Journals / Turkish Journal of Chemistry / 2014 / Cilt: 38 - Sayı: 5

Simultaneous determination of dexpanthenol, lidocaine hydrochloride, and mepyramine maleate in combined pharmaceutical gel by capillary electrophoresis

Pages
756–764
Publication Date
2014-05-01
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The developed method is accurate, precise, sensitive, selective, and repeatable.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:A new capillary electrophoresis method was developed for the simultaneous determination of dexpanthenol (DEX), lidocaine (LID), and mepyramine (MEP) in pharmaceutical preparations.
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Key Findings & Data:The best results were obtained using 20 mM (pH 3.0) phosphate buffer as the background electrolyte.
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Conclusion & Impact:The developed method is accurate, precise, sensitive, selective, and repeatable.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Capillary electrophoresis · dexpanthenol · lidocaine

Abstract

A new capillary electrophoresis method was developed for the simultaneous determination of dexpanthenol (DEX), lidocaine (LID), and mepyramine (MEP) in pharmaceutical preparations. The best results were obtained using 20 mM (pH 3.0) phosphate buffer as the background electrolyte. Separation was obtained using a fused-silica capillary (75 m m internal diameter, 50 cm total length, 41 cm effective length) and a potential of +30 kV at 20 °C. Standards and samples were injected using a pressure injection at 50 mbar for 5 s and the analytes were monitored at a detection wavelength of 200 nm. Under optimum conditions, migration times were 2.457 min for MEP, 3.520 min for LID, and 7.363 min for DEX. The method was linear over the ranges of 25--200 m g mL-1 for DEX, 7.5--60 m g mL-1 for MEP, and 7.5--60 m g mL-1 for LID. Limit of detection (LOD) values were 0.8 m g mL-1 for MEP, 1.8 m g mL-1 for LID, and 3.1 m g mL-1 for DEX. The developed method is accurate, precise, sensitive, selective, and repeatable.

Özet

A new capillary electrophoresis method was developed for the simultaneous determination of dexpanthenol (DEX), lidocaine (LID), and mepyramine (MEP) in pharmaceutical preparations. The best results were obtained using 20 mM (pH 3.0) phosphate buffer as the background electrolyte. Separation was obtained using a fused-silica capillary (75 m m internal diameter, 50 cm total length, 41 cm effective length) and a potential of +30 kV at 20 °C. Standards and samples were injected using a pressure injection at 50 mbar for 5 s and the analytes were monitored at a detection wavelength of 200 nm. Under optimum conditions, migration times were 2.457 min for MEP, 3.520 min for LID, and 7.363 min for DEX. The method was linear over the ranges of 25--200 m g mL-1 for DEX, 7.5--60 m g mL-1 for MEP, and 7.5--60 m g mL-1 for LID. Limit of detection (LOD) values were 0.8 m g mL-1 for MEP, 1.8 m g mL-1 for LID, and 3.1 m g mL-1 for DEX. The developed method is accurate, precise, sensitive, selective, and repeatable.

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Cite This Article

AKYIL, G. B., KARA, H. E. Ş., BAŞ, S. Y., ERTAŞ, N., GÖĞER, N. G. (2014). Simultaneous determination of dexpanthenol, lidocaine hydrochloride, and mepyramine maleate in combined pharmaceutical gel by capillary electrophoresis. Turkish Journal of Chemistry, Cilt: 38 - Sayı: 5, 756–764. https://ajindex.com/articles/184772

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