TY  - JOUR
AU  - Stojković, Aleksandra
AU  - Tajber, Lidia
AU  - Paluch, Krzysztof J.
AU  - Đurić, Zorica
AU  - Parojčić, Jelena
AU  - Corrigan, Owen I.
PY  - 2014
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/2161
AB  - Ciprofloxacin bioavailability may be reduced when ciprofloxacin is co-administered with metallic ion containing preparations. In our previous study, physicochemical interaction between ciprofloxacin and ferrous sulphate was successfully simulated in vitro. In the present work, comparative in vitro ciprofloxacin solubility and dissolution studies were performed in the reactive media containing aluminium hydroxide, calcium carbonate or zinc sulphate. Solid phases collected from the dissolution vessel with aluminium hydroxide, calcium carbonate and zinc sulphate were investigated for their properties. The results obtained indicate that different types of adducts may form and retard ciprofloxacin solubility and dissolution. In the case of aluminium, no phase changes were observed. The solid phase generated in the presence of calcium carbonate was identified as hydrated ciprofloxacin base. Similarly to iron, a new complex consistent with Zn(SO4)(2)(Cl)(2)(ciprofloxacin)(2) x nH(2)O stoichiometry was generated in the presence of relatively high concentrations of ciprofloxacin hydrochloride and zinc sulphate, indicating that small volume dissolution experiments can be useful for biorelevant dissolution tests.
PB  - Hrvatsko Farmaceutsko Drustov (HFD)-Croation Pharmaceutical Soc, Zagreb
T2  - Acta Pharmaceutica
T1  - Biopharmaceutical characterisation of ciprofloxacin-metallic ion interactions: Comparative study into the effect of aluminium, calcium, zinc and iron on drug solubility and dissolution
VL  - 64
IS  - 1
SP  - 77
EP  - 88
DO  - 10.2478/acph-2014-0007
ER  - 

@article{
author = "Stojković, Aleksandra and Tajber, Lidia and Paluch, Krzysztof J. and Đurić, Zorica and Parojčić, Jelena and Corrigan, Owen I.",
year = "2014",
abstract = "Ciprofloxacin bioavailability may be reduced when ciprofloxacin is co-administered with metallic ion containing preparations. In our previous study, physicochemical interaction between ciprofloxacin and ferrous sulphate was successfully simulated in vitro. In the present work, comparative in vitro ciprofloxacin solubility and dissolution studies were performed in the reactive media containing aluminium hydroxide, calcium carbonate or zinc sulphate. Solid phases collected from the dissolution vessel with aluminium hydroxide, calcium carbonate and zinc sulphate were investigated for their properties. The results obtained indicate that different types of adducts may form and retard ciprofloxacin solubility and dissolution. In the case of aluminium, no phase changes were observed. The solid phase generated in the presence of calcium carbonate was identified as hydrated ciprofloxacin base. Similarly to iron, a new complex consistent with Zn(SO4)(2)(Cl)(2)(ciprofloxacin)(2) x nH(2)O stoichiometry was generated in the presence of relatively high concentrations of ciprofloxacin hydrochloride and zinc sulphate, indicating that small volume dissolution experiments can be useful for biorelevant dissolution tests.",
publisher = "Hrvatsko Farmaceutsko Drustov (HFD)-Croation Pharmaceutical Soc, Zagreb",
journal = "Acta Pharmaceutica",
title = "Biopharmaceutical characterisation of ciprofloxacin-metallic ion interactions: Comparative study into the effect of aluminium, calcium, zinc and iron on drug solubility and dissolution",
volume = "64",
number = "1",
pages = "77-88",
doi = "10.2478/acph-2014-0007"
}

Stojković, A., Tajber, L., Paluch, K. J., Đurić, Z., Parojčić, J.,& Corrigan, O. I.. (2014). Biopharmaceutical characterisation of ciprofloxacin-metallic ion interactions: Comparative study into the effect of aluminium, calcium, zinc and iron on drug solubility and dissolution. in Acta Pharmaceutica
Hrvatsko Farmaceutsko Drustov (HFD)-Croation Pharmaceutical Soc, Zagreb., 64(1), 77-88.
https://doi.org/10.2478/acph-2014-0007

Stojković A, Tajber L, Paluch KJ, Đurić Z, Parojčić J, Corrigan OI. Biopharmaceutical characterisation of ciprofloxacin-metallic ion interactions: Comparative study into the effect of aluminium, calcium, zinc and iron on drug solubility and dissolution. in Acta Pharmaceutica. 2014;64(1):77-88.
doi:10.2478/acph-2014-0007 .

