Ivanović, Ivana

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  • Ivanović, Ivana (2)
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Author's Bibliography

Development and validation of a solid phase extraction-HPLC method for the determination of carbamazepine and its metabolites, carbamazepine epoxide and carbamazepine trans-diol, in plasma

Džodić, Predrag; Živanović, Ljiljana; Protić, Ana; Ivanović, Ivana; Veličković-Radovanović, Radmila; Spasić, Mirjana; Lukić, Stevo; Živanović, Slavoljub

(Srpsko hemijsko društvo, Beograd, 2012)

TY  - JOUR
AU  - Džodić, Predrag
AU  - Živanović, Ljiljana
AU  - Protić, Ana
AU  - Ivanović, Ivana
AU  - Veličković-Radovanović, Radmila
AU  - Spasić, Mirjana
AU  - Lukić, Stevo
AU  - Živanović, Slavoljub
PY  - 2012
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/1823
AB  - A solid phase extraction-HPLC method has been developed and validated for the rapid analysis of carbamazepine and its two metabolites, carbamazepine epoxide and carbamazepine trans-diol, in human plasma. The analysis was performed using a C18 Bakerbond-BDC analytical column (250 mm×4.6 mm i.d., particle size 5 μm). The optimal conditions for the separation were established with the mobile phase acetonitrile - 10 mM phosphate buffer, pH 7.0 (30:70, v/v) at a flow rate of 1.5 mL min-1 and temperature of 35°C, with UV detection at 210 nm. The total run time was about 8 minutes. The SPE procedure for the extraction of the analytes from a plasma sample was developed using Oasis HLB cartridges and subsequently, the eluate was injected into the HPLC system for analysis. Afterwards, the SPE-HPLC method was subjected to validation. Linearity was obtained over the concentration range of 0.2-25 μg mL-1 for carbamazepine, carbamazepine epoxide and carbamazepine trans-diol, with correlation coefficients higher than 0.995. The method showed good intra-day and inter-day precision with a relative standard deviation below 7.96 %, while the accuracy ranged from 92.09 to 108.5 % for all analytes. Finally, the method was successfully applied to the analysis of the plasma samples of epileptic patients in mono- and polytherapy.
AB  - SPE-HPLC metoda je razvijena i validirana u cilju brzog analiziranja karbamazepina i metabolita karbamazepin epoksida i karbamazepin trans-diola u humanoj plazmi. C18 Bakerbond-BDC analitička kolona (250 mm x 4,6 mm; 5 μm) je korišćena radi izvođenja analize. Optimalni uslovi za hromatografsko razdvajanje su mobilna faza acetonitril - 10 mM fosfatni pufer, pH 7,0 (30:70, v/v), protok od 1,5 ml min-1, temperatura 35°C i detekcija na 210 nm. Ukupno trajanje hromatografskog rana iznosi oko 8 min. SPE procedura za ekstrakciju analita iz uzoraka plazme je razvijena uz korišćenje Oasis HLB ketridža nakon čega se eluat injektuje u HPLC sistem radi analiziranja. Zatim je izvršena validacija SPE-HPLC metode. Linearnost je potvrđena u koncentracionom opsegu 0,2-25 μg/ml za karbamazepin, karbamazepin epoksid i karbamazepin trans-diol sa vrednošću korelacionih koeficijenata višom od 0,995. Preciznost metode u toku jednog i u toku više dana je dobra sa relativnom standardnom devijacijom nižom od 7,96 %, dok tačnost metode obuhvata vrednosti u opsegu od 92,09 do 108,5 % za sve analite. Na kraju je metoda uspešno primenjena u cilju analiziranja uzoraka plazme pacijenata obolelih od epilepsije na monoterapiji i politerapiji.
PB  - Srpsko hemijsko društvo, Beograd
T2  - Journal of the Serbian Chemical Society
T1  - Development and validation of a solid phase extraction-HPLC method for the determination of carbamazepine and its metabolites, carbamazepine epoxide and carbamazepine trans-diol, in plasma
T1  - Razvoj i validacija spe-HPLC metode za određivanje karbamazepina i metabolita karbamazepin epoksida i karbamazepin trans-diola u plazmi
VL  - 77
IS  - 10
SP  - 1423
EP  - 1436
DO  - 10.2298/JSC120106084D
ER  - 
@article{
author = "Džodić, Predrag and Živanović, Ljiljana and Protić, Ana and Ivanović, Ivana and Veličković-Radovanović, Radmila and Spasić, Mirjana and Lukić, Stevo and Živanović, Slavoljub",
year = "2012",
