SIMULTANEOUS QUANTITATIVE 1H NMR ANALYSIS OF METHANOL, ETHANOL AND THEIR METABOLIC PRODUCTS IN HUMAN PLASMA: EARLY DIANOSIS AND MONITORING DURING TREATMENT OF ACUTE METHANOL POISONING IN VIETNAM

被引:0
作者
Ta Thi Thao [1 ]
Nguyen Thi Ngan [1 ]
Vu Anh Phuong [1 ]
Ha Tran Hung [2 ]
Nguyen Van Thuc [2 ]
Pham Quang Trung [3 ]
机构
[1] VNU Univ Sci Hanoi, Fac Chem, Le Thanh Tong Str 19, Hanoi 110401, Vietnam
[2] Bach Mai Hosp, Poison Control Ctr, Hanoi 116301, Vietnam
[3] Hanoi Med Univ, Dept Emergency Intens Care Med & Toxicol, 1 Dong Da, Hanoi 116001, Vietnam
来源
IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENII KHIMIYA I KHIMICHESKAYA TEKHNOLOGIYA | 2021年 / 64卷 / 02期
关键词
methanol; ethanol; Vietnam; magnetic; proton; SPECTROSCOPY; BLOOD; SERUM;
D O I
10.6060/ivkkt.20216402.6294
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The H-1-NMR method for simultaneous quantification of methanol, ethanol and their metabolic products (formic acid and acetic acid) in human plasma was established. The effect of protein in plasma sample was removed by 25% trichloroacetic acid (TCA) with the ratio of TCA and plasma sample at 1/5 (v/v). The small amount of D2O (estimated 1/10 v/v) was chosen due to the effect of water signal was eliminated by using the advance water suppression with NOESY pulse sequence. The different analytical parameters such as linearity, precision, accuracy, and specificity, instrument detection limit (IDL) and instrument quantification limit (IQL) were validated. The instrument detection limit of four compounds in blank plasma varied from 0.68 (for methanol) to 2.88 mg/L (for formic acids). The average recoveries of concentration in dynamic ranges were found to be 96 to 105%. The good linearity between concentration calculated by integrated signal and measured obtained by calibration curves confirmed that concentration of analytes in plasma can be directly determined from the H-1-NMR signal. The proposed method has been successfully applied for direct determination of five compounds in 9 patient's plasma samples with the satisfactory results compared to GC/FID method. The analytical procedure can be useful for diagnosis and evaluation of treatment of methanol poisoning in Vietnamese hospitals.
引用
收藏
页码:41 / 48
页数:8
相关论文
共 25 条
[1]  
[Anonymous], 2015, BRIT NATL FORMULARY, V42
[2]   Analysis of methanol and its derivatives in illegally produced alcoholic beverages [J].
Arslan, M. Mustafa ;
Zeren, Cem ;
Aydin, Zeki ;
Akcan, Ramazan ;
Dokuyucu, Recep ;
Keten, Alper ;
Cekin, Necmi .
JOURNAL OF FORENSIC AND LEGAL MEDICINE, 2015, 33 :56-60
[3]   A novel method for quantification of ethanol and methanol in distilled alcoholic beverages using Raman spectroscopy [J].
Boyaci, Ismail Hakki ;
Genis, Huseyin Efe ;
Guven, Burcu ;
Tamer, Ugur ;
Alper, Neslihan .
JOURNAL OF RAMAN SPECTROSCOPY, 2012, 43 (08) :1171-1176
[4]  
Clary JJ., 2013, The Toxicology of methanol, P14, DOI [10.1002/9781118353110, DOI 10.1002/9781118353110]
[5]   A review on nuclear overhauser enhancement (NOE) and rotating-frame overhauser effect (ROE) NMR techniques in food science: Basic principles and applications [J].
Doost, Ali Sedaghat ;
Akbari, Marzieh ;
Stevens, Christian V. ;
Setiowati, Arima Diah ;
Van der Meeren, Paul .
TRENDS IN FOOD SCIENCE & TECHNOLOGY, 2019, 86 :16-24
[6]  
Ellis DI, 2019, ANALYST, V144, P324, DOI [10.1039/C8AN01702F, 10.1039/c8an01702f]
[7]   Applications of NMR spectroscopy to systems biochemistry [J].
Fan, Teresa W. -M. ;
Lane, Andrew N. .
PROGRESS IN NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY, 2016, 92-93 :18-53
[8]   Analysis of Methanol in the Presence of Ethanol, Using a Hybrid Capillary Electrophoresis Device with Electrochemical Derivatization and Conductivity Detection [J].
Ferreira Santos, Mauro Sergio ;
da Costa, Eric Tavares ;
Rolf Gutz, Ivano Gebhardt ;
Garcia, Carlos D. .
ANALYTICAL CHEMISTRY, 2017, 89 (02) :1362-1368
[9]   Expanding the Limits of Human Blood Metabolite Quantitation Using NMR Spectroscopy [J].
Gowda, G. A. Nagana ;
Gowda, Yashas N. ;
Raftery, Daniel .
ANALYTICAL CHEMISTRY, 2015, 87 (01) :706-715
[10]  
Hovda K.E., 2017, CRITICAL CARE TOXICO, P3058, DOI [10.1007/978-3-319-20790-2_78-2., DOI 10.1007/978-3-319-20790-2_78-2]