Utilizing Nanoparticle Catalyzed TMB/H2O2 System for Determination of Aspirin in Exhaled Breath Condensate

Author:

Mohammadzadeh Abachi Samineh12,Rezaei Homa13,Khoubnasabjafari Maryam45,Jouyban-Gharamaleki Vahid6,Rahimpour Elaheh17ORCID,Jouyban Abolghasem18

Affiliation:

1. Pharmaceutical Analysis Research Center and Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran.

2. Student Research Committee, Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran

3. Drug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran

4. Tuberculosis and Lung Diseases Research Center, Tabriz University of Medical Sciences, Tabriz, Iran

5. Department of Anesthesiology and Intensive Care, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran

6. Kimia Idea Pardaz Azarbayjan (KIPA) Science Based Company, Tabriz University of Medical Sciences, Tabriz 51664, Iran

7. Infectious and Tropical Diseases Research Center, Tabriz University of Medical Sciences, Tabriz

8. Faculty of Pharmacy, Near East University, PO BOX: 99138 Nicosia, North Cyprus, Mersin 10, Turkey

Abstract

Background: According to the poison center data for most countries, more than thousands of people’s exposure to aspirin or salicylate-containing products. So, this work aimed was to offer a rapid colorimetric method for monitoring aspirin concentration in exhaled breath condensate (EBC). Methods: A method based on a redox reaction catalyzed by nanoparticles was validated for the analysis of aspirin. 3,3 ,5,5 –Tetramethyl benzidine /H2O2 and sodium dodecyl sulfate modified silver nanoparticles were used as the redox reagents and catalyst, respectively. Results: Detection mechanism of aspirin using this system is based on the inhibitory effect of aspirin on the signal intensity of the colorimetric systems. Since the decrement in signal intensity was proportional to aspirin level, a colorimetric method was proposed for its quantification in EBC samples. This method shows a linear relationship with aspirin concentration in the range of 10‒250 mg.L−1 with a relative standard deviation of < 3.5%. Conclusion: This method has great potential for aspirin determination due to some features such as high reliability, and fast response time.

Publisher

Maad Rayan Publishing Company

Subject

General Pharmacology, Toxicology and Pharmaceutics,Pharmaceutical Science

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