Serveur d'exploration Chloroquine

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Therapeutic effect of chloroquine(CQ)-containing immunoliposomes in rats infected with Plasmodium berghei parasitized mouse red blood cells: comparison with combinations of antibodies and CQ or liposomal CQ

Identifieur interne : 003110 ( Main/Exploration ); précédent : 003109; suivant : 003111

Therapeutic effect of chloroquine(CQ)-containing immunoliposomes in rats infected with Plasmodium berghei parasitized mouse red blood cells: comparison with combinations of antibodies and CQ or liposomal CQ

Auteurs : Pierre A. M. Peeters [Pays-Bas] ; Bardo G. Brunink [Pays-Bas] ; Wijnand M. C. Eling [Pays-Bas] ; Daan J. A. Cromelin [Pays-Bas]

Source :

RBID : ISTEX:0CD486514356EEC65804E9D6D106541EB84A6846

English descriptors

Abstract

Abstract: The potential therapeutic application of chloroquine-containing immunoliposomes (Fab′-lipCQ) in a Plasmodium berghei malaria model was studied. Extending a previously described in vivo model (Peeters et al. (1988) Biochim. Biophys. Acta 943, 137–147) it was demonstrated that injection of antimouse red blood cell (anti-mRBC) Fab′-lipCQ was significantly more effective than liposome-encapsulated chloroquine (lipCQ) or free chloroquine in delaying or preventing a patent infection after intravenous injection of parasitized mouse red blood cells (p-mRBC) in rats. The results could be improved by injecting synchronized infected cells instead of non-synchronous p-mRBC in order to minimize the presence of free parasites which could easily infect rat RBC. It was further demonstrated that sequential injection of anti-mRBC IgG and lipCQ or chloroquine resulted in complete inactivation of the injected parasitized cells while Fab′-lipCQ administration resulted in a maximum score of 50% at an equal chloroquine, protein and phospholipid dose. In this report the potential of the concept of drug targeting for the effective treatment of a disease, which manifests in blood cells, was demonstrated.

Url:
DOI: 10.1016/0005-2736(89)90037-0


Affiliations:


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<term>Blood stream</term>
<term>Complete medium</term>
<term>Control lipcq</term>
<term>Days period</term>
<term>Density centrifugation</term>
<term>Diethyl ether</term>
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<term>Free parasites</term>
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<term>Immunoliposomes</term>
<term>Independent experiments</term>
<term>Infection</term>
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<term>Lipcq</term>
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<term>Lower ratios</term>
<term>Merozoite</term>
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<term>Reaction medium</term>
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<term>Tail vein</term>
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<term>Therapeutic efficacy</term>
<term>Therapeutic efficiency</term>
<term>Total amount</term>
<term>Total volume</term>
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<div type="abstract" xml:lang="en">Abstract: The potential therapeutic application of chloroquine-containing immunoliposomes (Fab′-lipCQ) in a Plasmodium berghei malaria model was studied. Extending a previously described in vivo model (Peeters et al. (1988) Biochim. Biophys. Acta 943, 137–147) it was demonstrated that injection of antimouse red blood cell (anti-mRBC) Fab′-lipCQ was significantly more effective than liposome-encapsulated chloroquine (lipCQ) or free chloroquine in delaying or preventing a patent infection after intravenous injection of parasitized mouse red blood cells (p-mRBC) in rats. The results could be improved by injecting synchronized infected cells instead of non-synchronous p-mRBC in order to minimize the presence of free parasites which could easily infect rat RBC. It was further demonstrated that sequential injection of anti-mRBC IgG and lipCQ or chloroquine resulted in complete inactivation of the injected parasitized cells while Fab′-lipCQ administration resulted in a maximum score of 50% at an equal chloroquine, protein and phospholipid dose. In this report the potential of the concept of drug targeting for the effective treatment of a disease, which manifests in blood cells, was demonstrated.</div>
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