2023
DOI: 10.1016/j.ijpharm.2023.123009
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Modeling of chitosan modified PLGA atorvastatin-curcumin conjugate (AT-CU) nanoparticles, overcoming the barriers associated with PLGA: An approach for better management of atherosclerosis

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Cited by 7 publications
(2 citation statements)
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“…Dash et al [ 112 ] synthesized chitosan-modified polylactic-co-glycolic acid (PLGA) atorvastatin–curcumin conjugate (AT-CU) nanoparticles for the management of atherosclerosis. Upon increasing the concentration of chitosan-modified PLGA AT-CU NPs, the particle size increased from 139.2 nm to 197.7 nm, the zeta potential ranged between 20.57 mV and 28.32 mV, and the drug encapsulation efficiency was enhanced from 71.81 to 90.57%.…”
Section: Herbal Bioactives Loaded Nanoformulations For Oral Deliverymentioning
confidence: 99%
“…Dash et al [ 112 ] synthesized chitosan-modified polylactic-co-glycolic acid (PLGA) atorvastatin–curcumin conjugate (AT-CU) nanoparticles for the management of atherosclerosis. Upon increasing the concentration of chitosan-modified PLGA AT-CU NPs, the particle size increased from 139.2 nm to 197.7 nm, the zeta potential ranged between 20.57 mV and 28.32 mV, and the drug encapsulation efficiency was enhanced from 71.81 to 90.57%.…”
Section: Herbal Bioactives Loaded Nanoformulations For Oral Deliverymentioning
confidence: 99%
“…Downregulating the intracellular transcription factors such as NF-kB, cyclooxygenase II, matrix metalloproteinase-9, activator protein 1, STAT3, and nitric oxide synthase has been remarkably induced apoptosis in different cell lines with curcumin treatment. [ 27 28 29 ] By inhibiting pyruvate kinase M2 (PKM2), curcumin has been found to offer a novel anticancer mechanism that lowers glucose absorption and lactate generation (the Warburg effect) in cancer cells. The PKM2 downregulation was accomplished by subduing the mammalian targets of rapamycin–hypoxia-inducible factor 1α.…”
Section: Role Of Natural Compounds In the Emerging Era Of Repurposingmentioning
confidence: 99%