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Comprehensive Ecotoxicity Studies on Quaternary Ammonium Salts Synthesized from Vitamin B(3) Supported by QSAR Calculations

Lately, ionic forms (namely, quaternary ammonium salts, QASs) of nicotinamide, widely known as vitamin B(3), are gaining popularity in the sectors developing novel pharmaceuticals and agrochemicals. However, the direct influence of these unique QASs on the development of various terrestrial plants,...

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Autores principales: Nowacka, Aleksandra, Olejniczak, Adriana, Stachowiak, Witold, Niemczak, Michał
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9960687/
https://www.ncbi.nlm.nih.gov/pubmed/36840262
http://dx.doi.org/10.3390/plants12040914
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author Nowacka, Aleksandra
Olejniczak, Adriana
Stachowiak, Witold
Niemczak, Michał
author_facet Nowacka, Aleksandra
Olejniczak, Adriana
Stachowiak, Witold
Niemczak, Michał
author_sort Nowacka, Aleksandra
collection PubMed
description Lately, ionic forms (namely, quaternary ammonium salts, QASs) of nicotinamide, widely known as vitamin B(3), are gaining popularity in the sectors developing novel pharmaceuticals and agrochemicals. However, the direct influence of these unique QASs on the development of various terrestrial plants, as well as other organisms, remains unknown. Therefore, three compounds comprising short, medium, and long alkyl chains in N-alkylnicotinamide were selected for phytotoxicity analyses, which were conducted on representative dicotyledonous (white mustard) and monocotyledonous (sorghum) plants. The study allowed the determination of the impact of compounds on the germination capacity as well as on the development of roots and stems of the tested plants. Interestingly, independently of the length of the alkyl chain or plant species, all QASs were established as non-phytotoxic. In addition, QSAR simulations, performed using the EPI Suite™ program pack, allowed the determination of the products’ potential toxicity toward fish, green algae, and daphnids along with the susceptibility to biodegradation. The obtained nicotinamide derivative with the shortest chain (butyl) can be considered practically non-toxic according to GHS criteria, whereas salts with medium (decyl) and longest (hexadecyl) substituent were included in the ‘acute II’ toxicity class. These findings were supported by the results of the toxicity tests performed on the model aquatic plant Lemna minor. It should be stressed that all synthesized salts exhibit not only a lack of potential for bioaccumulation but also lower toxicity than their fully synthetic analogs.
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spelling pubmed-99606872023-02-26 Comprehensive Ecotoxicity Studies on Quaternary Ammonium Salts Synthesized from Vitamin B(3) Supported by QSAR Calculations Nowacka, Aleksandra Olejniczak, Adriana Stachowiak, Witold Niemczak, Michał Plants (Basel) Article Lately, ionic forms (namely, quaternary ammonium salts, QASs) of nicotinamide, widely known as vitamin B(3), are gaining popularity in the sectors developing novel pharmaceuticals and agrochemicals. However, the direct influence of these unique QASs on the development of various terrestrial plants, as well as other organisms, remains unknown. Therefore, three compounds comprising short, medium, and long alkyl chains in N-alkylnicotinamide were selected for phytotoxicity analyses, which were conducted on representative dicotyledonous (white mustard) and monocotyledonous (sorghum) plants. The study allowed the determination of the impact of compounds on the germination capacity as well as on the development of roots and stems of the tested plants. Interestingly, independently of the length of the alkyl chain or plant species, all QASs were established as non-phytotoxic. In addition, QSAR simulations, performed using the EPI Suite™ program pack, allowed the determination of the products’ potential toxicity toward fish, green algae, and daphnids along with the susceptibility to biodegradation. The obtained nicotinamide derivative with the shortest chain (butyl) can be considered practically non-toxic according to GHS criteria, whereas salts with medium (decyl) and longest (hexadecyl) substituent were included in the ‘acute II’ toxicity class. These findings were supported by the results of the toxicity tests performed on the model aquatic plant Lemna minor. It should be stressed that all synthesized salts exhibit not only a lack of potential for bioaccumulation but also lower toxicity than their fully synthetic analogs. MDPI 2023-02-17 /pmc/articles/PMC9960687/ /pubmed/36840262 http://dx.doi.org/10.3390/plants12040914 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Nowacka, Aleksandra
Olejniczak, Adriana
Stachowiak, Witold
Niemczak, Michał
Comprehensive Ecotoxicity Studies on Quaternary Ammonium Salts Synthesized from Vitamin B(3) Supported by QSAR Calculations
title Comprehensive Ecotoxicity Studies on Quaternary Ammonium Salts Synthesized from Vitamin B(3) Supported by QSAR Calculations
title_full Comprehensive Ecotoxicity Studies on Quaternary Ammonium Salts Synthesized from Vitamin B(3) Supported by QSAR Calculations
title_fullStr Comprehensive Ecotoxicity Studies on Quaternary Ammonium Salts Synthesized from Vitamin B(3) Supported by QSAR Calculations
title_full_unstemmed Comprehensive Ecotoxicity Studies on Quaternary Ammonium Salts Synthesized from Vitamin B(3) Supported by QSAR Calculations
title_short Comprehensive Ecotoxicity Studies on Quaternary Ammonium Salts Synthesized from Vitamin B(3) Supported by QSAR Calculations
title_sort comprehensive ecotoxicity studies on quaternary ammonium salts synthesized from vitamin b(3) supported by qsar calculations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9960687/
https://www.ncbi.nlm.nih.gov/pubmed/36840262
http://dx.doi.org/10.3390/plants12040914
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