Chloroquine diphosphate bearing dextran nanoparticles augmented drug delivery and overwhelmed drug resistance in Plasmodium falciparum parasites

• Published in: International journal of biological macromolecules 2018-07, Vol.114, p.161-168
• Main Authors: Kashyap, Aman, Kaur, Rupinder, Baldi, Ashish, Jain, Upendra Kumar, Chandra, Ramesh, Madan, Jitender
• Format: Article
• Language: English
• Subjects: Chloroquine diphosphate; Dextran nanoparticles; Drug resistance; In vitro antimalarial activity; Sensitive and resistant Plasmodium falciparum
• ISSN: 0141-8130; 1879-0003
• DOI: 10.1016/j.ijbiomac.2018.03.102

Chloroquine diphosphate (CHQ) is primarily used for the treatment of Plasmodium falciparum malaria at the dose of 500mg orally or 10mg/kg parenterally. However, point mutations in Plasmodiumfalciparum chloroquine resistance transporter (PfCRT) protein and Plasmodium falciparum multidrug resistance protein 1 (Pfmdr1) localized in digestive vacuole membrane, are responsible for CHQ resistance. Therefore, in present investigation, dextran nanoparticles bearing chloroquine diphosphate (CHQ-DEX-NPs) were formulated by solvent diffusion method of size below 70nm with zeta-potential of −20.1±3.2mV. FT-IR, DSC and PXRD techniques confirmed the successful loading of drug in nanomatrix system with amorphous attributes. In vitro drug release analysis indicated the Higuchi pattern with diffusion controlled drug release. The IC50 of CHQ-DEX-NPs in sensitive (3D7) and resistant (RKL9) Plasmodium falciparum strains was estimated to be 0.031-μg/ml and 0.13-μg/ml significantly lower than 0.059-μg/ml and 0.36-μg/ml of CHQ. The augmented therapeutic efficacy of CHQ-DEX-NPs may be credited to deposition of tailored nanoparticles in food vacuoles of malaria parasites owing to the affinity of parasite towards DEX that consequently lower the drug resistance and improved the therapeutic index. In conclusion, CHQ-DEX-NPs must be evaluated under a set of stringent in vivo parameters to establish its therapeutic efficacy in preclinical model. •Plasmodium falciparum developed resistant against chloroquine•Plasmodium falciparum engulfs dextran through duct•Engineering nanochloroquine using dextran surmounted drug resistance in Plasmodium falciparum parasites