Indirect spectrophotometric estimation of lidocaine using crystal violet

A simple, quick and perceptive method was developed to estimate Lidocaine in its pure and pharmaceutical forms spectrally using a spectrometer for ultraviolet visible rays, and the method was summarized: by oxidation of the drug using a mixture of bromate and potassium bromide KBr-KBrO3 with an acidic medium, where the remaining oxidizing agent reacts with the dye Crystal violet (CV) to be a dark blue product It gave peak absorption value at 612 nm, with Beer-lambert law (linear concentration) was between (15) and (100) μg/ml while the molar absorption coefficient was equal to (1945.022) L/mol/cm , limit of detection (0.36) μg/ml, while the quantity limit was (1.08) μg/ml. The method has been effictively applied to the measurement of Lidocaine in both its pure form and its pharmaceutical preparations.

Authors

Publication Details

Journal
Springer Link (Chiba Institute of Technology)
Published
2026-01-07
DOI
https://doi.org/10.1051/epjconf/202634501075/pdf
Primary Topic
Analytical Methods in Pharmaceuticals
Type
article
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article

Indirect spectrophotometric estimation of lidocaine using crystal violet

Qabas Naji Rashid, Sura Ismail Ibrahim
Springer Link (Chiba Institute of Technology)
Analytical Methods in Pharmaceuticals
article

Indirect spectrophotometric estimation of lidocaine using crystal violet

Qabas Naji Rashid, Sura Ismail Ibrahim
article en

Abstract

A simple, quick and perceptive method was developed to estimate Lidocaine in its pure and pharmaceutical forms spectrally using a spectrometer for ultraviolet visible rays, and the method was summarized: by oxidation of the drug using a mixture of bromate and potassium bromide KBr-KBrO3 with an acidic medium, where the remaining oxidizing agent reacts with the dye Crystal violet (CV) to be a dark blue product It gave peak absorption value at 612 nm, with Beer-lambert law (linear concentration) was between (15) and (100) μg/ml while the molar absorption coefficient was equal to (1945.022) L/mol/cm , limit of detection (0.36) μg/ml, while the quantity limit was (1.08) μg/ml. The method has been effictively applied to the measurement of Lidocaine in both its pure form and its pharmaceutical preparations.

Springer Link (Chiba Institute of Technology)
Openalex Percentile: Top 93%
Analytical Methods in Pharmaceuticals
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