LOWER LIMITS OF DETECTION FOR SINGLE BIOLOGICAL PARTICLES USING IMPEDANCE SPECTROSCOPY

机译：阻抗谱法检测单个生物颗粒的下限

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Single-cell impedance spectroscopy integrated with lab-on-a-chip systems provides a direct and minimally invasive approach for monitoring and characterizing properties of individual cells in real-time. Here we investigate the theoretical potential and limitations of this technique for analyzing single membrane-bound particles as small as 100 nm in diameter. Our theoretical model suggests a lower limit of detection for single cells on the order of a few microns.

机译：与单芯片实验室系统集成的单细胞阻抗谱学提供了一种直接且微创的方法，用于实时监控和表征单个细胞的特性。在这里，我们研究了该技术用于分析直径最小为100 nm的单个膜结合颗粒的理论潜力和局限性。我们的理论模型建议单个细胞的检测下限为几微米。

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《American Society of Mechanical Engineers(ASME) Integrated Nanosystems Conference: Design, Synthesis, and Applications; 20050914-16; Berkeley,CA(US)》|2005年|P.17-18|共2页
会议地点 BerkeleyCA(US)
作者
Pahnit Seriburi; Ashutosh Shastry; Angelique Vant Wout; John Mittler; Shih-Hui Chao; John Koschwanez; Deirdre Meldrum;
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作者单位

Microscale Life Sciences Center, University of Washington Seattle, WA 98195-2500;

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原文格式 PDF
正文语种 eng
中图分类半导体技术;
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LOWER LIMITS OF DETECTION FOR SINGLE BIOLOGICAL PARTICLES USING IMPEDANCE SPECTROSCOPY

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