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淀粉材料作为生物相容性的支持物以及快速分离巨噬细胞的方法。

Starch materials as biocompatible supports and procedure for fast separation of macrophages.

机构信息

Department of Chemistry and Biomed Center, Université du Québec à Montréal, C.P. 8888, Branch A, Montréal, Québec, H3C 3P8, Canada.

Department of Biological Sciences and Biomed Center, Université du Québec à Montréal, C.P. 8888, Branch A, Montréal, Québec H3C 3P8, Canada.

出版信息

Carbohydr Polym. 2017 May 1;163:108-117. doi: 10.1016/j.carbpol.2017.01.053. Epub 2017 Jan 18.

Abstract

Different starch derivatives were evaluated as supports for attachment and recovery of macrophages (RAW 264.7 line). Gelatinized starch (G-St), acetate starch (Ac-St), carboxymethyl starch and aminoethyl starch were synthesized and characterized by FTIR, H NMR, SEM and static water contact angle. These polymers are filmogenic and may coat well the holder devices used for macrophage adhesion. They also present a susceptibility to mild hydrolysis with alpha-amylase, liberating the adhered macrophages. Cell counts, percentage of dead cells and level of tumor necrosis factor (TNF-α) were used to evaluate the possible interaction between macrophages and starch films. The high percentage of cell adhesion (90-95% on G-St and on Ac-St) associated with enzymatic detachment of macrophages from film-coated inserts, resulted in higher viabilities compared with those obtained with cells detached by current methods scrapping or vortex. This novel method allows a fast macrophage separation, with excellent yields and high viability of recovered cells.

摘要

不同的淀粉衍生物被评估为附着和回收巨噬细胞(RAW 264.7 系)的载体。对糊化淀粉(G-St)、醋酸淀粉(Ac-St)、羧甲基淀粉和氨乙基淀粉进行了合成和表征,通过傅里叶变换红外光谱(FTIR)、核磁共振氢谱(H NMR)、扫描电子显微镜(SEM)和静态水接触角进行了表征。这些聚合物具有成膜性,可以很好地涂覆用于巨噬细胞黏附的支架装置。它们还具有对α-淀粉酶的轻度水解的敏感性,从而释放黏附的巨噬细胞。细胞计数、死亡细胞的百分比和肿瘤坏死因子(TNF-α)水平用于评估巨噬细胞与淀粉薄膜之间的可能相互作用。高细胞黏附率(G-St 和 Ac-St 上为 90-95%)与酶法从涂有薄膜的小室中分离巨噬细胞相关联,与当前通过刮擦或涡旋方法分离细胞相比,细胞活力更高。这种新方法允许快速分离巨噬细胞,具有出色的产率和高回收率的细胞活力。

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