Jovanov, Pavle

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orcid::0000-0002-6225-2655
  • Jovanov, Pavle (3)
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Author's Bibliography

Determination of the acetamiprid residues in selected vegetables and fruit

Lazić, Sanja; Šunjka, Dragana; Jovanov, Pavle; Grahovac, Nada; Mojašević, Milica; Stojanović, Irena

(Belgrade : Plant Protection Society of Serbia, 2015)

TY  - CONF
AU  - Lazić, Sanja
AU  - Šunjka, Dragana
AU  - Jovanov, Pavle
AU  - Grahovac, Nada
AU  - Mojašević, Milica
AU  - Stojanović, Irena
PY  - 2015
UR  - http://fiver.ifvcns.rs/handle/123456789/3310
AB  - Increased use of pesticides has resulted in contamination of the environment causing
also many associated long-term effects on human health. Therefore, validated analytical
methods that produce reliable results for the assessment of pesticide residues in fruits
and vegetables are highly needed. The main objective of this study was validation of
the method for the analysis of acetamiprid in tomato and determination of its residues
after the application at recommended rates under controlled conditions. Obtained
results of acetamiprid half-life in tomato are compared with DTso in sweet cherry. For
sample pre-treatment QUEChERS procedure was used. Insecticide determination and
quantification were performed by HPLC with diode-array detection (Agilent 1100 Series)
and Zorbax Eclipse C18 column (50 mm x 4.6 mm internal diameter, 1.8 pm particle size)
This method fulfilled validation criteria described in the European Union guidelines (SANCO
12571/2013), by evaluating the accuracy, precision, linearity, limit of detection (LOD) and
limit of quantification (LOQ), as well as matrix-effect (ME), The accuracy and precision were
satisfactory, showing mean recovery values higher than 80% and precision below 20%,
in all cases. The validated method was applied for the analysis of acetamiprid residues in
real samples. Half-life of acetamiprid in tomato was 4.33 day and it is quite similar to DT,
obtained in the experiment with sweet cherries. On the sixth day after the acetamiprid
application residues in tornato were at MRL level, as well as in sweet cherries (according
to Serbian MRL, 2010), while the PHI was 14 days
PB  - Belgrade : Plant Protection Society of Serbia
C3  - Proceedings, 7th Congress on Plant Protection "Integrated Plant Protection – a Knowledge-Based Step towards Sustainable Agriculture, Forestry and Landscape Architecture", 24-28 November 2014, Zlatibor, 2015
T1  - Determination of the acetamiprid residues in selected vegetables and fruit
EP  - 348
SP  - 343
UR  - https://hdl.handle.net/21.15107/rcub_fiver_3310
ER  - 
@conference{
author = "Lazić, Sanja and Šunjka, Dragana and Jovanov, Pavle and Grahovac, Nada and Mojašević, Milica and Stojanović, Irena",
year = "2015",
abstract = "Increased use of pesticides has resulted in contamination of the environment causing
also many associated long-term effects on human health. Therefore, validated analytical
methods that produce reliable results for the assessment of pesticide residues in fruits
and vegetables are highly needed. The main objective of this study was validation of
the method for the analysis of acetamiprid in tomato and determination of its residues
after the application at recommended rates under controlled conditions. Obtained
results of acetamiprid half-life in tomato are compared with DTso in sweet cherry. For
sample pre-treatment QUEChERS procedure was used. Insecticide determination and
quantification were performed by HPLC with diode-array detection (Agilent 1100 Series)
and Zorbax Eclipse C18 column (50 mm x 4.6 mm internal diameter, 1.8 pm particle size)
This method fulfilled validation criteria described in the European Union guidelines (SANCO
12571/2013), by evaluating the accuracy, precision, linearity, limit of detection (LOD) and
limit of quantification (LOQ), as well as matrix-effect (ME), The accuracy and precision were
satisfactory, showing mean recovery values higher than 80% and precision below 20%,
in all cases. The validated method was applied for the analysis of acetamiprid residues in
real samples. Half-life of acetamiprid in tomato was 4.33 day and it is quite similar to DT,
obtained in the experiment with sweet cherries. On the sixth day after the acetamiprid
application residues in tornato were at MRL level, as well as in sweet cherries (according
to Serbian MRL, 2010), while the PHI was 14 days",
publisher = "Belgrade : Plant Protection Society of Serbia",
journal = "Proceedings, 7th Congress on Plant Protection "Integrated Plant Protection – a Knowledge-Based Step towards Sustainable Agriculture, Forestry and Landscape Architecture", 24-28 November 2014, Zlatibor, 2015",
title = "Determination of the acetamiprid residues in selected vegetables and fruit",
pages = "348-343",
url = "https://hdl.handle.net/21.15107/rcub_fiver_3310"
}
Lazić, S., Šunjka, D., Jovanov, P., Grahovac, N., Mojašević, M.,& Stojanović, I.. (2015). Determination of the acetamiprid residues in selected vegetables and fruit. in Proceedings, 7th Congress on Plant Protection "Integrated Plant Protection – a Knowledge-Based Step towards Sustainable Agriculture, Forestry and Landscape Architecture", 24-28 November 2014, Zlatibor, 2015
Belgrade : Plant Protection Society of Serbia., 343-348.
https://hdl.handle.net/21.15107/rcub_fiver_3310
Lazić S, Šunjka D, Jovanov P, Grahovac N, Mojašević M, Stojanović I. Determination of the acetamiprid residues in selected vegetables and fruit. in Proceedings, 7th Congress on Plant Protection "Integrated Plant Protection – a Knowledge-Based Step towards Sustainable Agriculture, Forestry and Landscape Architecture", 24-28 November 2014, Zlatibor, 2015. 2015;:343-348.
https://hdl.handle.net/21.15107/rcub_fiver_3310 .
Lazić, Sanja, Šunjka, Dragana, Jovanov, Pavle, Grahovac, Nada, Mojašević, Milica, Stojanović, Irena, "Determination of the acetamiprid residues in selected vegetables and fruit" in Proceedings, 7th Congress on Plant Protection "Integrated Plant Protection – a Knowledge-Based Step towards Sustainable Agriculture, Forestry and Landscape Architecture", 24-28 November 2014, Zlatibor, 2015 (2015):343-348,
https://hdl.handle.net/21.15107/rcub_fiver_3310 .

