Secondary Faculty Mentor (Name, Affiliation, website and Email\/Phone):<\/b><\/p>\n
Carsten Schroeder MD PhD, Georgia Regents University, Department of Surgery, CSCHROEDER@gru.edu<\/span><\/a>, 706-721-4726<\/p>\n Graduate Student\/PostDoc mentors (Name, Affiliation and Email\/Phone):<\/b><\/p>\n Wujun Zhao, UGA College of Engineering, zhaowj@uga.edu, 706-542-1482<\/p>\n Project Description:<\/b> Access to tumor samples without the need for painful and expensive tumor biopsies, would allow clinicians and researchers to frequently analyze patient samples and have significant impact on patent care. Thus the great potential in recent circulating tumor cell (CTC) research\u00a0lies in the use of these rare cells present in the peripheral blood\u00a0as an accessible biopsy that would permit repeated minimally invasive sampling of tumor cells. The concentration of CTCs is also believed to be an important indicator of cancer progression and metastasis. As a result accurate\u00a0counting and analysis of CTCs are critical to diagnosis and therapeutic response monitoring of various types of cancer, including\u00a0lung cancer. However, only 1-100 CTCs exist in 1 mL of whole blood (that is around 10^9\u00a0red blood cells and 10^6\u00a0white blood cells), which makes the enrichment,\u00a0characterization and analysis of CTCs challenging. Recent advances in microfluidic systems at the Dr.Mao\u2019s lab have lead to the development of a label-free micro-scale ferrofluidic cell separation platform that can enrich cells of interest based on their sizes with high throughput, high enrichment ratio, high purity and very low cost.\u00a0\u00a0The specific hypothesis for project is that microfluidic cell\u00a0enrichment will increase the detection rate of lung cancer circulating tumor cells (CTCs) in patient samples.<\/p>\n REU Student Role and Responsibility:<\/b> The student project will work with a graduate student and collaborators at Georgia Regents University to develop an optimized magnetic microfluidic system based on the previous generation of enrichment chip that can be used to process lung cancer specimens at a CTC\u00a0recovery ratio of over 90% with a cell-processing throughput of\u00a0over 109\u00a0cells\/hour. Our initial experimental results indicate that ferrofluids under magnetic fields can be used to enrich cancer cells from whole blood at approximately 10^8\u00a0cell\/hour with the current design. The throughput this\u00a0separation scheme needs to be systematically optimized to allow for over 10^9\u00a0cell\/hour throughput for CTC detection. In addition,\u00a0the dependence of separation efficiency on the channel geometry needs to be characterized in order to fashion a separator that performs optimally with lung\u00a0cancer specimens. The student will investigate: 1) The cross section of the microchannel will be increased to allow for faster flow rates (~100 \u03bcL\/min) to \u00a0process more cells; 2) Multiple microchannels\u00a0will be integrated together onto one chip to increase the throughput by at least one order; 3)\u00a0CTC traps will be included into the chip to retain sorted cells for further analysis.<\/p>\n Expected Outcome for REU student:<\/b> The student is expected to contribute and co-author journal and conference papers.<\/p>\n
![\"DSC_0093\"](\"https:\/\/reu.engr.uga.edu\/wp-content\/uploads\/2015\/07\/DSC_0093.jpg\")
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