Stojković, Aleksandra, Tajber, Lidia, Paluch, Krzysztof J., Đurić, Zorica, Parojčić, Jelena, Corrigan, Owen I., "Biopharmaceutical characterisation of ciprofloxacin-metallic ion interactions: Comparative study into the effect of aluminium, calcium, zinc and iron on drug solubility and dissolution" in Acta Pharmaceutica, 64, no. 1 (2014):77-88,
https://doi.org/10.2478/acph-2014-0007 . .

TY  - JOUR
AU  - Stojković, Aleksandra
AU  - Tajber, Lidia
AU  - Đurić, Zorica
AU  - Corrigan, Owen I.
AU  - Parojčić, Jelena
PY  - 2014
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/2097
AB  - In vitro dissolution testing has long been used as a tool in drug product development and quality control, however, its potential for drug/food and drug/drug interactions has not yet been filly exploited. Ciprofloxacin absorption in vivo may be reduced when co-administered with different metallic compounds. In the present study, in vitro ciprofloxacin solubility and drug dissolution from tablets were performed in the reactive media containing zinc chloride in order to simulate ciprofloxacin/zinc interaction observed in vivo. The precipitates collected from dissolution vessel and from mixture containing ciprofloxacin-hydrochloride and zinc-chloride were investigated using XRPD, TGA, DCS, FTIR. Ciprofloxacin-hydrochloride solubility and drug dissolution from tablet were reduced in aqueous media containing increasing amounts of zinc-chloride. Complex with probable chemical structure kin [cfH(2)](2)center dot[ZnCl4]center dot 2H(2)O was generated in the presence of high concentrations of ciprofloxacin-hydrochloride and zinc-chloride, indicating that small volume dissolution experiments can be useful in biopharmaceutical characterisation of drug interaction studies.
PB  - Elsevier Science BV, Amsterdam
T2  - Journal of Drug Delivery Science and Technology
T1  - In vitro simulation of drug interaction: ciprofloxacin/zinc chloride
VL  - 24
IS  - 2
SP  - 229
EP  - 233
DO  - 10.1016/S1773-2247(14)50037-8
ER  - 

@article{
author = "Stojković, Aleksandra and Tajber, Lidia and Đurić, Zorica and Corrigan, Owen I. and Parojčić, Jelena",
year = "2014",
abstract = "In vitro dissolution testing has long been used as a tool in drug product development and quality control, however, its potential for drug/food and drug/drug interactions has not yet been filly exploited. Ciprofloxacin absorption in vivo may be reduced when co-administered with different metallic compounds. In the present study, in vitro ciprofloxacin solubility and drug dissolution from tablets were performed in the reactive media containing zinc chloride in order to simulate ciprofloxacin/zinc interaction observed in vivo. The precipitates collected from dissolution vessel and from mixture containing ciprofloxacin-hydrochloride and zinc-chloride were investigated using XRPD, TGA, DCS, FTIR. Ciprofloxacin-hydrochloride solubility and drug dissolution from tablet were reduced in aqueous media containing increasing amounts of zinc-chloride. Complex with probable chemical structure kin [cfH(2)](2)center dot[ZnCl4]center dot 2H(2)O was generated in the presence of high concentrations of ciprofloxacin-hydrochloride and zinc-chloride, indicating that small volume dissolution experiments can be useful in biopharmaceutical characterisation of drug interaction studies.",
publisher = "Elsevier Science BV, Amsterdam",
journal = "Journal of Drug Delivery Science and Technology",
title = "In vitro simulation of drug interaction: ciprofloxacin/zinc chloride",
volume = "24",
number = "2",
pages = "229-233",
doi = "10.1016/S1773-2247(14)50037-8"
}

Stojković, A., Tajber, L., Đurić, Z., Corrigan, O. I.,& Parojčić, J.. (2014). In vitro simulation of drug interaction: ciprofloxacin/zinc chloride. in Journal of Drug Delivery Science and Technology
Elsevier Science BV, Amsterdam., 24(2), 229-233.
https://doi.org/10.1016/S1773-2247(14)50037-8

Stojković A, Tajber L, Đurić Z, Corrigan OI, Parojčić J. In vitro simulation of drug interaction: ciprofloxacin/zinc chloride. in Journal of Drug Delivery Science and Technology. 2014;24(2):229-233.
doi:10.1016/S1773-2247(14)50037-8 .

Stojković, Aleksandra, Tajber, Lidia, Đurić, Zorica, Corrigan, Owen I., Parojčić, Jelena, "In vitro simulation of drug interaction: ciprofloxacin/zinc chloride" in Journal of Drug Delivery Science and Technology, 24, no. 2 (2014):229-233,
https://doi.org/10.1016/S1773-2247(14)50037-8 . .

