Skip navigation

Solid-state flurbiprofen and methyl-β-cyclodextrin inclusion complexes prepared using a single-step, organic solvent-free supercritical fluid process

Solid-state flurbiprofen and methyl-β-cyclodextrin inclusion complexes prepared using a single-step, organic solvent-free supercritical fluid process

Rudrangi, Shashi Ravi Suman, Kaialy, Waseem, Ghori, Muhammad U., Trivedi, Vivek ORCID: 0000-0001-9304-9214 , Alexander, Bruce David and Snowden, Martin J. ORCID: 0000-0002-1087-2692 (2016) Solid-state flurbiprofen and methyl-β-cyclodextrin inclusion complexes prepared using a single-step, organic solvent-free supercritical fluid process. European Journal of Pharmaceutics and Biopharmaceutics, 104. pp. 164-170. ISSN 0939-6411 (doi:https://doi.org/10.1016/j.ejpb.2016.04.024)

[img]
Preview
PDF (Author's Accepted Manuscript)
15496_Trivedi_Solid state flurbiprofen (AAM) 2016.pdf - Accepted Version
Available under License Creative Commons Attribution Non-commercial No Derivatives.

Download (341kB) | Preview
[img] PDF (Acceptance Email)
15496_Trivedi_Solid state flurbiprofen - publication confirmation 2016.pdf - Additional Metadata
Restricted to Repository staff only

Download (65kB)

Abstract

The aim of this study was to enhance the apparent solubility and dissolution properties of flurbiprofen through inclusion complexation with cyclodextrins. Especially, the efficacy of supercritical fluid technology as a preparative technique for the preparation of flurbiprofen-methyl–β–cyclodextrin inclusion complexes was evaluated. The complexes were prepared by supercritical carbon dioxide processing and were evaluated by solubility, differential scanning calorimetry, X-ray powder diffraction, scanning electron microscopy, practical yield, drug content estimation and in vitro dissolution studies. Computational molecular docking studies were conducted to study the possibility of molecular arrangement of inclusion complexes between flurbiprofen and methyl-β-cyclodextrin. The studies support the formation of stable molecular inclusion complexes between the drug and cyclodextrin in a 1:1 stoichiometry. In vitro dissolution studies showed that the dissolution properties of flurbiprofen were significantly enhanced by the binary mixtures prepared by supercritical carbon dioxide processing. The amount of flurbiprofen dissolved into solution alone was very low with 1.11 ± 0.09% dissolving at the end of 60 min, while the binary mixtures processed by supercritical carbon dioxide at 45 °C and 200 bar released 99.39 ± 2.34% of the drug at the end of 30 min. All the binary mixtures processed by supercritical carbon dioxide at 45 °C exhibited a drug release of more than 80% within the first 10 min irrespective of the pressure employed. The study demonstrated the single step, organic solvent-free supercritical carbon dioxide process as a promising approach for the preparation of inclusion complexes between flurbiprofen and methyl–β–cyclodextrin in solid-state.

Item Type: Article
Additional Information: This release is under a CC BY-NC-ND Creative Commons License
Uncontrolled Keywords: Dissolution rate, Flurbiprofen, Inclusion complexes, Methyl–β–cyclodextrin, Solubility, Supercritical fluid technology
Subjects: Q Science > QD Chemistry
Faculty / School / Research Centre / Research Group: Faculty of Engineering & Science
Faculty of Engineering & Science > School of Science (SCI)
Last Modified: 19 Jun 2020 15:53
URI: http://gala.gre.ac.uk/id/eprint/15496

Actions (login required)

View Item View Item

Downloads

Downloads per month over past year

View more statistics