Zakład Fizyki Biomedycznej
Strona główna
Zespół
Badania
Aparatura
Seminaria
Publikacje
Nasze
konferencje
Aktywność
konferencyjna
Projekty
Programy
Najbliższe
wydarzenia
Linki
Kontakt

wizyta

od 2020-09-20


Authors: Paczkowska M., Mizera M, Salat K., Furgała A., Popik P., Knapik-Kowalczuk J., Krause A., Szymanowska-Powałowska D., Fojud Z., Kozak M., Paluch M., Cielecka-Piontek J

Title: Enhanced pharmacological efficacy of sumatriptan due to modification of its physicochemical properties by inclusion in selected cyclodextrins

Source: Scientific Reports

Year : 2018


Abstract:

The study focused on the pharmacological action of sumatriptan, in particular its antiallodynic and antihyperalgesic properties, as an effect of cyclodextrinic inclusion of sumatriptan, resulting in changes of its physicochemical qualities such as dissolution and permeability through artificial biological membranes, which had previously been examined in vitro in a gastro-intestinal model. The inclusion of sumatriptan into beta-cyclodextrin and 2-hydroxylpropylo-beta-cyclodextrin by kneading was confirmed with the use of spectral (fourier-transform infrared spectroscopy (FT-IR); solid state nuclear magnetic resonance spectroscopy with magic angle spinning condition, H-1 and C-13 MAS NMR) and thermal (differential scanning calorimetry (DSC)) methods. A precise indication of the domains of sumatriptan responsible for its interaction with cyclodextrin cavities was possible due to a theoretical approach to the analysis of experimental spectra. A high-performance liquid chromatography with a diode-array detector method (HPLC-DAD) was employed to determine changes in the concentration of sumatriptan during dissolution and permeability experiments. The inclusion of sumatriptan in complex with cyclodextrins was found to significantly modify its dissolution profiles by increasing the concentration of sumatriptan in complexed form in an acceptor solution compared to in its free form. Following complexation, sumatriptan manifested an enhanced ability to permeate through artificial biological membranes in a gastro-intestinal model for both cyclodextrins at all pH values. As a consequence of the greater permeability of sumatriptan and its increased dissolution from the complexes, an improved pharmacological response was observed when cyclodextrin complexes were applied.

DOI: 10.1038/s41598-018-34554-w   (Pobrane:  2019-03-19)

 © Opisy i zdjęcia: Zakład Fizyki Makromolekularnej  | Ta stona używa ciasteczek
     Zaktualizowano: podstrony  2021-06-21  / bazę danych:   2024-04-23  by Webmaster: Zbigniew Fojud