Development of a film-based immunochromatographic microfluidic device for malaria diagnosis

• Published in: Biomedical microdevices 2019-12, Vol.21 (4), p.86-8, Article 86
• Main Authors: Choi, Jihye, Cho, Sung-Jin, Kim, Yong Tae, Shin, Heungsop
• Format: Article
• Language: English
• Subjects: Antibodies; Antibody Specificity; Antigens; Avidin; Biological and Medical Physics; Biomedical Engineering and Bioengineering; Biophysics; Biotin; Chromatography, Affinity - instrumentation; Conjugates; Diagnosis; Engineering; Engineering Fluid Dynamics; Enzyme-Linked Immunosorbent Assay; Erythrocytes; Fluorescence; Food safety; Immobilization; Immunoglobulin G; L-Lactate dehydrogenase; L-Lactate Dehydrogenase - metabolism; Lab-On-A-Chip Devices; Lactate dehydrogenase; Lactic acid; Limit of Detection; Malaria; Malaria - diagnosis; Medical diagnosis; Microfluidic devices; Microfluidics; Monoclonal antibodies; Nanotechnology; Oxygen plasma; Plasmodium falciparum; Plasmodium falciparum - enzymology; Plasmodium falciparum - immunology; Plasmodium falciparum - physiology; Plasmodium vivax - enzymology; Plasmodium vivax - immunology; Plasmodium vivax - physiology; Polycarbonate; Polycarbonate resins; Polyethylene; Polyethylene terephthalate; Vector-borne diseases; Viruses
• ISSN: 1387-2176; 1572-8781
• DOI: 10.1007/s10544-019-0431-8

In this study, a novel film-based immunochromatographic microfluidic device (IMD) has been developed for malaria diagnosis. A microfluidic channel was patterned on a polyethylene terephthalate (PET) double-sided adhesive film using a plotting cutter and was assembled with a polycarbonate (PC) film. The PC film used for the probe immobilization layer was activated using oxygen plasma treatment to modify the film surface with avidin-biotin linker to immobilize a capture antibody. A fluorescent labeled Pan type mAb conjugate was prepared for signal indicator after undergoing a sandwich enzyme-linked immunosorbent assay (ELISA). Target antigens include Plasmodium falciparum ( P. falciparum ) lactate dehydrogenase (LDH) and Plasmodium vivax ( P. vivax ) LDH which were injected into the sample inlet. Target antigens combined with the conjugate and then flowed to the detection chamber where two test dots and a control dot (Ctrl) exist. In the presence of P. falciparum LDH, three detection dots including test dot 1 (T1), test dot 2 (T2) and Ctrl revealed fluorescence signals where P. falciparum mAb, Pan type pLDH mAb and goat anti-mouse IgG were immobilized, respectively. When P. vivax LDH was present, T2 and Ctrl dots showed fluorescence signals while no signal was detected with the negative control. P. falciparum LDH and P. vivax LDH were successfully detected on the IMD with a detection limit of 50 ng/mL and 100 ng/mL, respectively. The IMD provides a point-of-care diagnosis platform which is able to analyze pathogenic bacteria and viruses that can be applied in the field of clinical diagnosis and food safety testing.