{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,13]],"date-time":"2026-02-13T06:06:56Z","timestamp":1770962816229,"version":"3.50.1"},"reference-count":52,"publisher":"Wiley","issue":"7","license":[{"start":{"date-parts":[[2010,5,20]],"date-time":"2010-05-20T00:00:00Z","timestamp":1274313600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Drug Testing and Analysis"],"published-print":{"date-parts":[[2010,7]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Dispersive liquid\u2010liquid microextraction (DLLME), coupled with gas chromatography\u2010flame ionization detection (GC\u2010FID), has been successfully used for the extraction and determination of valproic acid (VPA) in pharmaceutical preparations. In the developed method, an appropriate mixture of extracting and disperser solvents was rapidly injected into an aqueous sample. Having formed a cloudy solution, the mixture was centrifuged and then the extracting solvent was sedimented at the bottom of a conical test tube. The extract was then injected into a GC system directly, without any further pretreatment. Initially, microextraction efficiency factors were optimized and the optimum experimental conditions found were as follows: tetrachloroethylene (9.0 \u00b5L) as extracting solvent; acetone (1.0 mL) as disperser solvent; 5 mL acidic aqueous sample (pH 1) without salt addition. Under the selected conditions, the calibration curve showed linearity in the range of 0.1\u20135.0 mg\/L with regression coefficient corresponding to 0.9998. The limit of detection was found to be 0.05 mg\/L. Finally, the method was applied for the determination of VPA in two different pharmaceutical preparations. A reasonable intra\u2010assay (3.9\u201310.8%, <jats:italic>n<\/jats:italic> = 3) and inter\u2010assay (5.6\u201311.4%, <jats:italic>n<\/jats:italic> = 3) precision illustrated the good performance of the analytical procedure. The protocol proved to be rapid and cost\u2010effective for screening purposes. Copyright \u00a9 2010 John Wiley &amp; Sons, Ltd.<\/jats:p>","DOI":"10.1002\/dta.131","type":"journal-article","created":{"date-parts":[[2010,5,22]],"date-time":"2010-05-22T20:16:43Z","timestamp":1274559403000},"page":"362-366","source":"Crossref","is-referenced-by-count":15,"title":["Quantitation of valproic acid in pharmaceutical preparations using dispersive liquid\u2010liquid microextraction followed by gas chromatography\u2010flame ionization detection without prior derivatization"],"prefix":"10.1002","volume":"2","author":[{"given":"Hamid Reza","family":"Sobhi","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Amir","family":"Kashtiaray","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hadi","family":"Farahani","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Farshad","family":"Abrahimpour","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ali","family":"Esrafili","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2010,8,31]]},"reference":[{"key":"e_1_2_6_2_2","doi-asserted-by":"publisher","DOI":"10.1111\/j.1528-1157.1975.tb04738.x"},{"key":"e_1_2_6_3_2","doi-asserted-by":"publisher","DOI":"10.2165\/00003495-197713020-00001"},{"key":"e_1_2_6_4_2","doi-asserted-by":"publisher","DOI":"10.1097\/00007691-198109000-00015"},{"key":"e_1_2_6_5_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0301-0082(98)00075-6"},{"key":"e_1_2_6_6_2","first-page":"43","volume":"37","author":"Willmore L. 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