Exploitation of erythrosine B as a fluorometric marker for lurasidone determination through electrostatic attraction; application to content uniformity test.


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:
Jul 2024
Historique:
revised: 05 07 2024
received: 06 04 2024
accepted: 15 07 2024
medline: 26 7 2024
pubmed: 26 7 2024
entrez: 26 7 2024
Statut: ppublish

Résumé

A recently developed antipsychotic drug, lurasidone, was determined using a simple, sensitive, and eco-friendly spectrofluorimetric approach. The suggested approach was based on the quantifiable quenching impact of lurasidone on the inherent fluorescence of erythrosine B in an acidic environment employing a Teorell-Stenhagen buffer (pH 4). Following excitation at 530 nm, the quenching of erythrosine B fluorescence was monitored at 552 nm. The system variables were systematically optimized to enhance the formation of the lurasidone-erythrosine B ion pair for analytical purposes. A linear calibration graph was built in the range of 20-600 ng mL

Identifiants

pubmed: 39054772
doi: 10.1002/bio.4845
doi:

Substances chimiques

Lurasidone Hydrochloride O0P4I5851I
Erythrosine PN2ZH5LOQY
Tablets 0
Antipsychotic Agents 0
Fluorescent Dyes 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e4845

Informations de copyright

© 2024 John Wiley & Sons Ltd.

Références

K. V. Sri, S. Sravani, M. S. Kumar, J. Pharm. Res. 2015, 5, 102.
Z. G. Khan, B. S. Vaidehi, G. N. Sarang, G. B. Shivam, P. B. Patil, J. PharmaSciTech 2017, 7, 2.
M. Y. Katteboina, N. R. Pilli, R. Mullangi, R. R. Seelam, S. R. Satla, Biomed. Chromatogr. 2016, 30, 1065.
N. K. Joshi, N. Shah, M. Dumasiya, A. Patel, Pharma Sci. Monit. 2012, 3, 2643.
S. M. Derayea, H. A. Elhamdy, K. M. B. El‐Din, M. Oraby, J. Mol. Liq. 2023, 391, 123264.
P. S. Monitor, J. Pharm. Sci. 2016, 2, 131.
M. D. Vaja, R. R. Patel, B. D. Patel, A. B. Chaudhary, Res. J. Pharm. Technol. 2022, 15, 4999.
T. Koo, S. Kim, J. Lee, D. Ha, M. Baek, H. Moon, Biomed. Chromatogr. 2011, 25, 1389.
K. Damodar, S. Bhogineni, B. Ramanjaneyulu, Drug Inven. Today 2011, 3, 305.
C. Liu, Q. Li, J. Fan, X. Bai, M. Wang, Y. Rong, China Pharm. 2014, 12, 1483.
S. A. Karaca, D. Y. UĞUR, Marmara Pharm. J. 2017, 21, 931.
K. V. Sri, M. S. Kumar, A. Sravani, Indian Drugs 2019, 56, 77.
S. S. Prasad, V. R. Anna, B. B. Kasimala, J. Crit. Rev. 2020, 7, 2155.
H. Jebaliya, A. Shah, S. C. Karad, S. Nakum, B. Dabhi, Results Chem. 2022, 4, 100427.
F. Logarinho, T. Rosado, C. Lourenço, M. Barroso, A. Araujo, E. Gallardo, J. Chromatogr., B 2016, 1038, 127.
S. Y. Al‐Nami, A. Q. Alorabi, Z. A. Al‐Ahmed, A. T. Mogharbel, H. M. Abumelha, M. A. Hussein, N. M. El‐Metwaly, ACS Omega 2023, 8, 10449.
A. S. Zaafan, S. M. Derayea, D. M. Nagy, M. Oraby, Acta Part a Mol. Biomol. Spectrosc. 2024, 319, 124519.
S. M. Derayea, M. Oraby, A. S. Zaafan, A. A. Hamad, D. M. Nagy, RSC Adv. 2024, 14, 8283.
I. C. H. H. T. Guideline, Q2, 2005, 1, 5.
S. M. Derayea, A. A. Hamad, R. Ali, H. R. H. Ali, Microchem. J. 2019, 149, 104024.
H. S. AlSalem, S. N. Alharbi, M. S. Binkadem, S. A. Mahmoud, M. A. Abdel‐Lateef, Luminescence 2024, 39, e4748.
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, 38, 1836.
M. A. Abdel‐Lateef, S. M. Derayea, D. A. El‐Deen, A. Almahri, M. Oraby, R. Soc. Open Sci. 2021, 8, 201545.
M. Rockville, United States Pharmacopeia and National Formulary (USP 30‐NF 25), The United States Pharmacopeial Convention, Rockville, MD 2007.
M. A. Abdel‐Lateef, R. J. Darling, I. A. Darwish, Luminescence 2024, 39, e4777.
S. M. Derayea, H. A. Elhamdy, M. Oraby, K. M. B. El‐Din, BMC Chem. 2024, 18, 92.
K. Van Aken, L. Strekowski, L. Patiny, Beilstein J. Org. Chem. 2006, 2, 3.
S. M. Derayea, A. S. Zaafan, D. A. Nagi, M. Oraby, Acta Part A Mol. Biomol. Spectrosc. 2023, 301, 122948.
J. Płotka‐Wasylka, Talanta 2018, 181, 204.
S. M. Derayea, H. A. Elhamdy, K. M. B. El‐Din, M. Oraby, RSC Adv. 2024, 14, 4065.
F. Pena‐Pereira, W. Wojnowski, M. Tobiszewski, Anal. Chem. 2020, 92, 10076.

Auteurs

Hadeer A Elhamdy (HA)

Department of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, Sohag University, Sohag, Egypt.

Mohamed Oraby (M)

Department of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, Sohag University, Sohag, Egypt.

Sayed M Derayea (SM)

Department of Analytical Chemistry, Faculty of Pharmacy, Minia University, Minia, Egypt.

Khalid M Badr El-Din (KM)

Department of Analytical Chemistry, Faculty of Pharmacy, Minia University, Minia, Egypt.

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Classifications MeSH