Abstract
In many parasitic diseases, the reticulo-endothelial system is the major site of infection. Linking antiparasitic drugs to macro-molecular carriers may therefore extensively improve their therapeutical properties. The drug-carrier complex is no longer able to diffuse through the cell plasma membranes, and will be taken up preferentially by the cells which display high endocytic capacity. Complexed drugs will also be excreted at lower rate than free drugs, leading to increased plasma levels, for prolonged periods. Not the least, cells with low or no endocytic activity will be protected from adverse action of the drug, thus improving the overall therapeutic index of the complex with regard to the free drug.
Chargé de Recherches of the Belgian F.N.R.S.
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References
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© 1979 Plenum Press, New York
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Tulkens, P., Trouet, A. (1979). The Concept of Drug-Carriers in the Treatment of Parasitic Diseases. In: Müller-Ruchholtz, W., Müller-Hermelink, H.K. (eds) Function and Structure of the Immune System. Advances in Experimental Medicine and Biology, vol 114. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-9101-6_66
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DOI: https://doi.org/10.1007/978-1-4615-9101-6_66
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