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Molecularly imprinted polymer-modified carbon paste electrodes (MIP-CPE): A review on sensitive electrochemical sensors for pharmaceutical determinations
TrAC - Trends in Analytical Chemistry ; 160 (no pagination), 2023.
Article in English | EMBASE | ID: covidwho-2248145
ABSTRACT
Recent years have been associated with the development of various sensor-based technologies in response to the undeniable need for the rapid and precise analysis of an immense variety of pharmaceuticals. In this regard, special attention has been paid to the design and fabrication of sensing platforms based on electrochemical detection methods as they can offer many advantages, such as portability, ease of use, relatively cheap instruments, and fast response times. Carbon paste electrodes (CPEs) are among the most promising conductive electrodes due to their beneficial properties, including ease of electrode modification, facile surface renewability, low background currents, and the ability to modify with different analytes. However, their widespread use is affected by the lack of sufficient selectivity of CPEs. Molecularly imprinted polymers (MIPs) composed of tailor-made cavities for specific target molecules are appealing complementary additives that can overcome this limitation. Accordingly, adding MIP to the carbon paste matrix can contribute to the required selectivity of sensing platforms. This review aims to present a categorized report on the recent research and the outcomes in the combinatory fields of MIPs and CPEs for determining pharmaceuticals in complex and simple matrices. CPEs modified with MIPs of various pharmaceutical compounds, including analgesic drugs, antibiotics, antivirals, cardiovascular drugs, as well as therapeutic agents affecting the central nervous system (CNS), will be addressed in detail.Copyright © 2023 Elsevier B.V.
Keywords
Carbon paste electrodes, Drugs, Electrochemical sensors, Molecularly imprinted polymers, Pharmaceutical, bipolar disorder/dt [Drug Therapy], blood analysis, complex formation, coronavirus disease 2019/dt [Drug Therapy], cross linking, cyclic voltammetry, density functional theory, depression/dt [Drug Therapy], differential pulse voltammetry, drug determination, drug monitoring, electrochemical detection, heart arrhythmia/dt [Drug Therapy], heart failure/dt [Drug Therapy], human, hydrogen bond, hypertension/dt [Drug Therapy], insomnia/dt [Drug Therapy], limit of detection, molecular dynamics, pain/dt [Drug Therapy], polymerization, review, seizure/dt [Drug Therapy], surface area, urinalysis, virus infection/dt [Drug Therapy], water analysis, analgesic agent/dt [Drug Therapy], antibiotic agent, antivirus agent/do [Drug Dose], antivirus agent/dt [Drug Therapy], azithromycin, benzodiazepine derivative/dt [Drug Therapy], beta adrenergic receptor blocking agent, bisoprolol fumarate, captopril, cardiovascular agent/dt [Drug Therapy], central nervous system agents, daclatasvir, diclofenac, dipyridamole, epinephrine, gemifloxacin, ivabradine, lamotrigine/dt [Drug Therapy], melitracen, meropenem, midazolam, minoxidil/dt [Drug Therapy], molecularly imprinted polymer, mosapride, mycophenolate mofetil, nevirapine, paracetamol, phenobarbital/dt [Drug Therapy], quetiapine, secnidazole, stavudine, tetracycline, theophylline, valaciclovir, vancomycin, zileuton, carbon paste electrode, electrochemical sensor, savapran

Full text: Available Collection: Databases of international organizations Database: EMBASE Language: English Journal: TrAC - Trends in Analytical Chemistry Year: 2023 Document Type: Article

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Full text: Available Collection: Databases of international organizations Database: EMBASE Language: English Journal: TrAC - Trends in Analytical Chemistry Year: 2023 Document Type: Article