کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1200780 1493600 2014 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Development of a flat membrane based device for electromembrane extraction: A new approach for exhaustive extraction of basic drugs from human plasma
ترجمه فارسی عنوان
توسعه یک دستگاه مبتنی بر غشاء تخت برای استخراج الکترومغناطیسی: یک رویکرد جدید برای استخراج کامل داروهای اساسی از پلاسمای انسانی
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
چکیده انگلیسی


• A technical device for electromembrane extraction was developed.
• A thin flat membrane of polypropylene was used to fabricate the device.
• Larger acceptor solution volume provided higher recovery.
• Exhaustive extraction of the basic drugs from human plasma was achieved.

In this work, a single-well electromembrane extraction (EME) device was developed based on a thin (100 μm) and flat porous membrane of polypropylene supporting a liquid membrane. The new EME device was operated with a relatively large acceptor solution volume to promote a high recovery. Using this EME device, exhaustive extraction of the basic drugs quetiapine, citalopram, amitriptyline, methadone and sertraline was investigated from both acidified water samples and human plasma. The volume of acceptor solution, extraction time, and extraction voltage were found to be important factors for obtaining exhaustive extraction. 2-Nitrophenyl octyl ether was selected as the optimal organic solvent for the supported liquid membrane. From spiked acidified water samples (600 μl), EME was carried out with 600 μl of 20 mM HCOOH as acceptor solution for 15 min and with an extraction voltage of 250 V. Under these conditions, extraction recoveries were in the range 89–112%. From human plasma samples (600 μl), EME was carried out with 600 μl of 20 mM HCOOH as acceptor solution for 30 min and with an extraction voltage of 300 V. Under these conditions, extraction recoveries were in the range of 83–105%. When combined with LC–MS, the new EME device provided linearity in the range 10–1000 ng/ml for all analytes (R2 > 0.990). The repeatability at low (10 ng/ml), medium (100 ng/ml), and high (1000 ng/ml) concentration level for all five analytes were less than 10% (RSD). The limits of quantification (S/N = 10) were found to be in the range 0.7–6.4 ng/ml.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Chromatography A - Volume 1326, 24 January 2014, Pages 7–12
نویسندگان
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