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1.
Rapid Commun Mass Spectrom ; 27(10): 1155-67, 2013 May 30.
Article in English | MEDLINE | ID: mdl-23592121

ABSTRACT

RATIONALE: Analog-to-digital converter (ADC)-based acquisition systems are widely applied in time-of-flight mass spectrometers (TOFMS) due to their ability to record the signal intensity of all ions within the same pulse. However, the acquisition system raises the requirement for data throughput, along with increasing the conversion rate and resolution of the ADC. It is therefore of considerable interest to develop a high-performance real-time acquisition system, which can relieve the limitation of data throughput. METHODS: We present in this work a high-efficiency real-time digital signal averager, consisting of a signal conditioner, a data conversion module and a signal processing module. Two optimization strategies are implemented using field programmable gate arrays (FPGAs) to enhance the efficiency of the real-time processing. A pipeline procedure is used to reduce the time consumption of the accumulation strategy. To realize continuous data transfer, a high-efficiency transmission strategy is developed, based on a ping-pong procedure. RESULTS: The digital signal averager features good responsiveness, analog bandwidth and dynamic performance. The optimal effective number of bits reaches 6.7 bits. For a 32 µs record length, the averager can realize 100% efficiency with an extraction frequency below 31.23 kHz by modifying the number of accumulation steps. In unit time, the averager yields superior signal-to-noise ratio (SNR) compared with data accumulation in a computer. CONCLUSIONS: The digital signal averager is combined with a vacuum ultraviolet single-photon ionization time-of-flight mass spectrometer (VUV-SPI-TOFMS). The efficiency of the real-time processing is tested by analyzing the volatile organic compounds (VOCs) from ordinary printed materials. In these experiments, 22 kinds of compounds are detected, and the dynamic range exceeds 3 orders of magnitude.


Subject(s)
Mass Spectrometry/instrumentation , Mass Spectrometry/methods , Time Factors , Volatile Organic Compounds/analysis
2.
Chin Med Sci J ; 22(2): 71-82, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17763577

ABSTRACT

OBJECTIVE: To provide basis of reference values for relevant parameters of Chinese Reference Man. METHODS: Eighteen kinds of major organ or tissue samples, including muscle, rib, liver, and so on, were obtained from 4 areas (Hebei, Shanxi, Jiangsu, and Sichuan provinces) with different dietary patterns in China in autopsy of 16 healthy adult men, who had just encountered sudden deaths. At the same time, whole blood samples were collected from 10 volunteers living in each of these areas. The concentrations of 56 elements in these samples were detected by using Inductively Coupled Plasma Mass Spectrometry (ICP-MS), Inductively Coupled Plasma Atomic Emission Spectrometry (ICP-AES), and Graphite Furnace Atomic Absorption Spectrometry (GF-AAS) techniques. Based on obtained concentrations and reference values of these organ or tissue weights for Chinese Reference Man, the relative elemental burdens in these organs or tissues as well whole body were also estimated. RESULTS: The concentrations of 56 elements in 18 main organs or tissues were determined all together and their elemental organ or tissue and whole body burdens were estimated. Furthermore, the distributions of important elements for radiation protection in these organs or tissues were emphatically discussed. CONCLUSION: By summing with past related results, the total results obtained from the series of research may provide more reliable and better representative basis of these reference values for Chinese Reference Man than before.


Subject(s)
Elements , Liver/chemistry , Lung/chemistry , Adult , Blood Chemical Analysis , Body Burden , China , Humans , Male , Reference Values
3.
Guang Pu Xue Yu Guang Pu Fen Xi ; 27(2): 374-7, 2007 Feb.
Article in Chinese | MEDLINE | ID: mdl-17514980

ABSTRACT

The research studied the influence of matrix effect on the determination of lead concentration and isotope ratio through simulating blood matrix, and its correction by common analyte internal standardization (CAIS) method. The experiment results showed that CAIS method was suitable for the multi-element-matrix. The relative errors between the determined and the true concentration values are 20% (without correction), 8% (by conventional internal reference correction) and 2% (by CAIS correction), respectively. Otherwise, the influence of matrix effect and its correction for isotope ratio determination are not that obvious. Similarity of the mass number and properties between internal reference and analyte elements seems not important for CAIS correction, since very close correction results were obtained by using Tl and Dy as internal reference elements. Besides, correction results are not affected by different matrix dilution. Reliability and practicality of CAIS were proved by bovine blood standard material determination.


