Lazić, S.

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  • Lazić, S. (12)
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Author's Bibliography

Disappearance of nicosulfuron residues in soil under laboratory conditions

Grahovac, Nada; Šunjka, D.; Lazić, S.; Vasin, Jovica; Kondić-Špika, Ankica; Jakšić, Snežana

(2017)

TY  - CONF
AU  - Grahovac, Nada
AU  - Šunjka, D.
AU  - Lazić, S.
AU  - Vasin, Jovica
AU  - Kondić-Špika, Ankica
AU  - Jakšić, Snežana
PY  - 2017
UR  - http://fiver.ifvcns.rs/handle/123456789/3702
AB  - Sulfunyluares (SUs) present a new generation of herbicides which selectively control broad- and narrow-leaved weeds. Nonethel iiened utilization of SUs leads to increased concern about herbicides residues as the « msequence of their prolonged persistence in some soils. Nicosulfuron belongs to the group of SUs herbicide. A laboratory experiment at termostat (temperature of 25°C) was carried out to evaluate the effect of temn< ‘ture on the dissipation dynamics and final residues of nicosulfuron in soil type Calcie Chernozem Clayic, Pachic. The dissipation of nicosulfuron in soi! was described by using the Mittag-Leffler function ¢ E, (-hr), ere obtained from the experimental data. The residues of nicosulfuron
iphy with diode array detection in the cted herbicide was applied as aqueous solution of commercial formulation nicosulfuron (K elvin", 40 ¢ L'). The starting coneentrations of nicosulfuron (measured in the samples soil taken on the ( th day, ! houirs afier the treatment)
Sulfunyluares (SUs) pre 1 new
 Model coefficients a, h. « v
were determined by uitra-performance liquid chromatog ultraviolet region. In order to invest gate dissipation
 
rye cs on 25°C were 389.84 ug ke ‘9.18 = : | ee E ¢ coe . pg kg, 649.02 ug kg 'and 797.69 ug kg! after the treatment with 40 grams active ingredient (a.i.) per hectare of nicosulfuron ig ai. ha'), 50 gal. ha”, 80.g ai. ha” and 100 gai. ha’. respectively. Atier two days, residues of nicosulfuron were lower more than 86% compared with the initial concentra ‘on. Pifty aays aficr the application of all doses the content of residues were below the LOQ for nicosulfuron (3.16 Hg kg'). The obtained half-time degradation (DT:») values of nicosulfuron vere in range of 0.34 d (80 g a.i. ha’ ') to 0.68 d (40 £att Significant reater Cissipation of nicosulfuron observed in this laboratory testing was influenced, most probably, by abiouc and biotic processes. Nicosulfuron poses low risks to the . imilar type soil because of their rapid dissipation,
C3  - 8th International Scientific Agriculture Symposium “AGROSYM 2017”,2017, Jahorina, Bosnia and Herzegovina
T1  - Disappearance of nicosulfuron residues in soil under laboratory conditions
SP  - 889
UR  - https://hdl.handle.net/21.15107/rcub_fiver_3702
ER  - 
@conference{
author = "Grahovac, Nada and Šunjka, D. and Lazić, S. and Vasin, Jovica and Kondić-Špika, Ankica and Jakšić, Snežana",
year = "2017",
abstract = "Sulfunyluares (SUs) present a new generation of herbicides which selectively control broad- and narrow-leaved weeds. Nonethel iiened utilization of SUs leads to increased concern about herbicides residues as the « msequence of their prolonged persistence in some soils. Nicosulfuron belongs to the group of SUs herbicide. A laboratory experiment at termostat (temperature of 25°C) was carried out to evaluate the effect of temn< ‘ture on the dissipation dynamics and final residues of nicosulfuron in soil type Calcie Chernozem Clayic, Pachic. The dissipation of nicosulfuron in soi! was described by using the Mittag-Leffler function ¢ E, (-hr), ere obtained from the experimental data. The residues of nicosulfuron
iphy with diode array detection in the cted herbicide was applied as aqueous solution of commercial formulation nicosulfuron (K elvin", 40 ¢ L'). The starting coneentrations of nicosulfuron (measured in the samples soil taken on the ( th day, ! houirs afier the treatment)
Sulfunyluares (SUs) pre 1 new
 Model coefficients a, h. « v
were determined by uitra-performance liquid chromatog ultraviolet region. In order to invest gate dissipation
 
rye cs on 25°C were 389.84 ug ke ‘9.18 = : | ee E ¢ coe . pg kg, 649.02 ug kg 'and 797.69 ug kg! after the treatment with 40 grams active ingredient (a.i.) per hectare of nicosulfuron ig ai. ha'), 50 gal. ha”, 80.g ai. ha” and 100 gai. ha’. respectively. Atier two days, residues of nicosulfuron were lower more than 86% compared with the initial concentra ‘on. Pifty aays aficr the application of all doses the content of residues were below the LOQ for nicosulfuron (3.16 Hg kg'). The obtained half-time degradation (DT:») values of nicosulfuron vere in range of 0.34 d (80 g a.i. ha’ ') to 0.68 d (40 £att Significant reater Cissipation of nicosulfuron observed in this laboratory testing was influenced, most probably, by abiouc and biotic processes. Nicosulfuron poses low risks to the . imilar type soil because of their rapid dissipation,",
journal = "8th International Scientific Agriculture Symposium “AGROSYM 2017”,2017, Jahorina, Bosnia and Herzegovina",
title = "Disappearance of nicosulfuron residues in soil under laboratory conditions",
pages = "889",
url = "https://hdl.handle.net/21.15107/rcub_fiver_3702"
}
Grahovac, N., Šunjka, D., Lazić, S., Vasin, J., Kondić-Špika, A.,& Jakšić, S.. (2017). Disappearance of nicosulfuron residues in soil under laboratory conditions. in 8th International Scientific Agriculture Symposium “AGROSYM 2017”,2017, Jahorina, Bosnia and Herzegovina, 889.
https://hdl.handle.net/21.15107/rcub_fiver_3702
Grahovac N, Šunjka D, Lazić S, Vasin J, Kondić-Špika A, Jakšić S. Disappearance of nicosulfuron residues in soil under laboratory conditions. in 8th International Scientific Agriculture Symposium “AGROSYM 2017”,2017, Jahorina, Bosnia and Herzegovina. 2017;:889.
https://hdl.handle.net/21.15107/rcub_fiver_3702 .
Grahovac, Nada, Šunjka, D., Lazić, S., Vasin, Jovica, Kondić-Špika, Ankica, Jakšić, Snežana, "Disappearance of nicosulfuron residues in soil under laboratory conditions" in 8th International Scientific Agriculture Symposium “AGROSYM 2017”,2017, Jahorina, Bosnia and Herzegovina (2017):889,
https://hdl.handle.net/21.15107/rcub_fiver_3702 .

Dissipation of nicosulfuron and oxasulfuron in soil under field condition

Grahovac, Nada; Suturović, Z; Kondić-Špika, Ankica; Sekulić, P.; Lazić, S.; Šunjka, D.; Jakšić, Snežana

(2013)

