Measuring single cell mass, volume, and density with dual suspended microchannel resonators

被引:139
作者
Bryan, Andrea K. [1 ,2 ]
Hecht, Vivian C. [1 ,2 ]
Shen, Wenjiang [3 ]
Payer, Kristofor
Grover, William H. [1 ,2 ,4 ]
Manalis, Scott R. [1 ,2 ]
机构
[1] MIT, Dept Biol Engn, Cambridge, MA 02139 USA
[2] MIT, Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
[3] Innovat Micro Technol, Santa Barbara, CA 93117 USA
[4] MIT, Microsyst Technol Labs, Cambridge, MA USA
基金
美国国家卫生研究院;
关键词
GROWTH;
D O I
10.1039/c3lc51022k
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Cell size, measured as either volume or mass, is a fundamental indicator of cell state. Far more tightly regulated than size is density, the ratio between mass and volume, which can be used to distinguish between cell populations even when volume and mass appear to remain constant. Here we expand upon a previous method for measuring cell density involving a suspended microchannel resonator (SMR). We introduce a new device, the dual SMR, as a high-precision instrument for measuring single-cell mass, volume, and density using two resonators connected by a serpentine fluidic channel. The dual SMR designs considered herein demonstrate the critical role of channel geometry in ensuring proper mixing and damping of pressure fluctuations in microfluidic systems designed for precision measurement. We use the dual SMR to compare the physical properties of two well-known cancer cell lines: human lung cancer cell H1650 and mouse lymphoblastic leukemia cell line L1210.
引用
收藏
页码:569 / 576
页数:8
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