Liquid chromatographic determination of malondialdehyde in plasma samples after liquid–liquid microextraction
Liquid chromatographic determination of malondialdehyde in plasma samples after liquid–liquid microextraction
نویسندگان: ابوالقاسم جویبان , سجاد عزیزی خواجه , جعفر سلیمانی , مریم خوب نسب جعفری , اعظم صمدی
کلمات کلیدی: Malondialdehyde, 2, 4-dinitrophenylhydrazine, vortex assisted liquid liquid microextraction, N2 assisted liquid liquid microextraction, validation, samples.
نشریه: 8538 , 3 , 13 , 2017
| نویسنده ثبت کننده مقاله |
ابوالقاسم جویبان |
| مرحله جاری مقاله |
تایید نهایی |
| دانشکده/مرکز مربوطه |
مرکز تحقیقات آنالیز دارویی |
| کد مقاله |
68882 |
| عنوان فارسی مقاله |
Liquid chromatographic determination of malondialdehyde in plasma samples after liquid–liquid microextraction |
| عنوان لاتین مقاله |
Liquid chromatographic determination of malondialdehyde in plasma samples after liquid–liquid microextraction |
| ناشر |
5 |
| آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ |
بلی |
| عنوان نشریه (خارج از لیست فوق) |
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| نوع مقاله |
Original Article |
| نحوه ایندکس شدن مقاله |
ایندکس شده سطح یک – ISI - Web of Science |
| آدرس لینک مقاله/ همایش در شبکه اینترنت |
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| Background: Malondialdehyde is a product of lipid peroxidation of polyunsaturated fatty acids in foods and biological samples and widely used as biomarker of oxidative stress in various diseases. We describe the validation of a new microextraction-LC-UV method for the determination of malondialdehyde (MDA) in the form of 2,4-dinitrophenylhydrazine (DNPH) derivatization in plasma samples.
Objective: A new microextraction technique called vortex and N2 assisted liquid-liquid microextraction has been developed for the determination MDA in plasma samples.
Method: The DNPH-derivatized MDA was extracted into ethyl acetate as an extraction solvent and measured by LC-UV at 310 nm after evaporation of ethyl acetate and re-dissolving in mobile phase composed of 0.2% acetic acid–acetonitrile (50:50; v/v). This method validated according to U.S. Food and Drug Administration guidelines.
Results: The limit of detection of MDA was 0.038 µmol L-1 (2.74 µg L-1) and the intra and interday relative standard deviations were in the range of 3.8-5.0% and 5.5-9.4%, respectively for different concentrations of MDA.
Conclusion: A precise and valid method to measure MDA as DNPH derivatization in plasma samples using LC was proposed. |
| نام فایل |
تاریخ درج فایل |
اندازه فایل |
دانلود |
| Curr Anal Chem 14 (2018) 416-422.pdf | 1398/06/24 | 366047 | دانلود |