Calibration of a cadmium IVNAA system

An in vivo neutron activation analysis (IVNAA) system for the measurement of cadmium in the human liver and kidney was calibrated using cadmium doped liver and kidney phantoms in a water tank. The effect on the number of cadmium gammas detected with changes in organ position and cross-organ interference was assessed. The lower limits of detection were found to be 12 mg cadmium in the kidney and 7 ppm cadmium in the liver. This system was compared to five others using a performance index which considers equipment specifications and dose to the subject, and was found to rank second best for the liver measurements and second worst for the kidney measurements. The results from the organ position studies showed that the depth of the organs in the body has a great effect on the results, and differences between systems could be partially due to differences in calibration geometry.     

Evaluation of amperometric detector for liquid chromatographic determination of 2-phenylphenol residues in orange rind

A modular component liquid chromatograph has been assembled which has on-stream ultraviolet (UV) and amperometric detectors connected to a dual pen recorder. In this method, the commonly used UV detection technique provides a reference for direct comparisons of results from the amperometric detector. The system has been evaluated and applied to the determination of 2-phenylphenol (2PP) fortified in orange rind. The method is not tedious; before liquid chromatographic analysis, the sample is extracted with methylene chloride and cleaned up on a Florisil column. The method is sensitive to less than 1 ppm 2PP fortified in orange rind; there are no electrically oxidizable interference, from control samples, in the chromatographic region of 2PP. Some background interference does appear from the same samples on the UV chromatogram. Thus, amperometric detection is more specific than UV detection for this application.     

A Monte Carlo study of the quality dependence of diamond thermoluminescent dosimeters in radiotherapy beams

Monte Carlo simulations with the EGS4 code system have been performed to determine the quality dependence of diamond TLDs in photon beams ranging from 25 kV to 25 MV x-rays and also in megavoltage electron beams. It has been shown that diamond TLDs in the form of discs of thickness 0.3 mm and diameter 5.64 mm show no significant dependence on the incident energy in clinical electron beams when irradiated close to dmax, but require an energy correction factor of 1.050 +/- 0.008 compared with diamond TLDs irradiated in 60Co gamma-rays. The correction factor increases with depth of irradiation and this effect is greater for thicker detectors. The Monte Carlo predicted sensitivity in x-ray beams is constant within 2.5% over the energy range 250 kV to 25 MV. However the sensitivity decreases by about 60% for 25 kV x-rays compared with 60Co gamma-rays.     

Cadmium resistance in A549 cells correlates with elevated glutathione content but not antioxidant enzymatic activities

Glutathione has been implicated to function in cytoprotection against cadmium toxicity. The mechanism by which glutathione plays this role has not been well understood. Because glutathione is an important antioxidant and several studies have shown that cadmium induces oxidative stress, this study was undertaken to determine whether development of cadmium resistance is linked to enhanced antioxidant activities. A cadmium-resistant subpopulation of human lung carcinoma A549 cells, which was developed by repeatedly exposing the cells to step-wise increased cadmium concentrations, was compared to a cadmium-sensitive one. The acquired cadmium resistance resulted from neither decreased cadmium uptake nor enhanced cellular metallothionein synthesis. Glutathione content, however, was markedly elevated in the cadmium-resistant cells. In contrast, the activities of the glutathione redox cycle related enzymes, glutathione peroxidase and reductase, were unchanged. Two other antioxidant enzymes, superoxide dismutase and catalase, were also not altered. The results suggest that the development of cadmium resistance in A549 cells unlikely results from enhanced antioxidant enzyme activities, although it is associated with elevated cellular glutathione levels. In addition, measurement of the mRNA and DNA levels for gamma-glutamylcysteine synthetase, the rate-limiting enzyme for glutathione biosynthesis, revealed that enhanced expression of the enzyme but not gene amplification is likely responsible for the elevation of cellular glutathione levels.     

A comparison of clinical results in brain scanning using germanium semiconductor detectors and sodium iodide detectors

A comparison is presented of the image quality obtained with a 70 mm Ge(Li) detector scanner and with routine techniques based on NaI (Tl) detectors. One hundred and sixty-five pairs of brain scans have been examined for which the patients have been scanned with both Ge(Li) and NaI (Tl) detectors. It is concluded that no major difficulties exist in introducing Ge(Li) scanners and that while a comparison of scans from different instruments is difficult there is evidence that improved diagnostic information may be obtained from scanners with Ge(Li) detectors.     

