Formulation and biopharmaceutical issues in the development of drug delivery systems for antiparasitic drugs.
The development of really new antiparasitic drugs to market level is a very rare event. A large number of lead structures have already been screened and discarded, the market is large but poor, and the administrative barriers are increasingly high and costly. Novel antiparasitics must not only be better, they must also be substantially safer than the existing repertoire. There are two major aspects to drug development. One is the strategy of pathogen-specific biochemical intervention, the other the strategy of optimal formulation and application. This review focuses on the latter. In finding and adapting innovative and "intelligent", i.e. parasite- and disease-specific formulations and delivery systems, established but deficient drugs might be optimised, enhancing their efficiency and reducing negative side effects at relatively low cost. Further, many promising new ideas are severely hampered by the low water solubility of the antiparasitic drug. Here as well, some of the innovative drug formulation and delivery systems discussed below might offer highly efficient, while technologically simple, solutions.
Item Type | Article |
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Keywords | Solid lipid nanoparticles, liposomal amphotericin-b, experimental visceral leishmaniasis, cutaneous leishmaniasis, beta-cyclodextrin, infected mice, sodium stibogluconate, canine, leishmaniasis, bearing liposomes, phagocytic uptake |
ISI | 184556200003 |