A sequential injection method for the determination of piroxicam in pharmaceutical formulations using europium sensitized fluorescence

Research output: Contribution to journalArticle

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Abstract

A simple, selective and sensitive luminescence method for the assay of piroxicam (PX) in pharmaceutical formulation is developed. The method is based on the luminescence sensitization of europium (Eu3+) by complexation with PX. The signal for PX-EU is monitored at λex=358 nm and λem=615 nm. Optimum conditions for the formation of the complex in methanol were 0.01 M TRIS buffer and 0.2 mM of Eu3+ which allows the determination of 100-2000 ppb of pX in batch method and 100-1000 ppb with limit of detection (LOD) = 23.0 ppb using sequential injection analysis (SIA). The relative standard deviations of the method range between 2 and 3% indicating excellent reproducibility of the method. The proposed method was successfully applied for he assay of PX in pharmaceutical formulations (Feldene capsules and tablets). Average recoveries of 101.0±0.3 and 98.8±2.7% were obtained for capsules in methanol using batch and sequential injection (SI) methods, respectively.

Original languageEnglish
Pages (from-to)1343-1350
Number of pages8
JournalTalanta
Volume64
Issue number5 SPEC. ISS.
DOIs
Publication statusPublished - Dec 15 2004

Fingerprint

Europium
Piroxicam
Drug Compounding
Fluorescence
Injections
Pharmaceutical Preparations
Capsules
Methanol
Luminescence
Assays
Complexation
Tablets
Buffers
Recovery
Limit of Detection

Keywords

  • Europium
  • Piroxicam
  • Sensitized fluorescence
  • Sequential injection

ASJC Scopus subject areas

  • Analytical Chemistry
  • Spectroscopy

Cite this

A sequential injection method for the determination of piroxicam in pharmaceutical formulations using europium sensitized fluorescence. / Al-Kindy, Salma M Z; Al-Wishahi, Aisha; Suliman, Fakhr Eldin O.

In: Talanta, Vol. 64, No. 5 SPEC. ISS., 15.12.2004, p. 1343-1350.

Research output: Contribution to journalArticle

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N2 - A simple, selective and sensitive luminescence method for the assay of piroxicam (PX) in pharmaceutical formulation is developed. The method is based on the luminescence sensitization of europium (Eu3+) by complexation with PX. The signal for PX-EU is monitored at λex=358 nm and λem=615 nm. Optimum conditions for the formation of the complex in methanol were 0.01 M TRIS buffer and 0.2 mM of Eu3+ which allows the determination of 100-2000 ppb of pX in batch method and 100-1000 ppb with limit of detection (LOD) = 23.0 ppb using sequential injection analysis (SIA). The relative standard deviations of the method range between 2 and 3% indicating excellent reproducibility of the method. The proposed method was successfully applied for he assay of PX in pharmaceutical formulations (Feldene capsules and tablets). Average recoveries of 101.0±0.3 and 98.8±2.7% were obtained for capsules in methanol using batch and sequential injection (SI) methods, respectively.

AB - A simple, selective and sensitive luminescence method for the assay of piroxicam (PX) in pharmaceutical formulation is developed. The method is based on the luminescence sensitization of europium (Eu3+) by complexation with PX. The signal for PX-EU is monitored at λex=358 nm and λem=615 nm. Optimum conditions for the formation of the complex in methanol were 0.01 M TRIS buffer and 0.2 mM of Eu3+ which allows the determination of 100-2000 ppb of pX in batch method and 100-1000 ppb with limit of detection (LOD) = 23.0 ppb using sequential injection analysis (SIA). The relative standard deviations of the method range between 2 and 3% indicating excellent reproducibility of the method. The proposed method was successfully applied for he assay of PX in pharmaceutical formulations (Feldene capsules and tablets). Average recoveries of 101.0±0.3 and 98.8±2.7% were obtained for capsules in methanol using batch and sequential injection (SI) methods, respectively.

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