红外探测材料的发展状况及未来发展

红外探测仪中，半导体红外探测技术相对较为成熟，逐步由传统半导体材料向半导体异质结、半导体超品格、半导体量子阱和半导体量子点等材料发展；人们发现超导的特性之后，设法研究超导红外探测仪，超导红外探测仪中又分STS、热电子和超导薄膜等类型；近些年又发展了超巨磁阻红外探测仪。技术的发展使材料的灵敏度、工作温度和探测率也在不断的向高层次发展，并不断的发现新的材料。在规模上，红外探测仪将会不断的向大规模焦平面方向发展(即热成像仪)；探测波长方面，要由单色向双色和多色发展；随技术的发展，红外探测仪应用也将大大的拓展。     

Methods for the measurement of benzodiazepines in biological samples

A review of methods for the measurement of benzodiazepines in biological specimens published over the last five years is presented. A range of immunoassay procedures using EIA, ELISA, FPIA, agglutination or kinetic interaction of microparticles, or RIA methods are now available. Cross reactivities to benzodiazepines are variable such that no one kit will recognise all benzodiazepines and their relevant metabolites at concentrations likely to be encountered during therapeutic use. Prior hydrolysis of urine to convert glucuronide metabolites to immunoreactive substances improves detection limits for many benzodiazepines. Several radioreceptor assays have now been published and show good sensitivity and specificity to benzodiazepines and offer the advantage (over immunoassay) of being able to detect these drugs with equal sensitivity. Solvent extraction techniques using a variety of solvents were still popular and offer acceptable recoveries and lack of significant interference from other substances. A number of papers describing solid phase extraction procedures were also published. Direct injection of specimens into a HPLC column with back flushing were also successfully described. Seventy two chromatographic methods using HPLC, LC-MS, GC and GC-MS methods were reviewed. HPLC was able to achieve detection limits for many benzodiazepines using UV or DAD detection down to 1-2 ng/ml using 1-2 ml of urine or serum (blood). ECD detectors gave detection limits better than 1 ng/ml from 1 ml of specimen, which was an order of magnitude lower than for NPD. EI-MS offered similar sensitivity, whilst NCI-MS was capable of detection down to 0.1 ng/ml. Methods suitable for the separation of enantiomers of benzodiazepines have been described using HPLC. Electrokinetic micellar chromatography has also been shown to be capable of the analysis of benzodiazepines in urine.     

Study of dosimetry consistency for kilovoltage x-ray beams

In this paper, the consistency of kilovoltage (tube potentials between 40 and 300 kV) x-ray beam dosimetry using the "in-air" method and the in-phantom measurement has been studied. The procedures for the measurement of the central-axis depth-dose curve, which serve as a link between the dose at the reference depth to the dose elsewhere in a phantom, were examined. The uncertainties on the measured dose distributions were analyzed with the emphasis on the surface dose measurement. The Monte Carlo method was used to calculate the perturbation correction factors for a photon diode and a NACP plane-parallel ionization chamber at different depths in a water phantom irradiated by 100-300 kV (2.43 mm Al-3.67 mm Cu half-value layer) x-ray beams. The depth-dose curves measured with these two detectors, after correcting for the perturbation effect (up to 15% corrections), agreed with each other to within 1.5%. Comparisons of the doses at the phantom surface and at 2 cm depth in water for photon beams of 100-300 kV tube potential obtained using the "backscatter" method and those using the "in-phantom" measurement have shown that the "in-air" method can be equally applied to this energy range if the depth-dose curve can be measured accurately. To this end, measured depth ionization curves require depth-dependent correction factors.     

The design of an animal PET: flexible geometry for achieving optimal spatial resolution or high sensitivity

We present the design of a positron emission tomograph (PET) with flexible geometry dedicated to in vivo studies of small animals (TierPET). The scanner uses two pairs of detectors. Each detector consists of 400 small individual yttrium aluminum perovskite (YAP) scintillator crystals of dimensions 2 x 2 x 15 mm3, optically isolated and glued together, which are coupled to position-sensitive photomultiplier tubes (PSPMT's). The detector modules can be moved in a radial direction so that the detector-to-detector spacing can be varied. Special hardware has been built for coincidence detection, position detection, and real-time data acquisition, which is performed by a PC. The single-event data are transferred to workstations where the radioactivity distribution is reconstructed. The dimensions of the crystals and the detector layout are the result of extensive simulations which are described in this report, taking into account sensitivity, spatial resolution and additional parameters like parallax error or scatter effects. For the three-dimensional (3-D) reconstruction a genuine 3-D expectation-maximization (EM)-algorithm which can include the characteristics of the detector system has been implemented. The reconstruction software is flexible and matches the different detector configurations. The main advantage of the proposed animal PET scanner is its high flexibility, allowing the realization of various detector-system configurations. By changing the detector-to-detector spacing, the system is capable of either providing good spatial resolution or high sensitivity for dynamic studies of pharmacokinetics.     

