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A High-Performance Thin Layer Chromatography (HPTLC) Method for Simultaneous Determination of Diphenhydramine Hydrochloride and Naproxen Sodium in Tablets

机译:高效薄层色谱法同时测定片剂中盐酸苯海拉明和萘普生钠的含量

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摘要

A rapid and simple high-performance thin layer chromatography (HPTLC) method with densitometry at 230 nm was developed and validated for simultaneous determination of diphenhydramine hydrochloride (DPH) and naproxen sodium (NPS) from pharmaceutical preparation. The separation was carried out on aluminum plates precoated with silica gel 60 F254 using mobile phase toluene:methanol:glacial acetic acid (7.5:1:0.2, v/v/v). The linearity range lies between 200 and 1200 ng/band for DPH and 1760 and 10,560 ng/band for NPS with correlation coefficients of 0.994 and 0.995, respectively. The Rf value for DPH is 0.20 ± 0.05 and for NPS is 0.61 ± 0.06. % Recoveries of DPH and NPS was in the range of 99.70%–99.95% and 99.63%–99.95%, respectively. Limit of detection value for DPH was 13.21 ng/band and for NPS was 8.03 ng/band. Limit of quantitation value for DPH was 40.06 ng/band and for NPS was 24.34 ng/band. The developed method was validated as per ICH guidelines. In stability testing, DPH was found unstable to acid and alkaline hydrolysis, and DPH and NPS were found unstable to oxidation, whereas both the drugs were stable to neutral and photodegradation. The proposed method was successfully applied for the routine quantitative analysis of dosage form containing DPH and NPS.
机译:开发了一种快速简便的高效薄层色谱法(HPTLC),其光密度法在230 nm处进行了测定,并验证了该方法可同时测定药物制剂中的盐酸苯海拉明(DPH)和萘普生钠(NPS)。使用流动相甲苯:甲醇:冰醋酸(7.5:1:0.2,v / v / v)在预先涂有硅胶60 F254的铝板上进行分离。对于DPH,线性范围在200到1200 ng /带之间;对于NPS,线性范围在1760和10,560 ng /带之间,相关系数分别为0.994和0.995。 DPH的Rf值为0.20±0.05,NPS的Rf值为0.61±0.06。 DPH和NPS的回收率分别在99.70%–99.95%和99.63%–99.95%之间。 DPH的检出限为13.21 ng / band,NPS的检出限为8.03 ng / band。 DPH的定量限为40.06 ng / band,NPS为24.34 ng / band。根据ICH指南验证了开发的方法。在稳定性测试中,发现DPH对酸和碱水解不稳定,而DPH和NPS对氧化不稳定,而两种药物对中性和光降解均稳定。该方法已成功应用于含有DPH和NPS的剂型的常规定量分析。

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