Novel API Coated Catheter Removes Amyloid-β from Plasma of Patients with Alzheimer's Disease.

Rishi Raj Chhipa, Omkar Gandbhir, Hao Le, Sadhana Sankar, Pazhani Sundaram
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Abstract

Alzheimer's disease (AD) is the most common cause of dementia, characterized by the deposition of Amyloid-beta (Aβ) plaques in the brain. We have previously developed Amytrap peptide (the active pharmacological ingredient, API) and linked it to a sepharose bead matrix by click chemistry to form Amytrapper matrix, which was able to bind and remove Aβ from human sera and plasma spiked with biotinylated Aβ42 (bio-Aβ42) in vitro. To extend the logic of the previous studies, the current study investigates whether the Amytrap peptide coated inside a medically viable polycarbonate catheter (Amytrapper catheter) could bind and retain Aβ from the human sera. The Amytrapper matrix and the novel Amytrapper catheter were able to bind and retain spiked bio-Aβ42 from human sera or native Aβ from plasma of AD patients. Additional characteristics of the Amytrapper catheter are evaluated and presented in this study. The results presented here provide a proof-of-principle for the first time that extracorporeal Amytrapper device aids clearance of native Aβ (from plasma of AD patients). Thus, our device Amytrapper, either in the form of Sepharose matrix or catheter, could become a novel therapeutic strategy to remove Aβ from circulation in AD patients.

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新型API涂层导管可从阿尔茨海默病患者血浆中去除淀粉样蛋白-β。
阿尔茨海默病(AD)是痴呆症最常见的原因,其特征是大脑中β淀粉样蛋白(Aβ)斑块的沉积。我们之前已经开发了Amytrap肽(活性药理成分,API),并通过点击化学将其与sepharose bead基质连接形成Amytrap基质,该基质能够在体外结合并去除含有生物素化a β42 (bio-Aβ42)的人血清和血浆中的a β。为了扩展先前研究的逻辑,目前的研究调查了包裹在医学上可行的聚碳酸酯导管(Amytrapper导管)内的Amytrap肽是否可以结合并保留人类血清中的a β。Amytrapper基质和新型Amytrapper导管能够结合并保留来自人血清的生物Aβ42或来自AD患者血浆的天然Aβ。本研究对amytraper导管的其他特性进行了评估和介绍。本文的结果首次提供了一个原理证明,即体外Amytrapper装置有助于清除(来自AD患者血浆的)天然a β。因此,我们的Amytrapper装置,无论是以Sepharose基质还是导管的形式,都可能成为一种新的治疗策略,从AD患者的循环中去除a β。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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