Evaluation of the Physicochemical and Biopharmaceutical properties of Fluoro-Indomethacin

Michela M. Mori, Anu J. Airaksinen, Jouni T. Hirvonen, Hélder A. Santos, Carla M. Caramella

Tutkimustuotos: ArtikkelijulkaisuArtikkeliTieteellinenvertaisarvioitu

Kuvaus

Drug nanocarriers have shown great potential in therapy and as diagnostic probes, such as in imaging of cancer and inflammation. Imaging can be applied to localize the carrier or the drug itself in the body and/or tissues. In this particular case it is important that drug molecules have the characteristics for possible detection, e.g. after modification with positron emission tomography (PET) compliant radioisotopes, without affecting their pharmacological behaviour. In order to easily and efficiently follow the ADME profile of the drug after loaded into nanocarriers, the drug can be radiolabelled with, e.g. 18F-label, in order to assess its biodistribution after enteral and parenteral administration in rats. However, this is only possible if the derivative compound behaves similarly to the parent drug compound. In this study, indomethacin (a poorly water-soluble drug) was chosen as a model compound and aimed to evaluate the physicochemical and biopharmaceutical properties of an analogue of indomethacin (IMC), fluoro-indomethacin (F-IMC). Although some of the physicochemical and biopharmaceutical properties of IMC are already known, in order to establish a feasible comparison between IMC and F-IMC, the behaviour of the former was also investigated in the same conditions as for F-IMC. In this context, both IMC and F-IMC were thermally and morphologically studied. Furthermore, the following properties were also studied for both compounds: pKa and log P, solubility and dissolution profiles at physiological pH values, and toxicity at different concentrations in Caco-2 cells. Finally, the transport across Caco-2 monolayers of the IMC and F-IMC at physiological pH range was also investigated. The results obtained showed similar values in pKa-logP, solubility, dissolution, cytotoxicity, and permeability for both compounds. Thus, there might be strong evidence that both IMC and F-IMC should have a similar ADME behaviour and profiles in vivo. The results provide fundamental tools and ideas for further research with nanocarriers of 18F-IMC.
Alkuperäiskielienglanti
LehtiCurrent Drug Metabolism
Vuosikerta14
Numero1
Sivut80-89
Sivumäärä9
ISSN1389-2002
DOI - pysyväislinkit
TilaJulkaistu - 2013
OKM-julkaisutyyppiA1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä, vertaisarvioitu

Tieteenalat

  • 317 Farmasia

Lainaa tätä

@article{19f7127878f8473fbc5d3458caa963ca,
title = "Evaluation of the Physicochemical and Biopharmaceutical properties of Fluoro-Indomethacin",
abstract = "Drug nanocarriers have shown great potential in therapy and as diagnostic probes, such as in imaging of cancer and inflammation. Imaging can be applied to localize the carrier or the drug itself in the body and/or tissues. In this particular case it is important that drug molecules have the characteristics for possible detection, e.g. after modification with positron emission tomography (PET) compliant radioisotopes, without affecting their pharmacological behaviour. In order to easily and efficiently follow the ADME profile of the drug after loaded into nanocarriers, the drug can be radiolabelled with, e.g. 18F-label, in order to assess its biodistribution after enteral and parenteral administration in rats. However, this is only possible if the derivative compound behaves similarly to the parent drug compound. In this study, indomethacin (a poorly water-soluble drug) was chosen as a model compound and aimed to evaluate the physicochemical and biopharmaceutical properties of an analogue of indomethacin (IMC), fluoro-indomethacin (F-IMC). Although some of the physicochemical and biopharmaceutical properties of IMC are already known, in order to establish a feasible comparison between IMC and F-IMC, the behaviour of the former was also investigated in the same conditions as for F-IMC. In this context, both IMC and F-IMC were thermally and morphologically studied. Furthermore, the following properties were also studied for both compounds: pKa and log P, solubility and dissolution profiles at physiological pH values, and toxicity at different concentrations in Caco-2 cells. Finally, the transport across Caco-2 monolayers of the IMC and F-IMC at physiological pH range was also investigated. The results obtained showed similar values in pKa-logP, solubility, dissolution, cytotoxicity, and permeability for both compounds. Thus, there might be strong evidence that both IMC and F-IMC should have a similar ADME behaviour and profiles in vivo. The results provide fundamental tools and ideas for further research with nanocarriers of 18F-IMC.",
keywords = "317 Pharmacy",
author = "Mori, {Michela M.} and Airaksinen, {Anu J.} and Hirvonen, {Jouni T.} and {A. Santos}, H{\'e}lder and Caramella, {Carla M.}",
year = "2013",
doi = "10.2174/138920013804545179",
language = "English",
volume = "14",
pages = "80--89",
journal = "Current Drug Metabolism",
issn = "1389-2002",
publisher = "Bentham Science Publishers, Ltd.",
number = "1",

}

Evaluation of the Physicochemical and Biopharmaceutical properties of Fluoro-Indomethacin. / Mori, Michela M.; Airaksinen, Anu J.; Hirvonen, Jouni T.; A. Santos, Hélder; Caramella, Carla M.

julkaisussa: Current Drug Metabolism, Vuosikerta 14, Nro 1, 2013, s. 80-89.

