Quality evaluation of synthesized modafinil used as pharmaceutical material
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https://doi.org/10.54939/1859-1043.j.mst.77.2022.98-103Keywords:
Modafinil; Smart drug; Bunte salt; USP.Abstract
Modafinil is a drug used in the treatment of narcolepsy, approved by the FDA in 1998. In previous studies, modafinil was easily synthesized through three stages, in the Bunte salt medium, the overall yield of 74,56 %. The quality of the modafinil was evaluated following USP 41. The results have shown that the synthesized modafinil satisfied quality requirements in pharmacopoeia.
References
[1]. Annas C. L., Annas G. J. (2009), “Enhancing the fighting force: Medical research on American soldiers”, Journal of Contemporary Health Law and Policy, 25 (2), pp. 283-308.
[2]. Bicherov A. V., Akopova A. R., Spiglazov V. I., Morkovik A. S. (2010), “New synthetic route to modafinil drug including desulfobenzhydrylation of sodium carbamoylmethyl thiosulfate: experimental and quantum chemical studies”, Rus. Chem. Bull., 59 (1), pp. 91-101.
[3]. Friedl K. E. (2015), “U. S. Army research on pharmacological enhancement of soldier performance: Stimulants, anabolic hormones, and blood doping”, Journal of Strenght and Conditioning Research”, 29 (11), pp. 71-76.
[4]. Urban K. R., Gao WJ. (2014), “Performance enhancement at the cost of potential brain plasticity: Neural ramifications of nootropic drugs in the healthy developing brain”, Frontiers in Systems Neuroscience, 8, pp. 1-10.
[5]. USP 41, Modafinil, 2018.