Enantioselective ecotoxicity of the herbicide dichlorprop and complexes formed with chitosan in two fresh water green algae
| Autor: | Yuezhong Wen, Xiaodong Kang, Yuli Yuan, Hui Chen, Dongmei Xu |
|---|---|
| Rok vydání: | 2011 |
| Předmět: |
Dichlorprop
Chlorella vulgaris Fresh Water Management Monitoring Policy and Law Polysaccharide Cell wall Chitosan chemistry.chemical_compound Chlorophyta Botany Ecosystem chemistry.chemical_classification biology Herbicides Public Health Environmental and Occupational Health Stereoisomerism General Medicine Pesticide biology.organism_classification chemistry Green algae Ecotoxicity 2 4-Dichlorophenoxyacetic Acid Water Pollutants Chemical Nuclear chemistry |
| Zdroj: | Journal of environmental monitoring : JEM. 13(4) |
| ISSN: | 1464-0333 |
| Popis: | To reduce the leaching potential, to prevent groundwater contamination and to maintain the efficacy of a pesticide, natural polysaccharides have received increasing attention due to their biocompatibility and useful biological reactivity for controlled release formulations (CRFs) of pesticides. In this paper, the toxicities of the chiral herbicide dichlorprop (DCPP) and its complexes with chitosan molecules (DCPP–CS) and chitosan nanoparticles (DCPP–NP) to two different green algae were determined and compared. The inhibition rates of DCPP, DCPP–CS and DCPP–NP were determined at 24, 48, 72, 96, 120, 144, 168 h, and the results show that (S)-DCPP was more toxic to Chlorella vulgaris than (R)-DCPP, while the (R)-DCPP was more toxic to Scenedesmus obliquus than (S)-DCPP. The study also found that the chiral selectivity of DCPP to Chlorella vulgaris and Scenedesmus obliquus could be changed when DCPP was complexed with chitosan molecules (CS) or chitosan nanoparticles (NP). For Chlorella vulgaris, the order of inhibition was (R)-DCPP–CS > (S)-DCPP–CS and (R)-DCPP–NP > (S)-DCPP–NP; for Scenedesmus obliquus, the order was (S)-DCPP–CS > (R)-DCPP–CS and (S)-DCPP–NP > (R)-DCPP–NP. This phenomenon suggests that the enantioselective behaviors of chiral compounds might shift when interactions with other chiral receptors coexist in different biological environments. Additionally, chitosan molecules and chitosan nanoparticles also showed different toxicities, which could be ascribed to the difference in the physicochemical properties between CS and NP or the differences in the cell walls of the two fresh water green algae. |
| Databáze: | OpenAIRE |
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