Emara Samy, Masujima Tsutomu, Zarad Walaa, Kamal Maha, El-Bagary Ramzia
Pharmaceutical Chemistry Department, Faculty of Pharmacy, Misr International University, Km 28 Ismailia Road, Cairo, Egypt.
Chem Cent J. 2012 Dec 12;6(1):155. doi: 10.1186/1752-153X-6-155.
Analysis of folic acid (FA) is not an easy task because of its presence in lower concentrations, its lower stability under acidic conditions, and its sensitiveness against light and high temperature. The present study is concerned with the development and validation of an automated environmentally friendly pre-column derivatization combined by solid-phase enrichment (SPEn) to determine low levels of FA.
Cerium (IV) trihydroxyhydroperoxide (CTH) as a packed oxidant reactor has been used for oxidative cleavage of FA into highly fluorescent product, 2-amino-4-hydroxypteridine-6-carboxylic acid. FA was injected into a carrier stream of 0.04 M phosphate buffer, pH 3.4 at a flow-rate of 0.25 mL/min. The sample zone containing the analyte was passed through the CTH reactor thermostated at 40°C, and the fluorescent product was trapped and enriched on a head of small ODS column (10 mm x 4.6 mm i.d., 5 μm particle size). The enriched product was then back-flush eluted by column-switching from the small ODS column to the detector with a greener mobile phase consisting of ethanol and phosphate buffer (0.04M, pH 3.4) in the ratio of 5:95 (v/v). The eluent was monitored fluorimetrically at emission and excitation wavelengths of 463 and 367 nm, respectively. The calibration graph was linear over concentrations of FA in the range of 1.25-50 ng/mL, with a detection limit of 0.49 ng/mL.
A new simple and sensitive green analytical procedure including on-line pre-column derivatization combined by SPEn has been developed for the routine quality control and dosage form assay of FA at very low concentration level. The method was a powerful analytical technique that had excellent sensitivity, sufficient accuracy and required relatively simple and inexpensive instrumentation.
由于叶酸(FA)浓度较低、在酸性条件下稳定性较差以及对光和高温敏感,其分析并非易事。本研究关注的是一种结合固相富集(SPEn)的自动化环保柱前衍生化方法的开发与验证,用于测定低水平的FA。
作为填充氧化剂反应器的四羟基过氧化铈(IV)(CTH)已用于将FA氧化裂解为高荧光产物2-氨基-4-羟基蝶啶-6-羧酸。FA以0.25 mL/min的流速注入pH 3.4的0.04 M磷酸盐缓冲液载流中。含有分析物的样品区通过恒温在40°C的CTH反应器,荧光产物被捕获并富集在小ODS柱(10 mm×4.6 mm内径,5μm粒径)柱头上。然后通过柱切换从小ODS柱将富集产物反冲洗脱至检测器,流动相为更环保的乙醇和磷酸盐缓冲液(0.04M,pH 3.4),比例为5:95(v/v)。分别在发射波长463 nm和激发波长367 nm处对洗脱液进行荧光监测。校准曲线在1.25 - 50 ng/mL的FA浓度范围内呈线性,检测限为0.49 ng/mL。
已开发出一种新的简单灵敏的绿色分析方法,包括结合SPEn的在线柱前衍生化,用于在极低浓度水平下对FA进行常规质量控制和剂型分析。该方法是一种强大的分析技术,具有出色的灵敏度、足够的准确度,且所需仪器相对简单且成本低廉。