TY  - CONF
AU  - Grahovac, Nada
AU  - Suturović, Z
AU  - Kondić-Špika, Ankica
AU  - Sekulić, P.
AU  - Lazić, S.
AU  - Šunjka, D.
AU  - Jakšić, Snežana
PY  - 2013
UR  - http://fiver.ifvcns.rs/handle/123456789/3731
AB  - Sulfonylureas represent a major advancement in global crop protection technology
and they have revolutionized weed control by introducing a unique mode of action.
These herbicides have low toxicity to mammals while they are highly toxic to plants.
The fate of sulfonylurea herbicides is directly related to their chemical structure and
mainly to the ionisation of the sulfonylurea bridge. The dissipation behavior of
nicosulfuron and oxasulfuron in soil were investigated. Soil was cored on
experimental site Rimski Sanéevi in Serbia four times (0-30 days after the spray).
The residue levels and dissipation rates of nicosulfuron and oxasulfuron in soil were
determined by liquid chromatography with diode array detection. The pesticide
formulations were applied in two different rates for nicosulfuron (50 g ai ha-1 and
100 g ai ha Nicogan 40SC) and oxasulfuron (80 g ai ha’' and 160 g ai ha’' Dynox).
The fortified recoveries were in the following range for nicosulfuron from 85.90% to
98.71% with relative standard deviations (RSDs) of 0.16—4.80% and for oxasulfuron
from 88.09% to 99.01% with relative standard deviations (RSDs) of 1.6-5.66%. The
limit of detections (LODs) for nicosulfuron and oxasulfuron in soil were 0.002 mg/kg
and 0.003 mg/kg, respectively. The dissipation of nicosulfuron and oxasulfuron
residues over the time in soil was described by the Mittag-Leffler function a*Ea,B (-
bt). Coefficients a, b, a, 8 were obtained from the experimental data, by using fitting
procedure. We got a=0.8, B=3.71, a=159.11, b=12.79 for nicosulfuron and a=0.8,
B=4.11, a=82.53, b=7.0 for oxasulfuron. The field dissipation half-life time for
nicosulfuron at the topsoil (0-30cm soil depth) was 5.2 days while for oxasulfuron
was 9.67days after application. These results could be utilized for the environmental
risks assessment and minimizing risk for contamination of natural water resources
and damage to following crops.
C3  - 8th International Symposium of Pesticides in Food and the Environment in Mediterranean Countries, Cappadocia (Urgup)/Nevsehir, Turkey
T1  - Dissipation of nicosulfuron and oxasulfuron in soil under field condition
EP  - 105
SP  - 105
UR  - https://hdl.handle.net/21.15107/rcub_fiver_3731
ER  - 
@conference{
author = "Grahovac, Nada and Suturović, Z and Kondić-Špika, Ankica and Sekulić, P. and Lazić, S. and Šunjka, D. and Jakšić, Snežana",
year = "2013",
abstract = "Sulfonylureas represent a major advancement in global crop protection technology
and they have revolutionized weed control by introducing a unique mode of action.
These herbicides have low toxicity to mammals while they are highly toxic to plants.
The fate of sulfonylurea herbicides is directly related to their chemical structure and
mainly to the ionisation of the sulfonylurea bridge. The dissipation behavior of
nicosulfuron and oxasulfuron in soil were investigated. Soil was cored on
experimental site Rimski Sanéevi in Serbia four times (0-30 days after the spray).
The residue levels and dissipation rates of nicosulfuron and oxasulfuron in soil were
determined by liquid chromatography with diode array detection. The pesticide
formulations were applied in two different rates for nicosulfuron (50 g ai ha-1 and
100 g ai ha Nicogan 40SC) and oxasulfuron (80 g ai ha’' and 160 g ai ha’' Dynox).
The fortified recoveries were in the following range for nicosulfuron from 85.90% to
98.71% with relative standard deviations (RSDs) of 0.16—4.80% and for oxasulfuron
from 88.09% to 99.01% with relative standard deviations (RSDs) of 1.6-5.66%. The
limit of detections (LODs) for nicosulfuron and oxasulfuron in soil were 0.002 mg/kg
and 0.003 mg/kg, respectively. The dissipation of nicosulfuron and oxasulfuron
residues over the time in soil was described by the Mittag-Leffler function a*Ea,B (-
bt). Coefficients a, b, a, 8 were obtained from the experimental data, by using fitting
procedure. We got a=0.8, B=3.71, a=159.11, b=12.79 for nicosulfuron and a=0.8,
B=4.11, a=82.53, b=7.0 for oxasulfuron. The field dissipation half-life time for
nicosulfuron at the topsoil (0-30cm soil depth) was 5.2 days while for oxasulfuron
was 9.67days after application. These results could be utilized for the environmental
risks assessment and minimizing risk for contamination of natural water resources
and damage to following crops.",
journal = "8th International Symposium of Pesticides in Food and the Environment in Mediterranean Countries, Cappadocia (Urgup)/Nevsehir, Turkey",
title = "Dissipation of nicosulfuron and oxasulfuron in soil under field condition",
pages = "105-105",
url = "https://hdl.handle.net/21.15107/rcub_fiver_3731"
}
Grahovac, N., Suturović, Z., Kondić-Špika, A., Sekulić, P., Lazić, S., Šunjka, D.,& Jakšić, S.. (2013). Dissipation of nicosulfuron and oxasulfuron in soil under field condition. in 8th International Symposium of Pesticides in Food and the Environment in Mediterranean Countries, Cappadocia (Urgup)/Nevsehir, Turkey, 105-105.
https://hdl.handle.net/21.15107/rcub_fiver_3731
Grahovac N, Suturović Z, Kondić-Špika A, Sekulić P, Lazić S, Šunjka D, Jakšić S. Dissipation of nicosulfuron and oxasulfuron in soil under field condition. in 8th International Symposium of Pesticides in Food and the Environment in Mediterranean Countries, Cappadocia (Urgup)/Nevsehir, Turkey. 2013;:105-105.
https://hdl.handle.net/21.15107/rcub_fiver_3731 .
Grahovac, Nada, Suturović, Z, Kondić-Špika, Ankica, Sekulić, P., Lazić, S., Šunjka, D., Jakšić, Snežana, "Dissipation of nicosulfuron and oxasulfuron in soil under field condition" in 8th International Symposium of Pesticides in Food and the Environment in Mediterranean Countries, Cappadocia (Urgup)/Nevsehir, Turkey (2013):105-105,
https://hdl.handle.net/21.15107/rcub_fiver_3731 .

Validation of the method for the determination of dithiocarbamates in fruits

Grahovac, Nada; Kondić-Špika, Ankica; Lazić, S.; Šunjka, D.; Jakšić, Snežana; Radović, B.

(Nacionalno drugtvo za procesnu tehniku i energetiku u poljoprivredi, Novi Sad, 2013)

TY  - CONF
AU  - Grahovac, Nada
AU  - Kondić-Špika, Ankica
AU  - Lazić, S.
AU  - Šunjka, D.
AU  - Jakšić, Snežana
AU  - Radović, B.
PY  - 2013
UR  - http://fiver.ifvcns.rs/handle/123456789/3723
AB  - Residues of active substances, which were frequently found in fruits and vegetables of market producers belonged to the dithiocarbamate group pesticide. According to their use dithiocarbamates belong to fungicides in terms dithiocarbamic acid. They are a group of compounds that exist as strong complexes with various metal ions, often in a polymeric form. This makes them difficult to analyse directly because of their limited solubility in most organic solvents. It is important to have a reliable method which enables the quick and simple detection of this group for official monitoring. This work reports a simple, rapid and sensitive method for the assessment residues dithiocarbamates in fruits. Dithiocarbamates were determined indirectly by measuring the amount of carbon disulfide (CS>) that is liberated by the chemical reaction. The fruit samples in undisturbed condition were heated with a solution of stannous (II) chloride and hydrochloric acid yielding carbon disulphide. Incurred carbon disulfide (CS) are determined "head-space" technique of gas-chromatography with mass detector. Linearity was verified by using the solutions of carbon disulphide in acetone. A linear dynamic range was obtained over a range of concentrations from 0.02 to 0.12 mg/kg for carbon disulfide with correlation coefficient r > 0.995. The accuracy of the method was acceptable since the average recoveries measured at four fortification levels were in the range of 83-103% (n = 4). The precision of the developed procedure expressed as the relative standard deviations (RSDs) were lower than 3.7% in all cases. Quantification was based on external standard calibration curves made with spiked blankmatrices.
PB  - Nacionalno drugtvo za procesnu tehniku i energetiku u poljoprivredi, Novi Sad
C3  - 3rd International Conference Sustainable postharvest and Food Technolologies - INOPTEP 2013 and XXV National Conference Processing and Energy in Agriculture PTEP , Vrnjačka Banja, 21 April 2013
T1  - Validation of the method for the determination of dithiocarbamates in fruits
EP  - 292
SP  - 292
UR  - https://hdl.handle.net/21.15107/rcub_fiver_3723
ER  - 
@conference{
author = "Grahovac, Nada and Kondić-Špika, Ankica and Lazić, S. and Šunjka, D. and Jakšić, Snežana and Radović, B.",
year = "2013",
abstract = "Residues of active substances, which were frequently found in fruits and vegetables of market producers belonged to the dithiocarbamate group pesticide. According to their use dithiocarbamates belong to fungicides in terms dithiocarbamic acid. They are a group of compounds that exist as strong complexes with various metal ions, often in a polymeric form. This makes them difficult to analyse directly because of their limited solubility in most organic solvents. It is important to have a reliable method which enables the quick and simple detection of this group for official monitoring. This work reports a simple, rapid and sensitive method for the assessment residues dithiocarbamates in fruits. Dithiocarbamates were determined indirectly by measuring the amount of carbon disulfide (CS>) that is liberated by the chemical reaction. The fruit samples in undisturbed condition were heated with a solution of stannous (II) chloride and hydrochloric acid yielding carbon disulphide. Incurred carbon disulfide (CS) are determined "head-space" technique of gas-chromatography with mass detector. Linearity was verified by using the solutions of carbon disulphide in acetone. A linear dynamic range was obtained over a range of concentrations from 0.02 to 0.12 mg/kg for carbon disulfide with correlation coefficient r > 0.995. The accuracy of the method was acceptable since the average recoveries measured at four fortification levels were in the range of 83-103% (n = 4). The precision of the developed procedure expressed as the relative standard deviations (RSDs) were lower than 3.7% in all cases. Quantification was based on external standard calibration curves made with spiked blankmatrices.",
publisher = "Nacionalno drugtvo za procesnu tehniku i energetiku u poljoprivredi, Novi Sad",
journal = "3rd International Conference Sustainable postharvest and Food Technolologies - INOPTEP 2013 and XXV National Conference Processing and Energy in Agriculture PTEP , Vrnjačka Banja, 21 April 2013",
title = "Validation of the method for the determination of dithiocarbamates in fruits",
pages = "292-292",
url = "https://hdl.handle.net/21.15107/rcub_fiver_3723"
}
Grahovac, N., Kondić-Špika, A., Lazić, S., Šunjka, D., Jakšić, S.,& Radović, B.. (2013). Validation of the method for the determination of dithiocarbamates in fruits. in 3rd International Conference Sustainable postharvest and Food Technolologies - INOPTEP 2013 and XXV National Conference Processing and Energy in Agriculture PTEP , Vrnjačka Banja, 21 April 2013
Nacionalno drugtvo za procesnu tehniku i energetiku u poljoprivredi, Novi Sad., 292-292.
https://hdl.handle.net/21.15107/rcub_fiver_3723
Grahovac N, Kondić-Špika A, Lazić S, Šunjka D, Jakšić S, Radović B. Validation of the method for the determination of dithiocarbamates in fruits. in 3rd International Conference Sustainable postharvest and Food Technolologies - INOPTEP 2013 and XXV National Conference Processing and Energy in Agriculture PTEP , Vrnjačka Banja, 21 April 2013. 2013;:292-292.
https://hdl.handle.net/21.15107/rcub_fiver_3723 .
Grahovac, Nada, Kondić-Špika, Ankica, Lazić, S., Šunjka, D., Jakšić, Snežana, Radović, B., "Validation of the method for the determination of dithiocarbamates in fruits" in 3rd International Conference Sustainable postharvest and Food Technolologies - INOPTEP 2013 and XXV National Conference Processing and Energy in Agriculture PTEP , Vrnjačka Banja, 21 April 2013 (2013):292-292,
https://hdl.handle.net/21.15107/rcub_fiver_3723 .

