نمایش پرونده ساده آیتم

dc.contributor.authorAbbaspour, M
dc.contributor.authorFarajzadeh, MA
dc.contributor.authorKhoubnasabjafari, M
dc.contributor.authorHaririan, S
dc.contributor.authorJouyban, A
dc.date.accessioned2018-08-26T08:56:01Z
dc.date.available2018-08-26T08:56:01Z
dc.date.issued2018
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/54385
dc.description.abstractRapid, highly efficient, and reliable liquid-liquid microextraction (LLME) methods followed by gas chromatography-flame ionization detection were developed for the extraction, preconcentration, and determination of valproate in human plasma and urine samples. Proteins of plasma sample are precipitated by adding methanol and urine sample was diluted prior to performing the microextraction procedures. Fine organic solvent droplets were formed by repeated suction and injection of the mixture of sample solution and extraction solvent into a test tube with a glass syringe. After extraction, phase separation was performed by centrifuging and the enriched analytes in the sedimented organic phase were determined by the separation system. The main factors influencing the extraction efficiency including extraction solvent type and volume, salt addition, pH, and extraction times are investigated. Under the optimized conditions, the proposed method showed good precision (relative standard deviation less than 8%). Limits of detection and lower limits of quantification for valproate were obtained in the ranges of 0.05-0.22 and 0.1-0.5آµg mL?1, respectively. The linear ranges were 0.5-500 and 0.1-200 آµg mL?1in plasma and urine, respectively (r2 ? 0.9995). The relative recoveries varied from 98-102 % and 93-100 %, respectively for plasma and urine samples. The mean relative standard deviations for intra-assay and inter-assay precisions were 3.4 % and 6.0 %, respectively. Preconcentration factors were in the range of 7-44. Good recoveries (55-86%) were obtained for the spiked samples. The proposed method was successfully used to analyze plasma and urine samples of epileptic receiving sodium valproate. آ© 2018 by Kermanshah University of Medical Sciences.
dc.language.isoEnglish
dc.relation.ispartofJournal of Reports in Pharmaceutical Sciences
dc.subjectacetylsalicylic acid
dc.subjectatorvastatin
dc.subjectbusentan
dc.subjectcalcium
dc.subjectchlordiazepoxide
dc.subjectcitalopram
dc.subjectcitrizine
dc.subjectclonazepam
dc.subjectdesmopressin
dc.subjectdiclofenac
dc.subjectdigoxin
dc.subjectergotamine
dc.subjectferrous sulfate
dc.subjectfluoxetine
dc.subjectfolic acid
dc.subjectfurosemide
dc.subjectimipramine
dc.subjectlamotrigine
dc.subjectmethanol
dc.subjectnortriptyline
dc.subjectomeprazole
dc.subjectphenobarbital
dc.subjectpropranolol
dc.subjectsildenafil
dc.subjectspironolactone
dc.subjecttrifluoperazine
dc.subjectunclassified drug
dc.subjectvalproic acid
dc.subjectvitamin D
dc.subjectwarfarin
dc.subjectaccuracy
dc.subjectanalytical parameters
dc.subjectArticle
dc.subjectblood transfusion
dc.subjectcalculation
dc.subjectcalibration
dc.subjectcapillary electrophoresis
dc.subjectcentrifugation
dc.subjectclinical evaluation
dc.subjectcomparative study
dc.subjectdrug blood level
dc.subjectdrug isolation
dc.subjectdrug selectivity
dc.subjectdrug specificity
dc.subjectdrug stability
dc.subjectdrug urine level
dc.subjectflame ionization detection
dc.subjectflow rate
dc.subjectgas chromatography
dc.subjecthuman
dc.subjectlimit of detection
dc.subjectlimit of quantitation
dc.subjectliquid chromatography
dc.subjectliquid phase microextraction
dc.subjectlower limit of quantification
dc.subjectmeasurement precision
dc.subjectmedical research
dc.subjectpH
dc.subjectphase separation
dc.subjectrepeatability
dc.subjectrobustness
dc.subjectseizure
dc.subjecttandem mass spectrometry
dc.subjecttemperature
dc.subjectultraviolet radiation
dc.subjectupper limit of quantification
dc.subjectvalidation process
dc.subjectvolatility
dc.titleGas chromatographic analysis of sodium valproate in plasma and urine after air assisted liquid-liquid microextraction
dc.typeArticle
dc.citation.volume7
dc.citation.issue1
dc.citation.spage27
dc.citation.epage43
dc.citation.indexScopus


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