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Cyanobacteria have been considered a major global threat because of their widespread ability to proliferate and contaminate inland and marine waters with toxic metabolites. For this reason, to avoid risks to humans and environmental health, regulatory legislation and guidelines have been established based on extensive toxicological data. However, most of what is known in this field come from works on microcystin (MC) variants, which effects were almost exclusively tested in metazoan models. In this work, we used acute end-point toxicological assays and high-resolution hybrid quadrupole time-of-flight mass spectrometer coupled with electrospray ionization source (ESI-Q-TOF-MS) analyses to evaluate the deleterious impact of aqueous extracts prepared from cultures of cyanobacteria and environmental bloom biomasses over a non-metazoan model organism, the cosmopolitan fresh/brackish water unicellular microeukaryote, Paramecium caudatum (Ciliophora). Our data suggest that all extracts produced time-dependent effects on P. caudatum survival, irrespective of their metabolite profile; and that this ciliate is more sensitive to extracts containing microginins than to extracts with only MCs, stressing that more toxicological investigations should be performed on the environmental impact of neglected cyanotoxins. Further, our data provide evidence that P. caudatum may be more sensitive to cyanotoxins than vertebrates, indicating that guidelines values, set on metazoans are likely to be inaccurate to protect organisms from basal food web positions. Thus, we highly recommend the widespread use of microeukaryotes, such as ciliates in environmental risk assessment frameworks for the establishment of more reliable cyanotoxin monitoring guideline values.Developmental toxicity refers to the occurrence of adverse effects on a developing organism as a consequence of exposure to hazardous chemicals. The assessment of developmental toxicity has become relevant to the safety assessment process of chemicals. The zebrafish embryo developmental toxicology assay is an emerging test used to screen the teratogenic potential of chemicals and it is proposed as a promising test to replace teratogenic assays with animals. Supported by the increased availability of data from this test, the developmental toxicity assay with zebrafish has become an interesting endpoint for the in silico modelling. The purpose of this study was to build up quantitative structure-activity relationship (QSAR) models. In this work, new in silico models for the evaluation of developmental toxicity were built using a well-defined set of data from the ToxCastTM Phase I chemical library on the zebrafish embryo. Categorical and continuous QSAR models were built by gradient boosting machine learning and the Monte Carlo technique respectively, in accordance with Organization for Economic Co-operation and Development principles and their statistical quality was satisfactory. The classification model reached balanced accuracy 0.89 and Matthews correlation coefficient 0.77 on the test set. The regression model reached correlation coefficient R2 0.70 in external validation and leave-one-out cross-validated Q2 0.73 in internal validation.This study investigated the ability of dual crosslinked interpenetrating polymer network (IPN) blend beads (DINSA/PVA-beads), composed of sodium alginate (SA) and poly (vinyl alcohol) (PVA), as a base-triggered carrier for the controlled release of dinotefuran (DIN) in Spodoptera litera midgut. The blend beads were characterized for morphology, encapsulation efficiency, swelling degree, and in vitro release of the blend beads were characterized. The results revealed that the double-crosslinked gel beads had a tightly interpenetrating network structure and exhibited a satisfactory embedding effect for DIN. The maximum of the DIN loading capacity was approximately 1.01%, with a high encapsulation efficiency of 83.19%. The triggered release of DIN from the blend beads was studied in deionized water (pH 3.0-11.0) via high-performance liquid chromatography (HPLC); it was found that the release rate was higher in alkaline pH conditions than in acidic and neutral conditions. [https://www.selleckchem.com/products/AZD0530.html Saracatinib mw] An in vivo dynamics and degradation study also demonstrated that the excellent release characteristics of DINSA/PVA-beads in the midgut of S. litera. This study provides a promising controlled-release form of dinotefuran that is more effective and can be used for the targeted control of pests with alkaline midgut.Parabens are used as antimicrobial preservatives in a range of consumer products. However, very limited information is available about the association between use of personal care products and paraben burden in human tissues. Accumulation of parabens in some non-destructive biomarkers (such as human fingernail) is essential for paraben biomonitoring. In this study, 50 human fingernail samples were collected from Nanjing, China. A subset of participants (n = 32) also provided their face cream samples (as the representative of personal care products). Six parabens, including methyl- (MeP), ethyl- (EtP), propyl- (PrP), butyl- (BuP), heptyl- (HeP), and benzyl-parabens (BzP), together with their major metabolites were measured in the fingernail and face cream samples. Total concentrations of parabens and their major metabolites were 39.9-27400 ng/g in fingernails. MeP, PrP and EtP were the three dominant parabens in fingernails with median values of 3140, 1290, and 127 ng/g, respectively. Significantly higher levels in female fingernails than those in male fingernails were observed for MeP, PrP, EtP, BuP, and the MeP metabolite (methyl protocatechuate, OH-MeP) (p less then 0.05). Adult fingernails contained greater concentrations of MeP and PrP than juvenile fingernails (p less then 0.05). Positive correlations were observed for EtP (R = 0.36, p less then 0.05) and BuP (R = 0.48, p = 0.008) concentrations between the fingernail and face cream samples. Our work is a preliminary study trying to explore the quantitative relationship between paraben concentrations in human body and use of personal care products. The result here provides a direct evidence that use of personal care products is one of the major sources for human exposure to parabens.