Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/85506
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dc.contributor.authorThamarath, Smitha Surendranen
dc.contributor.authorXiong, Aolien
dc.contributor.authorLin, Po-Hanen
dc.contributor.authorPreiser, Peter Raineren
dc.contributor.authorHan, Jongyoonen
dc.date.accessioned2019-05-16T03:57:49Zen
dc.date.accessioned2019-12-06T16:05:07Z-
dc.date.available2019-05-16T03:57:49Zen
dc.date.available2019-12-06T16:05:07Z-
dc.date.issued2019en
dc.identifier.citationThamarath, S. S., Xiong, A., Lin, P.-H., Preiser, P. R., & Han, J. (2019). Enhancing the sensitivity of micro magnetic resonance relaxometry detection of low parasitemia Plasmodium falciparum in human blood. Scientific Reports, 9, 2555-. doi:10.1038/s41598-019-38805-2en
dc.identifier.urihttps://hdl.handle.net/10356/85506-
dc.identifier.urihttp://hdl.handle.net/10220/48224en
dc.description.abstractUpon Plasmodium falciparum infection of the red blood cells (RBCs), the parasite replicates and consumes haemoglobin resulting in the release of free heme which is rapidly converted to hemozoin crystallites. The bulk magnetic susceptibility of infected RBCs (iRBCs) is changed due to ferric (Fe3+) paramagnetic state in hemozoin crystallites which induce a measurable change in spin-spin relaxation (transverse relaxation) rate in proton nuclear magnetic resonance (NMR) of iRBCs. Earlier, our group reported that this transverse relaxation rate (R2) can be measured by an inexpensive, portable 0.5 Tesla bench top magnetic resonance relaxometry (MRR) system with minimum sample preparation and is able to detect very low levels of parasitemia in both blood cultures as well as animal models. However, it was challenging to diagnose malaria in human blood using MRR, mainly due to the inherent variation of R2 values of clinical blood samples, caused by many physiological and genotypic differences not related to the parasite infection. To resolve the problem of baseline R2 rates, we have developed an improved lysis protocol for removing confounding molecular and cellular background for MRR detection. With this new protocol and by processing larger volume of blood (>1 ml), we are able to reliably detect very low level of parasitemia (representing early stage of infection, ~0.0001%) with a stable baseline and improved sensitivity using the current MRR system.en
dc.description.sponsorshipNRF (Natl Research Foundation, S’pore)en
dc.format.extent9 p.en
dc.language.isoenen
dc.relation.ispartofseriesScientific Reportsen
dc.rights© 2019 The Author(s) (Nature Publishing Group). Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.en
dc.subjectDRNTU::Science::Biological sciencesen
dc.subjectBiochemical Assaysen
dc.subjectMalariaen
dc.titleEnhancing the sensitivity of micro magnetic resonance relaxometry detection of low parasitemia Plasmodium falciparum in human blooden
dc.typeJournal Articleen
dc.contributor.schoolSchool of Biological Sciencesen
dc.identifier.doihttp://dx.doi.org/10.1038/s41598-019-38805-2en
dc.description.versionPublished versionen
item.grantfulltextopen-
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