Evidence map›Paper›PMID 40413264›Full record

ArticleScientific reports2025

Graphene oxide doped polyacrylonitrile-co-maleic acid nanofibers for high-performance liquid chromatography determination of amoxicillin and Oxytetracycline in milk.

Shaymaa A Mohamed, Waleed Alahmad, Ibrahim A Darwish, Mohamed Aly Saad Aly, Puttaruksa Varanusupakul

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Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Shaymaa A MohamedDepartment of Chemistry, Faculty of Science, Chulalongkorn University, Bangkok, 10330, Thailand.
Waleed AlahmadDepartment of Chemistry, Faculty of Science, Chulalongkorn University, Bangkok, 10330, Thailand.
Ibrahim A DarwishDepartment of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, P.O. Box 2457, Riyadh, 11451, Saudi Arabia.
Mohamed Aly Saad AlySchool of Electrical and Computer Engineering, Georgia Institute of Technology, Atlanta, GA, 30332, USA.
Puttaruksa VaranusupakulDepartment of Chemistry, Faculty of Science, Chulalongkorn University, Bangkok, 10330, Thailand. puttaruksa.w@chula.ac.th.

Funding

King Saud University, Riyadh, Saudi Arabia RSPD2025R944the Second Century Fund, Chulalongkorn University C2F
6 · The paper itself

Abstract

Detecting and quantifying trace amounts of antibiotics like amoxicillin and oxytetracycline in milk and environmental water samples is crucial for public health and environmental monitoring. This research focuses on developing a novel sorbent for solid-phase extraction (SPE) of amoxicillin and oxytetracycline from milk and environmental water samples, using electrospun graphene oxide-doped poly(acrylonitrile-co-maleic acid) nanocomposite fibers, followed by high-performance liquid chromatography with diode array detection (HPLC-DAD). The fibers were successfully fabricated and characterized using a suite of techniques: SEM-EDX, FTIR, XRD, BET, XPS, TGA, and Raman spectroscopy. The extraction process was optimized by carefully adjusting parameters like desorption solvent (0.60 mL of 0.2 M HCl in methanol), extraction time (60 min), and sample pH (3) to achieve efficient and reliable extraction. Under optimal conditions, the developed method demonstrated good linearity (5-100 µg/L, R² > 0.9925), low detection and quantification limits (1.50 µg/L and 5.0 µg/L for amoxicillin and 1.46 µg/L and 4.8 µg/L for oxytetracycline) and high enrichment factor (21 for amoxicillin and 47 for oxytetracycline). The achievable accuracy and precision of the developed sorbent were satisfying, for incidence, relative recovery range of 90.3-106.3% and 87.6-95.9% with RSD range of 1.9-4.3% and 1.1-4.7% for amoxicillin and oxytetracycline, respectively. The method demonstrates reliable and efficient extraction and quantification of antibiotics from two different classes at maximum residue levels, making it suitable for monitoring antibiotic contamination in food and environmental samples, ultimately promoting better public health outcomes.

Indexed as

Acrylic ResinsAmoxicillinGraphiteMaleatesMilkNanofibersOxytetracyclineAnimalsAnti-Bacterial AgentsChromatography, High Pressure LiquidLimit of DetectionSolid Phase ExtractionAcrylic ResinsAmoxicillinAnti-Bacterial Agentsgraphene oxideGraphiteMaleatesmaleic acidOxytetracyclinepolyacrylonitrileAmoxicillinAntibioticsElectrospun fibersGraphene oxideOxytetracyclinePolyacrylonitrile-co-maleic acidSolid phase extraction

Identifiers

PMID40413264
PMCPMC12103578

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