Journals / Turkish Journal of Chemistry / 2002 / Cilt: 26 - Sayı: 4

HPLC Method for the Analysis of Paracetamol, Caffeine and Dipyrone

Pages
521–528
Publication Date
2002-04-01
DOI
—
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AI Summary & Key Takeaways

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

The method was shown to be linear, reproducible, specific, sensitive and rugged.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:An accurate, simple, reproducible and sensitive method for the determination of paracetamol, caffeine and dipyrone was developed and validated.
📊
Key Findings & Data:Paracetamol, caffeine and dipyrone were separated using a m -Bondapack C 8 column by isocratic elution with a flow rate of 1.0 ml/min.
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Conclusion & Impact:The method was shown to be linear, reproducible, specific, sensitive and rugged.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Paracetamol · Acetaminophen · Caffeine

Abstract

An accurate, simple, reproducible and sensitive method for the determination of paracetamol, caffeine and dipyrone was developed and validated. Paracetamol, caffeine and dipyrone were separated using a m -Bondapack C 8 column by isocratic elution with a flow rate of 1.0 ml/min. The mobile phase composition was 0.01 M KH2PO4- -methanol-acetonitrile-isopropyl alcohol (420: 20: 30: 30) (v/v/v/v) and spectrophotometric detection was carried out at 215 nm. The linear range of determination for paracetamol, caffeine and dipyrone were 0.409-400 m g/ml, 0.151-200 m g/ml and 0.233-600 m g/ml, respectively. The method was shown to be linear, reproducible, specific, sensitive and rugged.

Özet

An accurate, simple, reproducible and sensitive method for the determination of paracetamol, caffeine and dipyrone was developed and validated. Paracetamol, caffeine and dipyrone were separated using a m -Bondapack C 8 column by isocratic elution with a flow rate of 1.0 ml/min. The mobile phase composition was 0.01 M KH2PO4- -methanol-acetonitrile-isopropyl alcohol (420: 20: 30: 30) (v/v/v/v) and spectrophotometric detection was carried out at 215 nm. The linear range of determination for paracetamol, caffeine and dipyrone were 0.409-400 m g/ml, 0.151-200 m g/ml and 0.233-600 m g/ml, respectively. The method was shown to be linear, reproducible, specific, sensitive and rugged.

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Cite This Article

ALTUN, M. L. (2002). HPLC Method for the Analysis of Paracetamol, Caffeine and Dipyrone. Turkish Journal of Chemistry, Cilt: 26 - Sayı: 4, 521–528. https://ajindex.com/articles/406211

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