用 ICP-MS 方法定量测定二水合乳清酸锌药物中的元素杂质

S. B, Gurupriya G, C. R, Niranjan Babu M
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摘要

如今,元素杂质通常存在于活性药物成分、原材料、化合物合成过程、药物辅料、成品、设备、容器和封口中。电感耦合等离子体质谱法(ICP-MS)是分析药物中元素杂质的先进技术之一。我们开发并验证了一种 ICP-MS 方法,用于检测乳清酸锌二水合物中的 17 种元素,即 V、Co、Ni、As、Se、Ru、Rh、Pd、Ag、Cd、Os、Ir、Pt、Au、Hg、Tl 和 Pb。样品用浓硝酸和浓盐酸稀释后进行分析。Li、Y、Tl、Co 和 Ce 被分配到调谐溶液中,以校正基线漂移和基质干扰。射频功率为 1550 W,射频匹配为 1.80 V,样品深度为 8.0 mm,雾化器气体流量为 1.01 L/min,雾化器泵流量为 0.10 rps,喷雾室温度为 2oC,He 流量为 4.3 mL/min,能量鉴别率为 3.0 V。所有 17 种元素在其检测范围内均表现出极佳的线性,测定系数≥ 0.9996。17 种元素的检测限为 0.0004 至 0.00411 ppm。日内和日间精密度(相对标准偏差)小于 6.4%。所有元素的加标回收率为 88.5%至 108.2%。在乳清酸锌二水合物的 17 种元素中,所有元素的测定结果均在规定范围内,结果均令人满意。所开发的方法简单、快速、有效。该方法可作为药物和制药工业中化合物定量的有力工具和必要技术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Quantitative Approach for the Determination of Elemental Impurities in Zinc Orotate Dihydrate Drug Substance by ICP-MS Method
These days elemental impurities are commonly present in active pharmaceutical ingredients, raw materials, during the synthesis of compounds, drug excipients, finished products, equipment, containers and closures. Inductively coupled plasma mass spectrometry (ICP-MS) is one of the advanced techniques to analyze elemental impurities in drug substances. An ICP-MS method was developed and validated for testing 17 elements, namely, V, Co, Ni, As, Se, Ru, Rh, Pd, Ag, Cd, Os, Ir, Pt, Au, Hg, Tl, and Pb in zinc orotate dihydrate. The samples were analyzed after diluting with concentrated nitric acid and concentrated hydrochloric acid. Li, Y, Tl, Co and Ce were assigned tuning solutions to correct the baseline drift and matrix interference. The RF power was 1550 W, RF matching was 1.80 V, sample depth was 8.0 mm, nebulizer gas flow was 1.01 L/min, nebulizer pump flow was 0.10 rps, spray chamber temperature 2oC, He flow rate was 4.3 mL/min and the energy discrimination rate was 3.0 V. All 17 elements exhibited excellent linearity in their testing range, with a coefficient of determination ≥ 0.9996. The limits of detection of the 17 elements were within the range of 0.0004 to 0.00411 ppm. The intra- and inter-day precision (relative standard deviation) was <6.4%. The recoveries of the spiked standard for all elements were 88.5 to 108.2%. Among the 17 elements of the zinc orotate dihydrate, the measured results of all the 17 elements were within the specified range, and the results of all the elements were also satisfactory. The developed method was simple, rapid, and effective. This method can be a powerful tool and imperative technology for the quantification of compounds in drug substances and pharmaceutical industries.
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