Research and application on the automatic measuring device for testing transverse thickness difference of cold-rolling steel sheet

Many advanced technologies have been applied in developing the automatic measuring device for testing transverse thickness difference of cold-rolling steel sheet,such as the technologies of automatic control,sensor measurement,marking identification,photographic location,computer application and information transmission.This measuring device can measure the transverse thickness difference of the steel plate accurately and quickly,with a high detection level of automation.It is an effective detection equipment for transverse thickness control of steel plate.Horizontal width of steel plate measuring 0.8-1.4 m, horizontal measurement point positioning accuracy±0.02 mm,thickness range 0.2-2.0 mm, measurement accuracy within±1μm.     

火焰原子吸收光谱法测定锑品中微量镉

利用火焰原子吸收光谱(FAAS)分析技术,对测定锑品中微量镉的基体和共存元素干扰、仪器分析参数等因素进行了研究,确定了最佳分析条件。试验结果表明:该方法准确、可靠、简便、适用。方法的检出限0.008 2μg/mL,相对标准偏差小于6%,回收率为92%～101%。     

提高鞍钢冷连轧机效能和产品精度的途径

通过对鞍钢1680mm冷连轧机力能参数、结构参数、带钢厚度和板形精度的大型综合测试,采用综合遗传神经网络建立轧制力模型,与实测误差不大于5％;采用综合改进遗传算法与冷连轧机辊型系统优化相结合,板形废品率从2．24％降至1．19％;运用缩合改进遗传算法与冷连轧机大系统参数相结合优化轧制规程,相同厚度来料成品由1mm扩大至0．8mm;运用“机电结合故障诊断法”,打出带钢厚差无法消除和易断带的原因。综合措施提高了轧机的效能和产品的精度。     

金属矿山选矿厂磨矿分级自动控制研究现状

自动控制技术在国内选矿厂磨矿分级流程中应用已有将近40年,为促进磨矿分级控制系统的工业化应用和深入研究,对磨矿分级控制系统的发展进行了综述。目前磨矿分级检测仪表主要分为给矿量、矿浆流量、矿浆浓度、矿浆粒度、矿仓料位、磨机负荷量等六个方面;检测手段分为直接测量和间接测量。磨矿分级控制策略从传统控制策略发展为现代控制技术和人工智能控制技术相互结合的控制策略。     

Numerical signal treatment for optimized alanine/ESR dosimetry in the therapy-level dose range

Electron spin resonance (ESR) spectra of alanine detectors irradiated to absorbed doses below 5 Gy are affected by a varying non-linear background which mainly influences the lower limit of detection in alanine/ESR dosimetry. A mathematical method based on fast Fourier transform is described capable of filtering simultaneously background and noise in the frequency domain of ESR spectra. It provides clearer alanine/ESR signals down to 50 mGy. Even in non-irradiated but long-term stored alanine detectors an ESR signal could be observed similar to irradiated alanine (pre-signal). A linear ESR signal vs absorbed dose relationship was found above 200 mGy, after correction for background and pre-signal. The number of repeated ESR read-out cycles and hence the time required for a precise and reliable low-dose evaluation have significantly been reduced. The method has been worked out for the therapy-level dosimetry range and tested on a Bruker ESP 300 and for comparison Bruker EMS 104 ESR spectrometer.     

Functionally null mutations in patients with the cblG-variant form of methionine synthase deficiency

A column-switching liquid chromatographic method is described for the simultaneous determination of aspirin and salicylic acid in human plasma. Blood samples are taken into chilled tubes containing a fluoride anticoagulant, and the plasma is isolated by centrifugation. Following a simple acidification step, a 200 microL aliquot of the sample is injected directly onto the HPLC system. The C-18 extraction column is washed with acidified water for 2 min, after which time the compounds are removed by back-flushing directly onto the analytical column (C-8 Nucleosil, 5 microns, 250 mm x 4.6 mm). The flow rate through both columns is 1 mL/min, and the analytes are quantified by measurement of their UV absorbance at 225 nm. The mobile phase is a mixture of water-methanol-acetonitrile-orthophosphoric acid (650:200:150:1 v/v/v/v). The method is linear in the concentration ranges 0.10-5.00 micrograms/mL for aspirin and 0.25-15.00 micrograms/mL for salicylic acid. Both compounds have a limit of quantitation of 0.10 microgram/mL and a limit of detection of 0.04 microgram/mL. Extensive stability tests have been carried out, and validation studies reveal the method to be reproducible and repeatable. Excellent recoveries from plasma obviate the need for an internal standard. The procedure is easier to execute and requires less sample handling than methods currently described in the literature. It has been successfully applied to the investigation of the levels of aspirin and salicylic acid in a healthy, nonfasting volunteer following a 600 mg oral dose of aspirin.     

