2017
DOI: 10.1016/j.ijpharm.2017.03.088
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Dehydroascorbate-derivatized chitosan particles for targeting antimalarial agents to infected erythrocytes

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Cited by 14 publications
(5 citation statements)
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“…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. 111 Liposomal formulations, including PEGylated liposomes, have been investigated for delivering antimalarial drugs such as maduramicin, chloroquine, artemisinin, and dihydroartemisinin. 115−118 In an in vivo study, a comparison between PEGylated and liposome-encapsulated artemisinin, administered both alone and in combination with curcumin, yielded remarkable results.…”
Section: Employment Of Nanotechnology In Parasitic Diseasesmentioning
confidence: 99%
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“…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. 111 Liposomal formulations, including PEGylated liposomes, have been investigated for delivering antimalarial drugs such as maduramicin, chloroquine, artemisinin, and dihydroartemisinin. 115−118 In an in vivo study, a comparison between PEGylated and liposome-encapsulated artemisinin, administered both alone and in combination with curcumin, yielded remarkable results.…”
Section: Employment Of Nanotechnology In Parasitic Diseasesmentioning
confidence: 99%
“…Various nanoparticle platforms, including liposomes, immunoliposomes, chitosan-based nanoparticles, peptide-associated liposomes, and solid lipid nanoparticles, have been explored for their ability to deliver drugs to infected red blood cells, enhancing drug efficacy and combating drug resistance. 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 .…”
Section: Employment Of Nanotechnology In Parasitic Diseasesmentioning
confidence: 99%
See 1 more Smart Citation
“…Parasite inhibition was achieved at 1 nM concentration, while free drug exhibited a comparative activity at 100 nM. It is convincing that specific targeting can reduce the dose and overcome the efflux-based drug resistance [22]. Table 2 summarizes some of the antimalarial formulations which are based on active drug targeting mechanism.…”
Section: Active Drug Targetingmentioning
confidence: 99%
“…Chloroquine phosphate is mainly used in the treatment of malaria and rheumatism in clinical [81][82][83]. Numerous studies have presented that it has broad-spectrum antiviral effect [84].…”
Section: Chloroquine Phosphatementioning
confidence: 99%