1,4-Anthraquinone: A new useful pre-column reagent for the determination of N-acetylcysteine and captopril in pharmaceuticals by high performance liquid chromatography

被引:11
作者
Gatti, Rita [1 ]
Morigi, Rita [1 ]
机构
[1] Univ Bologna, Alma Mater Studiorum, Dept Pharm & Biotechnol, Via Belmeloro 6, I-40126 Bologna, Italy
关键词
HPLC; 1.4-Anthraquinone; Pre-column derivatization; Pharmaceuticals; N-Acetylcysteine; Captopril; MOLECULAR-MASS THIOLS; HPLC-UV METHOD; DERIVATIZATION REAGENT; ULTRAVIOLET DERIVATIZATION; CAPILLARY-ELECTROPHORESIS; BIOLOGICAL SAMPLES; ALIPHATIC THIOLS; HUMAN PLASMA; ACID; CYSTEINE;
D O I
10.1016/j.jpba.2017.06.011
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
1,4-Anthraquinone (ANQ) is proposed as a novel pre-column reagent for high performance liquid chromatography (HPLC) determination of N-acetylcysteine (NAC) and captopril (CAP) in pharmaceutical formulations. The derivatization reactions were carried out at room temperature: NAC at pH 8 for 1 min, while CAP at pH 7.5 for 20 min. Both reactions reached completeness at a reagent to thiol molar ratio of about 2.5. The synthesised derivatives were characterized by H-1 NMR and IR The chromatographic separations were performed on a C-18 Phenomenex Synergi Fusion 4 mu m (250 mm x 4.6 mm I.D.) stainless steel column with detection at lambda=300 nm. The mobile phase consisted of methanol/triethylammonium (TEA) phosphate buffer (pH 3; 0.05 mol/L) 75:25 (v/v) at a flow-rate of 0.4 mL/min for NAC and 88:12 (v/v), at a flow-rate of 0.6 mL/min for CAP. The validation parameters (linearity, sensitivity, accuracy, precision, specificity and stability) were highly satisfactory. Linear response was observed (determination coefficient >= 0.9996). Detection limits were about 8 and 18 ng/mL for NAC and CAP, respectively. Intra-day precision (relative standard deviation, R.S.D.) was <= 1.58%, for thiol to internal standard (IS) peak area ratio and <= 0.33%, for thiol and IS retention times (t(R)), without significant differences between intra- and inter-day data. Thiol recovery studies were satisfactory (99.50%) with R.S.D. <= 0.56%. The results highlight the high sensitivity of the method and the remarkable reactivity and selectivity of the reagent towards the thiol function. The developed method is suitable for the quality control of both thiols in commercial products. The method can be applied in any analytical laboratory not requiring a sophisticated instrumentation. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:299 / 304
页数:6
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