-forming polymers and crosslinkers can be modified. In addition, postmodification with cell-recognition moieties, grafting of antibiofouling polymers, or chemical degradation of the core to yield nanocages allow the use of these robust nanostructures as "smart" nanocarriers. The building principles of these multifunctional nanoparticles borrow analogy from the synthesis, supramolecular assembly, stabilization, and dynamic activity of the naturally driven biological nanoparticles such as proteins, lipoproteins, and viruses. In this review, the chemistry involved during the buildup from small molecules to polymers to covalently stabilized nanoscopic objects is detailed, with contrast of the strategies of the supramolecular assembly of polymer building blocks followed by intramicellar stabilization into shell-, core-, or core-shell-crosslinked knedel-like nanoparticles versus polymerization of polymers into nanoscopic molecular brushes followed by further intramolecular covalent stabilization events. The rational design of shell-crosslinked knedel-like nanoparticles is then elaborated for therapeutic packaging and delivery, with emphasis on the polymer chemistry aspects to accomplish the synthesis of such nanoparticulate systems.

摘要

聚合物纳米颗粒是用于各种生物医学应用的有前景的递送平台。治疗性纳米颗粒开发面临的主要挑战之一是包封药物的过早解体和释放。在增强聚合物纳米颗粒动力学稳定性的不同策略中,壳交联和核交联已被证明能提供强大的特性,同时为包封各种治疗剂创造合适的环境,这些治疗剂包括亲水性、疏水性、金属性以及大小生物分子,并且还能控制它们的释放。壳交联和核交联纳米颗粒的多功能性源于壳形成聚合物和核形成聚合物以及交联剂的结构易于修饰。此外,用细胞识别部分进行后修饰、接枝抗生物污损聚合物或对核进行化学降解以产生纳米笼,使得这些坚固的纳米结构能够用作“智能”纳米载体。这些多功能纳米颗粒的构建原理借鉴了天然驱动的生物纳米颗粒(如蛋白质、脂蛋白和病毒)的合成、超分子组装、稳定化和动态活性。在这篇综述中,详细介绍了从小分子到聚合物再到共价稳定的纳米级物体形成过程中涉及的化学,对比了聚合物构建块超分子组装策略,随后在胶束内稳定化为壳交联、核交联或核壳交联的类克内德尔纳米颗粒,与聚合物聚合成纳米级分子刷随后进行进一步分子内共价稳定化事件。然后阐述了壳交联类克内德尔纳米颗粒用于治疗性包装和递送的合理设计,重点是聚合物化学方面以完成此类纳米颗粒系统的合成。

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