PubMed · 13743846
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L E ROTH. 1961. A method for reducing methacrylate sublimation from thin sections.. https://doi.org/10.1016/s0022-5320(61)90010-7
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A uniformly sized molecularly imprinted polymer (MIP) for (S)-naproxen has been prepared by a multi-step swelling and polymerization method using 4-vinylpyridine (4-VPY) and ethylene glycol dimethacrylate (EDMA) as a functional monomer and cross-linker, respectively. We optimized the preparation method of the MIP by changing the molar amounts of the template molecule and functional monomer. Further, we examined the effects of organic modifier type, column temperature and flow-rate on the retentivity and enantioselectivity for naproxen using a mixture of phosphate buffer and organic modifier (acetonitrile, ethanol and 2-propanol) as an eluent. When the amounts of (S)-naproxen, 4-VPY and EDMA used were 4, 6 and 25 mmol, respectively, the enantioselectivity and resolution for naproxen were good despite the shorter retention. When acetonitrile was used as an organic modifier, the highest column efficiency was obtained for the separation of naproxen enantiomers. With regard to the effects of column temperature and flow-rate, the column performance was improved by elevating a column temperature and decreasing a flow-rate.
OBJECTIVE: The purpose of this study was to measure the viscosity of resin formulations and investigate the relationship between diluent percentage and temperature. METHODS: Resin formulations were prepared using UDMA and either TEGDMA or HEMA, or HPMA, as diluents at different percentages. Viscosities were obtained with a Bohlin Rheometer at 23 degrees C for all formulations, and at 37 and 60 degrees C for selected formulations. RESULTS: The viscosity of the formulations exhibited Newtonian behaviour and decreased as the percentage of the diluent monomer increased, especially up to 40% of diluent. Linear regressions relating log(viscosity) and mass percent diluent, were obtained in the range 20-80% diluent. Viscosity also decreased as the temperature increased. Activation energies were calculated from Arrhenius plots, and ranged from 16.2-23.4 kJ mol-1. SIGNIFICANCE: The viscosity of the resins controls the flow properties and thus has a significant effect on the deployment of the respective monomers.
The effects of storing 2-hydroxyethyl methacrylate (HEMA) solutions for embedding tissues for light microscopy were studied using three commercially available HEMA embedding kits: Technovit 7100, Technovit 8100, and JB-4. These HEMA solutions were examined at various times of storage over a period of one year using a panel of physicochemical techniques including gas chromatography, titration, viscosimetry, determination of the maximum polymerization temperature and the time required to reach the maximum temperature, and detection of degradation products of HEMA monomers by histochemical procedures. The quality of the resin blocks was examined by the observation of mini-folds in sections. Data obtained from these tests showed that the release of by-products as a result of the degradation of the HEMA monomer during storage of HEMA solutions does not occur. Development of cross-linking agents by transesterification of HEMA monomer was not detected either. Gradual decrease of the inhibitor concentration during storage proved to be the main cause of the reduction of shelf-life of HEMA solutions. Inconsistent tissue infiltration after storage may be due to decreased rates of tissue penetration as a result of HEMA chain lengthening. Guidelines for safe and economical handling of HEMA mixtures are given.