Dissipation rate of acetamiprid in sweet cherries

Lazić, Sanja; Šunjka, Dragana B.; Panić, Srđan; Inđić, Dušanka; Grahovac, Nada; Guzsvány, Valéria; Jovanov, Pavle

(Beograd : Institut za pesticide i zaštitu životne sredine, 2014)

TY  - JOUR
AU  - Lazić, Sanja
AU  - Šunjka, Dragana B.
AU  - Panić, Srđan
AU  - Inđić, Dušanka
AU  - Grahovac, Nada
AU  - Guzsvány, Valéria
AU  - Jovanov, Pavle
PY  - 2014
UR  - http://fiver.ifvcns.rs/handle/123456789/1373
AB  - Degradation of acetamiprid in sweet cherry samples was evaluated at several intervals from the product application until the end of the pre-harvest interval. An orchard of sweet cherries located at Stepanovićevo village near Novi Sad was used in this study. Acetamiprid was applied according to the manufacturer's recommendation for protecting sweet cherries from their most important pests. Sweet cherry fruit samples were collected at eight intervals: immediately after acetamiprid application and 2, 4, 6, 8, 10, 12 and 14 days after application. The extraction of acetamiprid from sweet cherry samples was performed using a QuEChERS-based method. Determination was carried out using an HPLC-UV diode array detection system (Agilent 1100, United States) with an Agilent Zorbax Eclipse C18 column (50 mm × 4.6 mm internal diameter, 1.8 μm particle size). The method was subjected to a thorough validation procedure. The recovery data were obtained by spiking blank sweet cherry samples at three concentration levels (0.1-0.3 mg/ kg), yielding 85.4% average recovery. Precision values expressed as relative standard deviation (RSD) were below 1.61% for the intraday precision. Acetamiprid showed linear calibrations from 0.05 to 2.5 μg/ml with correlation coefficient (R2) of 0.995%. The limit of detection and limit of quantification were found to be 5 μg/kg and 14 μg/kg, respectively. The validated method was applied in the analysis of acetamiprid in sweet cherry samples. During the study period, the concentration of acetamiprid decreased from 0.529 mg/kg to 0.111 mg/kg. The content of acetamiprid in sweet cherry samples at the end of the pre-harvest interval was below the maximum permissible level specified by the Serbian and EU MRLs.
AB  - U cilju praćenja razgradnje acetamiprida u plodovima trešanja u periodu od primene preparata do isteka karence, izvršen je tretman preparatom na bazi ove aktivne materije u preporučenoj dozi. Ogled je postavljen u zasadu srednje kasne sorte trešnje na lokalitetu Stepanovićevo u okolini Novog Sada. Plodovi su uzorkovani osam puta - odmah nakon primene preparata, 2, 4, 6, 8, 10, 12 i 14 dana. Ekstrakcija acetamiprida iz trešanja izvedena je QuEChERS metodom. Za određivanje acetamiprida korišćena je tečna hromatografija sa DAD detektorom (Agilent 1100, United States) i Agilent Zorbax Eclipse C18 kolonom (unutrašnji prečnik 50 mm x 4.6 mm, veličina čestica 1.8 μm). Kao mobilna faza upotrebljeni su acetonitril i 1.5% rastvor CH3COOH (30/70), sa protokom 1 ml/min, temperaturom kolone 25 oC i injektovanom zapreminom 2,5 μl, dok je kao odgovarajuća talasna dužina usvojena vrednost od 254 nm. Validacija metode je u potpunosti sprovedena u skladu sa zahtevima standarda SANCO/12495/2011 (EU Commission