Guzsvány, Valéria

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  • Guzsvány, Valéria (3)
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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

Stability test of bentazone and dicamba in water.

Lazić, Sanja; Šunjka, Dragana; Grahovac, Nada; Guzsvány, Valéria

(SZAB Kémiai Szakbizottsag Analitikai és Koernyezetvédelmi Munkabizottsaga, 2013)

TY  - CONF
AU  - Lazić, Sanja
AU  - Šunjka, Dragana
AU  - Grahovac, Nada
AU  - Guzsvány, Valéria
PY  - 2013
UR  - http://fiver.ifvcns.rs/handle/123456789/3302
AB  - A reduction in pesticide effectiveness, in general, may be due to hydrolysis. The rate of hydrolysis is dependent on pH, pesticide chemistry, length of time in the spray tank and water
temperature in the spray tank. The exposure of the spray tank to sunlight will also impact the
rate of hydrolysis. The present work describes stability test of bentazon and dicamba in water
under different conditions, such as pH, presence or absence of sunlight and different
temperatures. Stability of bentazon and dicamba aqueous solution was assessed by exposing
aqueous samples to different temperatures, different pH (4, 7 and 10) and presence or absence
of sunlight. The stability study under laboratory conditions revealed high stability of both
compounds in aqueous solution pH 10, when exposed to sunlight or darkness. Dicamba was
stabile at pH 7, while in aqueous solution pH 3 degraded 30% of initial concentration of
dicamba. Bentazon degraded more that 50% after two weeks at pH 4 and 7.
PB  - SZAB Kémiai Szakbizottsag Analitikai és Koernyezetvédelmi Munkabizottsaga
C3  - Proceedings, 19th International Symposium on Analytical and Environmental Problems, 23 September 2013, Szeged, Hungary
T1  - Stability test of bentazone and dicamba in water.
EP  - 300
SP  - 297
UR  - https://hdl.handle.net/21.15107/rcub_fiver_3302
ER  - 
@conference{
author = "Lazić, Sanja and Šunjka, Dragana and Grahovac, Nada and Guzsvány, Valéria",
year = "2013",
abstract = "A reduction in pesticide effectiveness, in general, may be due to hydrolysis. The rate of hydrolysis is dependent on pH, pesticide chemistry, length of time in the spray tank and water
temperature in the spray tank. The exposure of the spray tank to sunlight will also impact the
rate of hydrolysis. The present work describes stability test of bentazon and dicamba in water
under different conditions, such as pH, presence or absence of sunlight and different
temperatures. Stability of bentazon and dicamba aqueous solution was assessed by exposing
aqueous samples to different temperatures, different pH (4, 7 and 10) and presence or absence
of sunlight. The stability study under laboratory conditions revealed high stability of both
compounds in aqueous solution pH 10, when exposed to sunlight or darkness. Dicamba was
stabile at pH 7, while in aqueous solution pH 3 degraded 30% of initial concentration of
dicamba. Bentazon degraded more that 50% after two weeks at pH 4 and 7.",
publisher = "SZAB Kémiai Szakbizottsag Analitikai és Koernyezetvédelmi Munkabizottsaga",
journal = "Proceedings, 19th International Symposium on Analytical and Environmental Problems, 23 September 2013, Szeged, Hungary",
title = "Stability test of bentazone and dicamba in water.",
pages = "300-297",
url = "https://hdl.handle.net/21.15107/rcub_fiver_3302"
}
Lazić, S., Šunjka, D., Grahovac, N.,& Guzsvány, V.. (2013). Stability test of bentazone and dicamba in water.. in Proceedings, 19th International Symposium on Analytical and Environmental Problems, 23 September 2013, Szeged, Hungary
SZAB Kémiai Szakbizottsag Analitikai és Koernyezetvédelmi Munkabizottsaga., 297-300.
https://hdl.handle.net/21.15107/rcub_fiver_3302
Lazić S, Šunjka D, Grahovac N, Guzsvány V. Stability test of bentazone and dicamba in water.. in Proceedings, 19th International Symposium on Analytical and Environmental Problems, 23 September 2013, Szeged, Hungary. 2013;:297-300.
https://hdl.handle.net/21.15107/rcub_fiver_3302 .
Lazić, Sanja, Šunjka, Dragana, Grahovac, Nada, Guzsvány, Valéria, "Stability test of bentazone and dicamba in water." in Proceedings, 19th International Symposium on Analytical and Environmental Problems, 23 September 2013, Szeged, Hungary (2013):297-300,
https://hdl.handle.net/21.15107/rcub_fiver_3302 .

