Biodegradability and ecotoxicitiy of tramadol, ranitidine, and their photoderivatives in the aquatic environment: Biologische Abbaubarkeit und Ökotoxizität von Tramadol, Ranitidin sowie ihren Photoderivate in der aquatischen Umwelt
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In: Environmental Science and Pollution Research, Vol. 19, No. 1, 01.2012, p. 72-85.
Research output: Journal contributions › Journal articles › Research › peer-review
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TY - JOUR
T1 - Biodegradability and ecotoxicitiy of tramadol, ranitidine, and their photoderivatives in the aquatic environment
T2 - Biologische Abbaubarkeit und Ökotoxizität von Tramadol, Ranitidin sowie ihren Photoderivate in der aquatischen Umwelt
AU - Bergheim, Marlies
AU - Gieré, Reto
AU - Kümmerer, Klaus
PY - 2012/1
Y1 - 2012/1
N2 - Purpose This study was designed to assess the fate and the overall potential impacts of the widely prescribed drugs ranitidine and tramadol after their introduction into the aquatic environment. Methods The probability to detect these two drugs in the aquatic environment was studied by analyzing their abiotic and biotic degradation properties. For this purpose, samples were irradiated with different light sources, and three widely used biodegradability tests from the OECD series, the closed bottle test (OECD 301 D), the manometric respirometry test (OECD 301 F) and the Zahn-Wellens test (OECD 302 B), were conducted. The ecotoxicity of the photolytically formed transformation products was assessed by performing the bacterial growth inhibition test (EN ISO 10712). Furthermore, quantitative structure-activity relationship analysis and a risk analysis based on the calculation of the predicted environmental concentrations have also been conducted to assess the environmental risk potential of the transformation products. The possible formation of stable products by microbial or photolytical transformation has been investigated with DOC and LC-MS analytics. Results In the present study, neither ranitidine, nor tramadol, nor their photoderivatives were found to be readily or inherently biodegradable according to test guidelines. The photolytic transformation was faster under a UV lamp compared to the reaction under an Xe lamp with a spectrum that mimics sunlight. No chronic toxicity against bacteria was found for ranitidine or its photolytic decomposition products, but a low toxicity was detected for the resulting mixture of the photolytic transformation products of tramadol. Conclusions The study demonstrates that transformation products may have a higher environmental risk potential than the respective parent compounds.
AB - Purpose This study was designed to assess the fate and the overall potential impacts of the widely prescribed drugs ranitidine and tramadol after their introduction into the aquatic environment. Methods The probability to detect these two drugs in the aquatic environment was studied by analyzing their abiotic and biotic degradation properties. For this purpose, samples were irradiated with different light sources, and three widely used biodegradability tests from the OECD series, the closed bottle test (OECD 301 D), the manometric respirometry test (OECD 301 F) and the Zahn-Wellens test (OECD 302 B), were conducted. The ecotoxicity of the photolytically formed transformation products was assessed by performing the bacterial growth inhibition test (EN ISO 10712). Furthermore, quantitative structure-activity relationship analysis and a risk analysis based on the calculation of the predicted environmental concentrations have also been conducted to assess the environmental risk potential of the transformation products. The possible formation of stable products by microbial or photolytical transformation has been investigated with DOC and LC-MS analytics. Results In the present study, neither ranitidine, nor tramadol, nor their photoderivatives were found to be readily or inherently biodegradable according to test guidelines. The photolytic transformation was faster under a UV lamp compared to the reaction under an Xe lamp with a spectrum that mimics sunlight. No chronic toxicity against bacteria was found for ranitidine or its photolytic decomposition products, but a low toxicity was detected for the resulting mixture of the photolytic transformation products of tramadol. Conclusions The study demonstrates that transformation products may have a higher environmental risk potential than the respective parent compounds.
KW - Chemistry
KW - Aquatic environment
KW - Degradation
KW - Ecotoxicology
KW - Irradiation
KW - Ranitidine
KW - Tramadol
KW - Transformation
KW - Sustainability Science
UR - http://www.scopus.com/inward/record.url?scp=84855269634&partnerID=8YFLogxK
U2 - 10.1007/s11356-011-0536-y
DO - 10.1007/s11356-011-0536-y
M3 - Journal articles
C2 - 21681613
VL - 19
SP - 72
EP - 85
JO - Environmental Science and Pollution Research
JF - Environmental Science and Pollution Research
SN - 1614-7499
IS - 1
ER -