Engineering a better device to capture — and release — circulating tumor cells

For many years, bioengineer Yaling Liu has remained in pursuit of the deadly tumor cell. Liu has been perfecting a microfluidic device the size of two quarters that has the ability to catch and release circulating tumor cells (CTCs) — cancer cells that circulate in a cancer patient’s blood. Such a gadget could lead to earlier detection of metastasis and primary tumors, as well as determine the effectiveness of the treatment — all via a simple blood test.

Liu, a faculty member in both mechanical engineering and bioengineering at Lehigh University, is in the early stages of testing his device in a clinical setting — and the results have been promising.

Liu’s “laboratory on a chip” is notable for its ability to not only capture tumor cells circulating in the blood, but to “release” those cells as well.

“Our circulating tumor cell device can release a tumor cell captured from a blood sample, enabling single cell analysis,” states Liu. “It could be used to check the effectiveness of a treatment, by identifying the amount of tumor cells circulating. Conducting genetic testing on a released single cell could also reveal whether the primary tumor had metastasized, as metastasized cells have unique genetic markers.”

The gadget could also be used to check the effectiveness of cancer gene therapy.

“Genetic tests could be performed on the released CTCs, indicating if the gene therapy is triggering changes in gene expression,” states Liu. In other words, such testing could help detect whether a treatment is working or if other methods should be explored.

Liu presented some of these on 18th Apri, at a conference taking place in Istanbul, Turkey called The Future of Medicine hosted by Royal Academy of Science International Trust (RASIT) and Bahçeşehir University. Liu presented via Skype from his office on Lehigh University’s campus in Bethlehem, Pennsylvania.

Liu’s device is part of a clinical drug trial for renal cancels and melanoma at the Lehigh Valley Cancer Institute. Funding for the study has been provided by the Andy Derr Foundation for Kidney Cancer Research. The aim is to gather preliminary data about whether the device can improve care.

The first stage of the trial, which involved an analysis of circulating tumor cells from a single blood draw of several dozen patients, has demonstrated very strong potential.

“The next step will be to track a few patients over the course of their treatment, taking several blood draws to see if the data captured by the microfluidic device correlates with the data their medical team is collecting through other methods,” states Liu.

Liu and his researcg team are preparing to undertake that next step within the next few months.

Magnetism, wavy-herringbone design key to CTC device’s success

Liu’s microfluidic device achieves two key standards by which the success of CTC devices is measured: high selectivity and high capture efficiency. Selectivity measures how well it rejects unwanted cells, such as white and red blood cells. Capture efficiency refers to the percentage of CTCs that the device collects.

The rectangular chip (same video above) — smaller than a few square centimeters and using as little as a few milliliters of blood–is made of the polymer PDMS. The chip’s key feature is a tiny flow channel on a hierarchically designed pad that is optimized to capture tumor cells from the blood flowing across it.

Using microfluidic design principles, Liu’s team engineered vortices in their device to increase the chance that tumor cells will collide with the surface of the flow channel. The group also arranged ripples in a wavy-herringbone pattern lining the bottom of the capture pad.

“The herringbone surface generates a passive vortex that mixes the cells and increases the chance that they will collide with the capture pad,” says Liu. “High selectivity is achieved by smoothing the sharp grooved herringbone pattern into a wavy one, helping to filter out unwanted cells.”

The group uses immunoaffinity — the specific chemical affinity between an antigen and an antibody — to make CTCs adhere to the device while normal blood cells flow past. They coat the pad with a layer of anti-epithelial cell adhesion molecules (anti-EpCAM) which bond with CTCs but not with healthy cells.

Liu and his research team recently improved upon the device’s release efficiency — or its ability to allow circulating tumor cells to be collected for further study. Instead of permanently depositing particles through immunoaffinity, anti-EpCAM coated magnetic microparticles were trapped over the untreated PDMS surface by an external magnetic field and were then released by readily removing the magnet for CTC collection. The results were published in the journal Lab on a Chip (Lab on a Chip 17 (19), 3291-3299) in an article called: “Magnetic particles assisted capture and release of rare circulating tumor cells using wavy-herringbone structured microfluidic devices.”

According to Liu, under optimimum conditions, the capture efficiency of the tumor cells were as high as 92% ± 2.9%. Capture experiments were also performed on whole blood samples, and the capture efficiency was in a high range of 82 – 96%, at different tumor cell concentrations.

[Ad] – YOU MAY LIKE: Cool Gadgets For GuysLatestGadgets.Tech – [Ad]

He states that such a method can potentially be used for CTC sorting from patient blood samples, CTC concentration monitoring, therapeutic guidance and drug dosage choice, and further study of tumors, such as tumor mutations. anddrug screening.

Adds Liu: “With metastatic cancers accounting for around 90% of deaths from solid tumors, the hope is that one day a device that can enable the analysis of single tumor cells circulating in the blood could make a big difference in early diagnosis, detection and monitoring of numerous types of cancer, without invasive biopsies.”

###

Disclaimer: We all make mistakes. Try and learn for them. Have a great day.

Recommended For You

About the Author: livescience

Leave a Reply

Your email address will not be published. Required fields are marked *