Solid-phase extraction followed by high-performance liquid chromatography with diode array detection for screening of dicamba herbicide in water

Lazić, S.; Grahovac, Nada; Šunjka, D.; Guzsvány, V.; Jakšić, Snežana

(2013)

TY  - CONF
AU  - Lazić, S.
AU  - Grahovac, Nada
AU  - Šunjka, D.
AU  - Guzsvány, V.
AU  - Jakšić, Snežana
PY  - 2013
UR  - http://fiver.ifvcns.rs/handle/123456789/3700
AB  - Chlorinated acids are selective agricultural herbicides which are widely employed in agriculture and gardening for control the growth of different unwanted
vegetable species in crops. Because of high water solubility and toxicological risk
of some acid herbicides and their metabolic products, monitoring of their concentration in surface and groundwater is very important task. The acidic herbicides
are manufactured in formulation as free acids, as their alkaline salts or as esters.
The unionized free acids vary in water solubility (Table 1), but the acidic herbicides most frequently exist in ionized form at environmental pH values. Acidic
herbicides formulated as salts are water soluble, while those formulations prepared as esters are less water soluble. In the environment, acidic herbicides formulated as esters have short hydrolysis half-life time (24-48 h) and therefore they are
generally present as ionized acids. For most analytes, especially for the acidic herbicides, solid phase extraction (SPE) is the choice of sample treatment, which is
followed by appropriate chromatographic separation and sensitive determination
of target components. For the acidic herbicides, combination of physico-chemical
parameters influences their extraction from aqueous solution. Ionogenicity (pKa)
and hydrophobicity (logkow) are especially important in determining the approach of SPE for efficient sample clean-up for further chromatographic analysis
of chlorophenoxy acid herbicide in water samples.
C3  - Knjiga izvoda, 6. Simpozijum „Hemija i zaštita životne sredine EnviroChem 2013“,  Vršac
T1  - Solid-phase extraction followed by high-performance liquid chromatography with diode array detection for screening of dicamba herbicide in water
EP  - 387
SP  - 386
UR  - https://hdl.handle.net/21.15107/rcub_fiver_3700
ER  - 
@conference{
author = "Lazić, S. and Grahovac, Nada and Šunjka, D. and Guzsvány, V. and Jakšić, Snežana",
year = "2013",
abstract = "Chlorinated acids are selective agricultural herbicides which are widely employed in agriculture and gardening for control the growth of different unwanted
vegetable species in crops. Because of high water solubility and toxicological risk
of some acid herbicides and their metabolic products, monitoring of their concentration in surface and groundwater is very important task. The acidic herbicides
are manufactured in formulation as free acids, as their alkaline salts or as esters.
The unionized free acids vary in water solubility (Table 1), but the acidic herbicides most frequently exist in ionized form at environmental pH values. Acidic
herbicides formulated as salts are water soluble, while those formulations prepared as esters are less water soluble. In the environment, acidic herbicides formulated as esters have short hydrolysis half-life time (24-48 h) and therefore they are
generally present as ionized acids. For most analytes, especially for the acidic herbicides, solid phase extraction (SPE) is the choice of sample treatment, which is
followed by appropriate chromatographic separation and sensitive determination
of target components. For the acidic herbicides, combination of physico-chemical
parameters influences their extraction from aqueous solution. Ionogenicity (pKa)
and hydrophobicity (logkow) are especially important in determining the approach of SPE for efficient sample clean-up for further chromatographic analysis
of chlorophenoxy acid herbicide in water samples.",
journal = "Knjiga izvoda, 6. Simpozijum „Hemija i zaštita životne sredine EnviroChem 2013“,  Vršac",
title = "Solid-phase extraction followed by high-performance liquid chromatography with diode array detection for screening of dicamba herbicide in water",
pages = "387-386",
url = "https://hdl.handle.net/21.15107/rcub_fiver_3700"
}
Lazić, S., Grahovac, N., Šunjka, D., Guzsvány, V.,& Jakšić, S.. (2013). Solid-phase extraction followed by high-performance liquid chromatography with diode array detection for screening of dicamba herbicide in water. in Knjiga izvoda, 6. Simpozijum „Hemija i zaštita životne sredine EnviroChem 2013“,  Vršac, 386-387.
https://hdl.handle.net/21.15107/rcub_fiver_3700
Lazić S, Grahovac N, Šunjka D, Guzsvány V, Jakšić S. Solid-phase extraction followed by high-performance liquid chromatography with diode array detection for screening of dicamba herbicide in water. in Knjiga izvoda, 6. Simpozijum „Hemija i zaštita životne sredine EnviroChem 2013“,  Vršac. 2013;:386-387.
https://hdl.handle.net/21.15107/rcub_fiver_3700 .
Lazić, S., Grahovac, Nada, Šunjka, D., Guzsvány, V., Jakšić, Snežana, "Solid-phase extraction followed by high-performance liquid chromatography with diode array detection for screening of dicamba herbicide in water" in Knjiga izvoda, 6. Simpozijum „Hemija i zaštita životne sredine EnviroChem 2013“,  Vršac (2013):386-387,
https://hdl.handle.net/21.15107/rcub_fiver_3700 .

Screening of pesticide residues in canal water in the Northern Serbia

Lazić, S.; Šunjka, D.; Milovanović, I; Grahovac, Nada

(2013)

