000 a
999 _c16339
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040 _aAIKTC-KRRC
_cAIKTC-KRRC
100 _916061
_aShah, Virag A.
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
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
700 _916062
_aJayvadan K. Patel
773 0 _dBhopal Innovare Academic Sciences Pvt Ltd
_x2656-0097
_tInternational journal of pharmacy and pharmaceutical science
856 _uhttps://innovareacademics.in/journals/index.php/ijpps/article/view/41137/24726
_yClick here
942 _2ddc
_cAR