The physical origins of transit time measurements for rapid, single cell mechanotyping-Reference-Cited by-同舟云学术

The physical origins of transit time measurements for rapid, single cell mechanotyping

Published:2016 Issue:17 Volume:16 Page:3330-3339
ISSN:1473-0197
Container-title:Lab on a Chip
language:en
Short-container-title:Lab Chip

Author:

Nyberg Kendra D.¹²³⁴⁵,Scott Michael B.¹²³⁴,Bruce Samuel L.¹²³⁴,Gopinath Ajay B.¹²³⁴,Bikos Dimitri⁶²³⁴,Mason Thomas G.⁶²³⁴⁷,Kim Jin Woong⁸⁹¹⁰¹¹¹²,Choi Hong Sung¹³¹⁴¹¹,Rowat Amy C.¹²³⁴⁵

Affiliation:

1. Department of Integrative Biology and Physiology

2. University of California

3. Los Angeles

4. USA

5. Department of Bioengineering

6. Department of Chemistry and Biochemistry

7. Department of Physics and Astronomy

8. Department of Bionano Technology

9. Hanyang University

10. Ansan

11. Republic of Korea

12. Department of Applied Chemistry

13. Shinsegae International Co. Ltd

14. Seoul

Abstract

Major physical contributors to cell transit times through microfluidic constrictions are identified with the goal of facilitating more precise mechanotyping.

Funder

National Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Biomedical Engineering,General Chemistry,Biochemistry,Bioengineering

Link

http://pubs.rsc.org/en/content/articlepdf/2016/LC/C6LC00169F

Reference50 articles.

1. Quantitative Diagnosis of Malignant Pleural Effusions by Single-Cell Mechanophenotyping

2. Passive mechanical behavior of human neutrophils: effect of cytochalasin B

3. Nanomechanical analysis of cells from cancer patients