Iodometric determination of quinine sulfate in tablets using N-oxidation with diperoxysebacic acid

None Ivan Iurchenko, None Mykola Blazheyevskiy, None Oksana Koretnik, None Oksana Shlusar
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Abstract

Using diperoxysebacic acid as an example, it was shown the interaction of diperoxycarboxylic acids with quinine alkaloid in an aqueous medium by kinetics method. The reaction proceeds quantitatively by the mechanism of nucleophilic substitution of β-peroxide oxygen atom in diperoxycarboxylic acid with the formation of the corresponding N-oxide, and the kinetics of the process is a subject to general rules of specific acid-base catalysis. New iodometric methods were developed, and the possibility of quinine sulfate quantification in pure form ‘Quinine sulfate’, as well as in the combined dosage form ‘Limpar® N 200 mg’ (Cassella Med GmbH, Germany) and in ‘Quinine sulfate 200 mg Tablets’ (Accord Healthcare Ltd, UK) by the reaction of oxidation with diperoxycarboxylic acid. They are characterized by high selectivity, and rate, simplicity of performing, and good accuracy. No toxic reagents or special conditions required. RSD ≤1.6% (δ =+0.40..+0.72%), LOQ=0.01 mg.
二过氧癸二酸- n -氧化法测定硫酸奎宁片剂中的碘量
以二过氧己二酸为例,用动力学方法研究了水溶液中二过氧羧酸与奎宁生物碱的相互作用。该反应定量地通过二过氧羧酸中β-过氧氧原子亲核取代生成相应的n -氧化物的机理进行,反应动力学遵循比酸碱催化的一般规律。开发了新的碘量测定方法,并通过与二过氧羧酸的氧化反应,确定了纯“硫酸奎宁”、联合剂型“Limpar®N 200 mg”(Cassella Med GmbH,德国)和“硫酸奎宁200 mg片剂”(Accord Healthcare Ltd,英国)中硫酸奎宁的定量可能性。其特点是选择性高,速度快,操作简单,准确性好。不需要有毒试剂或特殊条件。RSD≤1.6% (δ =+0.40 ~ +0.72%),定量限=0.01 mg。
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