Simplified uv spectrophotometric analysis of abiraterone acetate in bulk and formulations

Authors

  • Ramakrishna .M Department of Pharmaceutical Analysis, Narasaraopeta Institute of Pharmaceutical Sciences, Kotappakonda road, Yallamanda, Narasaraopeta, Palnadu, Andhra Pradesh, India
  • J.N.Suresh Kumar Department of Pharmaceutical Analysis, Narasaraopeta Institute of Pharmaceutical Sciences, Kotappakonda road, Yallamanda, Narasaraopeta, Palnadu, Andhra Pradesh, India
  • Lakshmi Roshini.J Department of Pharmaceutical Analysis, Narasaraopeta Institute of Pharmaceutical Sciences, Kotappakonda road, Yallamanda, Narasaraopeta, Palnadu, Andhra Pradesh, India
  • Sai Tejaswini.T Department of Pharmaceutical Analysis, Narasaraopeta Institute of Pharmaceutical Sciences, Kotappakonda road, Yallamanda, Narasaraopeta, Palnadu, Andhra Pradesh, India
  • Jagadeesh.N Department of Pharmaceutical Analysis, Narasaraopeta Institute of Pharmaceutical Sciences, Kotappakonda road, Yallamanda, Narasaraopeta, Palnadu, Andhra Pradesh, India
  • Jessie Snehita.K Department of Pharmaceutical Analysis, Narasaraopeta Institute of Pharmaceutical Sciences, Kotappakonda road, Yallamanda, Narasaraopeta, Palnadu, Andhra Pradesh, India
  • Siva Reddy.A Department of Pharmaceutical Analysis, Narasaraopeta Institute of Pharmaceutical Sciences, Kotappakonda road, Yallamanda, Narasaraopeta, Palnadu, Andhra Pradesh, India

DOI:

https://doi.org/10.47957/ijpda.v12i1.582

Keywords:

Abiraterone acetate, UV spectrophotometric method, solubility, ?max, linearity, LOD, LOQ, RSD

Abstract

Abiraterone acetate is an orally administered selective androgen biosynthesis inhibitor It is an irreversible inhibitor of cytochrome CYP17AThis enzyme is expressed in testicular, adrenal, and prostatic tumour tissues and is required for androgen biosynthesis.Abiraterone is used in combination with prednisone to treat a certain type of prostate cancer that has spread to other parts of the body.A Novel, simple, accurate, precise and reproducible UV spectrophotometric method has been developed and validated for estimation of Abiraterone acetate bulk and its formulations. After determining the solubility we had selected methanol as a solvent and Abiraterone acetate has absorbance at the wavelength of maximum ?max254nm. The drug was characterized by the melting point test. Proposed method was precise with RSD less than 2%. linearity test was approved within the range of 10-60µg/ml for with the correlation coefficient (R2) of 0.9991. Accuracy was 100.03%. LOD and LOQ were 0.006µg/ml and 0.018µg/ml respectively. The spike recovery of Abiraterone acetate in tablet was 99.88%.

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References

Beg S, Malik AK, Afzal O, Alta Mimi AS, Kazmi I, Al-Abbasi FA, Almalki WH, Barkat MA, Kawish SM, Pradhan DP, Rahman M. Systematic development and validation of a RP-HPLC method for estimation of abiraterone acetate and its degradation products. Journal of Chromatographic Science. 2021 Jan; 59(1):79-87.

Kavitapu D, Maruthapillai A, Mahapatra S, Selvi JA. New stability indicating RP-HPLC method for the determination of Abiraterone acetate, its related substances and degradation products in bulk and dosage form. Materials Today: Proceedings. 2021 Jan 1; 34:469-78.

Solymosi T, Tóth F, Orosz J, Basa-Dénes O, Angi R, Jordán T, O?tvo?s Z, Glavinas H. Solubility measurements at 296 and 310 K and physicochemical characterization of abiraterone and abiraterone acetate. Journal of Chemical & Engineering Data. 2018 Nov 12; 63(12):4453-8.

Goud VM, Rani BS, Sharma JV, Sirisha P. Development and Validation for estimation of Abiraterone acetate in Bulk and Pharmaceutical Dosage Form by UPLC. Research Journal of Pharmacy and Technology. 2019; 12(6):3029-32.

Kumar SV, Rudresha G, Gurav S, Zainuddin M, Dewang P, Kethiri RR, Rajagopal S, Mullangi R. Validated RP?HPLC/UV method for the quantitation of abiraterone in rat plasma and its application to a pharmacokinetic study in rats. Biomedical Chromatography. 2013 Feb; 27(2):203-7.

Gong a, Zhu X. ?-cyclodextrin sensitized spectrofluorimetry for the determination of abiraterone acetate and abiraterone. Journal of fluorescence. 2013 Nov; 23(6):1279-86.

Khedr A, Darwish I, Bamane F. Analysis of abiraterone stress degradation behaviour using liquid chromatography coupled to ultraviolet detection and electrospray ionization mass spectrometry. Journal of pharmaceutical and biomedical analysis. 2013 Feb 23; 74:77-82.

Chandra Reddy BJ, Sarada NC. Development and validation of a novel RP-HPLC method for stability-indicating assay of Abiraterone acetate. Journal of Liquid Chromatography & Related Technologies. 2016 Apr 20; 39(7):354-63.

Pharmaceutical analysis volume-II- Dr.A.Kasture UV Visible spectroscopy 2007; 169-181.

Instrumental method of drug analysis- applications of UV spectroscopy G.Vidya sagar; 2009: 176-8.

Pharmaceutical titrimetric analysis- A.A.Napolean introduction to pharmaceutical analysis; 2006:1.1-3.

Instrumental method of chemical analysis- G.R.Chatwal introduction to UV spectroscopy: 2.149-2.184.

Instrumental method of analysis-7th edition- Willard meritt dean settle

Published

2024-04-14
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How to Cite

M, R., S. K. J.N, L. R. J, S. T. T, J. N, J. S. K, and S. R. A. “Simplified Uv Spectrophotometric Analysis of Abiraterone Acetate in Bulk and Formulations”. International Journal of Pharmaceutics and Drug Analysis, vol. 12, no. 1, Apr. 2024, pp. 37-42, doi:10.47957/ijpda.v12i1.582.

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