“…These nanoparticles not only were able to deliver drug at a specific site which reduces the required doses but also can help fight efflux-associated drug resistance. ,,,, An ingenious chloroquine formulation, rooted in chitosan and infused with dehydroascorbic acid (DHA), exhibited a remarkable surge in the level of drug uptake by infected red blood cells (iRBCs). DHA’s strategic competition for glucose uptake facilitated drug delivery to the cells, leading to a profound inhibition of parasite growth at an astonishingly low 1 nM concentration, dwarfing the effects of free chloroquine, which required a far higher 100 nM concentration to produce similar results . Liposomal formulations, including PEGylated liposomes, have been investigated for delivering antimalarial drugs such as maduramicin, chloroquine, artemisinin, and dihydroartemisinin. − In an in vivo study, a comparison between PEGylated and liposome-encapsulated artemisinin, administered both alone and in combination with curcumin, yielded remarkable results.…”