Green and sensitive detection of olopatadine in aqueous humor using a signal‐on fluorimetric approach: GREEnness assessment

Author:

Mostafa Islam M.1ORCID,Omar Mahmoud A.23ORCID,Noureldeen Deena A. M.1,Zeid Abdallah M.45ORCID,Halawa Mohamed Ibrahim467ORCID,Mohamed Abobakr A.8ORCID

Affiliation:

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

2. Department of Pharmacognosy and Pharmaceutical Chemistry, College of Pharmacy Taibah University Al‐Madinah Al‐Munawwarah Saudi Arabia

3. Pharmaceutical Analysis Department, Faculty of Pharmacy Minia University Minia Egypt

4. Department of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy Mansoura University Mansoura Egypt

5. Department of Chemistry University of Michigan Ann Arbor Michigan USA

6. Guangdong Laboratory of Artificial Intelligence & Digital Economy (SZ) Shenzhen University Shenzhen China

7. Department of Chemistry, College of Science United Arab Emirates University Al Ain United Arab Emirates

8. Pharmaceutical Analytical Chemistry Department, Faculty of Pharmacy Fayoum University Faiyum Egypt

Abstract

AbstractOlopatadine (OLP) is widely utilized as an effective antihistaminic drug for alleviating ocular itching associated with allergic conjunctivitis. With its frequent usage in pharmacies, there arises a pressing need for a cost‐effective, easily implementable, environmentally sustainable detection method with high sensitivity. This study presents a novel signal‐on fluorimetric method for detecting OLP in both its pure form and aqueous humor. The proposed approach depends on enhancing the weak intrinsic fluorescence emission of OLP, achieving a remarkable increase of up to 680% compared to its intrinsic fluorescence. This enhancement is achieved by forming micelles around protonated OLP using an acetate buffer (pH 3.6) and incorporating a solution of sodium dodecyl sulfate (SDS) surfactant. A strong correlation (R = 0.9996) is observed between the concentration of OLP and fluorescence intensities ranging from 1.0 to 100.0 ng mL−1 with a limit of detection of 0.22 ng mL−1. This described method is successfully employed for quantifying OLP in both its powder form and pharmaceutical eye drops. Furthermore, it demonstrates robust performance in determining OLP in artificial aqueous humor with a percentage recovery of 99.05 ± 1.51, with minimal interference from matrix interferents. Moreover, the greenness of the described method was evaluated.

Publisher

Wiley

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