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Modelling the chloroquine chemotherapy of falciparum malaria: the value of spacing a split dose
We have attempted to provide a rational basis for improving the protocols for chemotherapy of malaria. We model the regression of parasitaemia by Plasmodium falciparum, its subsequent elimination from the body, or recrudescence, for populations of cells treated with chloroquine. Our model assumes th...
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Published in: | Parasitology 1998-05, Vol.116 (5), p.407-416 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | We have attempted to provide a rational basis for improving the
protocols
for chemotherapy of malaria. We model the
regression of parasitaemia by Plasmodium falciparum,
its subsequent elimination from the body, or recrudescence, for
populations of cells treated with chloroquine. Our model assumes that the
drug forms a complex with some receptor in
the parasite and that parasites possessing this complex die at a defined
rate. We take into account that chloroquine is
eliminated exponentially from the body. We show how the parameters of the
model can be derived from observations in
the field. The model correctly predicts the effects of drug dose, degree
of initial parasitaemia, rate of parasite multiplication
and degree of drug resistance to chloroquine chemotherapy. The level of
parasitaemia will reduce to a minimum at
sufficiently high concentrations of chloroquine, but only if the
parasitaemia is reduced to below that of 1 parasite per
infected person will a cure of malaria be obtained. Otherwise,
recrudescence will, sooner or later, occur. We show that,
even for drug-resistant malaria, if 2 doses of chloroquine are given to
a patient with an interval of some 10 days between
them, parasites can be eliminated from the body without toxic levels of
chloroquine being reached. |
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ISSN: | 0031-1820 1469-8161 |
DOI: | 10.1017/S0031182098002480 |