Sensitive Cloud Point Extraction Method for the Determination of Isoxsuprine Hydrochloride in Pharmaceutical forms using Spectrophotometry

Authors

  • Hind Hadi university of Baghdad, college of science, chemistry departmewnt
  • Wasan A. Al-Uzri

DOI:

https://doi.org/10.31351/vol31iss2pp83-90

Keywords:

Keywords: Isoxsuprine hydrochloride; Triton X-114; Cloud point extraction; sulfadimidine; diazotization reaction.

Abstract

      A simple and highly sensitive cloud point extraction process was suggested for preconcentration of micrograms amount of isoxsuprine hydrochloride (ISX) in pure and pharmaceutical samples. After diazotization coupling of ISX with diazotized sulfadimidine in alkaline medium, the azo-dye product quantitatively extracted into the Triton X-114 rich phase, dissolved in ethanol and determined spectrophotometrically at 490 nm. The suggested reaction was studied with and without extraction and simple comparison between the batch and CPE methods was achieved. Analytical variables including concentrations of reagent, Triton X-114 and base, incubated temperature, and time were carefully studied. Under the selected optimum conditions, the linearity ranges of calibration curves were 1-9 and 0.5-8 µg/mL with detection limits of 0.26 and 0.09 µg/mL of ISX for batch and CPE methods respectively. A relative standard deviation (RSD %) best than 1.98 and 2.67 % with the percentage recoveries range 100.14 and 99.63 % were obtained for both methods respectively. The proposed methods were successfully used in routine analysis of ISX in pharmaceutical forms with high accuracy and reproducibility.

How to Cite

1.
Hadi H, A. Al-Uzri W. Sensitive Cloud Point Extraction Method for the Determination of Isoxsuprine Hydrochloride in Pharmaceutical forms using Spectrophotometry. Iraqi Journal of Pharmaceutical Sciences [Internet]. 2022 Dec. 23 [cited 2024 Nov. 21];31(2):83-90. Available from: https://bijps.uobaghdad.edu.iq/index.php/bijps/article/view/1571

Publication Dates

References

“British Pharmacopoeia on CD-ROM”, Version 5, 3rd Ed., Vol. 1,Copyright by System Simulation Ltd, The Stationery Office Ltd., London, 2001.

D.S. Tatro, A–Z Drug Facts, Facts and Comparisons, St. Louis, 1999

T. Kalsang, B. Kanakapura, D.R. Hosakere, B.V. Kanakapura, Talanta., 2010; 81(4–5): 1216–23.

S. Shahrokhian, M. Hafezi-Kahnamouei, J. Electroanal. Chem., 2018;825: 30-39.

H. Ayman, L. Benedikt, J. Chromatogr. B: Biomed. Sci. Appl. 1991;563:216.

F. Belal, H.A. Al-malaq, A.A. Al-majed, E.A. Gadkariem, J. Liq. Chroma. Relat. Tech. 2000; 23:3175.

N. W. Beyene, J. F. V. Staden, R. I. Stefan and H. Y. Aboul-Enein, Farmaco ;60 : 613–619;

8-D. Suo, R. Wang, P. Wang, X. Fan, X. Su, J. Chromatogr. A, 2017;1526: 23-30.

C. Bozzolino, M. Leporati, F. Gani, C. Ferrero, M. Vincenti, J.pharm. and biomed. 2018; 150 15–24.

A. A. Gouda, A. M. Summan, A. H. Amin. RSC adv. 2016; 6: 94048-94057.

L.G. Hargis, Analytical Chemistry: Principles and Techniques, New Jersey: Prentice-Hall, 1998.

12-J. Inczedy, Analytical Application of Complex Equilibria, Budapest: AkademiaiKiado, 1976.

J.C. Miller, J.N. Miller, 1993. Statistics for Analytical Chemistry, Ellis Horwood, Chichester, UK.

Downloads

Published

2022-12-23