Green spectrophotometric and spectrofluorimetric determination of biperiden hydrochloride using erythrosine B sensing probe.
biperiden hydrochloride
colorimetry
erythrosin B sensor
fluorimetry
quenching
Journal
Luminescence : the journal of biological and chemical luminescence
ISSN: 1522-7243
Titre abrégé: Luminescence
Pays: England
ID NLM: 100889025
Informations de publication
Date de publication:
Apr 2024
Apr 2024
Historique:
revised:
15
02
2024
received:
10
01
2024
accepted:
27
02
2024
medline:
27
3
2024
pubmed:
27
3
2024
entrez:
27
3
2024
Statut:
ppublish
Résumé
Erythrosine B (EB) is a food colorant antiviral xanthene dye that has many applications as a color additive in pharmaceuticals and cosmetics. Its use as a sensor for spectrofluorimetric and spectrophotometric analysis of amine-based pharmaceuticals renders many advantages because of its availability, low cost, rapid labeling, and high sensitivity. Herein, two fast and sensitive spectrofluorimetric and spectrophotometric methods were established for the estimation of the anti-Parkinson drug, biperiden (BIP) hydrochloride (HCl), in its raw material and tablet forms. The proposed methods depended on the interaction between the phenolic group of EB and the tertiary amino group of the studied analyte to form an ion-pair complex at pH 4 using the Britton Robinson buffer. The spectrofluorimetric method is based on the measurement of the quenching power of BIP HCl on the fluorescence intensity of EB at λ
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e4725Informations de copyright
© 2024 John Wiley & Sons Ltd.
Références
L. M. De Lau, M. M. Breteler, Lancet Neurol. 2006, 5, 525.
K. Kawabata, M. Katsuno, Trihexyphenidyl, biperiden, and other anticholinergics in the treatment of Parkinson's disease, in NeuroPsychopharmacotherapy, Springer, Cham 2021. https://doi.org/10.1007/978-3-319-56015-1_221-1
The British Pharmacopoeia, The Stationary Office, London, Electronic version 2013.
S. C. Sweetman, Martindale: the complete drug reference, Pharmacutical Press, London 2005.
The United States Pharmacopoeia 30, the National Formulary 25, US Pharmacopeial Convention, Rockville, MD, Electronic version, 2007.
A. Mohammadi, A. Mehramizi, F. A. Moghaddam, H. Kashani, J. Chromatogr., B 2007, 854, 152.
H. M. Lotfy, E. M. Abdel‐Moety, E. G. Nouman, Y. Baghdady, M. Al‐Ghobashy, A. Abdel‐Aleem, S. Weshahy, Anal. Chem. Indian J. 2014, 14, 106.
V.r. Čápka, Y. Xu, J. Chromatogr., B 2001, 762, 181.
K. A. Hadidi, Legal Med. 2004, 6, 233.
R. Mandrioli, A. Musenga, S. S. Lasaponara, M. A. Saracino, S. Fanali, M. A. Raggi, Anal. Chim. Acta 2006, 560, 57.
E. Khaled, H. N. Hassan, M. A. Ahmed, R. O. El‐Attar, Electroanalysis 2017, 29, 975.
E. Khaled, I. A. El‐Sabbagh, N. El‐Kholy, E. A. Ghahni, Talanta 2011, 87, 40.
Z. Li, S. Sakamuru, R. Huang, M. Brecher, C. A. Koetzner, J. Zhang, H. Chen, C.‐F. Qin, Q.‐Y. Zhang, J. Zhou, L. D. Kramer, M. Xia, H. Li, Antiviral Res. 2018, 150, 217.
