Development and Validation of Fast and Simple Fourier Transform Infrared Spectrophotometric Method for Analysis of Thiamphenicol in Capsule Dosage Form

Q2 Pharmacology, Toxicology and Pharmaceutics
N. Nerdy, Linda Margata, N. Zebua, P. Lestari, T. K. Bakri, Faisal Yusuf, Vonna Aulianshah
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Abstract

The development of a method for identification and determination of thiamphenicol by Fourier Transform Infrared will provide convenience to developers because it is fast and easy for analysis. The research was carried out by utilizing the solubility of thiamphenicol in methanol with three stages, namely method development, sample analysis, and method validation. The method development stage showed that the specific peak of thiamphenicol was at a peak with a wavenumber of 1694.1 cm−1; this specific peak of thiamphenicol was used for qualitative analysis and quantitative analysis of thiamphenicol in the capsule dosage form. The sample analysis showed that all analyzed thiamphenicol in capsule dosage form showed good results both qualitatively and quantitatively. Qualitatively all the samples analyzed showed a specific peak at specific positions and specific wavenumbers. These results meet the requirements for containing thiamphenicol in the dosage form. Quantitatively all the samples analyzed ranged from 97.97% to 102.24% by peak height and peak area. These results meet the requirements for active substance levels in general preparations within 90.0% to 110.0%. The method validation for peak height and peak area showed that the accuracy parameter had a recovery percentage of 100.28% and 100.41% (between 98.0% to 102.0%), the precision parameter with a relative standard deviation of 0.31% and 0.37% (not more than 2.0%), and the linearity parameter with a correlation coefficient of 0.9999 and 0.9997 (not less than 0.99). The limit of detection value was 0.2971 mg/mL and 0.5338 mg/mL, the limit of quantitation value was 0.9004 mg/mL and 1.6176 mg/mL, the range for both was 80% to 120%, and the specificity for both met the requirement. The Fourier Transform Infrared method has been successfully developed, applied, and validated for qualitative analysis and quantitative analysis of thiamphenicol in capsule dosage form.
快速简便傅里叶变换红外分光光度法分析胶囊剂型中硫胺霉素的建立与验证
傅里叶变换红外光谱法对硫胺霉素的鉴定和测定具有快速、简便的特点,为开发人员提供了方便。本研究利用硫霉素在甲醇中的溶解度,分方法开发、样品分析和方法验证三个阶段进行。方法发展阶段表明,硫霉素的特异峰位于波数为1694.1 cm−1的峰上;利用该特定峰对胶囊剂型中硫胺霉素进行定性和定量分析。样品分析表明,所分析的硫霉素胶囊剂型均具有较好的定性和定量结果。定性分析的所有样品都在特定位置和特定波数处显示出特定的峰值。这些结果符合制剂中含有硫霉素的要求。定量分析的样品峰高和峰面积在97.97% ~ 102.24%之间。这些结果满足一般制剂中活性物质含量在90.0% ~ 110.0%的要求。对峰高和峰面积的方法验证表明,准确度参数的回收率分别为100.28%和100.41%(98.0% ~ 102.0%),精密度参数的相对标准偏差分别为0.31%和0.37%(不大于2.0%),线性参数的相关系数分别为0.9999和0.9997(不小于0.99)。检测限分别为0.2971 mg/mL和0.5338 mg/mL,定量限分别为0.9004 mg/mL和1.6176 mg/mL,检测范围为80% ~ 120%,特异性均满足要求。傅里叶变换红外方法成功地建立、应用于硫霉素胶囊剂型的定性和定量分析。
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来源期刊
Science and Technology Indonesia
Science and Technology Indonesia Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
CiteScore
1.80
自引率
0.00%
发文量
72
审稿时长
8 weeks
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