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Rapid identification of bluetongue virus by nucleic acid hybridization in solution.

A liquid phase hybridization format has been adapted for the identification of bluetongue virus (BTV) with respect to serogroup and serotype. In this paper we present experiments which demonstrate the identification of bluetongue virus with respect to both serogroup and serotype. BTV serogroup-specific and BTV serotype 17-specific single-stranded RNA probes labeled with 35S-CTP were used to identify BTV viral nucleic acids in infected cell culture lysates. Cell lysates were prepared for testing by rapid solubilization in a guanidine isothiocyanate/EDTA/dithiothreitol medium. Hybridizations were done in 12.5 microliter reaction volumes for 2 h or overnight using nanogram quantities of probe. An RNAse solution was added subsequent to hybridization and incubated for 30 min. TCA-precipitable counts were collected and quantitated by scintillation counting. Specific hybridization signals were obtained in as little as 3 h in assays consisting of uninfected controls, cells infected with different BTV serotypes, and cells infected with a strain of epizootic hemorrhagic disease of deer (EHDV-1). By using asymmetric single-stranded RNA probes we were able to distinguish viral mRNA and viral double-stranded RNA components. We propose this technique as an ancillary or replacement procedure for the confirmation and classification of viral isolates using an appropriate battery of nucleic acid probes. Potential applications and methods of enhancing the technique are discussed.

Bluetongue virus↗

Correction of sample absorption of radioactivity.

In the method presented here for the correction of sample absorption of C(14) activity, the only requirement is the availability of any C(14)-labeled compound of sufficiently high specific activity to permit addition, in negligible mass, of a number of counts equal to or greater than that in unknown samples and with solubility characteristics that exclude preferential layering during drying of samples. The principle may be applied to liquid scintillation counting. Absorption curves are dispensed with, and the weights of the assayed samples need not be determined.

Radioactivity↗

A rapid assay for DNA repair synthesis using neutral and alkaline sodium iodide gradients.

A modification to the method for estimation of repair DNA synthesis in cultured mammalian cells using density labeling which reduces the time and labor involved is described. Centrifugation times are reduced by using high-molecular-weight DNA which is loaded onto the top of a preformed sodium iodide gradient. Cerenkov counting is used to locate the region of the gradient containing light DNA for rebanding and likewise to identify appropriate fractions from alkaline gradients for acid precipitation for scintillation counting. The procedures give results indistinguishable from cesium chloride equilibrium gradients in a shorter time, with less effort, and at a lower cost.

Centrifugation, Density Gradient↗

LSC measurements of the half-life of 40K.

Liquid scintillation counting techniques combined with the CIEMAT/NIST method have been applied to measure the specific activity of natural potassium salts. Samples have been prepared with three different scintillators. The individual atomic composition as well as the density of the cocktails have been taken into account for the efficiency calculation. With the specific activity the half-life is calculated to be T1/2 = 1.248(3) x 10(9) a. The result is in reasonable agreement with other measurement results provided the same isotopic concentration of 40K is used.

Algorithms↗

Measurement of 90Sr in bone ash.

Bone is a critical organ for the accumulation of many radionuclides, including 90Sr. A bone ash has been prepared by NIST to become a standard reference material and the assaying of the 90Sr activity concentration is reported. A radiochemical procedure, based on extraction chromatography using a crown ether, has been developed to separate Sr from the bone ash. The natural Sr content of the bone ash has been determined by isotope dilution inductively coupled plasma mass spectrometry. The 90Sr activity concentration has been measured by low-level liquid scintillation counting.

Animals↗

The standardization of samarium-153.

Samarium-153 has been standardized by 4 pi beta liquid-scintillation counting, with an uncertainty of 0.4%. The probability per decay for the 103.2-keV gamma ray was measured, using two germanium detectors, to be 0.298 +/- 0.004. The half life, based on liquid-scintillation measurements over 6.4 half lives and pressurized-ionization-chamber measurements over four half lives, was found to be 46.27 +/- 0.02 h. The uncertainties given are one estimated standard deviation (of the mean when applicable) for random and non-random components.

Gamma Rays↗

Decoloration and solubilization of plant tissue prior to determination of 3H, 14C, and 35S by liquid scintillation.

A method is described for the decoloration and partial solubilization of plant tissue with 2% sodium hypochlorite. Following treatment of the digest with ammonia, the samples are suitable for the determination of 3H, 14C, and 35S by liquid scintillation counting. The color quenching is negligible and counting efficiencies are high: 30-40% for 3H and 90-95% for 14C.

Carbon Radioisotopes↗

Comparison of calculated spectra for the interaction of photons in a liquid scintillator. Example of 54Mn 835 keV emission.

