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1.
A. R. Jalilian L. Mirsadeghi Y. Yari-kamrani P. Rowshanfarzad M. Kamali-dehghan M. Sabet 《Journal of Radioanalytical and Nuclear Chemistry》2007,274(3):563-568
Copper-64 was produced as a by-product of 55Co via 64Ni(p,n)64Cu by 15 MeV proton bombardment of natNi resulting in a thick target yield of 5.31 MBq/μAh (143.5 μCi/μAh) and a radiochemical separation yield of 95% (radionuclide
purity >97% after 25 hours of bombardment). Rituximab was successively labeled with [64Cu]-CuCl2. N-succinimidyl-1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA-NHS) was prepared at 25 °C using DOTA and
N-hydroxy succinimide (NHS) in CH2Cl2 followed by the addition of 1 ml of a Rituximab pharmaceutical solution. Radiolabeling was performed at 37 °C in 3 hours.
Radio thin-layer chromatography showed an overall radiochemical purity of 90–95% at optimized conditions (specific activity=30
GBq/mg, labeling efficacy; 82%) using various chromatography systems. The final isotonic 64Cu-DOTA-Rituximab complex was passed through a 0.22 μm filter and checked by gel electrophoresis for radiolysis control. Stability
of the final product was checked in the formulation and in presence of human serum at 37 °C. 相似文献
2.
L. Canella M. L. Bonardi F. Groppi E. Persico C. Zona E. Menapace Z. B. Alfassi M. Chinol S. Papi G. Tosi 《Journal of Radioanalytical and Nuclear Chemistry》2008,276(3):813-818
Thanks to its favorable decay characteristics, 177gLu is finding several applications in nuclear medicine, especially for palliative metabolic radiotherapy of cancer and radioimunotherapy.
177gLu is produced in thermal nuclear reactor either by direct neutron capture 176Lu(n,γ)177(m+g)Lu on either natural or enriched 176Lu target, or by reaction on enriched 176Yb target followed by negatron decay. The latter method does produce a high radionuclidic purity and high specific activity
radionuclide in no-carrier-added form, since 177Yb decays solely to the ground state 177gLu. Conversely, the first method does produce a low specific activity 177gLu in carrier-added form,1 contaminated by the long-lived radioisotopic impurity 177mLu. The accurate determination of radionuclidic purity and half-life of 177gLu carried out by HPGe and LSCS is presented in some details. 相似文献
3.
M. Reková F. Budský V. Miler Z. Málek V. Jedináková-Křížová 《Journal of Radioanalytical and Nuclear Chemistry》2010,286(3):853-859
The aim of the study of labeling of ligand–antibody conjugates was to find optimal conditions of preparing of these conjugates
and appropriate radioactivity of selected nuclide for applications in nuclear medicine. Conjugation of the γ-immunoglobulin
G (human or bovine IgG, polyclonal antibodies) and bifunctional chelating agent, diethylenetriaminepentaacetic acid dianhydride
(cDTPAA), was carried out. Various values of the cDTPAA/antibody ratio, the weight concentration of polyclonal or monoclonal
antibodies (MEM-97) and buffers were used. Further, the labeling conditions of the DTPA–IgG conjugate by radionuclides 90Y and 177Lu were optimized, and the labeling yield and the conjugation ratio of prepared radionuclide–DTPA–IgG conjugates was determined.
Optimal incubation time of the immunoglobulin conjugation was obtained at 30 min from mixing of individual components. The
labeling yield of radionuclide–DTPA–antibody conjugate higher than 95% was achieved. Higher values of conjugation ratio of
radionuclide–DTPA–antibody conjugate were achieved in 0.1 mol L−1 carbonate buffer, pH 8.5, and the 0.1 mol L−1 carbonate buffer is suitable for studied conjugation systems. This study showed that the labeling yield as well as the conjugation
ratio of tested systems depend on the amount of antibody substance, bifunctional chelating agent/antibody molar ratio and
pH value of the buffer used. 相似文献
4.
