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   N-Octyl-Modified Magnetite Nps For Optimization of Solid Phase Extraction For Trace Analysis of Phenytoin in Real Samples  
   
نویسنده Raeisi Shaghayegh ,Qomi Mahnaz ,Dadras Orkideh ,Mousavi Zahra
منبع Nanomedicine Research Journal - 2019 - دوره : 4 - شماره : 1 - صفحه:40 -47
چکیده    Objective: phenytoin is an anti-seizure medication used to treat epilepsy, as well as to control arrhythmias and treat migraine headaches and nerve pain. it is recommended to determine the amount of this drug in the blood to control the seizure and prevent its toxicity. in the present study, a simplified and practical procedure based on the dispersive solid phase extraction was implemented and validated to determine phenytoin in plasma samples. hydrophobic n-octylmodified magnetic iron oxide nps (ionps) were employed as the sorbent. methods: the studied drug was detected using high-performance liquid chromatography with a diode array detector. the parameters affecting the extraction efficiency such as ph of the sample, amount of sorbent, time, salt, type and volume of the desorption eluent and desorption time were optimized. after the extraction procedure, magnetic nanoparticless (nps) were easily separated from the aqueous solution by applying an external magnetic field without the need to filtration or centrifugation. results: the separation and preconcentration procedures were fast and completed in less than 6 min. under the condition that was optimized, this method achieved a low limits of detection (3.0 ng ml-1), wide linear dynamic ranges (10 to 1000 ng ml-1), high enrichment factors (226), good correlation coefficients (r = 0.996), and good repeatability (6.7 to 7.3%). conclusion: this method was used to analyze plasma samples with good efficiency (≥ 90). based on the results, the proposed method may be more efficient for the analysis of phenytoin in plasma samples from epileptic patients for the aim of therapeutic drug monitoring.
کلیدواژه Dispersive ,Magnetic Nps ,Phenytoin ,Plasma ,Solid Microextraction
آدرس Islamic Azad University, Tehran Medical Sciences, Faculty Of Pharmaceutical Chemistry, Department Of Medicinal Chemistry, ایران, Islamic Azad University, Tehran Medical Sciences, Active Pharmaceutical Ingredients Research Center, ایران, Islamic Azad University, Tehran Medical Sciences, Faculty Of Pharmacy, Department Of Medicinal Chemistry, ایران, Islamic Azad University, Tehran Medical Sciences, Faculty Of Pharmacy, Department Of Pharmacology And Toxicology, ایران
پست الکترونیکی mosavi50@yahoo.com
 
     
   
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