Bio-Inspired, Zwitterionic Copolymers with Amphiphilic Character.

IF 4.2 3区 化学 Q2 POLYMER SCIENCE
Theresa M Lutz, Cevin P Braksch, Jonas De Breuck, Matthias Hartlieb, Meike N Leiske
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引用次数: 0

Abstract

Selectively targeting diseases with therapeutics remains a crucial yet still unsatisfied challenge in (nano)medicine. In recent years, a large body of biologically based drug carrier systems are produced which have proven to be suitable for the efficient transport of active compounds such as biopharmaceuticals and biotechnological drugs. However, those naturally occurring materials often entail risks, for example, due to accessible, functional groups created by uncontrolled protein denaturation processes of enzymes (e.g., proteases) which can lead to unwanted side effects in the body. To deal with this issue, designing bio-inspired synthetic copolymers offers a suitable alternative compared to systems based on materials derived from natural sources. Owing to the variety of electrostatically interacting motifs abundant in nature, synthetic statistical copolymers are developed with different polarity and zwitterionic arginine-derived units. To achieve the required physicochemical demands, a simple one-step synthesis approach is applied, the so-called xanthate-supported photo-iniferter reversible-addition-fragmentation chain-transfer (XPI-RAFT) polymerization. The cellular association of these polymers is compared to a fully non-ionic polymer. The results highlight new findings in the design of zwitterionic macromolecule structures for medical applications and further progress the understanding of the driving forces of the cell specificity of polyzwitterions.

具有两亲性的仿生两性离子共聚物
在(纳米)医学中,有选择地靶向治疗疾病仍然是一个至关重要但仍未得到满足的挑战。近年来,大量基于生物的药物载体系统被生产出来,这些系统已被证明适用于有效运输活性化合物,如生物制药和生物技术药物。然而,这些天然存在的材料通常会带来风险,例如,由于酶(例如蛋白酶)的不受控制的蛋白质变性过程产生的可接近的官能团,这可能导致体内不必要的副作用。为了解决这一问题,与基于天然材料的系统相比,设计仿生合成共聚物提供了一种合适的替代方案。由于自然界中具有丰富的静电相互作用基序,因此合成的统计共聚物具有不同极性和两性离子精氨酸衍生的单元。为了达到所需的物理化学要求,采用了一种简单的一步合成方法,即所谓的黄原酸支持的光不变性可逆加成-破碎链转移(XPI-RAFT)聚合。将这些聚合物的细胞结合与完全非离子聚合物进行比较。这些结果突出了用于医学应用的两性离子大分子结构设计的新发现,并进一步推动了对多两性离子细胞特异性驱动力的理解。
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来源期刊
Macromolecular Rapid Communications
Macromolecular Rapid Communications 工程技术-高分子科学
CiteScore
7.70
自引率
6.50%
发文量
477
审稿时长
1.4 months
期刊介绍: Macromolecular Rapid Communications publishes original research in polymer science, ranging from chemistry and physics of polymers to polymers in materials science and life sciences.
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