Evidence map›Paper›PMID 42215797›Full record

ArticleMikrochimica acta2026

AuNi alloy deposited heteroatom-doped porous carbon for the simultaneous detection of biogenic amines.

Tahera Lasker, Kyubin Shim, Md Mobarok Karim, Khatun A Jannath, Deog-Su Park

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Article in Mikrochimica acta, 2026. 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

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5 authors.

Tahera Lasker *Department of Chemistry, Pusan National University, Busan, 46241, Republic of Korea.ORCID 0000-0003-0830-4319
Kyubin Shim *Gyeongnam Aerospace and Defense Institute of Science and Technology (GADIST), Gyeongsang National University, Jinju, Gyeongnam, 52828, Republic of Korea.ORCID 0000-0003-4153-9611
Md Mobarok KarimDepartment of Chemical Materials, Pusan National University, Busan, 46241, Republic of Korea.ORCID 0000-0002-1001-0136
Khatun A JannathDepartment of Chemistry, Pusan National University, Busan, 46241, Republic of Korea.ORCID 0000-0003-2988-3081
Deog-Su ParkDepartment of Chemistry, Pusan National University, Busan, 46241, Republic of Korea. dsupark@pusan.ac.kr.ORCID 0000-0001-8177-5200

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Simultaneous determination of dopamine, serotonin, and melatonin was demonstrated using a disposable non-enzymatic electrochemical biosensor modified with AuNi alloy-deposited S, N-doped porous carbon. Initially, ZnO/S rich a S, N-doped carbon precursor was synthesized from Zn-rubeanic acid coordination polymer, followed by the acid treatment and pyrolysis under nitrogen to obtain S, N-doped porous carbon (SNPC). Then, a composite layer of benzoic acid functionalized polyterthiophene (pTBA) and SNPC was electrochemically formed (SNPC-pTBA) on the screen-printed electrode with additional subsequent casting of SNPC on the layer, followed by the deposition of AuNi nanoparticles (SNPC-pTBA/SNPC@AuNi) to further enhance the catalytic performance. To optimize the AuNi deposition conditions, the mole ratio, alloy deposition potential and time, SNPC content, and electrolyte pH were changed. Each sensing layer of the final sensor was characterized by electrochemical and surface analysis methods. Under the optimized condition, the proposed sensor exhibited well-defined oxidation peaks at 0.023 V, 0.182 V, and 0.40 V for dopamine, serotonin, and melatonin, respectively. The linear dynamic range was observed over the range 0.25 µM-500.0 µM, with detection limits of 65.8 ± 2.0 nM, 76.1 ± 1.3 nM, and 71.3 ± 2.7 nM for dopamine, serotonin, and melatonin, respectively. The sensor performance was almost unchanged in the presence of other interfering amines and non-amine molecules. The sensing platform reveals stability until 49 days with the relative standard deviation (RSD) of < 7.8%, and the sensor reliability was evaluated by detecting targeted biogenic amines in the real serum samples and the supplement tablet.

Indexed as

AlloysBiogenic AminesCarbonGoldMetal NanoparticlesBiosensing TechniquesDopamineElectrochemical TechniquesElectrodesHumansLimit of DetectionPorositySerotoninAlloysBiogenic AminesCarbonDopamineGoldSerotoninDopamineElectrochemical sensorGold alloysMelatoninScreen-printed electrodeSerotoninS, N-doped porous carbon (SNPC)Square-wave voltammetry

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.