Paper-based microchip electrophoresis for point-of-care hemoglobin testing

Nearly 7% of the world's population live with a hemoglobin variant. Hemoglobins S, C, and E are the most common and significant hemoglobin variants worldwide. Sickle cell disease, caused by hemoglobin S, is highly prevalent in sub-Saharan Africa and in tribal populations of Central India. Hemog...

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Published inAnalyst (London) Vol. 145; no. 7; pp. 2525 - 2542
Main Authors Hasan, Muhammad Noman, Fraiwan, Arwa, An, Ran, Alapan, Yunus, Ung, Ryan, Akkus, Asya, Xu, Julia Z, Rezac, Amy J, Kocmich, Nicholas J, Creary, Melissa S, Oginni, Tolulope, Olanipekun, Grace Mfon, Hassan-Hanga, Fatimah, Jibir, Binta W, Gambo, Safiya, Verma, Anil K, Bharti, Praveen K, Riolueang, Suchada, Ngimhung, Takdanai, Suksangpleng, Thidarat, Thota, Priyaleela, Werner, Greg, Shanmugam, Rajasubramaniam, Das, Aparup, Viprakasit, Vip, Piccone, Connie M, Little, Jane A, Obaro, Stephen K, Gurkan, Umut A
Format Journal Article
LanguageEnglish
Published England Royal Society of Chemistry 07.04.2020
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Summary:Nearly 7% of the world's population live with a hemoglobin variant. Hemoglobins S, C, and E are the most common and significant hemoglobin variants worldwide. Sickle cell disease, caused by hemoglobin S, is highly prevalent in sub-Saharan Africa and in tribal populations of Central India. Hemoglobin C is common in West Africa, and hemoglobin E is common in Southeast Asia. Screening for significant hemoglobin disorders is not currently feasible in many low-income countries with the high disease burden. Lack of early diagnosis leads to preventable high morbidity and mortality in children born with hemoglobin variants in low-resource settings. Here, we describe HemeChip, the first miniaturized, paper-based, microchip electrophoresis platform for identifying the most common hemoglobin variants easily and affordably at the point-of-care in low-resource settings. HemeChip test works with a drop of blood. HemeChip system guides the user step-by-step through the test procedure with animated on-screen instructions. Hemoglobin identification and quantification is automatically performed, and hemoglobin types and percentages are displayed in an easily understandable, objective way. We show the feasibility and high accuracy of HemeChip via testing 768 subjects by clinical sites in the United States, Central India, sub-Saharan Africa, and Southeast Asia. Validation studies include hemoglobin E testing in Bangkok, Thailand, and hemoglobin S testing in Chhattisgarh, India, and in Kano, Nigeria, where the sickle cell disease burden is the highest in the world. Tests were performed by local users, including healthcare workers and clinical laboratory personnel. Study design, methods, and results are presented according to the Standards for Reporting Diagnostic Accuracy (STARD). HemeChip correctly identified all subjects with hemoglobin S, C, and E variants with 100% sensitivity, and displayed an overall diagnostic accuracy of 98.4% in comparison to reference standard methods. HemeChip is a versatile, mass-producible microchip electrophoresis platform that addresses a major unmet need of decentralized hemoglobin analysis in resource-limited settings. We present a versatile, mass-producible, paper-based microchip electrophoresis platform that enables rapid, affordable, decentralized hemoglobin testing at the point-of-care.
Bibliography:Electronic supplementary information (ESI) available. See DOI
10.1039/c9an02250c
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AUTHOR CONTRIBUTIONS
MNH, AF, YA, RU, CMP, JAL, UAG conceived the idea and performed the initial development of the technology. MNH, AF, YA, RU, AA contributed to the proof-of-concept experiments and initial development. PT, AJR, NJK, TO, GMO, FH, BJ, SG, JAL, and SKO helped with the planning and execution of clinical studies in Nigeria, including human subject research protocol development, subject recruitment, blood sample collection, and testing. PT, AKV, PKB, RS, and AD helped with the planning and execution of clinical studies in India, including human subject research protocol development, subject recruitment, blood sample collection, and testing. PT, JZX, SR, TN, TS, and VV helped with the planning and execution of clinical studies in Thailand, including human subject research protocol development, subject recruitment, blood sample collection, and testing. GW helped with the adaptation of HemeChip design for high volume manufacturing. MSC edited the manuscript and authored the public health significance section. MNH, AF, RA, and UAG performed the data analysis, prepared the tables, figures, figure captions, and supplementary information. MNH, AF, RA, UAG drafted and edited the manuscript. All authors read and/or edited the manuscript.
ISSN:0003-2654
1364-5528
DOI:10.1039/c9an02250c