开发和验证微波辅助消解技术,作为一种利用 ICP-OES 估算药物剂型中硒含量的快速样品制备方法。

Q3 Veterinary
A K Pal, S Raja
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引用次数: 0

摘要

根据国际协调理事会 Q3D 准则,硒属于 2B 类元素。硫化硒是一种抗感染剂,具有抗真菌和抗菌特性,可用于治疗头皮屑和脂溢性皮炎。文献调查显示,大多数估算硒含量的分析技术都非常耗时和/或需要很高的技术水平。这一过程包括确定同位素、选择测量方法和优化典型的微波辅助消化程序。样品中加入二氟化氢铵、水和浓硝酸。经确认的微波消解程序分为两步:第一步,样品在 200°C 下升温 20 分钟并保持 5 分钟。之后,样品被冷却并用硼酸中和,然后在 180°C 的温度下升温 20 分钟并保持 10 分钟。通过电感耦合等离子体光发射光谱(ICP-OES)在 196.090 纳米波长处对硒进行估算。在开始分析前进行系统适用性测试,以确保系统性能的一致性。分析验证参数,如在 196.090 纳米波长下该方法的特异性、硒浓度在 10 ppm 至 150 ppm 范围内的线性、检测限为 1.28 ppm、定量限为 3.89 ppm。在 ICP-OES 操作条件发生微小变化时,该方法的稳健性也得到了证实。通过分析六次进样的相对标准偏差百分比,发现该方法的精确度低于 2.0%。准确度范围为 10 ppm 至 150 ppm,所有样品的准确度都在 95% 至 105% 之间。此外,还开发并验证了一种常用的微波辅助消解技术。该方法的精密度、特异性、线性、准确性和稳健性良好,可用于硫化硒药物和各种药物剂型中硒的测定。这种新开发的微波辅助消解技术具有最佳的灵敏度,与现有方法相比重现性高且省时。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development and validation of a microwave-assisted digestion technique as a rapid sample preparation method for the estimation of selenium in pharmaceutical dosage forms by ICP-OES.

Selenium is a class 2B element according to the International Council for Harmonization Q3D guidelines. Selenium sulfide is an anti-infective agent with antifungal and antibacterial properties used to treat dandruff and seborrheic dermatitis. The literature survey revealed that most of the analytical techniques to estimate selenium were time-consuming and/or required high skill levels. The process involved identifying the isotopes, selecting the measurement approach, and optimizing a typical microwave-aided digesting procedure. Ammonium hydrogen difluoride, water, and concentrated nitric acid were added to the samples. The confirmed microwave digestion program was a two-step program where in the initial step, the samples were ramped at 200°C for 20 min and held for 5 min. Later, samples were cooled and neutralized by boric acid, then ramped for 20 min to a temperature of 180°C and held for 10 min. Selenium was estimated at 196.090 nm by inductively coupled plasma optical emission spectroscopy (ICP-OES). System suitability was run before initiating analysis to ensure that system performance was consistent. Analytical validation parameters, such as the specificity of the method, were demonstrated at 196.090 nm, linearity was proven from 10 ppm to 150 ppm of selenium concentration, the detection limit was 1.28 ppm, and the limit of quantification was 3.89 ppm. Robustness was confirmed for small changes to ICP-OES operating conditions. The precision of the method demonstrated by analyzing the percentage relative standard deviation for six injections was found to be less than 2.0%. Accuracy was confirmed from 10 ppm to 150 ppm, and all the samples were observed to be within the range of 95%-105%. A common microwave-assisted digestion technique was developed and validated as well. The precision, specificity, linearity, accuracy, and robustness of the method for estimating selenium in selenium sulfide drug substances and various pharmaceutical dosage forms were demonstrated. This newly developed microwave-assisted digestion technique has optimum sensitivity and is highly reproducible and time-saving than the existing methods This method can be applied to numerous matrices for a finished dosage of selenium sulfide formulations.

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来源期刊
Archives of Razi Institute
Archives of Razi Institute Veterinary-Veterinary (all)
CiteScore
1.50
自引率
0.00%
发文量
108
审稿时长
12 weeks
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