H. Poorbaygi Sh. Sheibani S. M. R. Aghamiri M. Azizi Shamami 《Journal of Radioanalytical and Nuclear Chemistry》2012,292(1):429-434
Intra-hepatic administration of radioactive glass microspheres is a treatment for patients with primary liver cancer and hepatic
metastases. The purpose of this study was radionuclide purity assessment of new glass particles containing two radionuclide,
90Y as a therapeutic source and also 177Lu as a source of diagnostic gamma. For the mixed source, activity measurement using a dose calibrator cannot be used and
we need new calibration methods. YAS (Yb) and YAS compositions were sol–gel derived glass particles and production of 90Y (177Lu) and 90Y particles was performed using the Tehran Research Reactor. The radionuclide purity was carried out using γ-spectrometry
with HPGe detector. A non-destructive spectroscopic assay was employed due to a newly updated low uncertainty positron branching
ratio of 90Y that emit 511 keV annihilation radiations. In another method, a new calibration of 90Y using a non-destructive spectroscopic assay of 88Y were investigated. Potential radionuclide impurity include: 88Y, 152Eu, 60Co with activity 100, 50 and 5 Bq per 1 mg of that are not harmful for patients due to delivering radioactive particles about
20–50 mg in 90Y(177Lu) glass microspheres. Among of radionuclide impurity, 152Er with a half life of 13.54 years and 88Y with a half life of 106.65 days was important in the residual delivery device. For calibration of 90Y with monitoring of 511 keV, errors were12.2–21%. In calibration of 90Y using gamma spectroscopic assay of 88Y, there was an error less than 14%. Spectroscopic assay of 88Y can be performed easily and has more repeat for our purpose. 相似文献
5.
S. Pommé E. García-Toraño G. Sibbens S. Richter R. Wellum A. Stolarz A. Alonso 《Journal of Radioanalytical and Nuclear Chemistry》2008,277(1):207-210
High-resolution alpha-particle spectrometry was performed on three uranium materials enriched in 235U. Besides the 235U peaks, separate peaks belonging to impurity traces of 234U could be quantified. Relying on the isotopic composition of the uranium, as determined by mass spectrometry, the ratio of
the half-lives of 238U and 235U was determined via the activity ratio of 234U and 235U in the materials. As an intermediate link, the 234U/238U half-life ratio was taken from published mass spectrometric analyses of ‘secular equilibrium’ uranium material. The resulting
half-life ratio T
1/2(238U)/T
1/2(235U) = 6.351±0.031 is in agreement with the commonly adopted half-life values determined by Jaffey et al. 相似文献
6.
Marin Ayranov Dorothea Schumann 《Journal of Radioanalytical and Nuclear Chemistry》2010,286(3):649-654
The station for pions cancer therapy was operated at PSI from 1980 to 1992. After a cooling time of 12 years it’s made of
copper beam dump was cut and samples were taken for analytical purposes. The sampling collected about 500 g of high active
copper chips that can be used for separation of exotic radionuclides. The analyses by gamma spectrometry, LSC and AMS showed
main nuclides present to be 60Co, 54Mn, 22Na, 65Zn, 26Al, 53Mn, 59Ni, 63Ni, 55Fe and 60Fe and 44Ti with a daughter nuclide 44Sc. In the frame of ERAWAST project a procedure combining selective precipitation and ion exchange for the separation of the
rare radionuclides from the copper beam dump was developed. The proposed separation procedure is easy for remote controlled
implementation in a hot cell. The ion exchange separation of Ni, Al, Mg, Ti and Fe was complete and high decontamination factors
for copper and cobalt were achieved. Based on the developed procedure a remotely controlled system for separation of exotic
radionuclides from the copper chips was set up. The full scale system was installed in a hot cell where high activity levels
can be handled. In order to evaluate the reliability and functionality of the system extensive tests have been done. During
the test period 13.86 g in total of the proton irradiated copper beam dump were processed for separation of 26Al, 59Ni, 53Mn, 44Ti and 60Fe. The results showed that the system was operational and the radionuclide separation was selective with high chemical yield.
The procedure manages as well the generated liquid wastes containing high level of 60Co activity. 相似文献
7.
A. D. Sajeniouk 《Journal of Radioanalytical and Nuclear Chemistry》2005,264(2):337-342
8.
Chang Heon Lee Moo Yul Suh Kwang Yong Jee Won Ho Kim 《Journal of Radioanalytical and Nuclear Chemistry》2007,272(1):187-194
A sequential separation procedure has been developed for the determination of 99Tc, 94Nb, 55Fe, 90Sr and 59/63Ni in various radioactive wastes generated from nuclear power plants. Ion exchange and extraction chromatography were adopted
for individual separation of the radionuclides. Precipitation was supplementarily utilized for both purification of the individual
radionuclides and preparation of the radionuclide sources for use in a radioactivity measurement. The chromatographic separation
behavior of the radionuclides both from the sample matrix metals and from one another was investigated using stable metals,
Re (as a surrogate of 99Tc), Nb, Fe, Sr and Ni. The validity of the procedure for reliability and applicability was evaluated by measuring the recovery
of the metal carriers added to synthetic radioactive waste solutions. The recoveries by the chromatographic separation were
in the range of 84.8 to 102.2% with 2s of less than 8.6%, the recoveries by the precipitation being in the range of 84.3 to 97.3% with 2s of less than 10.9%. 相似文献
9.