Health and Consumer Protection Directorate- General, 2011). Prosečna vrednost prinosa ekstrakcije acetamiprida iz trešanja proverena na tri nivoa obogaćenja (0.1-0.3 mg/kg) iznosila je 85.4%. Preciznost merenja razmotrena proverom ponovljivosti određivanja acetamiprida izražena je relativnom standardnom devijacijom (RSD) sa vrednošću manjom od 1.61%. U opsegu masenih koncentracija acetamiprida od 0,05 do 2,5 μg/ml postignuta je dobra linearnost odziva detektora sa koeficijentom varijacije od 0,995%. Limit detekcije i kvantifikacije za određivanje acetamiprida u trešnjama prikazanom metodom iznose 5 μg/kg i 14 μg/kg. Tokom ispitivanog perioda koncentracija acetamiprida u trešnjama se smanjivala od 0,592 mg/kg neposredno nakon primene insekticida do 0,111 mg/kg po isteku karence od 14 dana. Analizom je utvrđeno da je sadržaj acetamiprida u uzorcima plodova trešnje nakon isteka perioda karence ispod maksimalno dozvoljene količine za ovu aktivnu materiju propisane Pravilnikom Republike Srbije (0,2 mg/kg) i Evropske Unije (1,5 mg/kg).
PB  - Beograd : Institut za pesticide i zaštitu životne sredine
PB  - Beograd : Društvo za zaštitu bilja Srbije
T2  - Pesticidi i fitomedicina
T1  - Dissipation rate of acetamiprid in sweet cherries
T1  - Razgradnja acetamiprida u plodovima trešanja
EP  - 82
IS  - 1
SP  - 75
VL  - 29
DO  - 10.2298/PIF1401075L
ER  - 
@article{
author = "Lazić, Sanja and Šunjka, Dragana B. and Panić, Srđan and Inđić, Dušanka and Grahovac, Nada and Guzsvány, Valéria and Jovanov, Pavle",
year = "2014",
abstract = "Degradation of acetamiprid in sweet cherry samples was evaluated at several intervals from the product application until the end of the pre-harvest interval. An orchard of sweet cherries located at Stepanovićevo village near Novi Sad was used in this study. Acetamiprid was applied according to the manufacturer's recommendation for protecting sweet cherries from their most important pests. Sweet cherry fruit samples were collected at eight intervals: immediately after acetamiprid application and 2, 4, 6, 8, 10, 12 and 14 days after application. The extraction of acetamiprid from sweet cherry samples was performed using a QuEChERS-based method. Determination was carried out using an HPLC-UV diode array detection system (Agilent 1100, United States) with an Agilent Zorbax Eclipse C18 column (50 mm × 4.6 mm internal diameter, 1.8 μm particle size). The method was subjected to a thorough validation procedure. The recovery data were obtained by spiking blank sweet cherry samples at three concentration levels (0.1-0.3 mg/ kg), yielding 85.4% average recovery. Precision values expressed as relative standard deviation (RSD) were below 1.61% for the intraday precision. Acetamiprid showed linear calibrations from 0.05 to 2.5 μg/ml with correlation coefficient (R2) of 0.995%. The limit of detection and limit of quantification were found to be 5 μg/kg and 14 μg/kg, respectively. The validated method was applied in the analysis of acetamiprid in sweet cherry samples. During the study period, the concentration of acetamiprid decreased from 0.529 mg/kg to 0.111 mg/kg. The content of acetamiprid in sweet cherry samples at the end of the pre-harvest interval