Development and validation of HPTLC method for the analysis of Olmutinib in Bulk drug
This paper describes a simple, precise, rapid and accurate high- performance thin layer chromatographic (HPTLC) method for determination of Olmutinib in bulk drug. Chroma to graphic separation was per formed on aluminium plates precoated with silicagel60F254 as the stationary phase using solvent sys...
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Veröffentlicht in: | International journal of pharmtech research 2020, Vol.13 (1), p.37-43 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | This paper describes a simple, precise, rapid and accurate high- performance thin
layer chromatographic (HPTLC) method for determination of Olmutinib in bulk drug. Chroma
to graphic separation was per formed on aluminium plates precoated with silicagel60F254 as the
stationary phase using solvent system consisted of chloro form: methanol: (9:1v/v). After the
application of bands using CAMAG Automatic TLC Sampler 4, the plate was developed in the
solvent system up to 70 mm in CAMAGT win Trough Chamber. This solvent system was
found to give compact spot for Olmutinib with Rfvalue of 0.32±0.02. The spots were scanned
at 267.68nm. The calibration curves were linear with co-relation coefficient of 0.995 for
Olmutinib. Linear regression analysis showed good linearity in the concentration range of 100-
1100 ng per spot. The method was validated in terms of Precision, specificity, and Linearity.
The average recovery of the standards in the samples was found to be 99.65% at the same time
we have checked the C.V. values of Reproducibility, intra-day and inter-day tabulated further.
The proposed method can be successfully applied to determine the drug content of bulk drug. |
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ISSN: | 0974-4304 0974-4304 |
DOI: | 10.20902/IJPTR.2019.130105 |