| Literature DB >> 36169675 |
Frances D Nicklen1, Alexia J Diaz1, Jiakun Lu1, Salil T Patel1, Elaine M Zheng1, Veronica R Campbell1, Benjamin M Wu1,2, Daniel T Kamei3.
Abstract
Malaria is an infectious disease that can cause severe sickness and death if not diagnosed and treated in a timely manner. The current gold standard technique for malaria diagnosis is microscopy, which requires a dedicated laboratory setting and trained personnel and can have a long time to result. These requirements can be alleviated using paper-based diagnostic devices that enable rapid and inexpensive diagnosis at the point of care, which can allow patients to receive treatment before their symptoms progress when used for early detection of diseases. The lateral-flow immunoassay (LFA) is one such device, but currently available LFAs are susceptible to false negative results caused by low parasite density. To improve sensitivity and detection, we utilized the aqueous two-phase system (ATPS) to concentrate and purify the sample, and nanozyme signal enhancement to increase the intensity of the visible signal on the test strip. We were able to achieve a limit of detection (LOD) of 0.01 ng/mL for the malaria biomarker Plasmodium lactate dehydrogenase (pLDH) in human serum using a multi-step assay combining the LFA format with the ATPS and nanozyme signal enhancement.Entities:
Keywords: Aqueous two-phase system (ATPS) preconcentration; Lateral-flow immunoassay (LFA); Malaria; Nanozyme signal enhancement; Platinum-coated gold nanozyme probes (PtGNP); Point-of-care diagnostics
Year: 2022 PMID: 36169675 DOI: 10.1007/s00216-022-04346-3
Source DB: PubMed Journal: Anal Bioanal Chem ISSN: 1618-2642 Impact factor: 4.478