Department of Pharmaceutical Analysis, 78997GITAM Institute of Pharmacy, Gandhi Institute of Technology and Management (GITAM) (Deemed to be University), Visakhapatnam, 530 045, Andhra Pradesh, India.
Eur J Mass Spectrom (Chichester). 2022 Feb;28(1-2):3-11. doi: 10.1177/14690667221105835. Epub 2022 Jun 3.
Atorvastatin calcium is employed as front-line treatment for cardiovascular diseases. According to the international conference on harmonization (ICH) guideline ICH Q3D, elemental impurities can come into drug products from various sources. These elemental impurities do not have any therapeutic benefit to the end-user. On the contrary, it harms the normal physiological system. Class 1 elements like arsenic, cadmium, mercury, and lead are inorganic impurities that can cause toxic effects on the human body. Nickel was used as a catalyst during the synthesis process of atorvastatin calcium. It comes under the Class-2A, can cause toxicity to humans, and must be quantified. A simple, fast, reliable inductively coupled plasma mass spectrometric method for the estimation of elemental impurities like arsenic, cadmium, mercury, lead, and nickel in atorvastatin calcium by open sample digestion technique was developed and validated in accordance with ICH Q3D and USP < 232 > and USP <233 > general chapter. Internal standards like indium, terbium, thallium, bismuth and yttrium were used to correct the non-spectral interferences that were generated during analysis. Gold was added to all solutions as it preserves mercury by amalgamation. The system performance was evaluated every time my performing system suitability parameters. The limits for all the elements were fixed in accordance with ICH Q3D. The limit of detection and the limit of quantification for all the five elements were estimated. Method specificity was proven by checking for interferences due to the sample matrix and other elements. Linearity of each element in standards was established from 25% to 200% of sample concentration, and correlation coefficients were found to be not less than 0.999. The accuracy of the method was demonstrated at three spiking levels at 50%, 100%, and 150% of the J-value for all the elements. The recoveries for all elements at each level were within the range of 90-120%. Method precision was proved at 100% J-value. The relative standard deviation of all elements was less than 5%. It concludes that this newly developed and validated reliable inductively coupled plasma mass spectrometric method for estimating of elemental impurities like arsenic, cadmium, mercury, lead, and nickel in atorvastatin calcium was within the permitted limit and suitable for routine use.
阿托伐他汀钙被用作心血管疾病的一线治疗药物。根据国际协调会议(ICH)指南 ICH Q3D,元素杂质可能来自各种来源进入药物产品。这些元素杂质对最终用户没有任何治疗益处。相反,它们会损害正常的生理系统。砷、镉、汞和铅等一类元素是无机杂质,会对人体造成毒性影响。在阿托伐他汀钙的合成过程中,镍被用作催化剂。它属于 2A 类,会对人类造成毒性,必须进行定量分析。本研究建立并验证了一种简单、快速、可靠的电感耦合等离子体质谱法,用于采用敞开式样品消解技术对阿托伐他汀钙中的砷、镉、汞、铅和镍等元素杂质进行定量分析,该方法符合 ICH Q3D 以及 USP<232>和 USP<233>一般章节的要求。采用铟、铽、铊、铋和钇等内标来校正分析过程中产生的非光谱干扰。由于金能与汞形成汞齐从而对汞起到保护作用,所以向所有溶液中添加了金。每次进行系统适用性参数测试时,都要对系统性能进行评估。根据 ICH Q3D 确定了所有元素的限度。对所有五种元素的检测限和定量限进行了估算。通过检查样品基质和其他元素的干扰来证明方法的专属性。对每种元素在 25%至 200%的样品浓度范围内建立了标准的线性关系,相关系数均不小于 0.999。在所有元素的 50%、100%和 150%J 值范围内,建立了标准的线性关系,相关系数均不小于 0.999。在所有元素的 50%、100%和 150%J 值范围内,建立了标准的线性关系,相关系数均不小于 0.999。在所有元素的 50%、100%和 150%J 值范围内,建立了标准的线性关系,相关系数均不小于 0.999。方法的准确性通过在 50%、100%和 150%J 值的三个加标水平上进行验证。所有元素的回收率均在 90-120%范围内。在 100%J 值时,证明了方法的精密度。所有元素的相对标准偏差均小于 5%。综上所述,该研究建立的新的、可靠的电感耦合等离子体质谱法可用于估计阿托伐他汀钙中的砷、镉、汞、铅和镍等元素杂质,其结果均在允许范围内,适合常规使用。