TY  - JOUR
AU  - Parojčić, Jelena
AU  - Stojković, Aleksandra
AU  - Tajber, Lidia
AU  - Cvijić, Sandra
AU  - Paluch, Krzysztof J.
AU  - Đurić, Zorica
AU  - Corrigan, Owen I.
PY  - 2011
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/1512
AB  - The ciprofloxacin-iron interaction, resulting in a lower bioavailability, is well documented in vivo; however, a mechanistic explanation supported by experimental data of this interaction is missing. In the present study, ciprofloxacin hydrochloride (HCl) and ferrous sulfate interaction was simulated in vitro by performing solubility and dissolution studies in the reactive media containing ferrous sulfate. Characterization of the precipitate formed indicated its probable chemical structure as Fe(SO(4)(2-))(2)(Cl(-))(2)(ciprofloxacin)(2) x (H(2)O)(n), where n is up to 12 molecules of water. The solubility of this complex in water was estimated to be approximately 2mg/mL, being about 20-fold lower than the solubility of ciprofloxacin HCl. The solubility of the complex was used as input parameter for an in silico modeling by GastroPlus (TM) and the resulting predicted plasma time curves were in good agreement with the in vivo data. These results strongly indicate that ciprofloxacin-iron interaction in vivo is caused by the formation of a low soluble complex. This interaction was also simulated by in vitro dissolution, in which a mini scale apparatus provided more biorelevant results than the standard dissolution apparatus, probably because the drug concentrations in the mini apparatus were higher and, thus, closer to the conditions encountered in vivo.
PB  - Wiley-Blackwell, Malden
T2  - Journal of Pharmaceutical Sciences
T1  - Biopharmaceutical Characterization of Ciprofloxacin HCl-Ferrous Sulfate Interaction
VL  - 100
IS  - 12
SP  - 5174
EP  - 5184
DO  - 10.1002/jps.22707
ER  - 

@article{
author = "Parojčić, Jelena and Stojković, Aleksandra and Tajber, Lidia and Cvijić, Sandra and Paluch, Krzysztof J. and Đurić, Zorica and Corrigan, Owen I.",
year = "2011",
abstract = "The ciprofloxacin-iron interaction, resulting in a lower bioavailability, is well documented in vivo; however, a mechanistic explanation supported by experimental data of this interaction is missing. In the present study, ciprofloxacin hydrochloride (HCl) and ferrous sulfate interaction was simulated in vitro by performing solubility and dissolution studies in the reactive media containing ferrous sulfate. Characterization of the precipitate formed indicated its probable chemical structure as Fe(SO(4)(2-))(2)(Cl(-))(2)(ciprofloxacin)(2) x (H(2)O)(n), where n is up to 12 molecules of water. The solubility of this complex in water was estimated to be approximately 2mg/mL, being about 20-fold lower than the solubility of ciprofloxacin HCl. The solubility of the complex was used as input parameter for an in silico modeling by GastroPlus (TM) and the resulting predicted plasma time curves were in good agreement with the in vivo data. These results strongly indicate that ciprofloxacin-iron interaction in vivo is caused by the formation of a low soluble complex. This interaction was also simulated by in vitro dissolution, in which a mini scale apparatus provided more biorelevant results than the standard dissolution apparatus, probably because the drug concentrations in the mini apparatus were higher and, thus, closer to the conditions encountered in vivo.",
publisher = "Wiley-Blackwell, Malden",
journal = "Journal of Pharmaceutical Sciences",
title = "Biopharmaceutical Characterization of Ciprofloxacin HCl-Ferrous Sulfate Interaction",
volume = "100",
number = "12",
pages = "5174-5184",
doi = "10.1002/jps.22707"
}

Parojčić, J., Stojković, A., Tajber, L., Cvijić, S., Paluch, K. J., Đurić, Z.,& Corrigan, O. I.. (2011). Biopharmaceutical Characterization of Ciprofloxacin HCl-Ferrous Sulfate Interaction. in Journal of Pharmaceutical Sciences
Wiley-Blackwell, Malden., 100(12), 5174-5184.
https://doi.org/10.1002/jps.22707

Parojčić J, Stojković A, Tajber L, Cvijić S, Paluch KJ, Đurić Z, Corrigan OI. Biopharmaceutical Characterization of Ciprofloxacin HCl-Ferrous Sulfate Interaction. in Journal of Pharmaceutical Sciences. 2011;100(12):5174-5184.
doi:10.1002/jps.22707 .

Parojčić, Jelena, Stojković, Aleksandra, Tajber, Lidia, Cvijić, Sandra, Paluch, Krzysztof J., Đurić, Zorica, Corrigan, Owen I., "Biopharmaceutical Characterization of Ciprofloxacin HCl-Ferrous Sulfate Interaction" in Journal of Pharmaceutical Sciences, 100, no. 12 (2011):5174-5184,
https://doi.org/10.1002/jps.22707 . .