{"title":"基于MIP技术的电化学传感器对盐酸西那卡塞片剂剂型和血清样品的灵敏测定","authors":"Ipek Kucuk, Selenay Sadak, Selda Zengin Kurnalı, Sacide Altınöz, Bengi Uslu","doi":"10.1007/s00604-025-07152-7","DOIUrl":null,"url":null,"abstract":"<div><p>Cinacalcet hydrochloride (CIN) is a calcium-sensing receptor agonist used to treat hypercalcemia in the parathyroid. The molecularly imprinted polymer (MIP)–based sensor (CIN@MIP/GCE) was electropolymerized using cyclic voltammetry (CV) of the functional monomer o-phenylenediamine (o–PD) with a template molecule CIN on a glassy carbon electrode (GCE). The optimum performance of the MIP-based electrode for CIN detection was obtained with parameters of a 1:7 monomer ratio, a 15-min removal time, ethanol as a removal solution, and a 15-min rebinding time. The surface characterization of the CIN@MIP/GCE sensor was conducted using atomic force microscopy (AFM) and scanning electron microscopy (SEM), while CV and electrochemical impedance spectroscopy (EIS) were employed for electrochemical characterization with [Fe(CN)<sub>6</sub>]<sup>3−</sup>/<sup>4−</sup> redox probe. AFM findings show that the MIP sensor with CIN-specific voids on the surface has a root-mean-square (RMS) value of 27.95, while the non-imprinted polymer (NIP) sensor without voids has a smoother surface formation and an RMS value of 21.30 nm. The analytical efficacy of the constructed sensor was assessed using differential pulse voltammetry (DPV). The limit of detection (LOD) was 0.17 × 10<sup>−12</sup>, with a linear range of 1.0 × 10<sup>−12</sup>–1.0 × 10<sup>−11</sup> M. The reliability of the constructed sensor was determined using CIN detection in real samples as tablet dosage form and human serum, yielding recovery results of 100.19% and 101.82%, respectively. The selectivity investigation was performed against prevalent interference substances. The relative imprinting factor (IF) values of CIN impurities confirmed the selectivity of the CIN sensor.</p><h3>Graphical Abstract</h3>\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":705,"journal":{"name":"Microchimica Acta","volume":"192 5","pages":""},"PeriodicalIF":5.3000,"publicationDate":"2025-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s00604-025-07152-7.pdf","citationCount":"0","resultStr":"{\"title\":\"A novel electrochemical sensor based on MIP technology for sensitive determination of cinacalcet hydrochloride in tablet dosage form and serum samples\",\"authors\":\"Ipek Kucuk, Selenay Sadak, Selda Zengin Kurnalı, Sacide Altınöz, Bengi Uslu\",\"doi\":\"10.1007/s00604-025-07152-7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Cinacalcet hydrochloride (CIN) is a calcium-sensing receptor agonist used to treat hypercalcemia in the parathyroid. The molecularly imprinted polymer (MIP)–based sensor (CIN@MIP/GCE) was electropolymerized using cyclic voltammetry (CV) of the functional monomer o-phenylenediamine (o–PD) with a template molecule CIN on a glassy carbon electrode (GCE). The optimum performance of the MIP-based electrode for CIN detection was obtained with parameters of a 1:7 monomer ratio, a 15-min removal time, ethanol as a removal solution, and a 15-min rebinding time. The surface characterization of the CIN@MIP/GCE sensor was conducted using atomic force microscopy (AFM) and scanning electron microscopy (SEM), while CV and electrochemical impedance spectroscopy (EIS) were employed for electrochemical characterization with [Fe(CN)<sub>6</sub>]<sup>3−</sup>/<sup>4−</sup> redox probe. AFM findings show that the MIP sensor with CIN-specific voids on the surface has a root-mean-square (RMS) value of 27.95, while the non-imprinted polymer (NIP) sensor without voids has a smoother surface formation and an RMS value of 21.30 nm. The analytical efficacy of the constructed sensor was assessed using differential pulse voltammetry (DPV). The limit of detection (LOD) was 0.17 × 10<sup>−12</sup>, with a linear range of 1.0 × 10<sup>−12</sup>–1.0 × 10<sup>−11</sup> M. The reliability of the constructed sensor was determined using CIN detection in real samples as tablet dosage form and human serum, yielding recovery results of 100.19% and 101.82%, respectively. The selectivity investigation was performed against prevalent interference substances. The relative imprinting factor (IF) values of CIN impurities confirmed the selectivity of the CIN sensor.</p><h3>Graphical Abstract</h3>\\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>\",\"PeriodicalId\":705,\"journal\":{\"name\":\"Microchimica Acta\",\"volume\":\"192 5\",\"pages\":\"\"},\"PeriodicalIF\":5.3000,\"publicationDate\":\"2025-04-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://link.springer.com/content/pdf/10.1007/s00604-025-07152-7.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Microchimica Acta\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s00604-025-07152-7\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microchimica Acta","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s00604-025-07152-7","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
A novel electrochemical sensor based on MIP technology for sensitive determination of cinacalcet hydrochloride in tablet dosage form and serum samples
Cinacalcet hydrochloride (CIN) is a calcium-sensing receptor agonist used to treat hypercalcemia in the parathyroid. The molecularly imprinted polymer (MIP)–based sensor (CIN@MIP/GCE) was electropolymerized using cyclic voltammetry (CV) of the functional monomer o-phenylenediamine (o–PD) with a template molecule CIN on a glassy carbon electrode (GCE). The optimum performance of the MIP-based electrode for CIN detection was obtained with parameters of a 1:7 monomer ratio, a 15-min removal time, ethanol as a removal solution, and a 15-min rebinding time. The surface characterization of the CIN@MIP/GCE sensor was conducted using atomic force microscopy (AFM) and scanning electron microscopy (SEM), while CV and electrochemical impedance spectroscopy (EIS) were employed for electrochemical characterization with [Fe(CN)6]3−/4− redox probe. AFM findings show that the MIP sensor with CIN-specific voids on the surface has a root-mean-square (RMS) value of 27.95, while the non-imprinted polymer (NIP) sensor without voids has a smoother surface formation and an RMS value of 21.30 nm. The analytical efficacy of the constructed sensor was assessed using differential pulse voltammetry (DPV). The limit of detection (LOD) was 0.17 × 10−12, with a linear range of 1.0 × 10−12–1.0 × 10−11 M. The reliability of the constructed sensor was determined using CIN detection in real samples as tablet dosage form and human serum, yielding recovery results of 100.19% and 101.82%, respectively. The selectivity investigation was performed against prevalent interference substances. The relative imprinting factor (IF) values of CIN impurities confirmed the selectivity of the CIN sensor.
期刊介绍:
As a peer-reviewed journal for analytical sciences and technologies on the micro- and nanoscale, Microchimica Acta has established itself as a premier forum for truly novel approaches in chemical and biochemical analysis. Coverage includes methods and devices that provide expedient solutions to the most contemporary demands in this area. Examples are point-of-care technologies, wearable (bio)sensors, in-vivo-monitoring, micro/nanomotors and materials based on synthetic biology as well as biomedical imaging and targeting.