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dc.contributor.authorJoseph O Muga, Jeremiah W Gathirwa, Matshawandile Tukulula, Walter GZO Jura
dc.date.accessioned2020-08-28T09:43:26Z
dc.date.available2020-08-28T09:43:26Z
dc.date.issued2018-12-01
dc.identifier.citation5en_US
dc.identifier.urihttps://repository.maseno.ac.ke/handle/123456789/2564
dc.description.abstractUse of chloroquine, an otherwise safe and relatively affordable anti-malarial drug, was discontinued due to widespread prevalence of resistant parasites. Many entrant anti-malarial drugs for treatment of chloroquine resistant malaria raises the concerns of cost and safety among other challenges. Innovative ways of circumventing chloroquine resistance is of paramount importance. Such may include nanoparticulate delivery strategies and targeting. This study evaluated physicochemical properties and in vitro antiplasmodial activity of chloroquine encapsulated heparin functionalized solid lipid nanoparticles (CQ-Hep-SLNs) and non-heparin functionalized SLNs (CQ-SLN) against Plasmodium falciparum.en_US
dc.publisherBioMed Centralen_US
dc.subjectHeparin;Chloroquine-encapsulated;Solid lipid nanoparticle;Antiplasmodial activityen_US
dc.titleIn vitro evaluation of chloroquine-loaded and heparin surface-functionalized solid lipid nanoparticlesen_US
dc.typeArticleen_US


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