稳定性指示高效液相色谱法测定盐酸赛庚啶、维生素B1、维生素B5、维生素B6的含量

Yayra Tuani, Seth Amo-Koi, D. Mingle, A. Gordon, A. Asor
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引用次数: 0

摘要

可靠、快速的分析方法对单一剂型中多种原料药的质量控制至关重要。本文建立了两种测定盐酸赛庚啶(CH)、单硝酸硫胺素(Vit)的方法,并进行了验证。b1)、泛酸钙(Vit);b5)和盐酸吡哆醇(Vit)。B 6)无包衣片剂。测定维生素时,流动相为pH为3.5的磷酸盐缓冲液和甲醇,比例为93:7,固定相为Eurospher ODS (150 × 4.5mm),室温下流速为1.0 mL/min。单硝酸硫胺素和盐酸吡哆醇的检测波长为270 nm,运行时间为0.00 ~ 5.50 min;泛酸钙的检测波长为205 nm,运行时间为5.50 ~ 11.00 min。在验证的条件下,获得了良好的分辨率和11分钟的运行时间。单硝酸硫胺素、盐酸吡哆醇和泛酸钙的保留时间分别为2.823±0.020、4.184±0.007和10.025±0.015。盐酸赛庚丁的流动相为甲醇和离子配对溶液(70:30),流速为1mL/min,运行时间为8 min,进样量为20µL,波长为285 nm,固定相为Eurospher ODS (150 × 4.5 mm)。盐酸赛庚啶的保留时间为4.961±0.006。在单硝酸硫胺素0.0192 mg/mL ~ 0.0288 mg/mL、盐酸吡啶醇0.0128 ~ 0.0192 mg/mL、泛酸钙0.032 ~ 0.048 mg/mL、盐酸赛七乙胺0.032 ~ 0.048 mg/mL的浓度范围内,两种方法均具有特异性、鲁棒性、准确性和精密度。盐酸赛戊乙胺、单硝酸硫胺素、盐酸吡哆醇、泛酸钙的相关系数r2均大于0.999。建立盐酸赛庚啶、维生素b1、维生素b5、维生素b6联合剂型的高效液相色谱测定方法并进行验证。结果表明,所建立的方法对盐酸赛庚啶、维生素b1、b5、b6的测定具有较好的精密度、专属性、准确度和稳健性。关键词:盐酸赛庚啶,单硝酸硫胺素,盐酸吡哆醇,泛酸钙,反相高效液相色谱,验证DOI: 10.7176/CMR/12-6-06
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Stability-Indicating HPLC Methods for the Quantification of Cyproheptadine Hydrochloride, Vitamins B1, B5 And B6 in Tablets using RP-HPLC with UV Detection
The availability of reliable and fast analytical method is crucial for the quality control of multi-API in a single dosage form. Herein, two methods have been developed and validated for the determination of Cyproheptadine hydrochloride (CH), Thiamine mononitrate (Vit. B 1 ), Calcium pantothenate (Vit. B 5 ) and Pyridoxine hydrochloride (Vit. B 6 ) in uncoated tablets. To assay the vitamins, a mobile phase combination of Phosphate buffer pH 3.5 and Methanol in the ratio 93:7, using Eurospher ODS (150 x 4.5mm) as the stationary phase with a flow rate set at 1.0 mL/min at ambient temperature conditions was adopted. Wavelength of detection was 270 nm with a run time of 0.00 to 5.50 minutes for Thiamine mononitrate and Pyridoxine hydrochloride, and 205 nm from 5.50 to 11.00 minutes for Calcium pantothenate. A good resolution and a short run time of 11 minutes were achieved with the validated conditions. The retention times of Thiamine mononitrate, Pyridoxine hydrochloride and Calcium pantothenate were 2.823±0.020, 4.184±0.007 and 10.025±0.015 respectively. The mobile phase for Cyproheptadine HCl was methanol and an ion-pairing solution (70:30), set at a flow rate of 1mL/min, a runtime of 8 minutes, an injection volume of 20 µL and a wavelength of 285 nm using Eurospher ODS (150 x 4.5 mm) as the stationary phase. The retention time for Cyproheptadine HCl was 4.961±0.006. Both methods were found to be specific, robust, accurate and precise over the concentration ranges of 0.0192 mg/mL–0.0288 mg/mL for Thiamine mononitrate, 0.0128–0.0192 mg/mL for Pyridoxine hydrochloride, 0.032–0.048 mg/mL for Calcium pantothenate and 0.032-0.048 mg/mL for Cyproheptadine hydrochloride. The Correlation Coefficient (r 2 ) for Cyproheptadine hydrochloride, Thiamine mononitrate, Pyridoxine hydrochloride and Calcium pantothenate were greater than 0.999. The purpose of this study was to develop and validate simple HPLC methods for the estimation of Cyproheptadine hydrochloride, Vitamins B 1 , B 5 and B 6 in combined dosage forms. The proposed methods were found to be precise, specific, accurate and robust for the estimation of Cyproheptadine hydrochloride, Vitamins B 1 , B 5 and B 6. Keywords: Cyproheptadine hydrochloride, Thiamine mononitrate, Pyridoxine hydrochloride, Calcium pantothenate, RP-HPLC, Validation DOI: 10.7176/CMR/12-6-06 Publication date: August 31 st 2020
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