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_aAIKTC-KRRC _cAIKTC-KRRC |
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_916061 _aShah, Virag A. |
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245 | _aOptimization and characterization of doxorubicin loaded solid lipid nanosuspension for nose to brain delivery using design expert software | ||
250 | _aVol.13(5) | ||
260 |
_aM P _bInnovare Academic Sciences Pvt Ltd _c2021 |
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300 | _a45-57p. | ||
520 | _aObjective: The goal of the current study was to investigate the possible use of solid lipid nanosuspension (SLNs) as a drug delivery method to boost doxorubicin (DOX) brain-targeting performance after intranasal (i. n.) administration.Methods: 33 factorial design was applied for optimization by using lipid concentration, surfactant concentration, and High-speed homogenizer (HSH) stirring time as dependent variables, and their effect was observed on particles size, Polydispersity index (PDI), and entrapment efficiency.Results: With the composition of Compritol® 888 ATO (4.6 % w/v), tween 80 (1.9 % w/v), and HSH stirring time, the optimized formula DOX-SLNs prepared (10 min). Particle size, PDI, zeta potential, entrapment efficiency, percent in vitro release were found to be 167.47±6.09 nm, 0.23±0.02, 24.1 mV, 75.3±2.79, and 89.35±3.27 percent in 24 h, respectively, for optimized formulation (V-O). No major changes in particle size, zeta potential, and entrapping efficiency were found in the stability studies at 4±2 °C (refrigerator) and 25±2 °C/60±5% RH up to 3 mo.Conclusion: Keywords: Solid lipid Nanosuspension, Homogenization and Ultrasonication, Characterization, Factorial design, Nose to brain deliveryFollowing the non-invasive nose-to-brain drug delivery, which is a promising therapeutic strategy, the positive findings confirmed the current optimized DOX-loaded SLNs formulation. | ||
650 | 0 |
_94639 _aPHARMACEUTICS |
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700 |
_916062 _aJayvadan K. Patel |
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773 | 0 |
_dBhopal Innovare Academic Sciences Pvt Ltd _x2656-0097 _tInternational journal of pharmacy and pharmaceutical science |
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_uhttps://innovareacademics.in/journals/index.php/ijpps/article/view/41137/24726 _yClick here |
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_2ddc _cAR |