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

Lazić, Sanja; Šunjka, Dragana B.; Grahovac, Nada; Guzsvány, Valéria; Bagi, Ferenc; Budakov, Dragana

(Institut za pesticide i zaštitu životne sredine, Beograd i Društvo za zaštitu bilja Srbije, Beograd, 2012)

TY  - JOUR
AU  - Lazić, Sanja
AU  - Šunjka, Dragana B.
AU  - Grahovac, Nada
AU  - Guzsvány, Valéria
AU  - Bagi, Ferenc
AU  - Budakov, Dragana
PY  - 2012
UR  - http://fiver.ifvcns.rs/handle/123456789/1131
AB  - A rapid and simple method for simultaneous determination of acetamiprid and its metabolite 6-chloronicotinic acid 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 diode-array detector and chromatograms were extracted at 230 nm. Extraction efficiency experiments demonstrated the ability of this method to extract neonicotinoids from sweet cherry samples. These insecticides were extracted with a mixture of acetonitril/0.1N ammonium-chloride (8/2, v/v). The 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)  lt 5%. Expanded measurement uncertainties for the analyzed compounds were 2.7 and 3.01%. The limit of quantification (LOQ) was 10 μg/kg and 30 μg/kg for acetamiprid and 6-chloronicotinic acid, respectively. Thus, the developed HPLC/DAD method can be considered a useful tool for 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.
AB  - U radu je predstavljena jednostavna metoda za određivanje acetamiprida i njegovog metabolita, 6-hlornikotinske kiseline, u uzorcima trešanja. Metoda je bazirana na primeni reverzno-faznog razdvajanja na C18 koloni primenom gradijentnog eluiranja. Određivanje i kvantifikacija analita je vršena tečnom hromatografijom (HPLC) sa DAD detektorom, pri čemu je korišćena talasna dužina od 230 nm. Tačnost metode je ocenjena procenom merne nesigurnosti. Ekstrakcija acetamiprida i 6-hlornikotinske kiseline iz uzoraka trešanja je vršena smešom acetonitril/amonijum-hlorid (0,1N) u odnosu 80:20 (v/v). Sva merenja su vršena u tri ponavljanja, pri čemu su dobijeni prinosi određivanja acetamiprida i 6-hlornikotinske kiseline u rasponima 95-101% i 73-83%, respektivno. Relativne standardne devijacije (RSD) merenja su u svim slučajevima bile ispod 5%. Limiti kvantifikacije za acetamiprid i 6-HNK iznosili su 10 i 30 μg/kg, respektivno. Kombinovana merna nesigurnost rezultata analize acetamiprida i njegovog metabolita procenjena je na 1,35, odnosno 1,50%, a proširena na 2,7 i 3,01%, upotrebom faktora pokrivanja (k=2) koji odgovara nivou poverenja od 95%, za normalnu raspodelu. Nakon validacije i procene merne neizvesnosti dobijeni rezultati pokazuju da se razvijena HPLC/DAD metoda može primeniti za određivanje sadržaja acetamiprida i 6-hlornikotinske kiseline u uzorcima trešanja i relevantnim matriksima kontaminiranim ovim jedinjenjima.
PB  - Institut za pesticide i zaštitu životne sredine, Beograd i Društvo za zaštitu bilja Srbije, Beograd
T2  - Pesticidi i fitomedicina
T1  - Application of liquid chromatography with diode-array detector for determination of acetamiprid and 6-chloronicotinic acid residues in sweet cherry samples
T1  - Primena tečne hromatografije sa DAD detektorom za određivanje ostataka acetamiprida i 6-hlornikotinske kiseline u uzorcima trešanja
EP  - 329
IS  - 4
SP  - 321
VL  - 27
DO  - 10.2298/PIF1204321L
ER  - 
@article{
author = "Lazić, Sanja and Šunjka, Dragana B. and Grahovac, Nada and Guzsvány, Valéria and Bagi, Ferenc and Budakov, Dragana",
year = "2012",
