2021
DOI: 10.1016/j.jddst.2021.102343
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Paclitaxel and curcumin co-loaded mixed micelles: Improving in vitro efficacy and reducing toxicity against Abraxane®

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Cited by 15 publications
(16 citation statements)
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“…In order to encapsulate both drugs, RIF and CUR, the solvent diffusion method was used, as previously described [ 17 , 20 ]. Briefly, RIF (100 mg) and CUR (50 mg) were dissolved in 20 mL of acetone; the solution was sonicated for 5 min (Digital Ultrasonic Cleaner, PS-10A 50/60 Hz, Shenzhen, China, 25 °C) and then added drop by drop using a programmable syringe infusion pump (PC11UB, APEMA, Buenos Aires, Argentina) to the aqueous dispersion of Soluplus ® (10% w / v ) at room temperature under constant magnetic stirring (50 RPM, 4 h) to let the complete evaporation of the organic solvent, as well.…”
Section: Methodsmentioning
confidence: 99%
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“…In order to encapsulate both drugs, RIF and CUR, the solvent diffusion method was used, as previously described [ 17 , 20 ]. Briefly, RIF (100 mg) and CUR (50 mg) were dissolved in 20 mL of acetone; the solution was sonicated for 5 min (Digital Ultrasonic Cleaner, PS-10A 50/60 Hz, Shenzhen, China, 25 °C) and then added drop by drop using a programmable syringe infusion pump (PC11UB, APEMA, Buenos Aires, Argentina) to the aqueous dispersion of Soluplus ® (10% w / v ) at room temperature under constant magnetic stirring (50 RPM, 4 h) to let the complete evaporation of the organic solvent, as well.…”
Section: Methodsmentioning
confidence: 99%
“…The CUR and RIF cumulative in vitro release from the nanomicelles with (0.7% w / v ) and without Gel(man) was studied by using dialysis method in SILF (pH 7.4) with the addition of ethanol (30% v / v ) [ 17 ] as external medium. Lyophilized micellar systems were redispersed in distilled water and further diluted with distilled water in order to achieve concentrations of 1 mg/mL for RIF and 0.5 mg/mL for CUR.…”
Section: Methodsmentioning
confidence: 99%
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“…Nanoxel ® is a polymeric amphiphilic micelle formulation approved for clinical use in India in 2006 and is currently undergoing clinical trials for FDA approval (ClinicalTrials.gov Identifier: NCT04066335), and Apealea, approved for use in the European Union in 2018, utilizes poly-(lglutamic acid) conjugated to PTX. Unfortunately, peripheral neuropathy remains a clinical challenge despite improved formulations, further necessitating continued optimization [136].…”
Section: Formulations For Enhanced Pk and Specific Targetingmentioning
confidence: 99%