Microparticles Containing Curcumin Solid Dispersion: Stability, Bioavailability and Anti-Inflammatory Activity

Journal Title: AAPS PharmSciTech - Year 2016, Vol 17, Issue 2

Abstract

This work aimed at improving the solubility of curcumin by the preparation of spray-dried ternary solid dispersions containing Gelucire®50/13-Aerosil® and quantifying the resulting in vivo oral bioavailability and anti-inflammatory activity. The solid dispersion containing 40% of curcumin was characterised by calorimetry, infrared spectroscopy and X-ray powder diffraction. The solubility and dissolution rate of curcumin in aqueous HCl or phosphate buffer improved up to 3600- and 7.3-fold, respectively. Accelerated stability test demonstrated that the solid dispersion was stable for 9 months. The pharmacokinetic study showed a 5.5-fold increase in curcumin in rat blood plasma when compared to unprocessed curcumin. The solid dispersion also provided enhanced anti-inflammatory activity in rat paw oedema. Finally, the solid dispersion proposed here is a promising way to enhance curcumin bioavailability at an industrial pharmaceutical perspective, since its preparation applies the spray drying, which is an easy to scale up technique. The findings herein stimulate further in vivo evaluations and clinical tests as a cancer and Alzheimer chemoprevention agent.

Authors and Affiliations

C. C. C. Teixeira, L. M. Mendonça, M. M. Bergamaschi, R. H. C. Queiroz, G. E. P. Souza, L. M. G. Antunes, L. A. P. Freitas

Keywords

Related Articles

Topical Lyogel Containing Corticosteroid Decreases IgE Expression and Enhances the Therapeutic Efficacy Against Atopic Eczema

Hydrocortisone cream intended for atopic eczema often produces unwanted side effects after long-term use. These side effects are essentially due to repeated percutaneous administration of the medication for skin dermatit...

Development and Validation of a Discriminative Dissolution Method for Atorvastatin Calcium Tablets using in vivo Data by LC and UV Methods

A dissolution method to analyze atorvastatin tablets using in vivo data for RP and test pilot (PB) was developed and validated. The appropriate conditions were determined after solubility tests using different media, and...

Process and Method Variability Modeling to Achieve QbD Targets

The online version of this article (doi:10.1208/s12249-015-0380-3) contains supplementary material, which is available to authorized users.

Development of Novel Docetaxel Phospholipid Nanoparticles for Intravenous Administration: Quality by Design Approach

The objective of this study was to develop novel docetaxel phospholipid nanoparticles (NDPNs) for intravenous administration. Modified solvent diffusion-evaporation method was adopted in the NDPN preparation. Central com...

Potential of Piperazinylalkylester Prodrugs of 6-Methoxy-2-Naphthylacetic Acid (6-MNA) for Percutaneous Drug Delivery

The online version of this article (doi:10.1208/s12249-014-0240-6) contains supplementary material, which is available to authorized users.

Download PDF file
  • EP ID EP682137
  • DOI  10.1208/s12249-015-0337-6
  • Views 80
  • Downloads 0

How To Cite

C. C. C. Teixeira, L. M. Mendonça, M. M. Bergamaschi, R. H. C. Queiroz, G. E. P. Souza, L. M. G. Antunes, L. A. P. Freitas (2016). Microparticles Containing Curcumin Solid Dispersion: Stability, Bioavailability and Anti-Inflammatory Activity. AAPS PharmSciTech, 17(2), -. https://europub.co.uk/articles/-A-682137