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040 _aAIKTC-KRRC
_cAIKTC-KRRC
100 _914909
_a Kathpalia, Harsha
245 _aFormulation and Optimization of Atovaquone Micronized Suspension by Top-down Method
250 _aVol.55(1), Jan-Man
260 _aKarnataka
_bAssociation of Pharmaceutical Teachers of India (APTI)
_c2021
300 _a77-85p.
520 _aAim: The present work aimed to tackle the solubility issue of a Biopharmaceutics Classification System (BCS) II drug, Atovaquone. Methods: Formulation of micronized suspension of atovaquone was optimized by employing a 32 full factorial design keeping poloxamer 188 (wetting agent) and phospholipon 90H (stabilizer) as the influential variables affecting the dependent variables viz. particle size and polydispersity index (PdI). Selected formulations from the optimized design space were further evaluated for dissolution and the formulation exhibiting maximum dissolution within 120 min was selected. The optimized batch consisting of atovaquone (15%), poloxamer 188 (2%), phospholipon 90H (1%), glycerin (10%) in the aqueous vehicle was microfluidized. Results: The particle size of resultant suspension was Zavg = 1313 ± 40 nm and PdI =0.1± 0.05. The zeta potential of the final micronized suspension was 0.0555 mV which indicated steric stabilization of the particles. The micronized suspension was adsorbed on a mixture of Kollidon CL SF and Aerosil 200 (2:1) and then dried and passed through 40# sieve. Conclusion: The solid-state characterization of the formulation revealed that the crystalline nature of the drug was retained after the milling process. The saturation solubility and in-vitro dissolution of adsorbed micronized suspension were 2.3-fold times enhanced as compared to the pure drug suspension due to a reduction in particle size. The top-down approach can be employed to improve the poor aqueous solubility of atovaquone.
650 0 _94639
_aPHARMACEUTICS
700 _914910
_a Das, Sukanya
773 0 _x0019-5464
_tIndian journal of pharmaceutical education and research
_dBengluru Association of Pharmaceutical Teachers of India (APTI)
856 _uhttps://www.ijper.org/sites/default/files/IndJPhaEdRes_55_1_77.pdf
_yClick here
942 _2ddc
_cAR