abstract = "A solid phase extraction-HPLC method has been developed and validated for the rapid analysis of carbamazepine and its two metabolites, carbamazepine epoxide and carbamazepine trans-diol, in human plasma. The analysis was performed using a C18 Bakerbond-BDC analytical column (250 mm×4.6 mm i.d., particle size 5 μm). The optimal conditions for the separation were established with the mobile phase acetonitrile - 10 mM phosphate buffer, pH 7.0 (30:70, v/v) at a flow rate of 1.5 mL min-1 and temperature of 35°C, with UV detection at 210 nm. The total run time was about 8 minutes. The SPE procedure for the extraction of the analytes from a plasma sample was developed using Oasis HLB cartridges and subsequently, the eluate was injected into the HPLC system for analysis. Afterwards, the SPE-HPLC method was subjected to validation. Linearity was obtained over the concentration range of 0.2-25 μg mL-1 for carbamazepine, carbamazepine epoxide and carbamazepine trans-diol, with correlation coefficients higher than 0.995. The method showed good intra-day and inter-day precision with a relative standard deviation below 7.96 %, while the accuracy ranged from 92.09 to 108.5 % for all analytes. Finally, the method was successfully applied to the analysis of the plasma samples of epileptic patients in mono- and polytherapy., SPE-HPLC metoda je razvijena i validirana u cilju brzog analiziranja karbamazepina i metabolita karbamazepin epoksida i karbamazepin trans-diola u humanoj plazmi. C18 Bakerbond-BDC analitička kolona (250 mm x 4,6 mm; 5 μm) je korišćena radi izvođenja analize. Optimalni uslovi za hromatografsko razdvajanje su mobilna faza acetonitril - 10 mM fosfatni pufer, pH 7,0 (30:70, v/v), protok od 1,5 ml min-1, temperatura 35°C i detekcija na 210 nm. Ukupno trajanje hromatografskog rana iznosi oko 8 min. SPE procedura za ekstrakciju analita iz uzoraka plazme je razvijena uz korišćenje Oasis HLB ketridža nakon čega se eluat injektuje u HPLC sistem radi analiziranja. Zatim je izvršena validacija SPE-HPLC metode. Linearnost je potvrđena u koncentracionom opsegu 0,2-25 μg/ml za karbamazepin, karbamazepin epoksid i karbamazepin trans-diol sa vrednošću korelacionih koeficijenata višom od 0,995. Preciznost metode u toku jednog i u toku više dana je dobra sa relativnom standardnom devijacijom nižom od 7,96 %, dok tačnost metode obuhvata vrednosti u opsegu od 92,09 do 108,5 % za sve analite. Na kraju je metoda uspešno primenjena u cilju analiziranja uzoraka plazme pacijenata obolelih od epilepsije na monoterapiji i politerapiji.",
publisher = "Srpsko hemijsko društvo, Beograd",
journal = "Journal of the Serbian Chemical Society",
title = "Development and validation of a solid phase extraction-HPLC method for the determination of carbamazepine and its metabolites, carbamazepine epoxide and carbamazepine trans-diol, in plasma, Razvoj i validacija spe-HPLC metode za određivanje karbamazepina i metabolita karbamazepin epoksida i karbamazepin trans-diola u plazmi",
volume = "77",
number = "10",
pages = "1423-1436",
doi = "10.2298/JSC120106084D"
}
Džodić, P., Živanović, L., Protić, A., Ivanović, I., Veličković-Radovanović, R., Spasić, M., Lukić, S.,& Živanović, S.. (2012). Development and validation of a solid phase extraction-HPLC method for the determination of carbamazepine and its metabolites, carbamazepine epoxide and carbamazepine trans-diol, in plasma. in Journal of the Serbian Chemical Society
Srpsko hemijsko društvo, Beograd., 77(10), 1423-1436.
https://doi.org/10.2298/JSC120106084D
Džodić P, Živanović L, Protić A, Ivanović I, Veličković-Radovanović R, Spasić M, Lukić S, Živanović S. Development and validation of a solid phase extraction-HPLC method for the determination of carbamazepine and its metabolites, carbamazepine epoxide and carbamazepine trans-diol, in plasma. in Journal of the Serbian Chemical Society. 2012;77(10):1423-1436.
doi:10.2298/JSC120106084D .
Džodić, Predrag, Živanović, Ljiljana, Protić, Ana, Ivanović, Ivana, Veličković-Radovanović, Radmila, Spasić, Mirjana, Lukić, Stevo, Živanović, Slavoljub, "Development and validation of a solid phase extraction-HPLC method for the determination of carbamazepine and its metabolites, carbamazepine epoxide and carbamazepine trans-diol, in plasma" in Journal of the Serbian Chemical Society, 77, no. 10 (2012):1423-1436,
https://doi.org/10.2298/JSC120106084D . .
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10
12