was below the maximum permissible level specified by the Serbian and EU MRLs., U cilju praćenja razgradnje acetamiprida u plodovima trešanja u periodu od primene preparata do isteka karence, izvršen je tretman preparatom na bazi ove aktivne materije u preporučenoj dozi. Ogled je postavljen u zasadu srednje kasne sorte trešnje na lokalitetu Stepanovićevo u okolini Novog Sada. Plodovi su uzorkovani osam puta - odmah nakon primene preparata, 2, 4, 6, 8, 10, 12 i 14 dana. Ekstrakcija acetamiprida iz trešanja izvedena je QuEChERS metodom. Za određivanje acetamiprida korišćena je tečna hromatografija sa DAD detektorom (Agilent 1100, United States) i Agilent Zorbax Eclipse C18 kolonom (unutrašnji prečnik 50 mm x 4.6 mm, veličina čestica 1.8 μm). Kao mobilna faza upotrebljeni su acetonitril i 1.5% rastvor CH3COOH (30/70), sa protokom 1 ml/min, temperaturom kolone 25 oC i injektovanom zapreminom 2,5 μl, dok je kao odgovarajuća talasna dužina usvojena vrednost od 254 nm. Validacija metode je u potpunosti sprovedena u skladu sa zahtevima standarda SANCO/12495/2011 (EU Commission Health and Consumer Protection Directorate- General, 2011). Prosečna vrednost prinosa ekstrakcije acetamiprida iz trešanja proverena na tri nivoa obogaćenja (0.1-0.3 mg/kg) iznosila je 85.4%. Preciznost merenja razmotrena proverom ponovljivosti određivanja acetamiprida izražena je relativnom standardnom devijacijom (RSD) sa vrednošću manjom od 1.61%. U opsegu masenih koncentracija acetamiprida od 0,05 do 2,5 μg/ml postignuta je dobra linearnost odziva detektora sa koeficijentom varijacije od 0,995%. Limit detekcije i kvantifikacije za određivanje acetamiprida u trešnjama prikazanom metodom iznose 5 μg/kg i 14 μg/kg. Tokom ispitivanog perioda koncentracija acetamiprida u trešnjama se smanjivala od 0,592 mg/kg neposredno nakon primene insekticida do 0,111 mg/kg po isteku karence od 14 dana. Analizom je utvrđeno da je sadržaj acetamiprida u uzorcima plodova trešnje nakon isteka perioda karence ispod maksimalno dozvoljene količine za ovu aktivnu materiju propisane Pravilnikom Republike Srbije (0,2 mg/kg) i Evropske Unije (1,5 mg/kg).",
publisher = "Beograd : Institut za pesticide i zaštitu životne sredine, Beograd : Društvo za zaštitu bilja Srbije",
journal = "Pesticidi i fitomedicina",
title = "Dissipation rate of acetamiprid in sweet cherries, Razgradnja acetamiprida u plodovima trešanja",
pages = "82-75",
number = "1",
volume = "29",
doi = "10.2298/PIF1401075L"
}
Lazić, S., Šunjka, D. B., Panić, S., Inđić, D., Grahovac, N., Guzsvány, V.,& Jovanov, P.. (2014). Dissipation rate of acetamiprid in sweet cherries. in Pesticidi i fitomedicina
Beograd : Institut za pesticide i zaštitu životne sredine., 29(1), 75-82.
https://doi.org/10.2298/PIF1401075L
Lazić S, Šunjka DB, Panić S, Inđić D, Grahovac N, Guzsvány V, Jovanov P. Dissipation rate of acetamiprid in sweet cherries. in Pesticidi i fitomedicina. 2014;29(1):75-82.
doi:10.2298/PIF1401075L .
Lazić, Sanja, Šunjka, Dragana B., Panić, Srđan, Inđić, Dušanka, Grahovac, Nada, Guzsvány, Valéria, Jovanov, Pavle, "Dissipation rate of acetamiprid in sweet cherries" in Pesticidi i fitomedicina, 29, no. 1 (2014):75-82,
https://doi.org/10.2298/PIF1401075L . .
10

