Optimizing the culture of plasmodium falciparum in hollow fiber bioreactors

The hollow fiber bioreactor (HFBR) is a cell culturing system allowing continuous perfusion of medium. It was designed to grow microorganisms in a dynamically altering medium mimicking change in the in vivo intravascular and extravascular compartments. The cell compartment (extra capillary space) an...

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Main Authors: P. Preechapornkul, K. Chotivanich, M. Imwong, A. M. Dondorp, S. J. Lee, N. P J Day, N. J. White, S. Pukrittayakamee
Other Authors: Mahidol University
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Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/29604
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spelling th-mahidol.296042018-09-24T16:25:03Z Optimizing the culture of plasmodium falciparum in hollow fiber bioreactors P. Preechapornkul K. Chotivanich M. Imwong A. M. Dondorp S. J. Lee N. P J Day N. J. White S. Pukrittayakamee Mahidol University Churchill Hospital Medicine The hollow fiber bioreactor (HFBR) is a cell culturing system allowing continuous perfusion of medium. It was designed to grow microorganisms in a dynamically altering medium mimicking change in the in vivo intravascular and extravascular compartments. The cell compartment (extra capillary space) and medium compartment (intra capillary space) are connected through pores of semipermeable fiber membranes. These membranes allow exchange of gas and nutrients. We have adapted this system for the ex vivo culture of Plasmodium falciparum at high parasite densities. A Thai P. falciparum isolate (TM036) cultured in RPMI, supplemented with 0.5% Albumax II, could be maintained continuously in the system by daily changes of a small volumes of medium. Under optimized conditions the HFBR cultures attained 8% parasitemia in 40% hematocrit, thereby providing a total parasite biomass of 6.0x109 parasitized erythrocytes. The main problem encountered was clogging of micropores in the hollow fiber system by cellular debris over time. Although 'reverse flushing' partly prevented this, a larger pore size might be needed to overcome this problem. The system opens new possibilities for the study of in vitro drug sensitivity under conditions mimicking in vivo pharmacokinetics, and the selection of anti-malarial drug resistance and associated parasite biological and genomic changes. 2018-09-24T09:25:03Z 2018-09-24T09:25:03Z 2010-07-01 Article Southeast Asian Journal of Tropical Medicine and Public Health. Vol.41, No.4 (2010), 761-769 01251562 2-s2.0-79952111423 https://repository.li.mahidol.ac.th/handle/123456789/29604 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79952111423&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Medicine
spellingShingle Medicine
P. Preechapornkul
K. Chotivanich
M. Imwong
A. M. Dondorp
S. J. Lee
N. P J Day
N. J. White
S. Pukrittayakamee
Optimizing the culture of plasmodium falciparum in hollow fiber bioreactors
description The hollow fiber bioreactor (HFBR) is a cell culturing system allowing continuous perfusion of medium. It was designed to grow microorganisms in a dynamically altering medium mimicking change in the in vivo intravascular and extravascular compartments. The cell compartment (extra capillary space) and medium compartment (intra capillary space) are connected through pores of semipermeable fiber membranes. These membranes allow exchange of gas and nutrients. We have adapted this system for the ex vivo culture of Plasmodium falciparum at high parasite densities. A Thai P. falciparum isolate (TM036) cultured in RPMI, supplemented with 0.5% Albumax II, could be maintained continuously in the system by daily changes of a small volumes of medium. Under optimized conditions the HFBR cultures attained 8% parasitemia in 40% hematocrit, thereby providing a total parasite biomass of 6.0x109 parasitized erythrocytes. The main problem encountered was clogging of micropores in the hollow fiber system by cellular debris over time. Although 'reverse flushing' partly prevented this, a larger pore size might be needed to overcome this problem. The system opens new possibilities for the study of in vitro drug sensitivity under conditions mimicking in vivo pharmacokinetics, and the selection of anti-malarial drug resistance and associated parasite biological and genomic changes.
author2 Mahidol University
author_facet Mahidol University
P. Preechapornkul
K. Chotivanich
M. Imwong
A. M. Dondorp
S. J. Lee
N. P J Day
N. J. White
S. Pukrittayakamee
format Article
author P. Preechapornkul
K. Chotivanich
M. Imwong
A. M. Dondorp
S. J. Lee
N. P J Day
N. J. White
S. Pukrittayakamee
author_sort P. Preechapornkul
title Optimizing the culture of plasmodium falciparum in hollow fiber bioreactors
title_short Optimizing the culture of plasmodium falciparum in hollow fiber bioreactors
title_full Optimizing the culture of plasmodium falciparum in hollow fiber bioreactors
title_fullStr Optimizing the culture of plasmodium falciparum in hollow fiber bioreactors
title_full_unstemmed Optimizing the culture of plasmodium falciparum in hollow fiber bioreactors
title_sort optimizing the culture of plasmodium falciparum in hollow fiber bioreactors
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/29604
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