TY  - CONF
AU  - Lazić, S.
AU  - Šunjka, D.
AU  - Milovanović, I
AU  - Grahovac, Nada
PY  - 2013
UR  - http://fiver.ifvcns.rs/handle/123456789/3724
AB  - Non-point-source contamination of surface water has emerged as an important environmental problem during the last decades. This is particularly obvious in areas with intensive pesticide application. Considering importance of water and soil quality, pesticide residues in our environment need to be more effectively documented. This study has focused on determination of pesticide residues in drainage water. Monitoring of pesticide residues were conducted at different locations in the northern part of Serbia, the main agricultural area of the country. The sampling was performed during spring and summer 2012 on twelve potential risk sites. The extraction of pesticides from water was carried out with ENVI™ C18 DSK 47 mm (Supelco 5-7171, Bellafonte, PA). Prior to extraction disc was conditioned with 5 ml of methanol and 5 ml of ultrapure water. Afterward, water sample was filtered through the disc under vacuum and disc was dried for 1 h at 25 °C. Pesticides were eluted from the disc with 5 ml of mixture dichloromethane/n-hexane (40/60, v/v) and evaporated to dryness. The extract was reconstituted in 1 ml of methanol, ultrasonically homogenized and analyzed. Analyses were performed on Agilent Technologies GC-MS Model 7890 A Series gas chromatograph coupled to 5975 C mass selective detector. A HP5MS (30 mx 0.25 mmi.d.) fused silica capillary column was used. Helium was used as the carrier gas at a constant pressure. Injection volume was 2.0 ul, in splitless mode at 280 °C. The total run time was 41.86 min. The interface was kept at 250 °C, the quadropole at 150 °C and the mass spectra were obtained at electron energy of 70 eV. After validation and measurement uncertainty evaluation steps, results obtained showed that the method can be applied to efficiently for monitoring of pesticide residues in water samples. In analyzed samples 22 pesticides were detected -8fungicides,9 herbicides and 5 insecticides. Herbicides were most frequently detected (in 41% of the samples), followed by fungicides (36%) and insecticides (23%)
C3  - 14th European Meeting on Enviromental Chemistry, Budva, 4 December 2013
T1  - Screening of pesticide residues in canal water in the Northern Serbia
EP  - 134
SP  - 134
UR  - https://hdl.handle.net/21.15107/rcub_fiver_3724
ER  - 
@conference{
author = "Lazić, S. and Šunjka, D. and Milovanović, I and Grahovac, Nada",
year = "2013",
abstract = "Non-point-source contamination of surface water has emerged as an important environmental problem during the last decades. This is particularly obvious in areas with intensive pesticide application. Considering importance of water and soil quality, pesticide residues in our environment need to be more effectively documented. This study has focused on determination of pesticide residues in drainage water. Monitoring of pesticide residues were conducted at different locations in the northern part of Serbia, the main agricultural area of the country. The sampling was performed during spring and summer 2012 on twelve potential risk sites. The extraction of pesticides from water was carried out with ENVI™ C18 DSK 47 mm (Supelco 5-7171, Bellafonte, PA). Prior to extraction disc was conditioned with 5 ml of methanol and 5 ml of ultrapure water. Afterward, water sample was filtered through the disc under vacuum and disc was dried for 1 h at 25 °C. Pesticides were eluted from the disc with 5 ml of mixture dichloromethane/n-hexane (40/60, v/v) and evaporated to dryness. The extract was reconstituted in 1 ml of methanol, ultrasonically homogenized and analyzed. Analyses were performed on Agilent Technologies GC-MS Model 7890 A Series gas chromatograph coupled to 5975 C mass selective detector. A HP5MS (30 mx 0.25 mmi.d.) fused silica capillary column was used. Helium was used as the carrier gas at a constant pressure. Injection volume was 2.0 ul, in splitless mode at 280 °C. The total run time was 41.86 min. The interface was kept at 250 °C, the quadropole at 150 °C and the mass spectra were obtained at electron energy of 70 eV. After validation and measurement uncertainty evaluation steps, results obtained showed that the method can be applied to efficiently for monitoring of pesticide residues in water samples. In analyzed samples 22 pesticides were detected -8fungicides,9 herbicides and 5 insecticides. Herbicides were most frequently detected (in 41% of the samples), followed by fungicides (36%) and insecticides (23%)",
journal = "14th European Meeting on Enviromental Chemistry, Budva, 4 December 2013",
title = "Screening of pesticide residues in canal water in the Northern Serbia",
pages = "134-134",
url = "https://hdl.handle.net/21.15107/rcub_fiver_3724"
}
Lazić, S., Šunjka, D., Milovanović, I.,& Grahovac, N.. (2013). Screening of pesticide residues in canal water in the Northern Serbia. in 14th European Meeting on Enviromental Chemistry, Budva, 4 December 2013, 134-134.
https://hdl.handle.net/21.15107/rcub_fiver_3724
Lazić S, Šunjka D, Milovanović I, Grahovac N. Screening of pesticide residues in canal water in the Northern Serbia. in 14th European Meeting on Enviromental Chemistry, Budva, 4 December 2013. 2013;:134-134.
https://hdl.handle.net/21.15107/rcub_fiver_3724 .
Lazić, S., Šunjka, D., Milovanović, I, Grahovac, Nada, "Screening of pesticide residues in canal water in the Northern Serbia" in 14th European Meeting on Enviromental Chemistry, Budva, 4 December 2013 (2013):134-134,
https://hdl.handle.net/21.15107/rcub_fiver_3724 .

Persistence and dissipation behavior of dicamba and bentazon herbicides in water under laboratory conditions

Lazić, S.; Šunjka, D.; Grahovac, Nada; Guzsvány, V.

(2013)

TY  - CONF
AU  - Lazić, S.
AU  - Šunjka, D.
AU  - Grahovac, Nada
AU  - Guzsvány, V.
PY  - 2013
UR  - http://fiver.ifvcns.rs/handle/123456789/3732
AB  - The characteristics of water used in a spray mix influence the
effectiveness of pesticides. It is important to know the pH of water used
with a pesticide and the susceptibility of the pesticide to hydrolysis.
In order to investigate the persistence, dissipation and degradation
kinetics of bentazone and dicamba, laboratory study was conducted
in deionized water (pH 7.0) at 2542°C (T1) and 442°C (T2). Herbicides
were dissolved at rate of 0.05 mg/ml. Concentration of analytes was
monitoried 0 (1h), 2, 4, 7, 10, 14, 18, 24 and 28 days after treatment and
analysing as triplicate samples. Samples were analyzed by high pressure
liquid chromatography (HPLC/DAD). The chromatographic separation
was carried out with Zorbax Eclipse XDB-C,, (50 mm x 4.6 mm x 1.8 pm)
analytical column, using reverse phase column with gradient conditions
of mobile phase consist of water (with 0.05% H PO,) and acetonitrile. In
T1 the dissipation were 1.3, 5.1, 7.5, 7.9, 8.1, 15.3, 24.1, 26.9% for dicamba
and 11.5, 33.3, 44.6, 46.9,48.8, 49.6, 50.1, 51.8% for bentazone in 2, 4, 7,
10, 14, 18, 24, and 28 days. Corresponding dissipation in T2 experiment
were 2.0, 2.7, 3.9, 5.0, 6.1, 6.9, 6.8, 8.0% for dicamba and 7.7, 15.2, 26.7;
29.4, 30.3, 30.6, 31.4, 31.9% for bentazone, respectively. The dissipation
data in water showed the DT, and DT,, values 57.3 and 114.9 days
ae for dicamba and 17.1 and 125.9 days for bentazone herbicide. Several
simulation models were used to evaluate the experimental data, such
as Exponential and Mittag-Leffler function. The dissipation of analized
eo . herbicides residues over the time in water were described by the MittagLeffler function, with the best-fit model for dicamba and bentazone [1].
The dissipation of dicamba and bentazone residues on 25+2°C and 442°C
es over the time in deinoized water were described by function a*Eo, (-bt).
ag Coefficients a, b, a, 8 were obtained from the experimental data by using
be fitting procedure. We got for dicamba and bentazone herbicides on
a 25+2°C coefficients a=0.8, R=3.71,a=159.11,b=12.79 and a=2.17, B=4.56,
Es a=1387.45, b=1.96 for 442 °C a=0.8, B=4.11, a=82.53, b=7.0 and a=0.99,
rs G=3.15, a=205.81, b=0.117, respectively. The hydrolysis study indicated 
that the dicamba and bentazone pesticides hydrolysed faster at 25+2°C.
These findings can be useful in the prediction of the dissipation behavior
of this pesticides in the spray tank immediately before application. The
dissipation rates of dicamba and bentazone pesticides depended on the
temperature and pH of water to be used.
C3  - 14th European Meeting on Enviromental Chemistry, Budva, Montenegro
T1  - Persistence and dissipation behavior of dicamba and bentazon herbicides in water under laboratory conditions
EP  - 86
SP  - 86
UR  - https://hdl.handle.net/21.15107/rcub_fiver_3732
ER  - 
@conference{
author = "Lazić, S. and Šunjka, D. and Grahovac, Nada and Guzsvány, V.",
year = "2013",
abstract = "The characteristics of water used in a spray mix influence the
effectiveness of pesticides. It is important to know the pH of water used
with a pesticide and the susceptibility of the pesticide to hydrolysis.
In order to investigate the persistence, dissipation and degradation
kinetics of bentazone and dicamba, laboratory study was conducted
in deionized water (pH 7.0) at 2542°C (T1) and 442°C (T2). Herbicides
were dissolved at rate of 0.05 mg/ml. Concentration of analytes was
monitoried 0 (1h), 2, 4, 7, 10, 14, 18, 24 and 28 days after treatment and
analysing as triplicate samples. Samples were analyzed by high pressure
liquid chromatography (HPLC/DAD). The chromatographic separation
was carried out with Zorbax Eclipse XDB-C,, (50 mm x 4.6 mm x 1.8 pm)
analytical column, using reverse phase column with gradient conditions
of mobile phase consist of water (with 0.05% H PO,) and acetonitrile. In
T1 the dissipation were 1.3, 5.1, 7.5, 7.9, 8.1, 15.3, 24.1, 26.9% for dicamba
and 11.5, 33.3, 44.6, 46.9,48.8, 49.6, 50.1, 51.8% for bentazone in 2, 4, 7,
10, 14, 18, 24, and 28 days. Corresponding dissipation in T2 experiment
were 2.0, 2.7, 3.9, 5.0, 6.1, 6.9, 6.8, 8.0% for dicamba and 7.7, 15.2, 26.7;
29.4, 30.3, 30.6, 31.4, 31.9% for bentazone, respectively. The dissipation
data in water showed the DT, and DT,, values 57.3 and 114.9 days
ae for dicamba and 17.1 and 125.9 days for bentazone herbicide. Several
simulation models were used to evaluate the experimental data, such
as Exponential and Mittag-Leffler function. The dissipation of analized
eo . herbicides residues over the time in water were described by the MittagLeffler function, with the best-fit model for dicamba and bentazone [1].
The dissipation of dicamba and bentazone residues on 25+2°C and 442°C
es over the time in deinoized water were described by function a*Eo, (-bt).
ag Coefficients a, b, a, 8 were obtained from the experimental data by using
be fitting procedure. We got for dicamba and bentazone herbicides on
a 25+2°C coefficients a=0.8, R=3.71,a=159.11,b=12.79 and a=2.17, B=4.56,
Es a=1387.45, b=1.96 for 442 °C a=0.8, B=4.11, a=82.53, b=7.0 and a=0.99,
rs G=3.15, a=205.81, b=0.117, respectively. The hydrolysis study indicated 
that the dicamba and bentazone pesticides hydrolysed faster at 25+2°C.
These findings can be useful in the prediction of the dissipation behavior
of this pesticides in the spray tank immediately before application. The
dissipation rates of dicamba and bentazone pesticides depended on the
temperature and pH of water to be used.",
journal = "14th European Meeting on Enviromental Chemistry, Budva, Montenegro",
title = "Persistence and dissipation behavior of dicamba and bentazon herbicides in water under laboratory conditions",
pages = "86-86",
url = "https://hdl.handle.net/21.15107/rcub_fiver_3732"
}
Lazić, S., Šunjka, D., Grahovac, N.,& Guzsvány, V.. (2013). Persistence and dissipation behavior of dicamba and bentazon herbicides in water under laboratory conditions. in 14th European Meeting on Enviromental Chemistry, Budva, Montenegro, 86-86.
https://hdl.handle.net/21.15107/rcub_fiver_3732
Lazić S, Šunjka D, Grahovac N, Guzsvány V. Persistence and dissipation behavior of dicamba and bentazon herbicides in water under laboratory conditions. in 14th European Meeting on Enviromental Chemistry, Budva, Montenegro. 2013;:86-86.
https://hdl.handle.net/21.15107/rcub_fiver_3732 .
Lazić, S., Šunjka, D., Grahovac, Nada, Guzsvány, V., "Persistence and dissipation behavior of dicamba and bentazon herbicides in water under laboratory conditions" in 14th European Meeting on Enviromental Chemistry, Budva, Montenegro (2013):86-86,
https://hdl.handle.net/21.15107/rcub_fiver_3732 .

