Parameterization of high magnetic field gradient fractionation columns for applications with Plasmodium falciparum infected human erythrocytes
Abstract Background Magnetic fractionation of erythrocytes infected with Plasmodium falicparum has several research uses including enrichment of infected cells from parasite cultures or enhanced detection of P. falciparum gametocytes. The aim of the present study was to quantitatively characterize t...
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ftdoajarticles:oai:doaj.org/article:ae45e2a42d3648e28acc9da28ca606e8 2023-05-15T15:14:25+02:00 Parameterization of high magnetic field gradient fractionation columns for applications with Plasmodium falciparum infected human erythrocytes Davis Timothy ME Karl Stephan St Pierre Tim G 2010-05-01T00:00:00Z https://doi.org/10.1186/1475-2875-9-116 https://doaj.org/article/ae45e2a42d3648e28acc9da28ca606e8 EN eng BMC http://www.malariajournal.com/content/9/1/116 https://doaj.org/toc/1475-2875 doi:10.1186/1475-2875-9-116 1475-2875 https://doaj.org/article/ae45e2a42d3648e28acc9da28ca606e8 Malaria Journal, Vol 9, Iss 1, p 116 (2010) Arctic medicine. Tropical medicine RC955-962 Infectious and parasitic diseases RC109-216 article 2010 ftdoajarticles https://doi.org/10.1186/1475-2875-9-116 2022-12-31T10:23:48Z Abstract Background Magnetic fractionation of erythrocytes infected with Plasmodium falicparum has several research uses including enrichment of infected cells from parasite cultures or enhanced detection of P. falciparum gametocytes. The aim of the present study was to quantitatively characterize the magnetic fractionation process and thus enable optimization of protocols developed for specific uses. Methods Synchronized cultures of P. falciparum parasites incubated with human erythrocytes were magnetically fractionated with commercially available columns. The timing of the fractionation experiments was such that the parasites were in second half of their erythrocytic life cycle with parasite densities ranging from 1 to 9%. Fractionations were carried out in a single pass through the columns. Cells were enumerated and differentiated in the initial samples as well as in the positive and negative fractions. The capture of cells by the fractionation column was described by a saturation binding model. Results The magnetic binding affinity to the column matrix was approximately 350 times greater for infected cells compared with uninfected cells. The purity of infected cells in the captured fraction was generally >80% but decreased rapidly (to less than 50%) when the number of infected cells that passed through the column was substantially decreased (to less than 9 ± 5 × 10 5 cells). The distribution of captured parasite developmental stages shifted to mature stages as the number of infected cells in the initial samples and flow rate increased. The relationship between the yield of infected cells in the captured fraction and flow rate of cells conformed to a complementary cumulative log-normal equation with flow rates >1.6 × 10 5 cells per second resulting in yields <50%. Conclusions A detailed quantitative analysis of a batchwise magnetic fractionation process for malaria infected erythrocytes using high gradient magnetic fractionation columns was performed. The models applied in this study allow the ... Article in Journal/Newspaper Arctic Directory of Open Access Journals: DOAJ Articles Arctic Malaria Journal 9 1 116 |
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Directory of Open Access Journals: DOAJ Articles |
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English |
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Arctic medicine. Tropical medicine RC955-962 Infectious and parasitic diseases RC109-216 |
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Arctic medicine. Tropical medicine RC955-962 Infectious and parasitic diseases RC109-216 Davis Timothy ME Karl Stephan St Pierre Tim G Parameterization of high magnetic field gradient fractionation columns for applications with Plasmodium falciparum infected human erythrocytes |
topic_facet |
Arctic medicine. Tropical medicine RC955-962 Infectious and parasitic diseases RC109-216 |
description |
Abstract Background Magnetic fractionation of erythrocytes infected with Plasmodium falicparum has several research uses including enrichment of infected cells from parasite cultures or enhanced detection of P. falciparum gametocytes. The aim of the present study was to quantitatively characterize the magnetic fractionation process and thus enable optimization of protocols developed for specific uses. Methods Synchronized cultures of P. falciparum parasites incubated with human erythrocytes were magnetically fractionated with commercially available columns. The timing of the fractionation experiments was such that the parasites were in second half of their erythrocytic life cycle with parasite densities ranging from 1 to 9%. Fractionations were carried out in a single pass through the columns. Cells were enumerated and differentiated in the initial samples as well as in the positive and negative fractions. The capture of cells by the fractionation column was described by a saturation binding model. Results The magnetic binding affinity to the column matrix was approximately 350 times greater for infected cells compared with uninfected cells. The purity of infected cells in the captured fraction was generally >80% but decreased rapidly (to less than 50%) when the number of infected cells that passed through the column was substantially decreased (to less than 9 ± 5 × 10 5 cells). The distribution of captured parasite developmental stages shifted to mature stages as the number of infected cells in the initial samples and flow rate increased. The relationship between the yield of infected cells in the captured fraction and flow rate of cells conformed to a complementary cumulative log-normal equation with flow rates >1.6 × 10 5 cells per second resulting in yields <50%. Conclusions A detailed quantitative analysis of a batchwise magnetic fractionation process for malaria infected erythrocytes using high gradient magnetic fractionation columns was performed. The models applied in this study allow the ... |
format |
Article in Journal/Newspaper |
author |
Davis Timothy ME Karl Stephan St Pierre Tim G |
author_facet |
Davis Timothy ME Karl Stephan St Pierre Tim G |
author_sort |
Davis Timothy ME |
title |
Parameterization of high magnetic field gradient fractionation columns for applications with Plasmodium falciparum infected human erythrocytes |
title_short |
Parameterization of high magnetic field gradient fractionation columns for applications with Plasmodium falciparum infected human erythrocytes |
title_full |
Parameterization of high magnetic field gradient fractionation columns for applications with Plasmodium falciparum infected human erythrocytes |
title_fullStr |
Parameterization of high magnetic field gradient fractionation columns for applications with Plasmodium falciparum infected human erythrocytes |
title_full_unstemmed |
Parameterization of high magnetic field gradient fractionation columns for applications with Plasmodium falciparum infected human erythrocytes |
title_sort |
parameterization of high magnetic field gradient fractionation columns for applications with plasmodium falciparum infected human erythrocytes |
publisher |
BMC |
publishDate |
2010 |
url |
https://doi.org/10.1186/1475-2875-9-116 https://doaj.org/article/ae45e2a42d3648e28acc9da28ca606e8 |
geographic |
Arctic |
geographic_facet |
Arctic |
genre |
Arctic |
genre_facet |
Arctic |
op_source |
Malaria Journal, Vol 9, Iss 1, p 116 (2010) |
op_relation |
http://www.malariajournal.com/content/9/1/116 https://doaj.org/toc/1475-2875 doi:10.1186/1475-2875-9-116 1475-2875 https://doaj.org/article/ae45e2a42d3648e28acc9da28ca606e8 |
op_doi |
https://doi.org/10.1186/1475-2875-9-116 |
container_title |
Malaria Journal |
container_volume |
9 |
container_issue |
1 |
container_start_page |
116 |
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1766344880516235264 |