Microfluidic Chip based direct triple antibody immunoassay for monitoring patient comparative response to leukemia treatment

dc.contributor.author Icoz, Kutay
dc.contributor.author Akar, Unal
dc.contributor.author Unal, Ekrem
dc.contributor.authorID 0000-0002-0947-6166 en_US
dc.contributor.authorID 0000-0002-0000-8999 en_US
dc.contributor.department AGÜ, Mühendislik Fakültesi, Elektrik - Elektronik Mühendisliği Bölümü en_US
dc.date.accessioned 2021-01-27T09:41:08Z
dc.date.available 2021-01-27T09:41:08Z
dc.date.issued 2020 en_US
dc.description Authors acknowledge TUBITAK (Project No: 115E020) for financial support. Authors also give thanks to Nazendenur Aksit and Ahsen Aydin for helping on taking the SEM images, Dr. Cengiz Gazeloglu from Isparta Suleyman Demirel University for valuable discussions on statistical analysis. en_US
dc.description.abstract We report a time and cost-efficient microfluidic chip for screening the leukemia cells having three specific antigens. In this method, the target blast cells are double sorted with immunomagnetic beads and captured by the 3rd antibody immobilized on the gold surface in a microfluidic chip. The captured blast cells in the chip were imaged using a bright-field optical microscope and images were analyzed to quantify the cells. First sorting was performed with nano size immunomagnetic beads and followed by 2nd sorting where micron size immunomagnetic beads were used. The low-cost microfluidic platform is made of PMMA and glass including micro size gold pads. The developed microfluidic platform was optimized with cultured B type lymphoblast cells and tested with the samples of leukemia patients. The 8 bone marrow samples of 4 leukemia patients on the initial diagnosis and on the 15th day after the start of the chemotherapy treatment were tested both with the developed microfluidic platform and the flow cytometry. A 99% statistical agreement between the two methods shows that the microfluidic chip is able to monitor the decrease in the number of blast cells due to the chemotherapy. The experiments with the patient samples demonstrate that the developed system can perform relative measurements and have a potential to monitor the patient response to the applied therapy and to enable personalized dose adjustment. en_US
dc.description.sponsorship Turkiye Bilimsel ve Teknolojik Arastirma Kurumu (TUBITAK) 115E020 en_US
dc.identifier.issn 1387-2176
dc.identifier.issn 1572-8781
dc.identifier.issue 3 en_US
dc.identifier.other PubMed ID: 32661698
dc.identifier.uri https://doi.org/10.1007/s10544-020-00503-6
dc.identifier.uri https://hdl.handle.net/20.500.12573/506
dc.identifier.volume Volume: 22 en_US
dc.language.iso eng en_US
dc.publisher SPRINGER, VAN GODEWIJCKSTRAAT 30, 3311 GZ DORDRECHT, NETHERLANDS en_US
dc.relation.isversionof 10.1007/s10544-020-00503-6 en_US
dc.relation.journal BIOMEDICAL MICRODEVICES en_US
dc.relation.publicationcategory Makale - Uluslararası - Editör Denetimli Dergi en_US
dc.relation.tubitak 115E020
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject comparative response en_US
dc.subject Microfluidic -based monitoring en_US
dc.subject Direct triple antibody en_US
dc.subject Leukemia en_US
dc.subject Biochip en_US
dc.subject Immunoassay en_US
dc.subject nano particles en_US
dc.subject Magnetic micro en_US
dc.title Microfluidic Chip based direct triple antibody immunoassay for monitoring patient comparative response to leukemia treatment en_US
dc.type article en_US

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