scholarly journals Determination of Pendimethalin Dynamic Residual Distribution in Crucian Carp Tissues and Associated Risk Assessment

2021 ◽  
Vol 2021 ◽  
pp. 1-9
Author(s):  
Lu Qiao ◽  
Na Yuan ◽  
Gang Han ◽  
Bo Cheng ◽  
Defu Zhang ◽  
...  

Pendimethalin has been considered a moderately to extremely toxic compound for fish and aquatic organism. This study developed the determination of dynamic residual distribution for pendimethalin in crucian carp tissues (muscle, liver, kidney, gill, and blood) under semistatic exposure system by high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) method. The pendimethalin residues in various fish tissues increased initially and then decreased, and the residue amount of pendimethalin varied from tissue to tissue of crucian carp. Particularly, the pendimethalin accumulation in most fish tissues made significant decreases at two-time points. Pendimethalin was initially absorbed and enriched by fish body, and then partial pendimethalin was discharged into the outside environment through the metabolism function of crucian carp. The residue levels of pendimethalin distributed in crucian carp were ranked in the following decreasing order: liver > kidney > gill or muscle > blood, attributed to the fact that pendimethalin tends to accumulate in lipid-rich tissues of fish. Risk assessment results indicated that the chronic risk from dietary exposure to pendimethalin through crucian carp consumption for Chinese residents was acceptable, along with a lower estimated exposure dose (EED) than acceptable daily intake (ADI) and risk quotient (RQ) < 1. This study performed the first analysis for pendimethalin residual distribution in crucian carp tissues under semistatic exposure condition and provided a reference for pollution control and risk assessment of pendimethalin aimed at aquatic products.

Nanomaterials ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 3319
Author(s):  
Nokwanda Hendricks ◽  
Olatunde Stephen Olatunji ◽  
Bhekumuzi Prince Gumbi

Fullerenes engineered nanomaterials are regarded as emerging environmental contaminants. This is as their widespread application in many consumer products, as well as natural release, increases their environmental concentration. In this work, an ultrasonic-assisted pressurized liquid extraction (UAPLE) method followed by high performance liquid chromatography with ultraviolet-visible detector (HPLC-UV-vis) was developed for extraction and determination of fullerene in sediments. The method was validated and found to be suitable for environmental risk assessment. Thereafter, the method was used for the determination of fullerene (C61-PCBM) in sediment samples collected from Umgeni River, South Africa. The current method allows for adequate sensitivity within the linear range of 0.01–4 µg g−1, method limit detection of 0.0094 µg g−1 and recoveries ranged between 67–84%. All the parameters were determined from fortified sediments samples. The measured environmental concentration (MEC) of fullerene in the sediment samples ranged from not detected to 30.55 µg g−1. To the best of our knowledge, this is the first report on the occurrence and ecological risk assessment of carbonaceous fullerene nanoparticles in African sediments and biosolids.


Author(s):  
E. Dimitrieska-Stojkovikj ◽  
A. Angeleska ◽  
B. Stojanovska-Dimzoska ◽  
Z. Hajrilai-Musliu ◽  
D. Koceva ◽  
...  

Background: Acrylamide (AA) is an important food contaminant resulted from Maillard reaction during thermal processing of carbohydrate rich food commodities. The present paper reports the data for the AA content in some types of thermally processed starch rich food, and assessment of dietary exposure for the population in North Macedonia. Methods: The AA level was determined employing modified and validated ultra high performance liquid chromatography with tandem quadrupole detector. A total of 160 samples divided in seven most frequently consumed commodity groups were collected for determination of their AA content. Finally, chronic exposure of AA in the population was estimated. Statistical analysis was performed applying OriginPro 8 SR4 v8.0951 software package Results: The average AA levels varied from 126.9±122.4 μg/kg for bread samples to 494.5±127.1 μg/kg for French fries samples. The dietary exposure of the population from North Macedonia for the tested food commodities was estimated at 0.643±0.171 μgAA/kgbw/day. The main contributor to the total AA intake was bread, with estimated value at 0.394±0.150 μgAA/kgbw/day. The margin of exposure values were 528 and 264, respectively for neurotoxicity and non-plastic effect calculated on average intake. Conclusion: The risk assessment analysis revealed increased concern for human health regarding the neoplastic effects, especially for infants, toddlers, and adolescents. This is the first study related to AA presence in different food commodities in North Macedonia, and implies that monitoring programs and mitigation strategies must be implemented.


2020 ◽  
Vol 51 (1) ◽  
pp. 23-33 ◽  
Author(s):  
Maryam Zahedi ◽  
Amir Shakerian ◽  
Ebrahim Rahimi ◽  
Reza Sharafati Chaleshtori

2009 ◽  
Vol 17 (3-4) ◽  
pp. 56-60 ◽  
Author(s):  
Dragan Milicevic ◽  
Verica Juric ◽  
Dubravka Vukovic ◽  
Miodrag Mandic ◽  
Tatjana Baltic

Background: Samples of blood, kidney, and liver per animal were randomly selected from slaughtered pigs (n=60) and analyzed for ochratoxin A. Methods: Determination of ochratoxin A concentration in samples of kidney and liver was performed by high-performance thinlayer chromatography after immunoaffnity column clean up, while for plasma samples, a spectrofluorometric procedure was used. Results: Of the 60 plasma samples, 60% contained ochratoxin A in the range of 2.5-33.3 ng/mL (mean 3.05?5.0 ng/mL), while the incidence of ochratoxin A in kidneys and liver were very similar (70% and 65%). The average ochratoxin A concentration in liver was 3.2?4.35 ng/g (1.2-19.5 ng/g) and in kidneys was 3.97?4.47 ng/g (1.3-22.0 ng/g). A statistically significant difference (p<0.01) was found between region Backa Topola and Kovilj for both liver and kidney samples. In kidney samples originating from region Kovilj and Senta, a statistically significant difference (p<0.01) was found. Mean distribution followed the pattern: kidney>liver>serum (100>80.8>77%). The results from this survey indicated that there was a strong correlation between the ochratoxin A level in serum and liver as well as in the ochratoxin A serum in kidney (r=0.884 and r=0.896, respectively) while the strongest correlation was found between the ochratoxin A level in liver and in kidney (r=0.970). Conclusion: The results of present study show that pork tissues as well as pork products are considered an important source of ochratoxin A in humans.


1989 ◽  
Vol 55 (7) ◽  
pp. 1273-1276 ◽  
Author(s):  
Ryuji Ueno ◽  
Kazuaki Uno ◽  
Saburoh S. Kubota ◽  
Yoshishige Horiguchi

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