Establishment and validation of HPLC methods for the determination of folic acid and parabens antimicrobial agents on folic acid oral solution

IF 4.3 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Wenhong Wu, Ying Liang, Renbang Zhao, Yude Shi, Jiahui Hou, Jiumei Peng, Jiadi Pan, Xiaoyi Li, Jingjing Zhou
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引用次数: 0

Abstract

Background

As the common antibacterial drugs in folic acid oral liquid, parabens are listed as mandatory substances in the quality standard. Both the Chinese Pharmacopoeia and the United States Pharmacopoeia use high performance liquid chromatography for the determination of folic acid, but the quantitative methods of parabens are different. Pharmacopoeias use different instruments to quantify folic acid and parabens, resulting in cumbersome and cumbersome detection methods.

Objective

Without changing the type of instrument and mobile phase, two methods were established for the determination of folic acid and parabens (methyl paraben; ethyl paraben; propyl paraben) using respective wavelengths and flow comparisons Propyl benzoate) high performance liquid chromatography method.

Method

Chromatographic separation was achieved on an Agilent 5 TC-C18 HPLC column (5 μm; 250 μm × 4.6 mm) maintained at 25 °C (column temperature). The mobile phase consisted of phosphate buffer (pH 4.0)-methanol. When the ratio is 99:1, it is used to determine the content of folic acid, and when the ratio is 79:21, it is used to determine the content of antimicrobial agents. The flow rate used was 1.2 mL/min, the injection volume of folic acid was 20 µL, and the injection volume of bacteriostatic agent was 50 µL. In addition, the blue applicability grade index (BAGI) and analytical greenness (AGREE) metric tools were used to evaluate the greenness and environmental friendliness of the developed methods.

Results

The method has a good linear relationship with R2 ≥ 0.9995, the average recovery rate of the two methods is ≥ 95%, and the relative standard deviation (RSD%) accuracy is less than 0.21%. The BAGI tool characterizes the developed method as green. The AGREE score is around 0.5, and the method is also largely consistent with the principles of green analytical chemistry.

Conclusions

The HPLC method was established for the rapid determination of folic acid and antibacterial agent of parabens in folic acid. The method has high accuracy, strong specificity, high recovery rate, good stability and environmental friendliness. Compared with the method in the pharmacopoeia, it has strong resistance to complex matrix interference, greatly shortens the detection time, and has little damage to the instrument and chromatographic column. It can be used for the quality standard of folic acid oral liquid.

HPLC法测定叶酸口服液中叶酸及对羟基苯甲酸酯类抗菌药物含量的方法建立及验证
背景对羟基苯甲酸酯作为叶酸口服液中常见的抗菌药物,在质量标准中被列为强制性物质。中国药典和美国药典均采用高效液相色谱法测定叶酸,但对羟基苯甲酸酯的定量方法不同。药典使用不同的仪器来定量叶酸和对羟基苯甲酸酯,导致检测方法繁琐和繁琐。目的在不改变仪器类型和流动相的情况下,建立两种测定叶酸和对羟基苯甲酸酯(对羟基苯甲酸甲酯;乙尼泊金;对羟基苯甲酸丙酯)分别用波长和流量比较苯甲酸丙酯)高效液相色谱法。方法采用Agilent 5 TC-C18高效液相色谱柱(5 μm;250 μm × 4.6 mm),在25°C(柱温)下保存。流动相为磷酸缓冲液(pH 4.0)-甲醇。当比例为99:1时,用于测定叶酸的含量,当比例为79:21时,用于测定抗菌药物的含量。流速1.2 mL/min,叶酸注射量20µL,抑菌剂注射量50µL。此外,采用蓝色适用性等级指数(BAGI)和分析绿色度(AGREE)度量工具对所开发方法的绿色度和环境友好性进行了评价。结果该方法线性关系良好,R2≥0.9995,两种方法的平均回收率≥95%,相对标准偏差(RSD%)准确度小于0.21%。BAGI工具将开发的方法描述为绿色。AGREE得分约为0.5,该方法也在很大程度上符合绿色分析化学的原则。结论建立了快速测定叶酸和对羟基苯甲酸酯类抗菌剂含量的高效液相色谱法。该方法具有准确度高、特异性强、回收率高、稳定性好、环境友好等特点。与药典中的方法相比,具有较强的抗复杂基质干扰能力,大大缩短了检测时间,对仪器和色谱柱的损坏很小。可作为叶酸口服液的质量标准。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Chemistry
BMC Chemistry Chemistry-General Chemistry
CiteScore
5.30
自引率
2.20%
发文量
92
审稿时长
27 weeks
期刊介绍: BMC Chemistry, formerly known as Chemistry Central Journal, is now part of the BMC series journals family. Chemistry Central Journal has served the chemistry community as a trusted open access resource for more than 10 years – and we are delighted to announce the next step on its journey. In January 2019 the journal has been renamed BMC Chemistry and now strengthens the BMC series footprint in the physical sciences by publishing quality articles and by pushing the boundaries of open chemistry.
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