Method validation and uncertainty evaluation of the insecticide chlorpyrifos in water samples by using HPLC analysis

Lazić, S.; Grahovac, Nada; Šunjka, D.; Pucarevic, M.; Jakšić, Snežana; Popović, Vera

(Beograd : Društvo za zaštitu bilja Srbije, 2012)

TY  - CONF
AU  - Lazić, S.
AU  - Grahovac, Nada
AU  - Šunjka, D.
AU  - Pucarevic, M.
AU  - Jakšić, Snežana
AU  - Popović, Vera
PY  - 2012
UR  - http://fiver.ifvcns.rs/handle/123456789/3726
AB  - Chlorpyrifos is one of organophosphorus (OPPs) insecticides, which are the most important and widely used classes of agricultural pesticides. Because of its intensive use of ecosystems are contaminated by chlorpyrifos and public concerns on safety have been increased.
The method has been developed for confirmation and quantitation of the chlorpyrifos in water samples reverse phase high performance liquid chromatography (HPLC) with photodiodes detection and chromatograms were extracted at 300 nm. This method was single-lab validate in order to demonstrate its performance for monitoring of the insecticide chlorpyrifos in water.
Method accuracy was quantified through measurement uncertainty estimate based on method validation data. Tap and groundwater samples were used to demonstrate linearity and accuracy. Linearity for chlorpyrifos was evaluated by calibration curves in the range of 0.01—10 pg/ml. The accuracy of the proposed method was evaluated as the mean recovery. The analytical method allowed us to quantify chlorpyrifos in tap water and groundwater in concentration level between 0.01-—10 pg/ml with recovery values between of 80.72-109.57 % for tap water and 89.99-97.45 % for groundwater and repeatability lower or equal than 0.6% for both the matrices. The experiments showed that there were no interference peaks from the water matrix (tap and ground) on the elution region of the chlorpyrifos. The RSD values were satisfactory being in the ranges of 0.283-1.237 % (for tap water) and 0.681-3.887 % (for groundwater). The variation of the retention time was less than 0.05 % during these experimental series. The combined relative uncertainty for water samples was 0.481 % (for tap water) and 0.654 % (for groundwater). The expanded uncertainty (Uc) was calculated as Uc= k*u,, where k is the coverage factor with level of confidence of approximately 95% considering a coverage factor of 2 (EURACHEMICITAC, 2000).
We proved that the method was specific for determination of chlorpyrifos in the relevant matrices. After validation and measurement uncertainty evaluation steps, results obtained showed that the method can be applied to efficiently for monitoring of chlorpyrifos in water samples.
PB  - Beograd : Društvo za zaštitu bilja Srbije
C3  - Annual MGPR Meeting 2012 and International Conference on Food and Health Safety: Moving Towards a Sustainable Agriculture, Belgrade, 11 October 2012
T1  - Method validation and uncertainty evaluation of the insecticide chlorpyrifos in water samples by using HPLC analysis
EP  - 73
SP  - 73
UR  - https://hdl.handle.net/21.15107/rcub_fiver_3726
ER  - 
@conference{
author = "Lazić, S. and Grahovac, Nada and Šunjka, D. and Pucarevic, M. and Jakšić, Snežana and Popović, Vera",
year = "2012",
abstract = "Chlorpyrifos is one of organophosphorus (OPPs) insecticides, which are the most important and widely used classes of agricultural pesticides. Because of its intensive use of ecosystems are contaminated by chlorpyrifos and public concerns on safety have been increased.
The method has been developed for confirmation and quantitation of the chlorpyrifos in water samples reverse phase high performance liquid chromatography (HPLC) with photodiodes detection and chromatograms were extracted at 300 nm. This method was single-lab validate in order to demonstrate its performance for monitoring of the insecticide chlorpyrifos in water.
Method accuracy was quantified through measurement uncertainty estimate based on method validation data. Tap and groundwater samples were used to demonstrate linearity and accuracy. Linearity for chlorpyrifos was evaluated by calibration curves in the range of 0.01—10 pg/ml. The accuracy of the proposed method was evaluated as the mean recovery. The analytical method allowed us to quantify chlorpyrifos in tap water and groundwater in concentration level between 0.01-—10 pg/ml with recovery values between of 80.72-109.57 % for tap water and 89.99-97.45 % for groundwater and repeatability lower or equal than 0.6% for both the matrices. The experiments showed that there were no interference peaks from the water matrix (tap and ground) on the elution region of the chlorpyrifos. The RSD values were satisfactory being in the ranges of 0.283-1.237 % (for tap water) and 0.681-3.887 % (for groundwater). The variation of the retention time was less than 0.05 % during these experimental series. The combined relative uncertainty for water samples was 0.481 % (for tap water) and 0.654 % (for groundwater). The expanded uncertainty (Uc) was calculated as Uc= k*u,, where k is the coverage factor with level of confidence of approximately 95% considering a coverage factor of 2 (EURACHEMICITAC, 2000).
We proved that the method was specific for determination of chlorpyrifos in the relevant matrices. After validation and measurement uncertainty evaluation steps, results obtained showed that the method can be applied to efficiently for monitoring of chlorpyrifos in water samples.",
publisher = "Beograd : Društvo za zaštitu bilja Srbije",
journal = "Annual MGPR Meeting 2012 and International Conference on Food and Health Safety: Moving Towards a Sustainable Agriculture, Belgrade, 11 October 2012",
title = "Method validation and uncertainty evaluation of the insecticide chlorpyrifos in water samples by using HPLC analysis",
pages = "73-73",
url = "https://hdl.handle.net/21.15107/rcub_fiver_3726"
}
Lazić, S., Grahovac, N., Šunjka, D., Pucarevic, M., Jakšić, S.,& Popović, V.. (2012). Method validation and uncertainty evaluation of the insecticide chlorpyrifos in water samples by using HPLC analysis. in Annual MGPR Meeting 2012 and International Conference on Food and Health Safety: Moving Towards a Sustainable Agriculture, Belgrade, 11 October 2012
Beograd : Društvo za zaštitu bilja Srbije., 73-73.
https://hdl.handle.net/21.15107/rcub_fiver_3726
Lazić S, Grahovac N, Šunjka D, Pucarevic M, Jakšić S, Popović V. Method validation and uncertainty evaluation of the insecticide chlorpyrifos in water samples by using HPLC analysis. in Annual MGPR Meeting 2012 and International Conference on Food and Health Safety: Moving Towards a Sustainable Agriculture, Belgrade, 11 October 2012. 2012;:73-73.
https://hdl.handle.net/21.15107/rcub_fiver_3726 .
Lazić, S., Grahovac, Nada, Šunjka, D., Pucarevic, M., Jakšić, Snežana, Popović, Vera, "Method validation and uncertainty evaluation of the insecticide chlorpyrifos in water samples by using HPLC analysis" in Annual MGPR Meeting 2012 and International Conference on Food and Health Safety: Moving Towards a Sustainable Agriculture, Belgrade, 11 October 2012 (2012):73-73,
https://hdl.handle.net/21.15107/rcub_fiver_3726 .

