苏州大学药学院
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魏同洪, 刘玲, 丁海洋, 等. 基于聚丙烯酸交联组装单层SiO2纳米粒粗糙表面及其细胞捕获[J]. 分析测试学报, 2017,36(8):1043-1046.
Rough Surface of One-layer SiO2 Nanoparticles Assembled by Polyacrylic Acid Cross-linking and Its Cell Capture[J]. 2017,36(8):1043-1046.
以玻片为载体(Subs),聚丙烯酸(PAA)为交联剂和柔性体,SiO2纳米粒为刚性体,人B淋巴细胞瘤Ramos细胞为目标细胞,TD05适体为细胞捕获配体(Apt),在载体上交联组装了结构为Subs-PAA1-SiO2-PAA2-Apt的细胞捕获支架。该支架既有小尺度的刚性结构,即SiO2纳米粒,又有柔性结构,即聚丙烯酸PAA1和PAA2。前者增加了载体的粗糙度,而后者不仅能够固载多重捕获配体,也能够有效降低宏观载体对细胞捕获的空间位阻。结果表明,支架具有良好的纳米粒结构,未发现纳米粒的融合甚至消失;支架的特异性捕获是非特异性吸附的16倍,被捕获细胞表现出较高的纯度;同时,支架具有较高的捕获效率,捕获细胞数是通常的单层刚性纳米粒支架的8.3倍。由此表明,该文构建的结构新颖的纳米粒柔性支架实现了目标细胞的高效率、高纯度捕获,将为肿瘤细胞的分析检测提供可靠的样本。
A cell capture scaffold with a structure of Subs-PAA1-SiO2-PAA2-Apt was assembled by using a glass slide as substrate carrier(Subs),polyelectrolyte polyacrylic acid(PAA) as cross-linking agent and flexible body,SiO2 nanoparticles as rigid body,and TD05 aptamer(Apt) as capture ligand of objective cell Ramos.Here there are a small scale and rigid structure(i.e.SiO2 nanoparticle),but also a flexible structure(i.e.polyacrylic acid PAA1 and PAA2).The former increased the roughness of carrier,and the latter could not only immobilized the multi-ligand Apt,but also decreased the steric hindrance from the scaffold itself and the carrier for cell capture.The results indicated that the as-assembled scaffold had a good nanoparticle structure and fusing even disappearing of the nanoparticle structure was not found.For the scaffold,its specific capture was 16 times of the non-specific adsorption,and the captured cell showed a higher purity.Meanwhile the captured cell has also a higher captureefficiency,and the capture cell number was 8.3 times of that of the usual rigid scaffold with one-layer nanoparticle.It was shown that the nanoparticle flexible scaffold with a novel structure was fabricated,which could realize the high purity and the high efficiency for cell capture.
支架细胞捕获纳米粒聚电解质
scaffoldcellcapturenanoparticlepolyelectrolyte
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