Published by Elsevier Ltd.”
“To investigate structural brain changes in inflammatory bowel disease (IBD). Brain

magnetic resonance imaging (MRI) was performed on 18 IBD patients (aged 45.16 +/- 14.71 years) and 20 aged-matched control subjects. The imaging protocol consisted of a sagittal-FLAIR, a T1-weighted high-resolution three-dimensional spoiled gradient-echo sequence, and a multisession spin-echo echo-planar diffusion-weighted sequence. Differences between patients and controls in brain volume and diffusion indices were evaluated using the voxel-based morphometry (VBM) and tract-based spatial GSK923295 statistics (TBSS) methods, respectively. The presence of white-matter hyperintensities (WMHIs) was evaluated on FLAIR images. VBM revealed decreased grey matter (GM) volume in patients in the fusiform and the inferior temporal gyrus bilaterally, the right precentral gyrus, the right supplementary motor area, the right middle frontal gyrus and the left superior parietal gyrus (p smaller than 0.05). TBSS showed decreased axial diffusivity (AD) in the right

corticospinal tract and the right superior longitudinal fasciculus in patients compared with controls. A larger number of WMHIs was observed in patients (p smaller than 0.05). Patients with IBD show an increase in WMHIs and GM atrophy, probably related to cerebral vasculitis and ischaemia. Decreased AD in major white matter tracts could be a secondary phenomenon, representing Wallerian degeneration. aEuro cent There is evidence of central nervous system involvement in IBD. aEuro cent Diffusion tensor imaging detects microstructural brain abnormalities in IBD. aEuro cent Voxel based morphometry reveals brain Screening Library atrophy in IBD.”
“Monophosphoryl lipid A (MPL) and Quil A are two immunological adjuvants

commonly used in vaccines. At present no simple, validated methods for the quantification of Quil A and MPL have been previously reported therefore the aim of the current study was to develop a simple, fast and validated method to quantify MPL and Quil A using high performance liquid chromatography evaporative light scattering detection (HPLC-ELSD). The HPLC-ELSD technique was carried out using a ZORBAX Eclipse XDB-C8 column (2.1 x 50 mm; particle size, 3.5 mu m) in an isocratic elution mode at 25 degrees C. MPL was CX-6258 mouse eluted at a retention time of 1.8 min with methanol-water as the mobile phase and a detector temperature of 75 degrees C. Quil A was resolved as three peaks with retention times of 4.1, 5.5 and 6.4 mm with a detector temperature of 30 degrees C and with water-acetonitrile and 0.01% formic acid as the mobile phase. The nebulizer pressure and gain were set at 3.5 bar and 10, respectively. Calibration curves plotted for both the adjuvants had an R-2 bigger than 0.997. Accuracy, intra- and inter-day precision were within the accepted limits. The limit of detection for MPL and Quil A were calculated as 1.343 and 2.06 mu g/mL, respectively. The limit of quantification was 2.