Subject(s)
Lead/blood , Lead/standards , Mass Spectrometry/methods , Animals , Calibration , Cattle , Humans , Isotopes/blood , Reproducibility of Results
4.
Guang Pu Xue Yu Guang Pu Fen Xi ; 26(11): 2120-4, 2006 Nov.
Article in Chinese | MEDLINE | ID: mdl-17260772

ABSTRACT

A method for determining 55 elements in human lung tissue was developed. Mixed acid (HNO3:HCl04) was added into samples, which were digested at room temperature over night, then heated at 180 degrees C. Arsenic and selenium in lung tissue were determined by hydride generation atomic fluorescence spectrometry (HG-AFS), potassium, sodium, calcium and magnesium were determined by atomic absorption spectrometer (AAS), while the rest of forty-eight elements were determined by inductively coupled plasma mass spectrometry (ICP-MS), respectively. Reference materials of GBW(E)080193 bovine hepar and GBWO9101 human hair were analyzed by the described method. The measured element values in two reference materials accorded with their reference values. The recovery rates for most of the studied elements were 90%-110%. The precisions of the method were 1.7%-10.0%. The concentrations of seventeen elements in the carcinomatous tissues were remarkably different from those in the pericarcinomatous tissues. The method is rapid, simple and accurate.


Subject(s)
Elements , Lung Neoplasms/chemistry , Spectrophotometry, Atomic , Animals , Cattle , Humans , Mass Spectrometry , Reproducibility of Results
5.
Biol Trace Elem Res ; 102(1-3): 39-49, 2004.
Article in English | MEDLINE | ID: mdl-15621926

ABSTRACT

The objective of the present study was to evaluate the potential effects of zinc, copper, and selenium on placental cadmium transport. From November 2002 through January 2003, a total of 47 healthy pregnant women from Da-Ye City, Hubei Province in Central China participated in the study. Their age, parity, gestational age, pregnancy history, and lifestyle data were obtained by questionnaire interview. The placental, whole-blood, and cord blood levels of cadmium were determined by inductively coupled plasma mass spectrometer (ICP-MS), whole-blood zinc was measured by flame atomic absorption spectrometry (F-AAS), whole-blood copper by ICP-MS, and selenium was by atomic fluorescence spectrophotometry (AFS). The cord blood cadmium concentration (0.020-1.48 microg/L) was significantly lower than in maternal blood (0.80-25.20 microg/L, p<0.01). The placental cadmium concentration was from 0.082 to 3.97 microg/g dry weight. Multiple linear regression analysis indicated that lower levels of maternal blood copper were significantly associated with higher cadmium concentrations in cord blood. Placental cadmium in women with lower levels of maternal blood zinc was significantly higher than in those with normal zinc levels. The placental cadmium level in women with lower whole-blood selenium was significantly lower than in subjects with normal selenium levels. It was concluded that the essential elements copper, selenium, and zinc might significantly affect placental cadmium transport.


Subject(s)
Cadmium/metabolism , Copper/blood , Placenta/metabolism , Selenium/blood , Zinc/blood , Adult , Biological Transport , Cadmium/blood , Female , Fetal Blood/chemistry , Humans , Nutritional Status , Pregnancy , Reference Values , Regression Analysis
6.
Zhongguo Zhong Yao Za Zhi ; 29(8): 753-9, 2004 Aug.
Article in Chinese | MEDLINE | ID: mdl-15506286

ABSTRACT

OBJECTIVE: To make an attempt at the multi-element speciation in the Chinese medicinal herbs by determining the concentrations of 25 elements in different extraction solutions. METHOD: Firstly, five Chinese medicinal herbs (Buddleja officinalis, Dictamnus dasycarpus, Myristica fragrans, Albizia judibrissin and Inula japonica) from the same region of China were treated to obtain water-soluble phase, lipid-soluble phase and non-soluble phase by water extraction, organic solvent extraction and acid digestion, respectively. Secondly, Phytolacca acinosa, a Chinese medicinal herb collected from 9 regions of China, was extracted by 0% EtOH, 50% EtOH, 75% EtOH, 95% EtOH, respectively, referring the Chinese Pharmacopoeia. Finally, the concentrations of 25 elements, such as Be, Cr, Cu, Zn, Ge, Sr, Y, Mo, Cd, Tl, Pb and REEs, in the above three phases were determined by ICP-MS. RESULT: Under the optimal conditions, all the 25 elements could be determined with detection limits ranged from 0.003 to 0.71 ng x g(-1). The average recoveries of the elements in P. acinosa were 88% approximately 119%, with the relative standard deviations 1.7% approximately 13.3%. It was observed that the determined 25 elements distributed in all the water-soluble, lipid-soluble and non-soluble phases, indicating that the inorganic species, organicspecies, as well as the protein bound species were coexisted in the herbs. Big differences of the element extraction rates could be found by using different ethanol solutions. CONCLUSION: With the aid of the obtained results, we may increase the extraction of necessary elements while decrease that of the toxic elements from the herbs by choosing a suitable solvent during the drug production.


