Abstract
The purpose of this study was to construct
biopolymer-based oil-in-water emulsion formulations for
encapsulation and release of poorly water soluble model
compounds naproxen and ibuprofen. Class II hydrophobin
protein HFBII from Trichoderma reesei was used as a
surfactant to stabilize the oil/water interfaces of the
emulsion droplets in the continuous aqueous phase.
Nanofibrillated cellulose (NFC) was used as a viscosity
modifier to further stabilize the emulsions and
encapsulate protein coated oil droplets in NFC fiber
network. The potential of both native and oxidized NFC
were studied for this purpose. Various emulsion
formulations were prepared and the abilities of different
formulations to control the drug release rate of naproxen
and ibuprofen, used as model compounds, were evaluated.
The optimal formulation for sustained drug release
consisted of 0.01% of drug, 0.1% HFBII, 0.15% oxidized
NFC, 10% soybean oil and 90% water phase. By comparison,
the use of native NFC in combination with HFBII resulted
in an immediate drug release for both of the compounds.
The results indicate that these NFC originated
biopolymers are suitable for pharmaceutical emulsion
formulations. The native and oxidized NFC grades can be
used as emulsion stabilizers in sustained and immediate
drug release applications. Furthermore, stabilization of
the emulsions was achieved with low concentrations of
both HFBII and NFC, which may be an advantage when
compared to surfactant concentrations of conventional
excipients traditionally used in pharmaceutical emulsion
formulations.
Original language | English |
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Pages (from-to) | 238-248 |
Journal | European Journal of Pharmaceutical Sciences |
Volume | 100 |
DOIs | |
Publication status | Published - 30 Mar 2017 |
MoE publication type | A1 Journal article-refereed |
Keywords
- nanofibrillated cellulose
- hydrophobin
- emulsions
- drug release
- ibuprofen
- naproxen