Mogućnost određivanja rezidua acetamiprida i njegovog metabolita u trešnjama primenom HPLC/DAD

Lazić, S.; Šunjka, D.; Grahovac, Nada; Komlen, V.; Bagi, F; Budakov, D.; Jakšić, Snežana

(2012)

TY  - CONF
AU  - Lazić, S.
AU  - Šunjka, D.
AU  - Grahovac, Nada
AU  - Komlen, V.
AU  - Bagi, F
AU  - Budakov, D.
AU  - Jakšić, Snežana
PY  - 2012
UR  - http://fiver.ifvcns.rs/handle/123456789/3730
AB  - U radu je razvijena brza i jednostavna metoda za istovremeno određivanje acetamiprida i njegovog metabolita, 6-hlornikotinske kiseline (6HNK) u uzorcima trešanja. Metoda se bazira na primeni reverzne faze razdvajanja na C18 koloni primenom gradijentne elucije. Za određivanje i kvantifikaciju analita primenjena je tečna hromatografija sa detektorom sa nizom diada (HPLC/DAD), pri talasnoj dužini od 230 nm. Ekstrakcija acetamiprida 6HNK izvedena je mešavinom acetonitril/0.IN NHyCl. Prosečne vrednosti prinosa ekstrakcije aceiamiprida 6HNK u uzorcima trešanja kretale su se u intervalima od 95-101% 1 73-83% (RSD<5%), respektivno,
AB  - A rapid and simple method for the simultaneous analysis and quantification of acetamiprid and 6-chloronicotinie acid (6CNA). as intermediate of acetamiprid decomposition in sweet cherry samples has been developed. This residue analysis method is based on the reversed phase separation on C8 column with gradient elution. Analytes’ determination and quantification were performed by HPLC/DAD and chromatograms were extracted at 230 nm. These insecticides were extracted with mixture acetonitril/0.1N NH)CL Average recoveries of acekumiprid and 6CNA from sweet cherry samples were in range between 95-101 % and 73- $3%, respectively. with RSDs<5%.
C3  - International Conference Submediterranean Agriculture-ICSA, Mostar, 22 November 2012
T1  - Mogućnost određivanja rezidua acetamiprida i njegovog metabolita u trešnjama primenom HPLC/DAD
T1  - Possibility for determination of acetamiprid and its metabolite residues in sweet cherry using HPLC/DAD
EP  - 18
SP  - 18
UR  - https://hdl.handle.net/21.15107/rcub_fiver_3730
ER  - 
@conference{
author = "Lazić, S. and Šunjka, D. and Grahovac, Nada and Komlen, V. and Bagi, F and Budakov, D. and Jakšić, Snežana",
year = "2012",
abstract = "U radu je razvijena brza i jednostavna metoda za istovremeno određivanje acetamiprida i njegovog metabolita, 6-hlornikotinske kiseline (6HNK) u uzorcima trešanja. Metoda se bazira na primeni reverzne faze razdvajanja na C18 koloni primenom gradijentne elucije. Za određivanje i kvantifikaciju analita primenjena je tečna hromatografija sa detektorom sa nizom diada (HPLC/DAD), pri talasnoj dužini od 230 nm. Ekstrakcija acetamiprida 6HNK izvedena je mešavinom acetonitril/0.IN NHyCl. Prosečne vrednosti prinosa ekstrakcije aceiamiprida 6HNK u uzorcima trešanja kretale su se u intervalima od 95-101% 1 73-83% (RSD<5%), respektivno,, A rapid and simple method for the simultaneous analysis and quantification of acetamiprid and 6-chloronicotinie acid (6CNA). as intermediate of acetamiprid decomposition in sweet cherry samples has been developed. This residue analysis method is based on the reversed phase separation on C8 column with gradient elution. Analytes’ determination and quantification were performed by HPLC/DAD and chromatograms were extracted at 230 nm. These insecticides were extracted with mixture acetonitril/0.1N NH)CL Average recoveries of acekumiprid and 6CNA from sweet cherry samples were in range between 95-101 % and 73- $3%, respectively. with RSDs<5%.",
journal = "International Conference Submediterranean Agriculture-ICSA, Mostar, 22 November 2012",
title = "Mogućnost određivanja rezidua acetamiprida i njegovog metabolita u trešnjama primenom HPLC/DAD, Possibility for determination of acetamiprid and its metabolite residues in sweet cherry using HPLC/DAD",
pages = "18-18",
url = "https://hdl.handle.net/21.15107/rcub_fiver_3730"
}
Lazić, S., Šunjka, D., Grahovac, N., Komlen, V., Bagi, F., Budakov, D.,& Jakšić, S.. (2012). Mogućnost određivanja rezidua acetamiprida i njegovog metabolita u trešnjama primenom HPLC/DAD. in International Conference Submediterranean Agriculture-ICSA, Mostar, 22 November 2012, 18-18.
https://hdl.handle.net/21.15107/rcub_fiver_3730
Lazić S, Šunjka D, Grahovac N, Komlen V, Bagi F, Budakov D, Jakšić S. Mogućnost određivanja rezidua acetamiprida i njegovog metabolita u trešnjama primenom HPLC/DAD. in International Conference Submediterranean Agriculture-ICSA, Mostar, 22 November 2012. 2012;:18-18.
https://hdl.handle.net/21.15107/rcub_fiver_3730 .
Lazić, S., Šunjka, D., Grahovac, Nada, Komlen, V., Bagi, F, Budakov, D., Jakšić, Snežana, "Mogućnost određivanja rezidua acetamiprida i njegovog metabolita u trešnjama primenom HPLC/DAD" in International Conference Submediterranean Agriculture-ICSA, Mostar, 22 November 2012 (2012):18-18,
https://hdl.handle.net/21.15107/rcub_fiver_3730 .

Procena merne neizvesnosti i validacija metode određivanja acetamiprida i 6-hlornikotinske kiseline u uzorcima trešanja

Lazić, S.; Grahovac, Nada; Šunjka, D.; Jakšić, Snežana; Ljubojević, M.

(Društvo za zaštitu bilja Srbije 11080 Beograd 80, Nemanjina 6; p.fah 123, 2012)

TY  - CONF
AU  - Lazić, S.
AU  - Grahovac, Nada
AU  - Šunjka, D.
AU  - Jakšić, Snežana
AU  - Ljubojević, M.
PY  - 2012
UR  - http://fiver.ifvcns.rs/handle/123456789/3709
AB  - Pojava ostataka pesticida u voću i povrću moguća je i pored poštovanja principa dobre poljoprivredne prakse. Identifikacija prisutnih pesticida i određivanje njihovih količina u ovim matriksima zahteva primenu metoda visoke osetljivosti i selektivnosti. Istraživanje je sprovedeno u cilju iznalaženja optimalnih eksperimentalnih uslova za razdvajanje i određivanje acetamiprida i njegovog metabolita, 6-hlornikotinske kiseline (6-HNK) u uzorcima trešanja, korišćenjem tečne hromatografije sa nizom fotoosetljivin dioda (DAD). Uzorci trešanja su korišćeni da bi se odredila selektivnost, linearnost, tačnost i limit kvantifikacije (LOQ). Tačnost metode je kvantifikovana kroz procenu merne neizvesnosti zasnovanu na podacima validacije metode.
PB  - Društvo za zaštitu bilja Srbije 11080 Beograd 80, Nemanjina 6; p.fah 123
C3  - Zbornik rezimea radova, 12. Simpozijum sa savetovanjem o zaštiti bilja, Zlatibor, 26-30. novembar 2012.
T1  - Procena merne neizvesnosti i validacija metode određivanja acetamiprida i 6-hlornikotinske kiseline u uzorcima trešanja
EP  - 81
SP  - 80
UR  - https://hdl.handle.net/21.15107/rcub_fiver_3709
ER  - 
@conference{
author = "Lazić, S. and Grahovac, Nada and Šunjka, D. and Jakšić, Snežana and Ljubojević, M.",
year = "2012",
abstract = "Pojava ostataka pesticida u voću i povrću moguća je i pored poštovanja principa dobre poljoprivredne prakse. Identifikacija prisutnih pesticida i određivanje njihovih količina u ovim matriksima zahteva primenu metoda visoke osetljivosti i selektivnosti. Istraživanje je sprovedeno u cilju iznalaženja optimalnih eksperimentalnih uslova za razdvajanje i određivanje acetamiprida i njegovog metabolita, 6-hlornikotinske kiseline (6-HNK) u uzorcima trešanja, korišćenjem tečne hromatografije sa nizom fotoosetljivin dioda (DAD). Uzorci trešanja su korišćeni da bi se odredila selektivnost, linearnost, tačnost i limit kvantifikacije (LOQ). Tačnost metode je kvantifikovana kroz procenu merne neizvesnosti zasnovanu na podacima validacije metode.",
publisher = "Društvo za zaštitu bilja Srbije 11080 Beograd 80, Nemanjina 6; p.fah 123",
journal = "Zbornik rezimea radova, 12. Simpozijum sa savetovanjem o zaštiti bilja, Zlatibor, 26-30. novembar 2012.",
title = "Procena merne neizvesnosti i validacija metode određivanja acetamiprida i 6-hlornikotinske kiseline u uzorcima trešanja",
pages = "81-80",
url = "https://hdl.handle.net/21.15107/rcub_fiver_3709"
}
Lazić, S., Grahovac, N., Šunjka, D., Jakšić, S.,& Ljubojević, M.. (2012). Procena merne neizvesnosti i validacija metode određivanja acetamiprida i 6-hlornikotinske kiseline u uzorcima trešanja. in Zbornik rezimea radova, 12. Simpozijum sa savetovanjem o zaštiti bilja, Zlatibor, 26-30. novembar 2012.
Društvo za zaštitu bilja Srbije 11080 Beograd 80, Nemanjina 6; p.fah 123., 80-81.
https://hdl.handle.net/21.15107/rcub_fiver_3709
Lazić S, Grahovac N, Šunjka D, Jakšić S, Ljubojević M. Procena merne neizvesnosti i validacija metode određivanja acetamiprida i 6-hlornikotinske kiseline u uzorcima trešanja. in Zbornik rezimea radova, 12. Simpozijum sa savetovanjem o zaštiti bilja, Zlatibor, 26-30. novembar 2012.. 2012;:80-81.
https://hdl.handle.net/21.15107/rcub_fiver_3709 .
Lazić, S., Grahovac, Nada, Šunjka, D., Jakšić, Snežana, Ljubojević, M., "Procena merne neizvesnosti i validacija metode određivanja acetamiprida i 6-hlornikotinske kiseline u uzorcima trešanja" in Zbornik rezimea radova, 12. Simpozijum sa savetovanjem o zaštiti bilja, Zlatibor, 26-30. novembar 2012. (2012):80-81,
https://hdl.handle.net/21.15107/rcub_fiver_3709 .