Performance evaluation of a whole-body PET scanner using the NEMA protocol. National Electrical Manufacturers Association

This study evaluates the performance of the newly developed high-resolution whole-body PET scanner ECAT EXACT HR+. METHODS: The scanner consists of four rings of 72 bismuth germanate block detectors each, covering an axial field of view of 15.5 cm with a patient port of 56.2 cm. A single block detector is divided into an 8 x 8 matrix, giving a total of 32 rings with 576 detectors each. The dimensions of a single detector element are 4.39 x 4.05 x 30 mm3. The scanner is equipped with extendable tungsten septa for two-dimensional two-dimensional measurements, as well as with three 68Ge line sources for transmission scans and daily quality control. The spatial resolution, scatter fraction, count rate, sensitivity, uniformity and accuracy of the implemented correction algorithms were evaluated after the National Electrical Manufacturers Association protocol using the standard acquisition parameters. RESULTS: The transaxial resolution in the two-dimensional mode is 4.3 mm (4.4 mm) in the center and increases to 4.7 mm (4.8 mm) tangential and to 8.3 mm (8.0 mm) radial at a distance of r = 20 cm from the center. The axial slice width measured in the two-dimensional mode varies between 4.2 and 6.6 mm FWHM over the transaxial field of view. In the three-dimensional mode the average axial resolution varies between 4.1 mm FWHM in the center and 7.8 mm at r = 20 cm. The scatter fraction is 17.1% (32.5%) for a lower energy discriminator level of 350 keV. The maximum true event count rate of 263 (345) kcps was measured at an activity concentration of 142 (26.9) kBq/ml. The total system sensitivity for true events is 5.7 (27.7) cps/Bq/ml. From the uniformity measurements, we obtained a volume variance of 3.9% (5.0%) and a system variance of 1.6% (1.7%). The implemented three-dimensional scatter correction algorithm reveals very favorable properties, whereas the three-dimensional attenuation correction yields slightly inaccurate results in low- and high-density regions. CONCLUSION: The ECAT EXACT HR+ has an excellent, nearly isotropic spatial resolution, which is advantageous for brain and small animal studies. While the relatively low slice sensitivity may hamper the capability for performing fast dynamic two-dimensional studies, the scanner offers a sufficient sensitivity and count rate capacity for fully three-dimensional whole-body imaging.     

Improved column-switching liquid chromatographic method for the determination of the enantiomers of mefloquine

A liquid chromatographic method for the determination of the enantiomers of mefloquine has been improved. The chromatography involved two columns: an achiral cyanopropyl stationary phase for the quantification of (+/-)-mefloquine and a chiral naphthyl-urea stationary phase for the determination of the enantiomeric ratio. Compared with the previous method, which needed two detectors, this one used one detector-integrator to which the two columns are connected alternately by an automated column-switching system. The method is suitable for the quantification (0.05 microgram/ml) of mefloquine and the determination of enantiomeric ratios from 500-microliters plasma samples with ultraviolet detection.     

Determination of SDZ ICM 567 in blood and muscle microdialysis samples by microbore liquid chromatography with ultraviolet and fluorescence detection

Fast, simple and accurate methods for the determination of SDZ ICM 567, the 7-methoxy derivative of tropisetron, in microdialysates have been developed. Sampling by microdialysis from freely moving rats in the portal and jugular vein offers a new technology for pharmacokinetic studies by direct and continuous measurement of unbound drug concentrations with time. SDZ ICM 567 can be identified in small sample volumes of dialysates on a microbore high-performance liquid chromatography column-switching system with ultraviolet detection. In addition, determination of SDZ ICM 567 by fluorimetric detection has been developed for muscle microdialysates from rats. [14C]SDZ ICM 567 was used as reference substance for the estimation of the amount of substance transferred through the dialysis membrane. The radioactive measurement (RA) gave the recovery information, whereas the liquid chromatographic method detected the sum of [14C]SDZ ICM 567 and dialyzed SDZ ICM 567.     

meso-四(4-三甲铵基苯基)卟啉流动注射分光光度法测定痕量镉

本文详细地研究了以meso-四(4-三甲铵基苯基)卟啉为显色剂,正相流路双通道流动注射分光光度法测定镉的实验条件.方法具有快速、灵敏和选择性好等特点.测定镉的相对误差<±3%.