Oral bioavailability of cinnarizine in dogs: relation to SNEDDS droplet size, drug solubility and in vitro precipitation
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Oral bioavailability of cinnarizine in dogs : relation to SNEDDS droplet size, drug solubility and in vitro precipitation. / Larsen, Anne T; Ohlsson, Anja G.; Polentarutti, Britta; Barker, Richard A; Phillips, Andrew R; Abu-Rmaileh, Ragheb; Dickinson, Paul A; Abrahamsson, Bertil; Ostergaard, Jesper; Müllertz, Anette.
In: European Journal of Pharmaceutical Sciences, Vol. 48, No. 1-2, 2013, p. 339-50.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Oral bioavailability of cinnarizine in dogs
T2 - relation to SNEDDS droplet size, drug solubility and in vitro precipitation
AU - Larsen, Anne T
AU - Ohlsson, Anja G.
AU - Polentarutti, Britta
AU - Barker, Richard A
AU - Phillips, Andrew R
AU - Abu-Rmaileh, Ragheb
AU - Dickinson, Paul A
AU - Abrahamsson, Bertil
AU - Ostergaard, Jesper
AU - Müllertz, Anette
N1 - Copyright © 2012 Elsevier B.V. All rights reserved.
PY - 2013
Y1 - 2013
N2 - The in vivo performance of self-nanoemulsifying drug delivery systems (SNEDDSs) with different in vitro physicochemical properties were determined with the purpose of elucidating the parameters determining the in vivo performance of SNEDDSs. The in vitro characterisation included the use of pulsed field gradient NMR and the dynamic lipolysis model. In vivo characterisation was carried out in dogs with elevated gastric pH. Four SNEDDSs containing cinnarizine were dosed orally, and the obtained PK profiles were related to in vitro characterisation data. The SNEDDSs with the lowest solubility of cinnarizine in the preconcentrates and the smallest droplet size had the highest AUC values after oral administration. No difference in C(max) and t(max) was observed between the SNEDDSs. Despite of precipitation occurring during in vitro lipolysis of one of the SNEDDS this SNEDDS performed as well in vivo as another SNEDDS that did not show any precipitation. The area under the colloidal dispersion curves as well as under the lipolysis curves could be used to rank order the in vivo performance of the SNEDDSs. Selection of in vitro optimisation parameters for SNEDDSs should be done carefully. It may not always be best to aim for the highest solubility in the preconcentrate and to avoid precipitation during in vitro lipolysis.
AB - The in vivo performance of self-nanoemulsifying drug delivery systems (SNEDDSs) with different in vitro physicochemical properties were determined with the purpose of elucidating the parameters determining the in vivo performance of SNEDDSs. The in vitro characterisation included the use of pulsed field gradient NMR and the dynamic lipolysis model. In vivo characterisation was carried out in dogs with elevated gastric pH. Four SNEDDSs containing cinnarizine were dosed orally, and the obtained PK profiles were related to in vitro characterisation data. The SNEDDSs with the lowest solubility of cinnarizine in the preconcentrates and the smallest droplet size had the highest AUC values after oral administration. No difference in C(max) and t(max) was observed between the SNEDDSs. Despite of precipitation occurring during in vitro lipolysis of one of the SNEDDS this SNEDDS performed as well in vivo as another SNEDDS that did not show any precipitation. The area under the colloidal dispersion curves as well as under the lipolysis curves could be used to rank order the in vivo performance of the SNEDDSs. Selection of in vitro optimisation parameters for SNEDDSs should be done carefully. It may not always be best to aim for the highest solubility in the preconcentrate and to avoid precipitation during in vitro lipolysis.
U2 - 10.1016/j.ejps.2012.11.004
DO - 10.1016/j.ejps.2012.11.004
M3 - Journal article
C2 - 23178440
VL - 48
SP - 339
EP - 350
JO - Norvegica Pharmaceutica Acta
JF - Norvegica Pharmaceutica Acta
SN - 0928-0987
IS - 1-2
ER -
ID: 44006268