Biodetection articles
A technology for products and detection reagents, which can be used in the determination/inspection of microorganisms, biochemical equipment and methods, and methods of sampling biological materials, etc., and can solve problems such as the complexity of living cell detection.
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preparation example 1
[0138] Incorporation of cell extractants into hydrogel beads during hydrogel polymerization .
[0139] Beads were prepared as described in Example 1 of International Patent Publication No. WO 2007 / 146722, where deionized water was replaced with the desired loading solution. By mixing 40 grams of 20 mole ethoxylated trimethylolpropane triacrylate (EO 20 - TMPTA) (SR415, available from Sartomer, Exeter, PA), 60 grams of deionized (DI) water, and 0.8 grams of photoinitiator (IRGACURE 2959, available from Ciba Specialty Chemicals, Tarrytown, NY) to prepare a uniform precursor combination thing. The precursor composition was poured into the funnel so that the precursor composition exited the funnel through a 2.0 mm diameter hole. The precursor composition was dropped along a vertical axis of a 0.91 m long, 51 mm diameter quartz tube extending through a UV exposure zone consisting of a light screen and a 240 W / cm irradiator equipped with a 25 cm long "H" bulb (available from Fu...
preparation example 2
[0143] Incorporation of cationic monomers into hydrogel beads during hydrogel polymerization .
[0144] Polymer beads with cationic monomers were prepared as described in Examples 30-34 of International Patent WO2007 / 146722. The precursor compositions used to prepare the beads are shown in Table 1. The components of the precursor composition were stirred together in a brown jar until the antimicrobial monomer dissolved.
[0145] Formation of DMAEMA-C in a three-necked round-bottomed reaction flask equipped with a mechanical stirrer, temperature probe, and condenser 8 Br. A reaction flask was charged with 234 parts dimethylaminoethyl methacrylate, 617 parts acetone, 500 parts 1-bromoethane, and 0.5 parts BHT antioxidant. The mixture was stirred at 35°C for 24 hours. At this point the reaction mixture was cooled to room temperature to give a clear slightly yellow solution. The solution was transferred to a round bottom flask and the acetone was removed by rotary evaporati...
preparation example 3
[0151] Incorporation of luciferin into hydrogel beads during hydrogel polymerization .
[0152] Luciferin-containing hydrogel beads were similarly prepared as follows: 20 parts of EO 20 - TMPTA was mixed with 30 parts of luciferin (2 mg in 30 ml of 14 mM phosphate buffer (pH 6.4)) and 0.4 part of photoinitiator (IRGACURE 2959) and exposed to ultraviolet light to prepare beads. The beads were then stored in jars at 4°C and labeled luciferin-1s.
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