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利用拟南芥细胞和幼苗修复双氯芬酸和磺胺甲恶唑。

Phytoremediation of diclofenac and sulfamethoxazole in Arabidopsis thaliana cells and seedlings.

机构信息

Department of Applied Science, School of Science and Technology, Hong Kong Metropolitan University, Ho Man Tin, Kowloon, Hong Kong SAR, China.

Department of Construction, Environment and Engineering, Technological and Higher Education Institute of Hong Kong, Shing Tai Road, Chai Wan, Hong Kong SAR, China.

出版信息

Chemosphere. 2024 Sep;364:142989. doi: 10.1016/j.chemosphere.2024.142989. Epub 2024 Aug 2.

Abstract

Diclofenac (DLF), a widely recognized non-steroidal anti-inflammatory drug (NSAID), and sulfamethoxazole (SMX), a broad-spectrum sulfonamide antibiotic, are commonly prescribed medications that have raised concerns as significant contributors to pharmaceutical pollution in natural ecosystems despite their clinical effectiveness. This study investigates the potential phytoremediation pathways for these two drugs in plant systems by tracking and quantifying the fate of the parent compounds and their metabolites in Arabidopsis thaliana using cell and seedling cultures. Results indicated significant differences in the dissipation of DLF according to the treatment and time interaction within the cell cultures. Viable plant cells showed complete dissipation of DLF from an initial concentration of 2758 ng/mL in 96 h, whereas non-viable cells and blank solutions remained stable. The dissipation of SMX was comparable across viable, non-viable, and blanks, showing a minor decrease from 842 to 799 ng/mL over 120 h following the treatment of viable cells. DLF metabolites including 4'-hydroxy-diclofenac, 5-hydroxy-diclofenac, acyl-glutamatyl-diclofenac, 1-(2,6-dichlorophenyl)-5-hydroxy-2-indolinone, 5-sulfooxy-diclofenac, 5-glucopyranosyloxy-diclofenac, 1-(2,6-dichloro-4-hydroxyphenyl)-2-indolinone, and 4'-glucopyranosyloxy-diclofenac were recognized, likely formed through acylation, glutamyl conjugation, hydroxylation, dehydration, cyclization, sulfonation, and glucosidation. While for SMX, metabolites including sulfamethoxazole-glucuronide, nitroso-sulfamethoxazole, N-acetylsulfamethoxazole, and N-acetyl-5-OH-sulfamethoxazole were identified, potentially produced through glucuronidation, nitrosation, acetylation, and hydroxylation. Phase I metabolite concentrations of DLF and SMX peaked earlier than those of phase II metabolites. Hydroponic A. thaliana demonstrated comparable efficiencies in the phytoremediation of DLF and SMX, with concentrations varying from 1 mg/L to 10 mg/L. Detectable levels of both parent compounds and their metabolites confirmed successful absorption and metabolism within the plant system. This study provides valuable insights into the potential of phytoremediation as a sustainable approach for reducing the environmental toxicity of DLF and SMX and suggests comparable metabolic efficiency. These findings contribute to the growing body of knowledge on phytoremediation and its application in addressing pollution from pharmaceuticals and personal care products.

摘要

双氯芬酸(DLF)是一种广泛认可的非甾体抗炎药(NSAID),磺胺甲恶唑(SMX)是一种广谱磺胺类抗生素,尽管它们在临床上有效,但由于它们是造成自然生态系统中药物污染的主要因素之一,因此已被广泛关注。本研究通过跟踪和量化拟南芥细胞和幼苗培养物中母体化合物及其代谢物的命运,研究了这两种药物在植物系统中的潜在植物修复途径。结果表明,在细胞培养物中,根据处理和时间的相互作用,DLF 的消散存在显著差异。有活力的植物细胞在 96 小时内将初始浓度为 2758ng/mL 的 DLF 完全消散,而无活力的细胞和空白溶液则保持稳定。SMX 的消散在有活力、无活力和空白之间是可比的,在处理有活力的细胞 120 小时后,从 842ng/mL 略有下降。检测到 DLF 代谢物,包括 4'-羟基双氯芬酸、5-羟基双氯芬酸、酰基谷氨酸酰基双氯芬酸、1-(2,6-二氯苯基)-5-羟基-2-吲哚酮、5-磺氧基双氯芬酸、5-葡糖苷酰氧基双氯芬酸、1-(2,6-二氯-4-羟基苯基)-2-吲哚酮和 4'-葡糖苷酰氧基双氯芬酸,可能通过酰化、谷氨酰基结合、羟化、脱水、环化、磺化和葡糖苷酸化形成。对于 SMX,鉴定出代谢物包括磺胺甲恶唑-葡糖醛酸苷、亚硝基磺胺甲恶唑、N-乙酰磺胺甲恶唑和 N-乙酰-5-OH-磺胺甲恶唑,可能通过葡糖醛酸化、亚硝化、乙酰化和羟化产生。DLF 和 SMX 的 I 相代谢物浓度早于 II 相代谢物浓度达到峰值。水培拟南芥在 DLF 和 SMX 的植物修复中表现出相当的效率,浓度范围从 1mg/L 到 10mg/L。在植物系统中检测到母体化合物及其代谢物的可检测水平,证实了它们的成功吸收和代谢。本研究为植物修复作为一种可持续的方法,降低双氯芬酸和磺胺甲恶唑的环境毒性提供了有价值的见解,并表明其具有相当的代谢效率。这些发现为植物修复及其在解决药品和个人护理产品污染方面的应用提供了更多的知识。

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