2013
DOI: 10.1016/j.ijpharm.2013.03.021
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Development and evaluation of a novel phytosome-loaded chitosan microsphere system for curcumin delivery

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Cited by 162 publications
(85 citation statements)
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“…The encapsulation efficiency was 92.83 ± 0,520 % which is in accordance with other methods of production of phyto-phospholipidic particles 9 .…”
Section: Encapsulation Efficiency Of Optimized Formulationsupporting
confidence: 88%
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“…The encapsulation efficiency was 92.83 ± 0,520 % which is in accordance with other methods of production of phyto-phospholipidic particles 9 .…”
Section: Encapsulation Efficiency Of Optimized Formulationsupporting
confidence: 88%
“…The first reports of phyto-phospholipid complex preparation used essentially organic aprotic solvents as dichloromethane, or dioxane as the reaction medium-8 catalase and thiobarbituric acid reactive substances with respect to carbon tetrachloride treated group (P < 0.05 and <0.01. Those harmful solvents have been progressively substituted by less toxic solvents as acetone or ethanol 9 . The phytosomes were generally obtained…”
Section: Introductionmentioning
confidence: 99%
“…In vitro curcumin release from Cur-PS-CMs was slower than that from curcumin-loaded chitosan microspheres (Cur-CMs) in pH 1.0, 4.0, 6.8, and 7.4 showing 1.67 and 1.07-fold increase in absorption of curcumin compared with Cur-PSs and Cur-CMs, respectively. The half-life of orally administered Cur-PS-CMs was longer than those of Cur-PSs and Cur-CMs by ~2 and 1.5-times, respectively, confirming oral absorption with prolonged retention time for sustained delivery of lipophilic compounds [240]. The MMC-soybean phosphatidylcholine complex-loaded PEG-lipid-PLA hybrid NPs were reported with Folate functionalization (FA-PEG-PE-PLA NPs@MMC-SPC) for targeted drug delivery and dual-controlled drug release involving hydrophobic core (PLA) loaded with MMC-SPC, an amphiphilic lipid interface layer (PE), a hydrophilic shell (PEG), and a targeting ligand (FA) on the surface, with a spherical shape, and high encapsulation efficiency (95%).…”
Section: Phytosomal Nanoparticulate Materialsmentioning
confidence: 67%
“…The entrapment efficiency was calculated according to the following formula: [15][16] Entrapment efficiency (%) = (Total amount of drug) -(Amount of free drug) / (Total amount of drug) × 100…”
Section: Drug Entrapment Efficiencymentioning
confidence: 99%