A. A. Hamad, R. Ali, H. R. H. Ali, D. M. Nagy, S. M. Derayea, RSC Adv. 2018, 8, 5373.
S. M. Derayea, A. A. Hamad, R. Ali, H. R. H. Ali, Microchem. J. 2019, 149, 104024.
F. Ibrahim, R. Aboshabana, H. Elmansi, R. Soc. Open Sci. 2022, 9, 220628.
E. Yosrey, H. Elmansi, Z. A. Sheribah, M. E. S. Metwally, Luminescence 2022, 37, 1785. https://doi.org/10.1002/bio.4358
M. Tolba, M. Salim, Spectrochim. Acta A Mol. Biomol. Spectrosc. 2021, 263, 120156.
M. E. El Sharkasy, M. M. Tolba, F. Belal, M. I. Walash, R. AboShabana, Luminescence 2023, 38, 2073.
A. Almahri, M. A. Abdel‐Lateef, E. Samir, S. M. Derayea, M. A. El Hamd, Luminescence 2021, 36, 651.
M. S. Binkadem, H. S. AlSalem, S. T. Al‐Goul, M. A. El Hamd, M. Oraby, F. M. Ali Zainy, M. A. Abdel‐Lateef, Luminescence 2023, 1836, 38.
K. Ramluckan, K. G. Moodley, F. Bux, Fuel 2014, 116, 103.
D. Snigur, M. Fizer, A. Chebotarev, O. Lukianova, O. Zhukovetska, Dyes Pigm. 2022, 198, 110028.
A. A. Hamad, R. Ali, S. M. Derayea, RSC Adv. 2022, 12, 7413.
ICH Harmonised Tripartite Guidelines, Validation of analytical procedures: text and methodology Q2 (R1). http://www.ich.org/products/guidelines/quality/article/quality-guidelines.html (Accessed August, 2023).
J. Miller, J. C. Miller, Statistics and chemometrics for analytical chemistry, Pearson Education, Harlow, England 2018.
N. A. Vodolazkaya, Y. A. Gurina, N. V. Salamanova, N. O. McHedlov‐Petrossyan, J. Mol. Liq. 2009, 145, 188.
J. Wang, Z. Liu, J. Liu, S. Liu, W. Shen, Spectrochim. Acta A Mol. Biomol. Spectrosc. 2008, 69, 956.
N. O. McHedlov‐Petrossyan, R. S. Mayorga, J. Chem. Soc., Faraday Trans. 1992, 88, 3025.
X. Tang, Z. Liu, S. Liu, X. Hu, Sci. China B Chem. 2007, 50, 54.
A. C. Moffat, M. D. Osselton, B. Widdop, J. Watts, Clarke's Analysis of Drugs and Poisons, Pharmaceutical Press, London, UK 2011.
C. Li, S. Liu, Z. Liu, X. Hu, J. Fluoresc. 2011, 21, 723.
M. A. Abdel‐Lateef, S. M. Derayea, D. A. M. N. El‐Deen, A. Almahri, M. Oraby, R. Soc. Open Sci. 2021, 8, 201545.
C. Würth, M. Grabolle, J. Pauli, M. Spieles, U. Resch‐Genger, Nat. Protoc. 2013, 8, 1535.
A. M. Zeid, A. A. El‐Masry, D. R. El‐Wasseef, M. Eid, I. A. Shehata, Sustain. Chem. Pharm. 2022, 29, 100795.
R. Aboshabana, A. M. Zeid, F. A. Ibrahim, Spectrochim. Acta A Mol. Biomol. Spectrosc. 2023, 295, 122626.
A. A. El‐Masry, A. M. Zeid, BMC Chem. 2023, 17, 93.
A. A. El‐Masry, A. M. Zeid, Microchem. J. 2024, 197, 109788.
J. Płotka‐Wasylka, Talanta 2018, 181, 204.
M. S. Imam, A. H. Abdelazim, S. Ramzy, A. S. Batubara, M. Gamal, S. Abdelhafiz, A. M. Zeid, BMC Chem. 2023, 17, 89.
F. Pena‐Pereira, W. Wojnowski, M. Tobiszewski, Anal. Chem. 2020, 92, 10076.