Radioactivity scintillators

Thymidine Uptake Studies. Tritiated thymidine (52 mCi/ anole 0.1 /rCi/ml) was added to cells for 60 min at 37°C. Cells were then washed with PBS, incubated at 4°C for 15 min in the presence of ice cold 5% TCA, rinsed with TCA and scraped from the flasks with a rubber policeman. Cells were again washed with PBS, and solubilized in 0.1N NaOH overnight. Aliquots were assayed for protein (62) and radioactivity (scintillation fluid 100 ml Biosolve (Beckman, Fullerton, CA.), 7g of PPO and 0.6 g of POPOP per liter of toluene). 

Output formats Cuvette or plate reader, microscope images, videos, radioactivity (scintillation or Geiger counting) Plate reader— Usts formats suitable for automated deposition into databases for processing and visualization. HCS—image files and calculated parameters and metadata... 

A further consideration is whether the solvent is likely to interfere with the analysis. Toluene is a poor first choice for a method that is to quantify the drug by ultraviolet detection. It is difficult to remove all traces of the solvent, and even a small residual amount can affect the detection limit seriously. Similarly, chlorinated solvents are best avoided if radioactive scintillation counting or electron-capture detection is to be used. Some solvents may not be suitable because they would react with the analyte, for example a ketone such as ethyl methyl ketone would react with primary amines. Solvent impurities and additives may be unknown to the analyst. Antioxidants such as hydroquinone and pyrogallol are added to diethyl ether to limit peroxide formation. These highly electroactive molecules can affect electrochemical detection methods adversely, particularly if they have been concentrated by solvent evaporation. Freshly distilled diethyl ether may be used, but it should not be stored as this is not only potentially dangerous, the peroxides that form may decompose the analyte. Methyl /-butyl ether (boiling point 55°C) is supplied without antioxidants and is a useful alternative to diethyl ether. Chloroform and dichloro-methane may be stabilized with ethanol although pentene is used by at least one manufacturer and may... 

Radiometric ore sorting has been used successfully for some uranium ores because uranium minerals emit gamma rays which may be detected by a scintillation counter (2). In this appHcation, the distribution of uranium is such that a large fraction of the ore containing less than some specified cut-off grade can be discarded with tittle loss of uranium values. Radioactivity can also be induced in certain minerals, eg, boron and beryllium ores, by bombarding with neutrons or gamma rays. 

Deuterium oxide [7789-20-0] M 20, f 3.8°/760mm, b 101.4°/760mm, d 1.105. Distd from alkaline KMnOa [de Giovanni and Zamenhof Biochem 7 92 79 I963. NOTE that D2O invariably contains tritiated water and will therefore be RADIOACTIVE always check the radioactivity of D2O in a scintillation counter before using. 

Physical methods Physical methods include photometric absorption and fluorescence and phosphorescence inhibition, which is wrongly referred to as fluorescence quenching [1], and the detection of radioactively labelled substances by means of autoradiographic techniques, scintillation procedures or other radiometric methods. These methods are nondestructive (Chapt. 2). 

The scintillators are a special type of fluorescence indicators they are employed for the fluorimetric detection of radioactively labelled substances. They are stimulated by ) -radiation to the emission of electromagnetic radiation and will be discussed in Volume 2. 

In the carbon-14 expts, HMX/RDX product was isolated qualitatively, separated Into its components, and each component assayed for carbon-14 beta radioactivity using a liquid scintillation counting technique (Ref 11). DPT-l4C was isolated as an intermediate product from the reaction mixt and similarly radioassayed. For the nitrogen-15 tagged AN expts, HMX and RDX were assayed mass spectrometrically for i5N/i4N ratios from which atom %1SN contents were calcd. In die course of these expts, each tagged species was added initially and also at subsequent stages of the reaction process. The important observations and results are summarized as ... 

Fluorescent materials are very important in medical research. Dyes such as fluorescein (21) can be attached to protein molecules, and the protein can be traced in a biological system by exciting the fluorescein and looking for its emissions. The use of a fluorescent material allows the detection of much smaller concentrations than would otherwise be possible. Because fluorescent materials can be activated by radioactivity, they are also used in scintillation counters to measure radiation (see Box 17.2). 

Radioactivity Analysis. Samples of urine, feces, and tissues were combusted to COo and analyzed for radioactivity (5). By using this method the recovery of radioactivity from samples spiked with C was 95 dt 5%. To determine the radioactivity expired as CO2, 5-ml aliquots of the solution used to trap the CO2 were added to 15 ml of a scintillation counting solution containing 4 grams 2,5-diphenyloxazole (PPO) and 0.1 grams l,4-bis-2(5-phenyloxazolyl)-benzene (POPOP) per liter of 1 1 toluene 2-methoxyethanol. Samples were counted for radioactivity in a Nuclear Chicago Mark II liquid scintillation counter. Counting eflSciency was corrected by the internal standard technique. 

Figure 2. Thin-layer radiochromatogram of urine (100 il) from rats injected with labeled PbTx-3. TLC plates were developed in two sequential solvent systems chloroform ethyl acetate ethanol (50 25 25 80 10 10). Radioactive zones were scraped and counted in a liquid scintillation counter. Native PbTx-3 runs at 13 cm.

Since cigarette tobacco already contains several micrograms of the TSNA, we determined the transfer rate of NNN into the smoke by spiking the tobacco column with NNN-2 - C. The smoke from such radiolabeled cigarettes is then analyzed by HPLC and the amount of unchanged NNN-2 - C is determined by liquid scintillation counting. Independent of the smoke pH, about 11% of the radioactive NNN is found in the mainstream smoke thus 41-46% of mainstream smoke NNN stems from the tobacco NNN and 54-59% are pyrosynthesized (11). 

PMT assays were performed as described by Vannier et al. [3] by adding an equal volume of an enzyme preparation to a 0.1 M Tris-HCl buffer containing 3.36 pM of [ C]SAM (1.8 GBq mmol, 740 kBq ml", NEN), 1% (WA ) BSA and 12% sucrose, with or without 0.2% pectic acceptor. The incubation was run at 28°C for 12 h. After precipitation of the reaction product in 70% ethanol, the methylated polymers were selectively extracted with 0.5% ammonium oxalate and radioactivity was measured in a Tricarb 2250 CA Packard scintillation counter. 

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