Tutkimustuotos: ArtikkelijulkaisuArtikkeliTieteellinenvertaisarvioitu

TY - JOUR

T1 - Evaluation of the Physicochemical and Biopharmaceutical properties of Fluoro-Indomethacin

AU - Mori, Michela M.

AU - Airaksinen, Anu J.

AU - Hirvonen, Jouni T.

AU - A. Santos, Hélder

AU - Caramella, Carla M.

PY - 2013

Y1 - 2013

N2 - Drug nanocarriers have shown great potential in therapy and as diagnostic probes, such as in imaging of cancer and inflammation. Imaging can be applied to localize the carrier or the drug itself in the body and/or tissues. In this particular case it is important that drug molecules have the characteristics for possible detection, e.g. after modification with positron emission tomography (PET) compliant radioisotopes, without affecting their pharmacological behaviour. In order to easily and efficiently follow the ADME profile of the drug after loaded into nanocarriers, the drug can be radiolabelled with, e.g. 18F-label, in order to assess its biodistribution after enteral and parenteral administration in rats. However, this is only possible if the derivative compound behaves similarly to the parent drug compound. In this study, indomethacin (a poorly water-soluble drug) was chosen as a model compound and aimed to evaluate the physicochemical and biopharmaceutical properties of an analogue of indomethacin (IMC), fluoro-indomethacin (F-IMC). Although some of the physicochemical and biopharmaceutical properties of IMC are already known, in order to establish a feasible comparison between IMC and F-IMC, the behaviour of the former was also investigated in the same conditions as for F-IMC. In this context, both IMC and F-IMC were thermally and morphologically studied. Furthermore, the following properties were also studied for both compounds: pKa and log P, solubility and dissolution profiles at physiological pH values, and toxicity at different concentrations in Caco-2 cells. Finally, the transport across Caco-2 monolayers of the IMC and F-IMC at physiological pH range was also investigated. The results obtained showed similar values in pKa-logP, solubility, dissolution, cytotoxicity, and permeability for both compounds. Thus, there might be strong evidence that both IMC and F-IMC should have a similar ADME behaviour and profiles in vivo. The results provide fundamental tools and ideas for further research with nanocarriers of 18F-IMC.

AB - Drug nanocarriers have shown great potential in therapy and as diagnostic probes, such as in imaging of cancer and inflammation. Imaging can be applied to localize the carrier or the drug itself in the body and/or tissues. In this particular case it is important that drug molecules have the characteristics for possible detection, e.g. after modification with positron emission tomography (PET) compliant radioisotopes, without affecting their pharmacological behaviour. In order to easily and efficiently follow the ADME profile of the drug after loaded into nanocarriers, the drug can be radiolabelled with, e.g. 18F-label, in order to assess its biodistribution after enteral and parenteral administration in rats. However, this is only possible if the derivative compound behaves similarly to the parent drug compound. In this study, indomethacin (a poorly water-soluble drug) was chosen as a model compound and aimed to evaluate the physicochemical and biopharmaceutical properties of an analogue of indomethacin (IMC), fluoro-indomethacin (F-IMC). Although some of the physicochemical and biopharmaceutical properties of IMC are already known, in order to establish a feasible comparison between IMC and F-IMC, the behaviour of the former was also investigated in the same conditions as for F-IMC. In this context, both IMC and F-IMC were thermally and morphologically studied. Furthermore, the following properties were also studied for both compounds: pKa and log P, solubility and dissolution profiles at physiological pH values, and toxicity at different concentrations in Caco-2 cells. Finally, the transport across Caco-2 monolayers of the IMC and F-IMC at physiological pH range was also investigated. The results obtained showed similar values in pKa-logP, solubility, dissolution, cytotoxicity, and permeability for both compounds. Thus, there might be strong evidence that both IMC and F-IMC should have a similar ADME behaviour and profiles in vivo. The results provide fundamental tools and ideas for further research with nanocarriers of 18F-IMC.

KW - 317 Pharmacy

U2 - 10.2174/138920013804545179

DO - 10.2174/138920013804545179

M3 - Article

VL - 14

SP - 80

EP - 89

JO - Current Drug Metabolism

JF - Current Drug Metabolism

SN - 1389-2002

IS - 1

ER -