Development and Validation of HPTLC Method for Estimation of Tenoxicam and its Formulations

Indian Journal of Pharmaceutical Sciences
S ChandelC J Kapadia

Abstract

A simple, precise, accurate and rapid high performance thin layer chromatographic method has been developed and validated for the estimation of tenoxicam in the microemulsion gels. Tenoxicam was chromatographed on silica gel 60 F(254) TLC plate, as a stationary phase. The mobile phase was toluene: ethyl acetate: formic acid (6:4:0.3 v/v/v), which gave a dense and compact spot of tenoxicam with a R(f) value of 0.38±0.03. The quantification was carried out at 379 nm. The method was validated in terms of linearity, accuracy, precision and specificity. To justify the suitability, accuracy and precision of the proposed method, recovery studies were performed at three concentration levels. Statistical analysis proved that the proposed method is accurate and reproducible with linearity in the range of 100 to 400 ng. The limit of detection and limit of quantification for tenoxicam were 25 and 50 μg/spot, respectively. The proposed method can be employed for the routine analysis of tenoxicam as well as in pharmaceutical formulations.

References

Jan 10, 1986·Journal of Chromatography·P HeizmannK Zinapold
Jul 2, 1993·Journal of Chromatography·M I Múnera-Jaramillo, S Botero-Garcés
Jun 1, 2002·Journal of Pharmaceutical and Biomedical Analysis·Horria A MohamedOthman A Farghaly
Jul 3, 2002·Journal of Pharmaceutical and Biomedical Analysis·Alaa S Amin
Jan 24, 2004·Journal of Pharmaceutical and Biomedical Analysis·Magda H BararyTarek S Belal
Oct 19, 2006·Journal of Pharmaceutical and Biomedical Analysis·Nitin G Tayade, Mangal S Nagarsenker

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