Formation and occurrence of transformation products of metformin in wastewater and surface water

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Formation and occurrence of transformation products of metformin in wastewater and surface water. / Tisler, Selina; Zwiener, Christian.

In: Science of the Total Environment, Vol. 628-629, 2018, p. 1121-1129.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Tisler, S & Zwiener, C 2018, 'Formation and occurrence of transformation products of metformin in wastewater and surface water', Science of the Total Environment, vol. 628-629, pp. 1121-1129. https://doi.org/10.1016/j.scitotenv.2018.02.105

APA

Tisler, S., & Zwiener, C. (2018). Formation and occurrence of transformation products of metformin in wastewater and surface water. Science of the Total Environment, 628-629, 1121-1129. https://doi.org/10.1016/j.scitotenv.2018.02.105

Vancouver

Tisler S, Zwiener C. Formation and occurrence of transformation products of metformin in wastewater and surface water. Science of the Total Environment. 2018;628-629:1121-1129. https://doi.org/10.1016/j.scitotenv.2018.02.105

Author

Tisler, Selina ; Zwiener, Christian. / Formation and occurrence of transformation products of metformin in wastewater and surface water. In: Science of the Total Environment. 2018 ; Vol. 628-629. pp. 1121-1129.

Bibtex

@article{e7cf12c1cd39449fbd4bc2dc4ca14f7d,
title = "Formation and occurrence of transformation products of metformin in wastewater and surface water",
abstract = "The aim of this work was to investigate the occurrence and fate of the antidiabetic metformin (MF) and its transformation products (TPs) in wastewater and surface water samples. New TPs of MF were approached by electrochemical degradation with a boron-doped-diamond electrode (at 1.5 V for 10 min). 2,4-Diamino-1,3,5-triazine (2,4-DAT), methylbiguanide (MBG), 2-amino-4-methylamino-1,3,5-triazine (2,4-AMT) and 4-amino-2-imino-1-methyl-1,2-dihydro-1,3,5-triazine (4,2,1-AIMT) were identified by hydrophilic interaction chromatography (HILIC) with quadrupole time-of-flight mass spectrometry (QTOF-MS) and accurate mass fragmentation. However, the well-known transformation product guanyl urea (GU) could not be formed electrochemically. In samples from wastewater treatment plants (WWTP), 2,4-AMT and 2,4-DAT showed an increasing trend from influents to effluents, which implies formation of the TPs during WWT. MBG is also formed by hydrolysis of MF and therefore didn't show this trend in WWTPs. Compared to GU, the concentrations of other TPs are generally three orders of magnitude lower. MBG and 2,4-DAT were also detected in surface water which was impacted by waste water, while 4,2,1-AIMT could not be detected in any sample. The concentrations of MF were in an expected range for influent (14 to 95 μg/l), effluent (0.7 to 6.5 μg/l), surface water (up to 234 ng/l) and tap water (34 ng/l). GU concentrations, however, were in one of the two investigated WWTP much higher in the influent (between 158 μg/l and 2100 μg/l) than in the effluent (between 26 and 810 μg/l). This is a rather unexpected result which has not been reported yet. Obviously, GU has been already formed in parts of the sewer system from MF or from other biguanide compounds like antidiabetics or disinfection chemicals. Furthermore, lower concentrations of GU in the effluents than in the influents indicate degradation processes of guanyl urea in the waste water treatment.",
keywords = "Guanyl urea, High-resolution mass spectrometry, LC-MS, Metformin, Methylbiguanide, Surface water, Transformation products, Wastewater treatment",
author = "Selina Tisler and Christian Zwiener",
year = "2018",
doi = "10.1016/j.scitotenv.2018.02.105",
language = "English",
volume = "628-629",
pages = "1121--1129",
journal = "Science of the Total Environment",
issn = "0048-9697",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Formation and occurrence of transformation products of metformin in wastewater and surface water