Determination of pesticide residues in drainage water

Lazić, Sanja; Šunjka, Dragana B.; Milovanović, I.; Jovanov, Pavle; Grahovac, Nada

(Global Nest, Secretariat, Athens, 2013)

TY  - CONF
AU  - Lazić, Sanja
AU  - Šunjka, Dragana B.
AU  - Milovanović, I.
AU  - Jovanov, Pavle
AU  - Grahovac, Nada
PY  - 2013
UR  - http://fiver.ifvcns.rs/handle/123456789/1211
AB  - Pesticides are used worldwide within agriculture to protect crops and ensure the quantity and quality of the harvest. However, intensive and inappropriate pesticides application can directly or indirectly affect different parts of the environment, especially water source. Besides the occurrence of pesticides in drinking water, control of pesticide presence in surface and groundwater is also very important. This primarily refers to the drainage water, river and groundwater, considering the importance of environmental protection and food safety production. The presence of pesticide residues in these matrices may cause yield reduction and decrease product quality, due to its uptake. Objectives of this study included drainage water investigations to identify residue levels of selected pesticides. The sampling was performed during June 2012. Water samples were taken from drainage canals, on twelve sampling points, in intensively cultivated regions of Serbia, Vojvodina Province. Pesticides were chosen based on the European Union Directive 2008/105/EC. This directive by Annex X defines the List of priority substances in the field of water policy. List includes 33 pollutant - 9 are pesticides. The extraction of pesticides from water was performed using 018 ENVI (TM) disc (47 mm). Prior to extraction disc was conditioned with 5 ml of methanol and 5 ml of deionized water. Afterward, water sample was filtered through the disc under vacuum. After drying under vacuum (25 degrees C for 1 h), pesticides were eluted from the disc with 5 ml of mixture of dichloromethane/n-hexane (40/60, v/v) and evaporated to dryness. The extract was dissolved in 1 ml of methanol, ultrasonically homogenized and analyzed. The pesticide residues concentrations analyzed by gas chromatography/electron capture detection with Ni-63. Identification is performed by the use of GC/MS. The mean recovery of this extraction method for all analyzed pesticides at 1 mu g/ml, 0.1 pg/ml and 0.01 pg/ml spiking levels was 93.6%, with associated standard deviations (RSD) of 2.7. The limit of quantification was 0.01 pg/ml. Method accuracy was quantified through measurement uncertainty estimate based on method validation data. The combined relative uncertainty for water samples was 0.481%, while the expanded uncertainty (Us) calculated as U-c=k*U-c, where k is the coverage factor with level of confidence of approximately 95% considering a coverage factor of 2 (EURACHEM/CITAC, 2000), was 0.962%. Obtained values of evaluated analytical parameters are completely in accordance with regulations for analysis of pesticides trace level. Described method was applied for determination of above mentioned pesticides in real water samples. Finally, acetochlor, alachlor and chlorpyrifos were detected in drainage water samples collected in the agricultural area of Serbia.
PB  - Global Nest, Secretariat, Athens
C3  - Proceedings of the 13th International Conference on Environmental Science & Technology
T1  - Determination of pesticide residues in drainage water
UR  - https://hdl.handle.net/21.15107/rcub_fiver_1211
ER  - 
@conference{
author = "Lazić, Sanja and Šunjka, Dragana B. and Milovanović, I. and Jovanov, Pavle and Grahovac, Nada",
year = "2013",
