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Analytical methods for the determination of paracetamol pseudoephedrine and brompheniramine in Comtrex tablets

机译:测定Comtrex片剂中对乙酰氨基酚伪麻黄碱和溴苯那敏的分析方法

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摘要

Comtrex® tablets composed of paracetamol, pseudoephedrine and brompheniramine are widely used for relieving symptoms related to common cold. This study has overcome the challenging dosage form ratio (250:15:1) and proposed chromatographic methods for analyzing the ternary combination were utilized displaying different apparatus, solvents and sensitivity ranges. Three chromatographic methods namely thin layer chromatography (TLC), high performance liquid chromatography with ultra-violet detection (HPLC–UV) and ultra-performance liquid chromatography coupled to tandem mass spectrometry (UPLC-MS/MS) were developed and validated for the simultaneous determination of the three drugs. Concerning the TLC method, aluminum TLC plates pre-coated with silica gel 60F254 were used and methanol:water:ammonia (9:1:0.1, v/v/v) was applied as a mobile phase; scanning of the plates was carried out at 254 nm. For the HPLC–UV method C18 column was used with an isocratic elution mobile phase composed of water:acetonitrile (75:25, v/v; pH 3.2) and the detection was at 210 nm. For the UPLC-MS/MS method; separation was performed on a UPLC-BEH C18 column with methanol: 0.1% ammonium formate (60:40, v/v) as the mobile phase utilizing diphenhydramine as an internal standard and mass spectrometry was used for detection. The methods were simple, sensitive, accurate and precise. Statistical analysis revealed no significant difference from the reported methods in regard to accuracy and precision.Electronic supplementary materialThe online version of this article (10.1186/s13065-019-0595-6) contains supplementary material, which is available to authorized users.
机译:由对乙酰氨基酚,伪麻黄碱和溴苯那敏组成的Comtrex ®片剂被广泛用于缓解与普通感冒有关的症状。这项研究克服了具有挑战性的剂型比例(250:15:1),并提出了用于分析三元组合的色谱方法,显示了不同的仪器,溶剂和灵敏度范围。开发了三种色谱方法,分别是薄层色谱(TLC),具有紫外检测的高效液相色谱(HPLC-UV)和与串联质谱联用的超高效液相色谱(UPLC-MS / MS),并进行了验证三种药物的测定。关于TLC方法,使用预先涂有硅胶60F254的铝TLC板,并以甲醇:水:氨水(9∶1∶0.1,v / v / v)作为流动相。板的扫描在254nm进行。对于HPLC-UV方法,C18色谱柱使用的等度洗脱流动相为水:乙腈(75:25,v / v; pH 3.2),检测波长为210nm。对于UPLC-MS / MS方法;使用苯海拉明作为内标,在甲醇:0.1%甲酸铵(60:40,v / v)作为流动相的UPLC-BEH C18色谱柱上进行分离,并使用质谱进行检测。该方法简单,灵敏,准确,准确。统计分析表明,与报道的方法在准确性和精密度上没有显着差异。电子补充材料本文的在线版本(10.1186 / s13065-019-0595-6)包含补充材料,授权用户可以使用。

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