VALIDATING THE ANALYTICAL METHOD FOR THE REFERENCE SAMPLE OF LAPPACONITINE


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Abstract

A method for the quantitative determinnation of the reference sample of lappaconitine by HPLC has been developed and included in the draft of the pharmacopoeic article for this drug. The proposed analytical technique is completely validated and includes the entire complex of characteristics for the specificity, suitability of the chromatographic system, and the linearity, accuracy, and reproducibility of the HPLC analyses.

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