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1.
J Chromatogr Sci ; 57(7): 592-599, 2019 Aug 01.
Article in English | MEDLINE | ID: mdl-30994892

ABSTRACT

Two chromatographic methods (high performance thin layer chromatography (HPTLC) and high performance liquid chromatography-diode array detector (HPLC-DAD)), were addressed for the analysis of a mixture consisted of phenylephrine hydrochloride and ibuprofen in two forms bulk and their combined dosage form. This binary mixture is considered to be a challenging one as the two drugs differ greatly in their chemical and physical properties. Not only this affects their simultaneous analysis, but also hinders their simultaneous extraction from biological fluids as plasma. That is the reason the literature lacks any report for the simultaneous extraction and analysis of these drugs from biological fluids. The concentration ranges of both drugs were 0.1-2.5 µg/spot and 0.1-100 µg/mL by HPTLC and HPLC, respectively. Not only was the HPLC-DAD method applied to the investigated drugs determination in pharmaceutical preparations, but also in spiked human plasma. Extensive study was conducted to optimize their simultaneous extraction from plasma as it was a crucial step for the in vivo analysis. The results obtained by proposed methods and a reference one were statistically comparable by analysis of variance test. No significant difference was recorded between the mean percent levels determined by the proposed methods and the reference one.


Subject(s)
Chromatography, High Pressure Liquid/methods , Chromatography, Thin Layer/methods , Ibuprofen/analysis , Phenylephrine/analysis , Drug Combinations , Humans , Ibuprofen/blood , Ibuprofen/chemistry , Ibuprofen/isolation & purification , Limit of Detection , Linear Models , Phenylephrine/blood , Phenylephrine/chemistry , Phenylephrine/isolation & purification , Reproducibility of Results , Solid Phase Extraction , Tablets
2.
Se Pu ; 34(1): 103-7, 2016 Jan.
Article in Chinese | MEDLINE | ID: mdl-27319173

ABSTRACT

A method for the separation and determination of optical isomers of phenylephrine was developed based on the promoting effect of non-chiral ionic liquid on chiral ligand-exchange capillary electrophoresis after the electrophoretic parameters were optimized systematically. R-phenylephrine and S-phenylephrine can be separated and determined effectively in 20 mmol/L Tris-H3PO4 buffer solution (pH 5.4) composed of 4.0 mmol/L Cu(II), 8.0 mmol/L L-proline (L-Pro) and 15 mmol/L 1-butyl-3-methylimidazolium chloride ([BMIM] Cl) with the applied voltage of 20 kV, capillary temperature of 25 °C , detection wavelength of 254 nm, and injection of 5 s at 3,447 Pa. The resolution of R- and S-phenylephrines was 1. 42. The linear ranges for the determination of R-phenylephrine and S-phenylephrine were 12. 5 - 150 mg/L and 15. 0-150 mg/L, respectively. The method has been satisfactorily used for the determination of R-phenylephrine and S-phenylephrine in the spiked blood and urine samples. The spiked recoveries in the urine sample were in the range of 93. 7% -108. 2% with the RSDs lower than 3. 18% (n= 3) , and the spiked recoveries in the blood sample were in the range of 91. 4% and 113. 1% with the RSDs lower than 4. 82% (n =3).


Subject(s)
Electrophoresis, Capillary , Ionic Liquids/chemistry , Phenylephrine/isolation & purification , Phenylephrine/chemistry
3.
Anal Chem ; 78(22): 7891-5, 2006 Nov 15.
Article in English | MEDLINE | ID: mdl-17105185

ABSTRACT

Different pharmaceutical preparations against the common cold contain acetaminophen, phenylephrine hydrochloride, and chlorpheniramine maleate. A degradation product had been discovered in these preparations after short- and long-term stability studies. This degradation product was isolated and found to be an adduct of phenylephrine and maleic acid. An account of the isolation and characterization of this compound was published. Our interest in this area led us to synthesize the compound, and we found that the synthesized compound does not have the same spectroscopic properties described in the original paper. Our subsequent work identified the structure of the degradation product as a "Michael addition" product of phenylephrine and maleic acid.


Subject(s)
Acetaminophen/analysis , Chemistry, Pharmaceutical , Chlorpheniramine/isolation & purification , Phenylephrine/isolation & purification , Acetaminophen/chemistry , Analgesics, Non-Narcotic/analysis , Analgesics, Non-Narcotic/pharmacology , Anti-Allergic Agents/analysis , Anti-Allergic Agents/pharmacology , Chlorpheniramine/chemistry , Common Cold/drug therapy , Drug Stability , Magnetic Resonance Spectroscopy , Maleates/isolation & purification , Nasal Decongestants/analysis , Nasal Decongestants/pharmacology , Phenylephrine/chemistry
4.
J Pharm Biomed Anal ; 12(11): 1379-96, 1994 Nov.
Article in English | MEDLINE | ID: mdl-7849134

ABSTRACT

Methyl and propyl parahydroxybenzoate (MPHB, PPHB), phenylephrine hydrochloride (PE) and chlorphenamine maleate (CPM) are often combined as ingredients in cough-syrups. Due to distinct chemical structures, pKa values among other chemical properties are different. This may result in a particular chromatographic behaviour on ion-pair reversed-phase liquid chromatographic (LC) systems. A face-centred central composite design was applied to study the impact of four LC mobile phase parameters and parameter interactions on the retention of these four compounds. The mobile phase parameters studied were the concentration of methanol as organic modifier, the concentration of sodium dioctylsulphosuccinate (SDSS) as counter-ion, the concentration of dimethyloctylamine (DMOA) as competitive base and the pH. By means of the proposed design, mathematical regression models and response surface plots were calculated, which could predict the compounds' retention times with good statistical reliability. Adequate combination of the most relevant of these mobile phase parameters enabled complete chromatographic separations within short times of analysis.


Subject(s)
Chlorpheniramine/isolation & purification , Chromatography, Liquid/methods , Parabens/isolation & purification , Phenylephrine/isolation & purification , Analysis of Variance , Chlorpheniramine/chemistry , Parabens/chemistry , Phenylephrine/chemistry , Regression Analysis
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