abstract = "Pesticides are used worldwide within agriculture to protect crops and ensure the quantity and quality of the harvest. However, intensive and inappropriate pesticides application can directly or indirectly affect different parts of the environment, especially water source. Besides the occurrence of pesticides in drinking water, control of pesticide presence in surface and groundwater is also very important. This primarily refers to the drainage water, river and groundwater, considering the importance of environmental protection and food safety production. The presence of pesticide residues in these matrices may cause yield reduction and decrease product quality, due to its uptake. Objectives of this study included drainage water investigations to identify residue levels of selected pesticides. The sampling was performed during June 2012. Water samples were taken from drainage canals, on twelve sampling points, in intensively cultivated regions of Serbia, Vojvodina Province. Pesticides were chosen based on the European Union Directive 2008/105/EC. This directive by Annex X defines the List of priority substances in the field of water policy. List includes 33 pollutant - 9 are pesticides. The extraction of pesticides from water was performed using 018 ENVI (TM) disc (47 mm). Prior to extraction disc was conditioned with 5 ml of methanol and 5 ml of deionized water. Afterward, water sample was filtered through the disc under vacuum. After drying under vacuum (25 degrees C for 1 h), pesticides were eluted from the disc with 5 ml of mixture of dichloromethane/n-hexane (40/60, v/v) and evaporated to dryness. The extract was dissolved in 1 ml of methanol, ultrasonically homogenized and analyzed. The pesticide residues concentrations analyzed by gas chromatography/electron capture detection with Ni-63. Identification is performed by the use of GC/MS. The mean recovery of this extraction method for all analyzed pesticides at 1 mu g/ml, 0.1 pg/ml and 0.01 pg/ml spiking levels was 93.6%, with associated standard deviations (RSD) of 2.7. The limit of quantification was 0.01 pg/ml. Method accuracy was quantified through measurement uncertainty estimate based on method validation data. The combined relative uncertainty for water samples was 0.481%, while the expanded uncertainty (Us) calculated as U-c=k*U-c, where k is the coverage factor with level of confidence of approximately 95% considering a coverage factor of 2 (EURACHEM/CITAC, 2000), was 0.962%. Obtained values of evaluated analytical parameters are completely in accordance with regulations for analysis of pesticides trace level. Described method was applied for determination of above mentioned pesticides in real water samples. Finally, acetochlor, alachlor and chlorpyrifos were detected in drainage water samples collected in the agricultural area of Serbia.",
publisher = "Global Nest, Secretariat, Athens",
journal = "Proceedings of the 13th International Conference on Environmental Science & Technology",
title = "Determination of pesticide residues in drainage water",
url = "https://hdl.handle.net/21.15107/rcub_fiver_1211"
}
Lazić, S., Šunjka, D. B., Milovanović, I., Jovanov, P.,& Grahovac, N.. (2013). Determination of pesticide residues in drainage water. in Proceedings of the 13th International Conference on Environmental Science & Technology
Global Nest, Secretariat, Athens..
https://hdl.handle.net/21.15107/rcub_fiver_1211
Lazić S, Šunjka DB, Milovanović I, Jovanov P, Grahovac N. Determination of pesticide residues in drainage water. in Proceedings of the 13th International Conference on Environmental Science & Technology. 2013;.
https://hdl.handle.net/21.15107/rcub_fiver_1211 .
Lazić, Sanja, Šunjka, Dragana B., Milovanović, I., Jovanov, Pavle, Grahovac, Nada, "Determination of pesticide residues in drainage water" in Proceedings of the 13th International Conference on Environmental Science & Technology (2013),
https://hdl.handle.net/21.15107/rcub_fiver_1211 .