聚合物的结构和形状改变了类似病毒的粒子-聚合物的抗原性
Parker W Lee, Sergey A Isarov, Jaqueline D Wallat
1Department of Chemistry and Biochemistry, Miami University , Oxford, Ohio 45056, United States.
Journal of the American Chemical Society
|January 26, 2017
概括
与传统的甲基聚乙烯 (mPEG) 相比,如聚诺烯 (PNB) 这样的刷型聚合物在附着于病毒样颗粒时提供更好的免疫屏蔽. PNB结合有效降低了抗体识别,提高了生物制药潜力.
科学领域:
- 生物制药发展
- 聚合物化学
- 免疫学
背景情况:
- 在生物制药中,共价聚合物与蛋白质的结合对于逃避免疫监测至关重要.
- 甲聚乙醇 (mPEG) 或PEGylation是一种常见的方法,导致批准的药物.
- 刷型聚合物有望提高体外和体内性能.
研究的目的:
- 将聚乙烯糖醇 (PEG),聚烯酸和聚乙烯 (PNB) 与病毒样颗粒结合时的聚合物构成进行比较.
- 评估这些结合颗粒与PEGylated颗粒的免疫识别.
主要方法:
- 使用小角度中子散射 (SANS) 来确定聚合物构造.
- 不同水溶性聚合物的结合,使其成为像病毒一样的微粒.
- 通过抗体结合试验评估免疫识别.
主要成果:
- 小角度中子散射显示了PEG,聚烯酸和PNB结合物的不同聚合物构造.
- 聚乙烯 (PNB) 结合提供了最有效的抗体识别屏蔽.
- 不同的聚合物结合策略之间的免疫识别有显著差异.
结论:
- 不同的聚合物结构在与病毒类似的颗粒相连时表现出独特的形状.
- 与PEGylation相比,多聚乙烯 (PNB) 具有更好的免疫逃避能力.
- PNB结合是开发具有增强隐形性能的下一代生物制药的一个有希望的策略.
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