Application of liquid chromatography with diode-array detector for determination of acetamiprid and 6-chloronicotinic acid residues in sweet cherry samples

Šunjka, D.; Lazić, S.; Grahovac, Nada; Ljubojević, M.

(Beograd : Društvo za zaštitu bilja Srbije, 2012)

TY  - CONF
AU  - Šunjka, D.
AU  - Lazić, S.
AU  - Grahovac, Nada
AU  - Ljubojević, M.
PY  - 2012
UR  - http://fiver.ifvcns.rs/handle/123456789/3727
AB  - Acetamiprid is a broad-spectrum neonicotinoids insecticide used on a wide range crops, especially fruits. Besides its positive effects, acetamiprid also has been posing various health risks to consumers. Due to the growing use of insecticides from the family of neonicotinoids, their increased presence in the environment is evident. For this reason, the concentration of acetamiprid residues, including its metabolite 6-chloronicotinic acid, in agricultural products should be monitored.
A rapid and simple method for the confirmation, simultaneous analysis and quantification of acetamiprid and 6-chloronicotinic acid as intermediate of acetamiprid decomposition in sweet cherry samples has been developed. This residue analysis method is based on the reversed phase separation on C18 column with gradient elution. Analytes’ determination and quantification were performed by high performance _ liquid chromatography (HPLC) with photodiodes detection and chromatograms were extracted at 230nm. Extraction efficiency experiments demonstrated the ability of this method to extract neonicotinoids from sweet cherry samples. These insecticides were extracted with mixture acetonitril/0.1N ammonium-chloride (8/2, v/v). The extract was filtered through layer of celit and evaporated, the residue dissolved with acetone and then analyzed by liquid chromatography. The standard addition method was used for acetamiprid and 6-chloronicotinic acid determination in order to eliminate the matrix effect. Sweet cherry samples spiked with the concentration levels of 0.5mg/kg and 1mg/kg was used to ensure method accuracy (recovery) and data precision. The repeatability of the retention times and peak areas were checked by injecting the standard mixture of acetamiprid and 6-chloronicotinic acid solution five times. Average recoveries of acetamiprid and 6-chlornicotinic acid from sweet cherry samples were in the range of 95-101% and 73-83%, respectively with the associated relative standard deviations (RSDs) < 5%. Limit of detection (LOD) for the analyzed acetamiprid and 6-chloronicotinic acid was estimated from fortified samples. The limit of quantification (LOQ) was 10 and 30u9/kg for acetamiprid and 6-chloronicotinic acid, respectively. Thus, it can be concluded that the developed HPLC-DAD method represents a useful tool for a sensitive and rapid determination of acetamiprid and 6-chloronicotinic acid. Hence, the method may find further application in the analysis of real sweet cherry samples contaminated with these insecticides at a ppb level.
PB  - Beograd : Društvo za zaštitu bilja Srbije
C3  - Annual MGPR Meeting 2012 and International Conference on Food and Health Safety: Moving Towards a Sustainable Agriculture, Belgrade, 11 October 2012
T1  - Application of liquid chromatography with diode-array detector for determination of acetamiprid and 6-chloronicotinic acid residues in sweet cherry samples
EP  - 65
SP  - 65
UR  - https://hdl.handle.net/21.15107/rcub_fiver_3727
ER  - 
@conference{
author = "Šunjka, D. and Lazić, S. and Grahovac, Nada and Ljubojević, M.",
year = "2012",
abstract = "Acetamiprid is a broad-spectrum neonicotinoids insecticide used on a wide range crops, especially fruits. Besides its positive effects, acetamiprid also has been posing various health risks to consumers. Due to the growing use of insecticides from the family of neonicotinoids, their increased presence in the environment is evident. For this reason, the concentration of acetamiprid residues, including its metabolite 6-chloronicotinic acid, in agricultural products should be monitored.
A rapid and simple method for the confirmation, simultaneous analysis and quantification of acetamiprid and 6-chloronicotinic acid as intermediate of acetamiprid decomposition in sweet cherry samples has been developed. This residue analysis method is based on the reversed phase separation on C18 column with gradient elution. Analytes’ determination and quantification were performed by high performance _ liquid chromatography (HPLC) with photodiodes detection and chromatograms were extracted at 230nm. Extraction efficiency experiments demonstrated the ability of this method to extract neonicotinoids from sweet cherry samples. These insecticides were extracted with mixture acetonitril/0.1N ammonium-chloride (8/2, v/v). The extract was filtered through layer of celit and evaporated, the residue dissolved with acetone and then analyzed by liquid chromatography. The standard addition method was used for acetamiprid and 6-chloronicotinic acid determination in order to eliminate the matrix effect. Sweet cherry samples spiked with the concentration levels of 0.5mg/kg and 1mg/kg was used to ensure method accuracy (recovery) and data precision. The repeatability of the retention times and peak areas were checked by injecting the standard mixture of acetamiprid and 6-chloronicotinic acid solution five times. Average recoveries of acetamiprid and 6-chlornicotinic acid from sweet cherry samples were in the range of 95-101% and 73-83%, respectively with the associated relative standard deviations (RSDs) < 5%. Limit of detection (LOD) for the analyzed acetamiprid and 6-chloronicotinic acid was estimated from fortified samples. The limit of quantification (LOQ) was 10 and 30u9/kg for acetamiprid and 6-chloronicotinic acid, respectively. Thus, it can be concluded that the developed HPLC-DAD method represents a useful tool for a sensitive and rapid determination of acetamiprid and 6-chloronicotinic acid. Hence, the method may find further application in the analysis of real sweet cherry samples contaminated with these insecticides at a ppb level.",
publisher = "Beograd : Društvo za zaštitu bilja Srbije",
journal = "Annual MGPR Meeting 2012 and International Conference on Food and Health Safety: Moving Towards a Sustainable Agriculture, Belgrade, 11 October 2012",
title = "Application of liquid chromatography with diode-array detector for determination of acetamiprid and 6-chloronicotinic acid residues in sweet cherry samples",
pages = "65-65",
url = "https://hdl.handle.net/21.15107/rcub_fiver_3727"
}
Šunjka, D., Lazić, S., Grahovac, N.,& Ljubojević, M.. (2012). Application of liquid chromatography with diode-array detector for determination of acetamiprid and 6-chloronicotinic acid residues in sweet cherry samples. in Annual MGPR Meeting 2012 and International Conference on Food and Health Safety: Moving Towards a Sustainable Agriculture, Belgrade, 11 October 2012
Beograd : Društvo za zaštitu bilja Srbije., 65-65.
https://hdl.handle.net/21.15107/rcub_fiver_3727
Šunjka D, Lazić S, Grahovac N, Ljubojević M. Application of liquid chromatography with diode-array detector for determination of acetamiprid and 6-chloronicotinic acid residues in sweet cherry samples. in Annual MGPR Meeting 2012 and International Conference on Food and Health Safety: Moving Towards a Sustainable Agriculture, Belgrade, 11 October 2012. 2012;:65-65.
https://hdl.handle.net/21.15107/rcub_fiver_3727 .
Šunjka, D., Lazić, S., Grahovac, Nada, Ljubojević, M., "Application of liquid chromatography with diode-array detector for determination of acetamiprid and 6-chloronicotinic acid residues in sweet cherry samples" in Annual MGPR Meeting 2012 and International Conference on Food and Health Safety: Moving Towards a Sustainable Agriculture, Belgrade, 11 October 2012 (2012):65-65,
https://hdl.handle.net/21.15107/rcub_fiver_3727 .

