Enantiomerization and enantioselective bioaccumulation of diclofop-methyl in tubifex worms

IF 2.8 4区 化学 Q2 CHEMISTRY, ANALYTICAL
Chirality Pub Date : 2023-09-18 DOI:10.1002/chir.23618
Tiantian Liu, Xinhong Duan
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引用次数: 0

Abstract

In this study, the hydrolysis of diclofop-methyl (DM) in aqueous system and the bioaccumulation of its main metabolite, Diclofop (DA), in the tubifex worms were investigated using enantioselective high-performance liquid chromatography. With the addition of tubifex, rapid hydrolysis was observed for DM. It is revealed that the hydrolysis of DM in the water and the accumulation of DA in the worms were both enantioselective. Meanwhile, either the hydrolysis amount or the levels of enantioselectivity were influenced by the tubifex. After incubated for 24 h, about 94.6% of the DM was hydrolyzed and the enantiomer fraction of metabolite (DA) deviated from 0.5 with R-DA significantly higher than S-DA. The enantiopure S-DM and R-DM and S-DA and R-DA were incubated, and enantiomerizations were detected between the two DM enantiomers with S-form inversing into R-form and vice versa. It was found that the S-DM exhibited a higher tendency to invert than the R-DM.

Abstract Image

双氯氟吡甲禾灵在管虫体内的对映体化和对映体选择性生物累积。
本研究采用对映体选择性高效液相色谱法研究了甲基双氯磷 (DM) 在水体系中的水解及其主要代谢产物双氯磷 (DA) 在管圆线虫体内的生物累积。加入管圆线虫后,观察到 DM 快速水解。结果表明,DM 在水中的水解和 DA 在蠕虫体内的积累都是对映体选择性的。同时,水解量或对映体选择性的水平都受到管虫的影响。培养24小时后,约94.6%的DM被水解,代谢产物(DA)的对映体部分偏离0.5,R-DA明显高于S-DA。将对映体纯度为 S-DM 和 R-DM、S-DA 和 R-DA 的对映体进行孵育,检测到两种 DM 对映体之间的对映体化,S-形式反转为 R-形式,反之亦然。结果发现,S-DM 比 R-DM 表现出更高的反转趋势。
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来源期刊
Chirality
Chirality 医学-分析化学
CiteScore
4.40
自引率
5.00%
发文量
124
审稿时长
1 months
期刊介绍: The main aim of the journal is to publish original contributions of scientific work on the role of chirality in chemistry and biochemistry in respect to biological, chemical, materials, pharmacological, spectroscopic and physical properties. Papers on the chemistry (physiochemical, preparative synthetic, and analytical), physics, pharmacology, clinical pharmacology, toxicology, and other biological aspects of chiral molecules will be published.
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