Department of Chemistry 'Ugo Schiff', University of Florence, Via della Lastruccia 3-13, 50019, Sesto Fiorentino, Italy.
Anal Bioanal Chem. 2022 Feb;414(4):1713-1722. doi: 10.1007/s00216-021-03804-8. Epub 2021 Nov 29.
In this paper is reported the selective detection and quantification of levodopa in co-presence of carbidopa. The method took advantage of the spontaneous oxidation and color development of levodopa at basic pH here driven by alkaline earth cations and co-solvent in solution. We have shown for the first time the generation and stabilization of the purple melanochrome from levodopa, by using magnesium acetate and dimethyl sulfoxide, which was here exploited for the development of a quantitative colorimetric assay for the active principle ingredient in commercial drugs for the treatment of Parkinson's disease. The calibration curves of levodopa in the two tablet formulations, containing carbidopa as decarboxylase inhibitor, showed a common linear trend between 10 mg L and 40 mg L with levodopa alone or in combination with carbidopa in standard solutions, with very good reproducibility (CV%, 3.3% for both brand and generic drug) and very good sensitivity, with limit of quantification about 0.6 mg L in any case. The colorimetric method here developed is very simple and effective, appearing as a rapid and low-cost alternative to other methodologies, involving large and expensive instrumentations, for drug estimation and quality control of pharmaceutical formulations.
本文报道了在卡比多巴共存下对左旋多巴的选择性检测和定量。该方法利用了碱性条件下,由碱土金属阳离子和共溶剂在溶液中驱动的左旋多巴的自发氧化和显色反应。我们首次展示了通过使用醋酸镁和二甲基亚砜,从左旋多巴中生成和稳定紫色黑素,这在开发用于治疗帕金森病的商业药物中左旋多巴的定量比色测定法方面得到了应用。在含有卡比多巴作为脱羧酶抑制剂的两种片剂制剂中,左旋多巴的校准曲线在 10mg L 和 40mg L 之间表现出共同的线性趋势,无论是在标准溶液中单独使用左旋多巴还是与卡比多巴联合使用,都具有非常好的重现性(CV%,两种品牌和仿制药均为 3.3%)和非常好的灵敏度,定量限约为 0.6mg L。这里开发的比色法非常简单有效,似乎是一种快速且低成本的替代方法,与其他涉及大型昂贵仪器的方法相比,用于药物估计和药物制剂的质量控制。