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Sökning: WFRF:(Boere Stijn)

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1.
  • Boere, Stijn, et al. (författare)
  • Tyre/road interaction model for the prediction of road texture influence on rolling resistance
  • 2014
  • Ingår i: International Journal of Vehicle Design. - 0143-3369 .- 1741-5314. ; 65:2-3, s. 202-221
  • Tidskriftsartikel (refereegranskat)abstract
    • A novel modelling approach to predict the influence of road texture on the rolling resistance of car tyres is presented where the large static tyre deformations and the small texture induced tyre vibrations are treated separately. The energy dissipation due to the large continuous cyclic deformation of the tyre cross section for a treadless tyre subject to nominal load on a smooth road is determined in a non-linear steady-state rolling analysis on an FEM tyre model. The additional energy dissipation resulting from the con tact forces and tyre vibrations due to the combined effect of the tread profile and the road texture, are determined based on a modal representation of the deformed tyre. The predicted rolling resistance coefficients are compared to experimental data. Although an offset in the absolute rolling resistance levels can be observed, the model predicts the correct trend regarding the increase of rolling resistance with increasing texture depth.
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2.
  • van Doorn, Leni, et al. (författare)
  • Effect of Scalp Cooling on the Pharmacokinetics of Paclitaxel
  • 2021
  • Ingår i: Cancers. - : MDPI. - 2072-6694. ; 13:15
  • Tidskriftsartikel (refereegranskat)abstract
    • Simple Summary This study investigated the correlation between scalp cooling used to prevent chemotherapy-induced alopecia and the pharmacokinetics of paclitaxel in female cancer patients with a solid tumor. In a prospective cohort study, 14 patients who were treated with weekly paclitaxel and scalp cooling were able to undergo pharmacokinetic sampling of paclitaxel during one cycle of treatment. In comparison to a control cohort of 24 patients treated with weekly paclitaxel without scalp cooling, our data showed that scalp cooling used concomitantly with one course of paclitaxel did not reduce or increase the clearance of paclitaxel. Therefore, it is unlikely that scalp cooling influences paclitaxel efficacy or toxicity. Finally, despite scalp cooling, half of the patients in our study developed a form of hair loss. Importantly, neither an association with difference in paclitaxel clearance nor change in hair loss was found. Chemotherapy-induced alopecia (CIA), a side effect with high impact, can be prevented by cooling the scalp during the administration of some cytotoxic drugs. However, the effects of this prolonged scalp cooling on the pharmacokinetics of chemotherapy have never been investigated. In this study, we compared the pharmacokinetics of the widely used chemotherapeutic agent paclitaxel (weekly dose of 80-100 mg/m(2)) in female patients with solid tumors using concomitant scalp cooling (n = 14) or not (n = 24). Blood samples were collected in all patients for pharmacokinetic analyses up to 6 h after one course of paclitaxel administration. The primary endpoint was the clearance (L/h) of paclitaxel. Paclitaxel clearance-expressed as relative difference in geometric means-was 6.8% (90% CI: -16.7% to 4.4%) lower when paclitaxel was administered with concomitant scalp cooling versus paclitaxel infusions without scalp cooling. Within the subgroup of patients using scalp cooling, paclitaxel clearance was not statistically significantly different between patients with CIA (alopecia grade 1 or 2) and those without CIA. Hence, scalp cooling did not negatively influence the clearance of paclitaxel treatment.
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