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Development of hot-melt extrusion as a novel technique for the ...

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55 exrudates (b) DPD/L100-55 PM (c) DPD/L100 extrudates and (d)DPD/L100 PM.6.4 Molecular modelling <strong>of</strong> drugs/polymers (Gaussian 09). 1146.5a XPS BE peaks <strong>of</strong> C 1s PRP, L100 and PRP/L100 <strong>for</strong>mulations 1166.5b C 1s BE peaks <strong>of</strong> DPD, L100 and DPD/L100 <strong>for</strong>mulations 1166.5c O 1s peaks <strong>of</strong> DPD, L100, DPD/L100 and PRP, L100-55, PRP/L100-55118<strong>for</strong>mulations.6.5d N 1s peaks <strong>of</strong> PRP and DPD <strong>for</strong>mulations. 1196.6a Molecular structure <strong>of</strong> PRP and DPD (NMR peak <strong>as</strong>signment) 1216.6b1 H NMR spectra <strong>of</strong> all PRP and DPD <strong>for</strong>mulations. 123CHAPTER 77.1 SEM images (magnification x 500) <strong>of</strong> <strong>the</strong> extruded <strong>for</strong>mulations (a)136PRP/L100 and (b) DPD/L100-55.7.2 Particle size distribution <strong>of</strong> L100 and L100-55 b<strong>as</strong>ed <strong>for</strong>mulations with136both drugs (milling time 5 min, 400 rpm).7.3a Sensory scores <strong>of</strong> all <strong>for</strong>mulations by panellist (n=6). 1377.3b Normalised DI (%) <strong>of</strong> all drug/L100 <strong>for</strong>mulations in four different time138scale.7.3c Normalised DI (%) <strong>of</strong> all drug/L100-55 <strong>for</strong>mulations in four different139time scale.7.3d Relationship between results <strong>of</strong> t<strong>as</strong>te sensors and human t<strong>as</strong>te scores <strong>for</strong>140similar t<strong>as</strong>tes. The standard deviations on <strong>the</strong> x- and y-axes are <strong>the</strong>difference between <strong>the</strong> panellists‘ scores and me<strong>as</strong>urement error (n = 6),respectively.xxiii | P a g e

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