RP-HPLC Method for Rhein Quantification in Cassia fistula L. (Fabaceae) Leaves.

Q4 Medicine Acta Medica Philippina Pub Date : 2024-12-18 eCollection Date: 2024-01-01 DOI:10.47895/amp.vi0.8803
Jade P Rodriguez
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Abstract

Objectives: The aim of this study is to establish a Reversed Phase - High Performance Liquid Chromatographic (RP-HPLC) method for the quantification of Rhein from Cassia fistula L. leaves.

Methods: A Shimadzu system equipped with a C18 Column (150 x 4.6 mm, 5 μm) with an isocratic elution of Acetonitrile (solvent A) and 0.1% trifluoroacetic acid aqueous solution (solvent B) (Merck, 1.08178.0050) with a 55:45 ratio, respectively and a flow rate of 1.0 mL/min and sample injection of 10 μL detection was done at 230 nm. Standard solution of Rhein (Chengdu Biopurify) was prepared for method development. This study was validated using the guidelines set under "ICH Topic Q2 R2 or the Validation of Analytical Procedures". Procedures for linearity, precision, accuracy, limit of detection, and limit of quantitation were performed.

Results: The retention time of Rhein standard was determined at 5.10 minutes. LOD and LOQ were determined to be 1.278 mcg/mL and 3.872 mcg/mL, respectively with good linearity (R2 ≥0.996) with a linear range of 2.5-20 ug/mL of the Rhein standard. The accuracy of the method was determined based on % recovery method and ranged from 94.75%-100.32% (intraday, n=3) with %RSD of 0.71. The intraday precision %RSD was 2.92 (n=6) while interday precision %RSD was 3.75 (n=3). The method was able to check the Rhein quantity among 10 samples of Cassia fistula L. leaves from different locations in the Philippines.

Conclusion: The method was found to be sensitive and accurate for the quantification of Rhein. The method was found to be useful for the quantification of the amount of Rhein and can be used as a Quality Control tool for the assessment of Cassia fistula.

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反相高效液相色谱法测定决明子叶中大黄碱含量。
目的:建立反相高效液相色谱(RP-HPLC)定量测定决明子叶中大黄碱含量的方法。方法:采用岛津系统,C18柱(150 × 4.6 mm, 5 μm),乙腈(溶剂A)和0.1%三氟乙酸水溶液(溶剂B) (Merck, 1.08178.0050),以55:45的比例等密度洗脱,流速为1.0 mL/min,进样量为10 μL,在230 nm处检测。制备了Rhein(成都生物纯化)标准溶液,用于方法开发。本研究使用ICH主题Q2 R2或分析方法验证指南进行验证。进行了线性度、精密度、准确度、检出限和定量限的测定程序。结果:测定莱茵标准品保留时间为5.10 min。测定的定量限和定量限分别为1.278微克/毫升和3.872微克/毫升,线性范围为2.5 ~ 20微克/毫升,R2≥0.996;方法的准确度为94.75% ~ 100.32%(日内,n=3), %RSD为0.71。日内精密度%RSD为2.92 (n=6),日间精密度%RSD为3.75 (n=3)。该方法能够对菲律宾不同产地的10份决明子叶样品进行莱茵含量的检测。结论:该方法灵敏、准确,可用于莱茵的定量分析。该方法可用于定量测定莱茵的含量,并可作为评价决明子瘘的质量控制工具。
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来源期刊
Acta Medica Philippina
Acta Medica Philippina Medicine-Medicine (all)
CiteScore
0.40
自引率
0.00%
发文量
199
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