AI Article Synopsis

  • Malaria is a serious infectious disease that needs quick diagnosis and treatment to prevent severe health issues or death, with microscopy being the standard but time-consuming method for diagnosis.
  • New paper-based diagnostic devices like lateral-flow immunoassays (LFAs) offer a faster and cheaper alternative for detecting malaria at the point of care, but they can sometimes miss infections if the parasite density is low.
  • To improve detection accuracy, researchers combined LFA with an aqueous two-phase system and nanozyme signal enhancement, achieving a highly sensitive detection limit for the malaria biomarker Plasmodium lactate dehydrogenase (pLDH) at 0.01 ng/mL in human serum.

Article 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.

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Source
http://dx.doi.org/10.1007/s00216-022-04346-3DOI Listing

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