10.
Dimitrios C. Xarchoulakos Konstantina Kehagia Nikolaos Kallithrakas-Kontos Constantinos Potiriadis 《Journal of Radioanalytical and Nuclear Chemistry》2017,312(2):285-292
For the first time, a radiological study for the dissolved 238U, 234U, 210Pb and 210Po was held in major Greek rivers across the country. 234U/238U activity ratios are above one in all samples and 210Po/210Pb activity ratios are respectively below the unit indicating the disequilibrium in the samples. Quite satisfactory correlations were observed among 234U and 238U as well as among 210Po and 210Pb values. Uranium isotopes were separated by ion exchange and electroplated on stainless steel plates. 210Po was spontaneously deposited on nickel plates, while 210Pb was indirectly determined through the ingrowth of 210Po. The sources were measured by a-spectrometry. 相似文献
11.
Chang Heon Lee Myung Ho Lee Sun Ho Han Yeoung-Keong Ha Kyuseok-Song 《Journal of Radioanalytical and Nuclear Chemistry》2011,288(2):319-325
A simple and rapid separation procedure was systemized for the determination of 99Tc, 90Sr, 94Nb, 55Fe and 59,63Ni in low and intermediate level radioactive wastes. The integrated procedure involves precipitation, anion exchange and extraction
chromatography for the separation and purification of individual radionuclide from sample matrix elements and from other radionuclides.
After separating Re (as a surrogate of 99Tc) on an anion change resin column, Sr, Nb, Fe and Ni were sequentially separated as follows; Sr was separated as Sr (Ca-oxalate)
co-precipitates from Nb, Fe and Ni followed by purification using Sr-Spec extraction chromatographic resin. Nb was separated
from Fe and Ni by anion exchange chromatography. Fe was separated from Ni by anion exchange chromatography. Ni was separated
as Ni-dimethylglyoxime precipitates after the removal of 134,137Cs and 110mAg by Cs-phosphotungstate and AgCl precipitation, respectively. Finally, the radionuclide sources were prepared by precipitation
for their radioactivity measurements. The reliability of the procedure was evaluated by measuring the recovery of chemical
carriers added to a synthetic radioactive waste solution. 相似文献
12.
Claudia Landstetter Christian Katzlberger 《Journal of Radioanalytical and Nuclear Chemistry》2009,282(2):467-471
Screening measurements for 3H, 226Ra, 222Rn and 238U in ground water were performed within a ground- and drinking water project in Austria. The aim of this project is to get
an overview of the distribution of natural radionuclide activity concentration levels in ground water bodies. In some cases
this water is used for drinking water abstraction. In this paper methods and results of the screening measurements are presented.
Regions with high activity concentrations were identified and in these regions further investigation for 228Ra, 210Pb and 210Po will be conducted. 相似文献
13.
Summary An extraction chromatography method was developed for the separation of 239Np from 243Am in nitric acid solution. A sorbent based on aliphatic quaternary amine Aliquat-336 and hydrophobized silica gel was prepared. 239Np reduced to the oxidation state(IV) with ferrous sulfamate in 2M or 6M HNO3 sorbs on the prepared silica gel column. After washing with 0.1M ferrous sulfamate in 2.5M HNO3, 239Np is eluted with 0.1M HNO3 containing 0.02M HF. The separation of 243Am from 239Np is very effective. The purity of 239Np was found to be better than 99.5%. The proposed 239Np milking procedure is suitable for the preparation of 239Np tracer that can be used for the determination of 237Np radiochemical yield. 相似文献
14.
M. Yamamoto A. Sakaguchi J. Tomita T. Imanaka K. Shiraishi 《Journal of Radioanalytical and Nuclear Chemistry》2009,279(1):93-103
To estimate the dietary intakes of 210Pb and 210Po for the Japanese adults and their annual effective doses, 210Pb and 210Po were measured for 240 daily diet samples collected at two locations of Ishikawa Prefecture in Japan over three years by
duplicate portion studies. No appreciable differences in intake rates of 210Pb and 210Po and their 210Po/210Pb ratios were seen among the years in each district, and between the two districts. The intake rates evaluated using 240
diet samples were 0.20 Bq/d/p for 210Pb and 0.61 Bq/d/p for 210Po as a median, respectively. Annual effective doses of 210Pb and 210Po for Japanese adults were estimated to be 0.050 and 0.053 mSv/y, respectively. 相似文献
15.