abstract = "A rapid and simple method for simultaneous determination of acetamiprid and its metabolite 6-chloronicotinic acid 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 diode-array detector and chromatograms were extracted at 230 nm. Extraction efficiency experiments demonstrated the ability of this method to extract neonicotinoids from sweet cherry samples. These insecticides were extracted with a mixture of acetonitril/0.1N ammonium-chloride (8/2, v/v). The 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)  lt 5%. Expanded measurement uncertainties for the analyzed compounds were 2.7 and 3.01%. The limit of quantification (LOQ) was 10 μg/kg and 30 μg/kg for acetamiprid and 6-chloronicotinic acid, respectively. Thus, the developed HPLC/DAD method can be considered a useful tool for 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., U radu je predstavljena jednostavna metoda za određivanje acetamiprida i njegovog metabolita, 6-hlornikotinske kiseline, u uzorcima trešanja. Metoda je bazirana na primeni reverzno-faznog razdvajanja na C18 koloni primenom gradijentnog eluiranja. Određivanje i kvantifikacija analita je vršena tečnom hromatografijom (HPLC) sa DAD detektorom, pri čemu je korišćena talasna dužina od 230 nm. Tačnost metode je ocenjena procenom merne nesigurnosti. Ekstrakcija acetamiprida i 6-hlornikotinske kiseline iz uzoraka trešanja je vršena smešom acetonitril/amonijum-hlorid (0,1N) u odnosu 80:20 (v/v). Sva merenja su vršena u tri ponavljanja, pri čemu su dobijeni prinosi određivanja acetamiprida i 6-hlornikotinske kiseline u rasponima 95-101% i 73-83%, respektivno. Relativne standardne devijacije (RSD) merenja su u svim slučajevima bile ispod 5%. Limiti kvantifikacije za acetamiprid i 6-HNK iznosili su 10 i 30 μg/kg, respektivno. Kombinovana merna nesigurnost rezultata analize acetamiprida i njegovog metabolita procenjena je na 1,35, odnosno 1,50%, a proširena na 2,7 i 3,01%, upotrebom faktora pokrivanja (k=2) koji odgovara nivou poverenja od 95%, za normalnu raspodelu. Nakon validacije i procene merne neizvesnosti dobijeni rezultati pokazuju da se razvijena HPLC/DAD metoda može primeniti za određivanje sadržaja acetamiprida i 6-hlornikotinske kiseline u uzorcima trešanja i relevantnim matriksima kontaminiranim ovim jedinjenjima.",
publisher = "Institut za pesticide i zaštitu životne sredine, Beograd i Društvo za zaštitu bilja Srbije, Beograd",
journal = "Pesticidi i fitomedicina",
title = "Application of liquid chromatography with diode-array detector for determination of acetamiprid and 6-chloronicotinic acid residues in sweet cherry samples, Primena tečne hromatografije sa DAD detektorom za određivanje ostataka acetamiprida i 6-hlornikotinske kiseline u uzorcima trešanja",
pages = "329-321",
number = "4",
volume = "27",
doi = "10.2298/PIF1204321L"
}
Lazić, S., Šunjka, D. B., Grahovac, N., Guzsvány, V., Bagi, F.,& Budakov, D.. (2012). Application of liquid chromatography with diode-array detector for determination of acetamiprid and 6-chloronicotinic acid residues in sweet cherry samples. in Pesticidi i fitomedicina
Institut za pesticide i zaštitu životne sredine, Beograd i Društvo za zaštitu bilja Srbije, Beograd., 27(4), 321-329.
https://doi.org/10.2298/PIF1204321L
Lazić S, Šunjka DB, Grahovac N, Guzsvány V, Bagi F, Budakov D. Application of liquid chromatography with diode-array detector for determination of acetamiprid and 6-chloronicotinic acid residues in sweet cherry samples. in Pesticidi i fitomedicina. 2012;27(4):321-329.
doi:10.2298/PIF1204321L .
Lazić, Sanja, Šunjka, Dragana B., Grahovac, Nada, Guzsvány, Valéria, Bagi, Ferenc, Budakov, Dragana, "Application of liquid chromatography with diode-array detector for determination of acetamiprid and 6-chloronicotinic acid residues in sweet cherry samples" in Pesticidi i fitomedicina, 27, no. 4 (2012):321-329,
https://doi.org/10.2298/PIF1204321L . .
12