AU - Tisler, Selina

AU - Zwiener, Christian

PY - 2018

Y1 - 2018

N2 - The aim of this work was to investigate the occurrence and fate of the antidiabetic metformin (MF) and its transformation products (TPs) in wastewater and surface water samples. New TPs of MF were approached by electrochemical degradation with a boron-doped-diamond electrode (at 1.5 V for 10 min). 2,4-Diamino-1,3,5-triazine (2,4-DAT), methylbiguanide (MBG), 2-amino-4-methylamino-1,3,5-triazine (2,4-AMT) and 4-amino-2-imino-1-methyl-1,2-dihydro-1,3,5-triazine (4,2,1-AIMT) were identified by hydrophilic interaction chromatography (HILIC) with quadrupole time-of-flight mass spectrometry (QTOF-MS) and accurate mass fragmentation. However, the well-known transformation product guanyl urea (GU) could not be formed electrochemically. In samples from wastewater treatment plants (WWTP), 2,4-AMT and 2,4-DAT showed an increasing trend from influents to effluents, which implies formation of the TPs during WWT. MBG is also formed by hydrolysis of MF and therefore didn't show this trend in WWTPs. Compared to GU, the concentrations of other TPs are generally three orders of magnitude lower. MBG and 2,4-DAT were also detected in surface water which was impacted by waste water, while 4,2,1-AIMT could not be detected in any sample. The concentrations of MF were in an expected range for influent (14 to 95 μg/l), effluent (0.7 to 6.5 μg/l), surface water (up to 234 ng/l) and tap water (34 ng/l). GU concentrations, however, were in one of the two investigated WWTP much higher in the influent (between 158 μg/l and 2100 μg/l) than in the effluent (between 26 and 810 μg/l). This is a rather unexpected result which has not been reported yet. Obviously, GU has been already formed in parts of the sewer system from MF or from other biguanide compounds like antidiabetics or disinfection chemicals. Furthermore, lower concentrations of GU in the effluents than in the influents indicate degradation processes of guanyl urea in the waste water treatment.

AB - The aim of this work was to investigate the occurrence and fate of the antidiabetic metformin (MF) and its transformation products (TPs) in wastewater and surface water samples. New TPs of MF were approached by electrochemical degradation with a boron-doped-diamond electrode (at 1.5 V for 10 min). 2,4-Diamino-1,3,5-triazine (2,4-DAT), methylbiguanide (MBG), 2-amino-4-methylamino-1,3,5-triazine (2,4-AMT) and 4-amino-2-imino-1-methyl-1,2-dihydro-1,3,5-triazine (4,2,1-AIMT) were identified by hydrophilic interaction chromatography (HILIC) with quadrupole time-of-flight mass spectrometry (QTOF-MS) and accurate mass fragmentation. However, the well-known transformation product guanyl urea (GU) could not be formed electrochemically. In samples from wastewater treatment plants (WWTP), 2,4-AMT and 2,4-DAT showed an increasing trend from influents to effluents, which implies formation of the TPs during WWT. MBG is also formed by hydrolysis of MF and therefore didn't show this trend in WWTPs. Compared to GU, the concentrations of other TPs are generally three orders of magnitude lower. MBG and 2,4-DAT were also detected in surface water which was impacted by waste water, while 4,2,1-AIMT could not be detected in any sample. The concentrations of MF were in an expected range for influent (14 to 95 μg/l), effluent (0.7 to 6.5 μg/l), surface water (up to 234 ng/l) and tap water (34 ng/l). GU concentrations, however, were in one of the two investigated WWTP much higher in the influent (between 158 μg/l and 2100 μg/l) than in the effluent (between 26 and 810 μg/l). This is a rather unexpected result which has not been reported yet. Obviously, GU has been already formed in parts of the sewer system from MF or from other biguanide compounds like antidiabetics or disinfection chemicals. Furthermore, lower concentrations of GU in the effluents than in the influents indicate degradation processes of guanyl urea in the waste water treatment.

KW - Guanyl urea

KW - High-resolution mass spectrometry

KW - LC-MS

KW - Metformin

KW - Methylbiguanide

KW - Surface water

KW - Transformation products

KW - Wastewater treatment

U2 - 10.1016/j.scitotenv.2018.02.105

DO - 10.1016/j.scitotenv.2018.02.105

M3 - Journal article

C2 - 30045535

AN - SCOPUS:85042228546

VL - 628-629

SP - 1121

EP - 1129

JO - Science of the Total Environment

JF - Science of the Total Environment

SN - 0048-9697

ER -

ID: 256508162