Determination of chlorpyrifos in water used for agricultural production

Lazić, S.; Šunjka, D.; Grahovac, Nada; Vuković, S.; Jakšić, Snežana

(2011)

TY  - JOUR
AU  - Lazić, S.
AU  - Šunjka, D.
AU  - Grahovac, Nada
AU  - Vuković, S.
AU  - Jakšić, Snežana
PY  - 2011
UR  - http://fiver.ifvcns.rs/handle/123456789/3718
AB  - The quality of the water for irrigation in conventional, but especially in
organic food production is very important. The presence of pesticide residues in
water may cause yield reduction and decrease product quality, due to its uptake.
Chlorpyrifos is one of the most widely used insecticide in the world and it ts
detected in surface and groundwaters more frequently than any other
organophosphorus insecticide. Also, chlorpyrifos is one of the most important
water pollutants (EU Directive 2008/105/EC).
The aim of this study was determination of chlorpyrifos in river and
ground water, wich are widely used for irrigation in agricultural production. The
Extraction of chlorpyrifos was performed using ENVI C18 SP disc (47 mm).
Prior to the extraction disc was conditioned with 5 ml of acetonitrile/methanol
(50/50, v/v) and 5 ml deionized water. Under vacuum 500 ml of river and ground
water with added chlorpyrifos standard solutions in concentration 0.01-1.0 ug ml
', was filtered through the disc. Disc was being dried at 25°C for I h.
Chlorpyrifos was eluted with 6 ml (23 ml) of acetonitrile/methanol (50/50, v/v)
mixture and evaporated to dryness. The extract was diluted in 2 ml of
acetonitrile/methanol (50/50, v/v). Analysis was performed with a Hewlett—
Packard (HP) model 5890 Series II gas chromatograph with EC Ni®’ detector.
Determination conditions were — t °C of column 190 °C with an increase of 30°C
min’! up to 275°C, t°C of injector 230°C and t°C of detector 300°C. The linearity
of the method was evaluated by chromatographing chlorpyrifos solution in
concentrations 0.001-1.0 pg mI'. Correlation coefficient (R°) was 0.995 and limit
of detection (LOD) and limit of quantification (LOQ) were 0.004 pg ml! and
0.01 wg mI', respectively. The average recovery for river water was 87.5% and
for groundwater 97.9%.
T2  - Poljoprivreda i šumarstvo
T1  - Determination of chlorpyrifos in water used for agricultural production
EP  - 25
IS  - 4
SP  - 17
VL  - 57
UR  - https://hdl.handle.net/21.15107/rcub_fiver_3718
ER  - 
@article{
author = "Lazić, S. and Šunjka, D. and Grahovac, Nada and Vuković, S. and Jakšić, Snežana",
year = "2011",
abstract = "The quality of the water for irrigation in conventional, but especially in
organic food production is very important. The presence of pesticide residues in
water may cause yield reduction and decrease product quality, due to its uptake.
Chlorpyrifos is one of the most widely used insecticide in the world and it ts
detected in surface and groundwaters more frequently than any other
organophosphorus insecticide. Also, chlorpyrifos is one of the most important
water pollutants (EU Directive 2008/105/EC).
The aim of this study was determination of chlorpyrifos in river and
ground water, wich are widely used for irrigation in agricultural production. The
Extraction of chlorpyrifos was performed using ENVI C18 SP disc (47 mm).
Prior to the extraction disc was conditioned with 5 ml of acetonitrile/methanol
(50/50, v/v) and 5 ml deionized water. Under vacuum 500 ml of river and ground
water with added chlorpyrifos standard solutions in concentration 0.01-1.0 ug ml
', was filtered through the disc. Disc was being dried at 25°C for I h.
Chlorpyrifos was eluted with 6 ml (23 ml) of acetonitrile/methanol (50/50, v/v)
mixture and evaporated to dryness. The extract was diluted in 2 ml of
acetonitrile/methanol (50/50, v/v). Analysis was performed with a Hewlett—
Packard (HP) model 5890 Series II gas chromatograph with EC Ni®’ detector.
Determination conditions were — t °C of column 190 °C with an increase of 30°C
min’! up to 275°C, t°C of injector 230°C and t°C of detector 300°C. The linearity
of the method was evaluated by chromatographing chlorpyrifos solution in
concentrations 0.001-1.0 pg mI'. Correlation coefficient (R°) was 0.995 and limit
of detection (LOD) and limit of quantification (LOQ) were 0.004 pg ml! and
0.01 wg mI', respectively. The average recovery for river water was 87.5% and
for groundwater 97.9%.",
journal = "Poljoprivreda i šumarstvo",
title = "Determination of chlorpyrifos in water used for agricultural production",
pages = "25-17",
number = "4",
volume = "57",
url = "https://hdl.handle.net/21.15107/rcub_fiver_3718"
}
Lazić, S., Šunjka, D., Grahovac, N., Vuković, S.,& Jakšić, S.. (2011). Determination of chlorpyrifos in water used for agricultural production. in Poljoprivreda i šumarstvo, 57(4), 17-25.
https://hdl.handle.net/21.15107/rcub_fiver_3718
Lazić S, Šunjka D, Grahovac N, Vuković S, Jakšić S. Determination of chlorpyrifos in water used for agricultural production. in Poljoprivreda i šumarstvo. 2011;57(4):17-25.
https://hdl.handle.net/21.15107/rcub_fiver_3718 .
Lazić, S., Šunjka, D., Grahovac, Nada, Vuković, S., Jakšić, Snežana, "Determination of chlorpyrifos in water used for agricultural production" in Poljoprivreda i šumarstvo, 57, no. 4 (2011):17-25,
https://hdl.handle.net/21.15107/rcub_fiver_3718 .

Pesticide residues in apple samples on the market of Republic of Serbia 2004-2007

Lazić, S.; Pucarevic, M.; Bursić, V.; Ostojić, Nada; Vuković, S.

(2009)

TY  - JOUR
AU  - Lazić, S.
AU  - Pucarevic, M.
AU  - Bursić, V.
AU  - Ostojić, Nada
AU  - Vuković, S.
PY  - 2009
UR  - http://fiver.ifvcns.rs/handle/123456789/3716
AB  - Our study comprised the determination of the pesticide residue content in 108 samples of
apples. The pesticide residues were determined by gas chromatography with NPD, ECD and GLC - MS.
The samples were iested for the content of 75 pesticides with LOD of 0.001 to 0.005 mg/kg which were
lower than MRLs according to the EU standards. The relative standard deviation was lower than 19% for
all the tested compounds. In the apple samples taken during 2004, the percentage of the samples positive to the pesticide residue content was 51.85% and the most frequent contaminants were *} HCH and
endosulfan. In the analyzed samples, taken during 2005, out of 70.91% samples in which the pesticide
residues were detected, endosulfan was present in 41.03%, captan in 35.9%, chlorpyrifos in 20.51% and
parathion in 17.95%. The content of the procymidone and lambda-cyhalothrin residues were over the EU
MALs. During 2006 all apple samples were residue-free. Out of 13 samples analyzed in 2007, five contained the pesticide residues below the EU MRLs with the most frequently detected dithiocarbamate.
T2  - Plant Science (Bulgaria)
T1  - Pesticide residues in apple samples on the market of Republic of Serbia 2004-2007
EP  - 310
IS  - 4
SP  - 306
VL  - 46
UR  - https://hdl.handle.net/21.15107/rcub_fiver_3716
ER  - 
@article{
author = "Lazić, S. and Pucarevic, M. and Bursić, V. and Ostojić, Nada and Vuković, S.",
year = "2009",
abstract = "Our study comprised the determination of the pesticide residue content in 108 samples of
apples. The pesticide residues were determined by gas chromatography with NPD, ECD and GLC - MS.
The samples were iested for the content of 75 pesticides with LOD of 0.001 to 0.005 mg/kg which were
lower than MRLs according to the EU standards. The relative standard deviation was lower than 19% for
all the tested compounds. In the apple samples taken during 2004, the percentage of the samples positive to the pesticide residue content was 51.85% and the most frequent contaminants were *} HCH and
endosulfan. In the analyzed samples, taken during 2005, out of 70.91% samples in which the pesticide
residues were detected, endosulfan was present in 41.03%, captan in 35.9%, chlorpyrifos in 20.51% and
parathion in 17.95%. The content of the procymidone and lambda-cyhalothrin residues were over the EU
MALs. During 2006 all apple samples were residue-free. Out of 13 samples analyzed in 2007, five contained the pesticide residues below the EU MRLs with the most frequently detected dithiocarbamate.",
journal = "Plant Science (Bulgaria)",
title = "Pesticide residues in apple samples on the market of Republic of Serbia 2004-2007",
pages = "310-306",
number = "4",
volume = "46",
url = "https://hdl.handle.net/21.15107/rcub_fiver_3716"
}
Lazić, S., Pucarevic, M., Bursić, V., Ostojić, N.,& Vuković, S.. (2009). Pesticide residues in apple samples on the market of Republic of Serbia 2004-2007. in Plant Science (Bulgaria), 46(4), 306-310.
https://hdl.handle.net/21.15107/rcub_fiver_3716
Lazić S, Pucarevic M, Bursić V, Ostojić N, Vuković S. Pesticide residues in apple samples on the market of Republic of Serbia 2004-2007. in Plant Science (Bulgaria). 2009;46(4):306-310.
https://hdl.handle.net/21.15107/rcub_fiver_3716 .
Lazić, S., Pucarevic, M., Bursić, V., Ostojić, Nada, Vuković, S., "Pesticide residues in apple samples on the market of Republic of Serbia 2004-2007" in Plant Science (Bulgaria), 46, no. 4 (2009):306-310,
https://hdl.handle.net/21.15107/rcub_fiver_3716 .