Matthias J. Brunnermeier Stefanie A. K. Schmied Robert Schupfner 《Journal of Radioanalytical and Nuclear Chemistry》2012,292(3):1285-1290
The period of date of death of an elephant can be assessed by analyzing four different radionuclides, 14C, 90Sr, 228Th and 232Th in its ivory. These nuclides are supposed to have variing concentrations at different parts of a tusk. The reason is the
procedure of growth which takes place at the butt-site of a tusk. Therefore the site of sampling could have a big influence
on the assessed date of death. However, to find out if the position of sampling is important a complete tusk was analyzed
regarding the distribution of these nuclides. Results show that the concentration activity of 14C and 228Th varies in different parts of a tusk. The activity concentration of 90Sr is very similar in all analyzed parts. The conclusion is that sampling at the butt of a tusk is recommended for age assessment. 相似文献
16.
S. K. Aggarwal D. Alamelu P. M. Shah N. N. Mirashi 《Journal of Radioanalytical and Nuclear Chemistry》2007,273(3):771-774
Determination of 241Am/243Am ratios is required for vanous purposes including assay of Am by isotope dilution techniques. Alpha-spectrometry on electrodeposited
sources is a preferred technique for this determination. However, there is an inherent problem of tail contribution which
necessitates the use of suitable algorithms to account for the same. Recently, in the frame of a Coordinated Research Program
(CRP) of the International Atomic Energy Agency (IAEA), WinALPHA software has been developed which is a combination of an
asymmetrical Gaussian for the main part of the peak and a low energy function. Therefore, it was of interest to compare the
use of this algorithm with the routinely used method, in our laboratory, based on geometric progression (G. P.) decrease.
Since, there are no reference materials available commercially for 241Am/243Am ratios, synthetic mixtures covening a wide range (0.3 to 2.0) of 241Am/243Am α-activity ratios were used and un-ignited electrodeposited sources were prepared for α-spectrometry. The α-spectra obtained using PIPS detector, were evaluated using the two algonthms The 241Am/243Am α-activity ratios obtained were also compared with those determined by thermal ionization mass spectrometry (TIMS). An agreement
of about 1% was obtained in the 241Am/243Am ratios determined by the two methods and also by using the two algorithms for α-spectrum evaluation. 相似文献
17.
S. Osaki S. Sugihara Y. Maeda T. Osaki 《Journal of Radioanalytical and Nuclear Chemistry》2007,272(1):135-140
Depth distribution of atmospheric 210Pb and 7Be and 90Sr and 137Cs fission products was measured in two types of aeolian soils (desert dust and volcanic ash), irrigated paddy soil and strongly
acidic soil. The depth dependence of 210Pb, 7Be and 137Cs show that these radionuclides have been diffused as solid soil particles in surface soil layers. In aeolian soil layers,
about 50% of 90Sr were diffused in surface soil layer and the remaining 50% had penetrated to deeper layers. The half of the fission particles
containing 90Sr were shown to have decomposed over the past 35 years. 相似文献
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20.
V. N. Yelgaonkar K. C. Jagadeesan V. Shivarudrappa V. K. Sharma S. Chitra 《Journal of Radioanalytical and Nuclear Chemistry》2007,274(2):277-280
Radiotracers are extensively used in many industries for trouble shooting and optimization of process parameters leading to
considerable savings in time and huge economic benefits. In chemical and petrochemical industries different gases and vapours
flowing in the conversion reactors play a major role in the final production. Gaseous radiotracers are ideal to study hydrodynamics
of gas phases in process vessels. 41Ar and 79Kr are the preferred gaseous radiotracers for such studies. Owing to the increase in demand from Indian industries for gas
phase radiotracers, efforts have been made to produce 41Ar and 79Kr indigenously by irradiation of 40Ar and enriched 78Kr gaseous targets in research reactors. Prequalification of the containers used, safety aspects concerning accidental rupture
and mandatory tests necessary for irradiation of gaseous targets in the reactors have been studied. The paper describes some
of the important safety aspects involved and the results of trial irradiations on the production of 41Ar and 79Kr radiotracers. Standardization of suitable assay protocols for their regular production and supply for applications in industries
is also described. 相似文献