The CIEMAT/NIST and TDCR methods in liquid scintillation counting, initially developed for the activity standardization of pure-beta radionuclides, have been extended to the standardization of electron capture and beta-gamma radionuclides. Both methods require the calculation of the energy spectrum absorbed by the liquid scintillator. For radionuclides emitting X-rays or gamma-rays, when the energy is greater than a few tens of keV the Compton interaction is important and the absorption is not total. In this case, the spectrum absorbed by the scintillator must be calculated using analytical or stochastic models. An illustration of this problem is the standardization of 54Mn, which is a radionuclide decaying by electron capture. The gamma transition, very weakly converted, leads to the emission of an 835 keV photon. The calculation of the detection efficiency of this radionuclide requires the calculation of the energy spectrum transferred to the scintillator after the absorption of the gamma ray and the associated probability of absorption. The validity of the method is thus dependent on the correct calculation of the energy transferred to the scintillator. In order to compare the calculation results obtained using various calculation tools, and to provide the metrology community with some information on the choice of these tools, the LS working group of the ICRM organised a comparison of the calculated absorbed spectra for the 835 keV photon of 54Mn. The result is the spectrum of the energy absorbed by the scintillator per emission of an 835 keV gamma ray. This exercise was proposed for a standard 20 ml LS glass vial and for LS cocktail volumes of 10 and 15 ml. The calculation was done for two different cocktails: toluene and a widely used commercial cocktail, Ultima Gold. The paper describes the results obtained by nine participants using a total of 12 calculation codes.

Algorithms↗

Sensitive radiochemical esterolytic assays for urokinase.

Two radiochemical esterolytic assays for urokinase are described. One assay is based on the urokinase-dependent hydrolysis of Nalpha-acetyl-glycyl-L-lysine [3H]methyl ester and the other on the urokinase-dependent activation of plasminogen and assay of generated plasmin with Nalpha-tosyl-L-arginine [3H]methyl ester. The assays are performed in tubes placed in liquid scintillation counting vials. At the end of the experiment generated [3H]methanol is extracted into the liquid scintillation cocktail and counted. Unhydrolyzed substrate largely remains in the aqueous phase and contributes only a small fraction of the counts. This facile separation of 3H-labeled alcohol from the ester substrate allows the simple and highly sensitive assay for urokinase. The assays give results in good agreement with the classical fibrin plate assay.

Adult↗

Assay of tritium-labelled terbutaline.

A method for the determination of unchanged 3H-labelled terbutaline in biological samples was developed for use in early pharmacokinetic investigations involving various species. Terbutaline was isolated from the biological sample by ion pair extraction with 0.015 mol/L bis(2-ethylhexyl)phosphoric acid in methylene chloride. To eliminate co-determination of conjugated terbutaline present in the samples, extraction was combined with partition chromatography. Quantification was achieved by liquid scintillation counting. The recovery of [3H]terbutaline from serum and urine was 96.1 +/- 0.7 (mean +/- SEM) in the concentration range 1-250 ng/mL.

Animals↗

An index to measure the healing potential of ischaemic ulcers using Thallium 201.

Prediction of healing of ulcers in ischaemic limbs can preclude unnecessary treatment for ulcers that cannot heal. Non-invasive methods are of marked value as the ischaemic limb is susceptible to further ulceration from local skin penetration. Relative hyperemia of the ulcer was measured by scintillation count over the ulcer and at points 2.5 cm from the edge of the ulcer. Relative hyperemia was determined by dividing the count per unit area of the ulcer by the counts per unit area of the surrounding tissue. All ulcers with a relative hyperemia over 1.5 healed.

Humans↗

The influence of exogenous oxytoxin on labelling of secretory epithelium of mouse mammary gland by [3H]leucine, evidenced by autoradiography.

It has been suggested that oxytocin, besides its milk-ejecting activity, is also involved in the hormonal regulation of the mammary gland secretory cells. The available data, however, are conflicting. In this study two independent experiments, separated by a certain time interval show that oxytocin intravenously administered to mice at days 10-14 of lactation diminished the incorporation of [3H]leucine into the mammary gland tissue by 32 and 53 per cent, respectively. The neurohormone was co-injected with the tracer amino acid. The radioactivity taken up by the secretory cells was estimated by light microscopic autoradiography. The autoradiograms were evaluated by visual silver grain counting. Tissue radioactivity was measured by liquid scintillation counting. A milk stasis in the mammary gland induced by depriving the mice of suckling two hours before tracer injection had no influence on the secretory activity of the glandular cells. It is assumed that oxytocin has a direct effect on the milk-producing cells, and that the reduction in measurable radioactivity caused by the neurohormone may be due to an accelerated intracellular passage of labelled milk proteins.

Animals↗

Occupational ingestion of P-32: the value of monitoring techniques to determine dose. A case report.

