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Spectrometric determination of trimethoprim and sulfamethoxazole in tablets by automated sequential injection technique

机译:通过自动顺序注射技术光谱法测定片剂中三甲双胍和磺胺甲恶唑

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摘要

An automated sequential injection analysis with spectrometric detection for the determination of trimethoprim and sulfamethoxazole in tablets is proposed. The concentration of sulfamethoxazole is determined by monitoring the absorbance at 540 nm due to the intensively colored complex formed by derivatization reaction of sulfamethoxazole with nitrite and N-(1-naphthyl)ethylenediamine in acidic media. With knowledge of the sulfamethoxazole concentration, the trimethoprim concentration can be calculated from the absorption of the sample solution at 264 nm, where both analytes absorb, and the additivity of individual absorbances according to Beer-Lambert law can be used. The developed method has a linear dynamic range of 0.03-5.0 mg dm(-3) and a detection limit of 0.03 mg dm(-3) for trimethoprim and a linear dynamic range of 0.1-10.0 mg dm(-3) and a detection limit of 0.01 mg dm(-3) for sulfamethoxazole. The sampling frequency of the method is 24 h(-1). The method was successfully applied on pharmaceutical dosage form of tablets, as the results of the determination are in a good agreement with the official pharmacopoeial method (HPLC). The developed sequential injection analysis is simpler, cheaper, and faster than already published methods and pharmacopoeial assay. So it appears to be suitable for quality control in the pharmaceutical industry. Graphic abstract
机译:提出了一种具有光谱检测的自动顺序注射分析,用于测定片剂中Trimethokim和磺胺甲恶唑的测定。由于磺胺甲氧唑与亚硝酸亚硝酸亚硝酸酯和N-(1-萘基)乙二胺在酸性介质中通过衍生化反应形成的强烈着色的复合物,通过监测540nm的吸光度来确定磺胺甲恶唑的浓度。通过了解磺胺甲恶唑浓度,可以根据可以使用264nm的样品溶液的吸收,其中分析物吸收和根据Beer-Lambert Law的单个吸收的添加性来计算三甲基巯基浓度。开发方法具有0.03-5.0mg DM(-3)的线性动态范围,对TiMethoprim的0.03mg DM(-3)的检出限,线性动态范围为0.1-10.0mg DM(-3)和检测磺胺甲恶唑的限制为0.01mg(-3)。该方法的采样频率为24小时(-1)。该方法成功地应用于片剂的药物剂型,因为测定结果与官方药典方法(HPLC)吻合良好。发达的顺序注射分析比已经发表的方法和药典测定更简单,更便宜,更快。因此,它似乎适用于制药行业的质量控制。图形摘要

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