Using experimental design in optimisation of VIS spektrophotometric method of investigation feroglicin sulfate in Orferon retard tablets

Zečević, Mira; Jocić, Biljana; Ivanović, Ivana

(Savez farmaceutskih udruženja Srbije, Beograd, 2004)

TY  - JOUR
AU  - Zečević, Mira
AU  - Jocić, Biljana
AU  - Ivanović, Ivana
PY  - 2004
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/536
AB  - Iron preparations are used in the treatment or prophylaxis of sideropenic anemia developed due to insuficiency of iron in the body. They can be used orally (tablets, capsules, suspensiones, wines ) and parenterally. The aim of this paper was to use experimental design to optimize a visible (VIS) spektrophotometric method for analyzing feroglicin sulfate in tablet formulations. Traditional approach of step-byspep procedure is time consuming, requires a large number of experiments and optimizes only one factor (experimental conditions) at the time, neglecting other factors as well as potential interaction. Using 23 factor design, a set of planed experiments was performed, and factors that significantly influence the sensitivity of the method were detected and optimized. Optimal experimental conditions have been found and sensitivity and selectivity of the spectrophotometric method have been improved ( 1 ).
AB  - Preparati gvožđa su namenjeni za oralnu upotrebu u obliku tableta, kapsula, suspenzija i vina kao i za parenteralnu upotrebu u obliku injekcija. U ovom radu ispitivane su Orferon retard ® tablete koje sadrže feroglicin sulfat. Sadržaj gvožđa u njima je određivan primenom VIS spektrofotometrijske metode. Eksperimentalni dizajn je korišćen u cilju definisanja optimalnih eksperimentalnih uslova. Uobičajeni način optimizacije ispitivanjem jednog po jednog faktora je neracionalan i sadrži veliki broj nepotrebnih eksperimenata, a takođe ne razmatra uticaje interakcija između faktora. Primenom 23 faktorskog dizajna po određenom matematičko-statističkom modelu pripremljena je serija planiranih eksperimenata i ispitan je uticaj svih značajnih faktora pri čemu je omogućeno da se neki faktori menjaju u isto vreme. Na taj način je omogućeno postavljanje pretpostavki o eksperimentalnim optimumima, čime se mogu poboljšati osetljivost, selektivnost i specifičnost metode (1).
PB  - Savez farmaceutskih udruženja Srbije, Beograd
T2  - Arhiv za farmaciju
T1  - Using experimental design in optimisation of VIS spektrophotometric method of investigation feroglicin sulfate in Orferon retard tablets
T1  - Primena eksperimentalnog dizajna u optimizaciji VIS spektrofotometrijske metode za određivanje feroglicin sulfata u Orferon retard tabletama
VL  - 54
IS  - 1-2
SP  - 51
EP  - 59
UR  - https://hdl.handle.net/21.15107/rcub_farfar_536
ER  - 
@article{
author = "Zečević, Mira and Jocić, Biljana and Ivanović, Ivana",
year = "2004",