Subject(s)
Drugs, Chinese Herbal/chemistry , Metals, Heavy/analysis , Phytolacca/chemistry , Plants, Medicinal/chemistry , Trace Elements/analysis , Buddleja/chemistry , Cadmium/analysis , Copper/analysis , Dictamnus/chemistry , Drugs, Chinese Herbal/isolation & purification , Ecosystem , Lead/analysis , Molybdenum/analysis , Myristica/chemistry , Solvents/chemistry , Zinc/analysis
7.
Article in English | MEDLINE | ID: mdl-15478940

ABSTRACT

The objective of the present study was to evaluate the potential effect of environmental exposure to cadmium on pregnancy outcome and fetal growth. Normal pregnant women were selected from Da-ye city of Hubei province, a cadmium-polluted area, from November 2002 through January 2003. Whole blood of pregnant women, cord blood, and placenta were collected and cadmium levels were determined by inductively coupled plasma emission mass spectroscopy. Incidence rate of preterm labor (gestational age < or = 37 weeks) and neonatal asphyxia, neonatal birth height, and birth weight were compared between lower and higher cadmium exposure level groups. Whole blood cadmium of 44 mothers ranged from 0.80 to 25.20 microg/L. Cadmium concentration in maternal blood was significantly higher than that in cord blood (t = 11.44, P < 0.01). Placenta cadmium ranged from 0.084 to 3.97 microg/g dry weight. After adjustment for maternal age, history of gestation, abortion and lactation, Logistic regression analysis showed that there was no significant association between cadmium exposure levels and pregnancy outcome (premature labor or neonatal asphyxia). Multiple linear regression analysis showed that, cord blood cadmium level, but not maternal blood cadmium and placenta cadmium, was significantly negatively associated with neonatal birth height (t= -2.33, P < 0.05). Compared with lower cord blood cadmium level (< or = 0.40 microg/L), higher level of cord blood cadmium (>0.40 microg/L) was associated with 2.24cm decrease in neonatal birth height. There was no significant association between cadmium exposure and birth weight. It was concluded that environmental exposure to cadmium significantly lower neonatal birth height.


Subject(s)
Birth Weight , Cadmium Poisoning , Environmental Exposure , Environmental Pollutants/poisoning , Fetal Development/drug effects , Pregnancy Outcome , Adult , Cadmium/blood , China , Environmental Pollutants/blood , Female , Fetal Blood/chemistry , Fetal Growth Retardation/etiology , Humans , Infant, Newborn , Male , Pregnancy
8.
Guang Pu Xue Yu Guang Pu Fen Xi ; 24(9): 1117-20, 2004 Sep.
Article in Chinese | MEDLINE | ID: mdl-15762538

ABSTRACT

This paper studied the trace elements Cs, Th and U in ten kinds of human autopsy tissues by ICP-MS. The instrumental operating conditions were optimized for the measurement of Cs, Th and U. Rhodium (Rh) was used as an internal standard element to compensate matrix effect. Detection limits for Th, U and Cs were 5.7-17.8 pg x mL(-1). The recoveries for spiking liver samples were 96%-107%, and their RSDs were 4.8%-8.9%. Reference materials of NIST SRM 8414 Bovine and NIST SRM 1486 Bone Meal were analyzed by the described method, and the analytical results agreed well with the reference values. Human autopsy tissues samples were digested by mixed acid (HNO3 + HClO4). The determination of Cs, Th and U in lung, liver, bone, heart, stomach, spleen, muscle, kidney, thyroid gland and intestinum tenue was performed by ICP-MS without separation and enrichment procedures. The obtained results indicated that this method is rapid, sensitive and accurate; the distribution of the three elements is different from one to another human organ sample; the main organ targets for Th and U are lungs and kidneys; and a coordinated variation of Cs, Th and U concentration in lungs was found in the samples collected from Hebei and Sichuan provinces.


Subject(s)
Autopsy , Cesium/analysis , Mass Spectrometry/methods , Reference Standards , Thorium/analysis , Uranium/analysis , Electrochemistry/methods , Environmental Monitoring/methods , Humans , Limit of Detection
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