The purpose of this article is to described the analytical methods used to assess the internal dose from a P-32-labeled compound that was inadvertently ingested. Bioassay data, using the International Commission on Radiation Protection (ICRP)-30 model, enabled the calculation of internal dose. Whole body counting (WBC) and urinary measurement with liquid scintillation counting were utilized to estimate the amount of radioactive material deposited in body organs. This metabolic model assumes that 80% of the material ingested is absorbed through the gastrointestinal tract because P-32 is soluble. The time of the intake, a critical variable in this method, was estimated on the basis of urine contamination of clothing. Twenty-four-hour urine sampling over a 6-week period, coupled with daily WBC over the same period, was performed. Because P-32 does not emit photons, WBC relied on measuring the bremsstrahlung radiation produced as a result of interaction of beta radiation with the body's tissues. A P-32-spiked phantom was used as a control. Over the 6-week monitoring period, urinary results indicated an ingestion of 560 microCi of P-32, whereas WBC estimated on intake of 580 microCi. An assessment of the laboratory where the accident occurred indicated that approximately 600 microCi of radioactive phosphorous was missing. The total effective dose equivalent was estimated at 4.8 rem (48 mSv). On the basis of this study, the ICRP model appears to fit the data obtained from urine measurements and WBC. No symptoms were noted from the ingestion of 580 microCi. The committed organ doses were well within the occupational nonstochastic limits of 50 (0.5 Sv) permitted by the Nuclear Regulatory Commission. These results were confirmed by NUREG/CR-4884 and commercial software (CINDY). This report confirms the value of using the ICRP-30 model with urinary measurements and WBC to estimate the dose received as a result of ingestion of radioactive P-32.

Accidents, Occupational↗

The measurement of activity contained in a 32P stainless-steel stent by destructive assay.

Destructive assays of stainless-steel stents containing 32P were performed. Prior to assay, 24 stents were intercompared on a NaI(Tl) well-type crystal. A subset of stents were then digested in a suitable carrier solution by the addition of concentrated hydrofluoric acid. The final solution was measured by the CIEMAT/NIST tritium efficiency tracing method for liquid scintillation counting. A separate experiment was performed which indicated no loss of activity during stent digestion. Expanded (k = 2) uncertainties on stent activity ranged from 1.0% to 2.6%.

Angioplasty, Balloon, Coronary↗

Thin-layer chromatography analysis of human CYP3A-catalyzed testosterone 6beta-hydroxylation.

Testosterone and other steroid hormones have been studied as prototypic examples of endogenous substrates for hepatic cytochrome P450 (P450) enzymes. CYP3A enzymes from various species, including human, metabolize testosterone by a 6beta-hydroxylation reaction, which is unique to this P450 subfamily. A thin-layer chromatographic method is described for the determination of 6beta-hydroxytestosterone formed enzymatically by incubation of [14C]-testosterone with cDNA-expressed CYP3A enzymes or liver microsomes. 14C-labeled enzymatic products are applied to silica gel thin-layer plates, which are developed sequentially with methylene chloride:acetone (80:20) followed by chloroform, ethyl acetate, and absolute ethanol (80:20:14). Metabolite quantification is performed by autoradiography and liquid scintillation counting. This method is applicable to enzymatic studies for the determination of CYP3A-dependent testosterone 6beta-hydroxylation activity in both human and animal liver microsomes.

Autoradiography↗

A modified Lucas cell for leakage measurement from encapsulated radium sources.

A new method to determine the leakage rate from encapsulated radium sources is proposed. The method is based on the principle of enclosing the source to be tested in a hermetically sealed container and measuring the radon radioactivity growth in the container as a function of time. A cylindrical modified Lucas cell, designed and built in our laboratory, is used for measuring the radon which are done by ZnS(Ag) alpha scintillation counting and can be easily compared with existing standard for leak tests. Results obtained show the applicability of the method for leak testing for radon leakage from sealed radium sources.

Kinetics↗

Standardization of 125I and 238Pu.

A simple distance-variable detection table on which two detectors can be mounted and moved back and forth facing each other centred on a sample source has been constructed for photon-photon and alpha-photon coincidence counting for 125I and 238Pu, respectively. Two NaI(Tl) detectors were used for the standardization of 125I. A Si detector and an NaI(Tl) detector were employed for the standardization of 238Pu. The NaI(Tl) detectors have a very thin aluminium window for measuring low-energy photons from 125I and 238Pu while the Si-detector is a usable-in-air ion-implanted detector for alpha particles from 238Pu. A thin collodion film was used for 238Pu samples, whereas a thick polyester film was used for 125I samples to prevent 125I from leaking from the sample. The key comparison result of 125I showed good agreement, and the result of 238Pu was also compared with that of liquid scintillation counting.

Algorithms↗

Systemic distribution of 14C-labeled formaldehyde applied in the root canal following pulpectomy.

The systemic distribution of 14C-labeled formaldehyde which had been placed in the root canals of the canines of cats following pulpectomies was studied using liquid scintillation counting and wholebody autoradiographic technique. Radioactive 14C which had been placed in the canals was found in the plasma 30 min after the root canal procedure. The recovery of systemic 14C radioactivity increased with time. In addition, it seemed that approximately 3% of the dose placed in the teeth was excreted in the urine within 36 h. Whole-body autoradiograms indicated extensive concentration of 14C radioactivity in tissues other than those analyzed with the liquid scintillation technique.

Animals↗