2015
DOI: 10.3109/10837450.2015.1116565
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Preparation andin vitroevaluation of 5-fluorouracil-loaded PCL nanoparticles for colon cancer treatment

Abstract: Nanoparticles loaded with 5-fluorouracil (5-FU) for colon cancer therapies were prepared using the solvent evaporation technique, which involved lyophilization by freeze-drying. Formulations produced a substantially high encapsulation efficiency of approximately 93%. A positive correlation was seen when increasing polycaprolactone (PCL) and/or PVA concentrations and the size of nanoparticles produced. Increasing PCL concentration had a considerable influence on PDI while increasing PVA concentration had a less… Show more

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Cited by 34 publications
(10 citation statements)
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“…[2][3][4][5] The anticancer drug 5-fluorouracil (5FU) is one of the most commonly used drugs for treating breast cancer, and various folate (FA)-based controlled drug delivery systems (DDSs) have been developed to deliver 5FU to MCF-7 breast cancer cells. 6,7 Several biodegradable polymer-based materials, including gellan gum, 8 poly(D,Llactic-co-glycolic acid), 9 polycaprolactone, 10 and L-lysinemodified hyperbranched polyester, 11 have been developed as 5FU delivery platforms to enhance the anticancer activity of 5FU. However, the size of these polymeric platforms is a major concern with regard to cell internalization of drugincorporated carriers.…”
Section: Introductionmentioning
confidence: 99%
“…[2][3][4][5] The anticancer drug 5-fluorouracil (5FU) is one of the most commonly used drugs for treating breast cancer, and various folate (FA)-based controlled drug delivery systems (DDSs) have been developed to deliver 5FU to MCF-7 breast cancer cells. 6,7 Several biodegradable polymer-based materials, including gellan gum, 8 poly(D,Llactic-co-glycolic acid), 9 polycaprolactone, 10 and L-lysinemodified hyperbranched polyester, 11 have been developed as 5FU delivery platforms to enhance the anticancer activity of 5FU. However, the size of these polymeric platforms is a major concern with regard to cell internalization of drugincorporated carriers.…”
Section: Introductionmentioning
confidence: 99%
“…A reduction in encapsulation efficiency observed in higher PVA concentrations might be due to an increase in aqueous solubility of drug . However, increasing PCL concentrations did not significantly affect the encapsulation efficiency . Taken together of particle size and encapsulation efficiency results, the CQ‐PCL NPs that fabricated using 20 mg/mL PCL and 0.5% w/v PVA, had the smallest particle size (334.22 ± 43.21 nm), good uniformity of size distribution (PDI = 0.13 ± 0.05) with high encapsulation efficiency of 95.54 ± 1.49%.…”
Section: Resultsmentioning
confidence: 95%
“…The measurements were performed with reference to the supernatant of the drug-free nanoparticles as blank. The amount of encapsulated 5-FU was determined by subtracting the amount of free drug in the collected supernatant aftercentrifugation from the added amount in the beginning of the preparation using the following equation [14].…”
Section: Characterization Of 5-fu-pcnsnanosystem Encapsulationefficiency (Ee%)mentioning
confidence: 99%