abstract = "Iron preparations are used in the treatment or prophylaxis of sideropenic anemia developed due to insuficiency of iron in the body. They can be used orally (tablets, capsules, suspensiones, wines ) and parenterally. The aim of this paper was to use experimental design to optimize a visible (VIS) spektrophotometric method for analyzing feroglicin sulfate in tablet formulations. Traditional approach of step-byspep procedure is time consuming, requires a large number of experiments and optimizes only one factor (experimental conditions) at the time, neglecting other factors as well as potential interaction. Using 23 factor design, a set of planed experiments was performed, and factors that significantly influence the sensitivity of the method were detected and optimized. Optimal experimental conditions have been found and sensitivity and selectivity of the spectrophotometric method have been improved ( 1 )., Preparati gvožđa su namenjeni za oralnu upotrebu u obliku tableta, kapsula, suspenzija i vina kao i za parenteralnu upotrebu u obliku injekcija. U ovom radu ispitivane su Orferon retard ® tablete koje sadrže feroglicin sulfat. Sadržaj gvožđa u njima je određivan primenom VIS spektrofotometrijske metode. Eksperimentalni dizajn je korišćen u cilju definisanja optimalnih eksperimentalnih uslova. Uobičajeni način optimizacije ispitivanjem jednog po jednog faktora je neracionalan i sadrži veliki broj nepotrebnih eksperimenata, a takođe ne razmatra uticaje interakcija između faktora. Primenom 23 faktorskog dizajna po određenom matematičko-statističkom modelu pripremljena je serija planiranih eksperimenata i ispitan je uticaj svih značajnih faktora pri čemu je omogućeno da se neki faktori menjaju u isto vreme. Na taj način je omogućeno postavljanje pretpostavki o eksperimentalnim optimumima, čime se mogu poboljšati osetljivost, selektivnost i specifičnost metode (1).",
publisher = "Savez farmaceutskih udruženja Srbije, Beograd",
journal = "Arhiv za farmaciju",
title = "Using experimental design in optimisation of VIS spektrophotometric method of investigation feroglicin sulfate in Orferon retard tablets, Primena eksperimentalnog dizajna u optimizaciji VIS spektrofotometrijske metode za određivanje feroglicin sulfata u Orferon retard tabletama",
volume = "54",
number = "1-2",
pages = "51-59",
url = "https://hdl.handle.net/21.15107/rcub_farfar_536"
}
Zečević, M., Jocić, B.,& Ivanović, I.. (2004). Using experimental design in optimisation of VIS spektrophotometric method of investigation feroglicin sulfate in Orferon retard tablets. in Arhiv za farmaciju
Savez farmaceutskih udruženja Srbije, Beograd., 54(1-2), 51-59.
https://hdl.handle.net/21.15107/rcub_farfar_536
Zečević M, Jocić B, Ivanović I. Using experimental design in optimisation of VIS spektrophotometric method of investigation feroglicin sulfate in Orferon retard tablets. in Arhiv za farmaciju. 2004;54(1-2):51-59.
https://hdl.handle.net/21.15107/rcub_farfar_536 .
Zečević, Mira, Jocić, Biljana, Ivanović, Ivana, "Using experimental design in optimisation of VIS spektrophotometric method of investigation feroglicin sulfate in Orferon retard tablets" in Arhiv za farmaciju, 54, no. 1-2 (2004):51-59,
https://hdl.handle.net/21.15107/rcub_farfar_536 .