Determination of Toxic and Essential Elements in Urine by Inductively Coupled Plasma Mass Spectrometry Текст научной статьи по специальности «Медицинские технологии»

Determination of Toxic and Essential Elements in Urine by Inductively Coupled Plasma Mass Spectrometry

DOI: 10.17691/stm2016.8.3.14 Received June 10, 2015

G.A. Veikhman, PhD, Leading Researcher, Laboratory of Elemental Analysis Methods1; Senior Lecturer, Department of General and Organic Chemistry2;

O.V. Gilyova, PhD, Leading Chemist, Laboratory of Elemental Analysis Methods1;

E.V. Stenno, Head of the Laboratory of Elemental Analysis Methods1;

T.S. Ulanova, DSc, Head of the Department of Chemical and Analytical Research Methods1; Professor, Department of Environmental Protection3

federal Scientific Center for Medical and Preventive Health Risk Management Technologies, 82 Monastyrskaya St., Perm, 614045, Russian Federation;

2Perm State Pharmaceutical Academy, 2 Polevaya St., Perm, 614000, Russian Federation; 3Perm National Research Polytechnic University, 29a Komsomol'skiy prospekt,

Perm, 614990, Russian Federation

The aim of the investigation was to optimize the conditions of a routine urinalysis by inductively coupled plasma mass spectrometry (ICP-MS) for diagnostic studies.

Materials and Methods. We determined the content of 12 elements (V, Cr, Mn, Ni, Cu, Zn, As, Se, Sr, Cd, Tl, Pb) in the urine of children in Russian industrial region (n=57, mean age being under 6 years) by ICP-MS on a quadrupole mass spectrometer Agilent 7500cx (Agilent Technologies, USA) with octopole collision/reaction cell according to the methodology developed by MUK 4.1.3230-14.

Results. The arithmetic mean of the elements in the group was 0.72 ^ig/L (V); 2.13 ^ig/L (Cr); 1.11 ^ig/L (Mn); 2.76 ^ig/L (Ni); 26.67 ^ig/L (Cu); 482.1 ^ig/L (Zn); 10.09 ^ig/L (As); 32.84 ^ig/L (Se); 1,275.35 ^ig/L (Sr); 0.122 ^ig/L (Cd); 1.16 ^ig/L (Tl); 2.16 ^ig/L (Pb). The urine samples were directly analyzed after diluting 1:10 by 1% nitric acid solution. The findings accuracy was confirmed by comparing with the values of standard urine samples performed by SERONORM™ urine.

Conclusion. The proposed easy method to determine the essential and toxic elements in urine using a mass spectrometer Agilent 7500cx with octopole collision/reaction cell can be recommended for diagnostic and screening tests in clinical settings.

Key words: mass spectrometry with octopole collision/reaction cell; ICP-MS; collision/reaction cell; essential and toxic elements; urinalysis.

The problem of establishing the relationship between environmental exposure and health status of the population is one of the most urgent and challenging in modern preventive medicine. The application of modern medical technologies for rehabilitation and treatment of the population under anthropogenic stress requires new rapid tests to determine the content of chemical compounds and elements in biological media. According to research associates [1], electrothermal atomization atomic absorption spectroscopy (ETA-AAS) with Zeeman background correction and inductively coupled plasma mass spectrometry (ICP-MS) are the most promising techniques used to study biological fluids without prior sample deterioration. However, the capability to determine a great number of elements in one sample, low detection limits, high reproducibility, a wide range of detectable concentrations, low consumption of substances sampled, high efficiency provide greater prospects when biomedia are studied by ICP-MS.

For contacts: Galina A. Veikhman, e-mail: veikhman_ga@mail.ru

Normative and methodological base of Russia has methodological instructions on determining chemical elements in biological media: MUK 4.1.1483-03 [2], which are advisory in nature. They have been elaborated on the basis of ICP-MS, however, they fail to meet current standardization requirements and metrological certification, and do not take into consideration particular conditions when samples are prepared, device setting parameters that causes difficulties in using the instructions in laboratory practice.

In the elemental analysis laboratory of Federal Scientific Center for Medical and Preventive Health Risk Management Technologies (Perm) there were developed and introduced the techniques of simultaneous determination of 12 chemical elements (vanadium, chrome, manganese, nickel, cuprum, zinc, selenium, strontium, thallium, lead, cadmium, arsenic) in biomedia [3-6]. The techniques (MUK 4.1.3161-14, MUK 4.1.3230-14) are registered in Federal information

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measurement assurance fund (FR.1.31.2014.17064) [7] and used in routine clinical diagnosis of health situation in population living in territories with negative impact of the environment, as well as for control after rehabilitation treatment in hospital environment.

Our choice of elements to be determined in biomedia is well-considered. The recommended diagnostic elements in urine are Cu, Zn, Mn, Ni, Pb, Cr, As, Cd, Tl and V [1, 8]. In addition, we think it necessary to control Sr content in biomedia, since within Perm territory there are regions with high concentration of strontium in drinking water. It should be noted that the data on concentration of some the above mentioned elements in urine reported by different researchers are conflicting. The Table shows the reference values of the elements in urine calculated in diagnostic laboratories ALS Scandinavia [9], ARUP USA [10], and represented in well-known Tietz clinical guide to laboratory tests [11]. The first use the data of Rodushkin and Odman obtained by ICP-MS [12], and the other refers to Komaromy-Hiller et al. [13]. There are differences in allowable levels for Cr, Mn, Cu, Cd, Pb.

Tietz presents reference levels determined by flame atomic absorption spectrometry and atomic absorption spectrometry with electrothermal atomisation (FAAS and ETA-AAS), which are close to those under discussion only for Cu, Zn, As. Moreover, the limits of detection (LOD) of the mentioned techniques are known to be able to differ by several orders [1].

Due to the existing problem we aimed at estimating the correctness of findings using the developed technique when a number of microelements were simultaneously determined in urine samples using IPC-MS in children living in industrial regions.

The aim of the investigation was to optimize the conditions of a routine urinalysis by inductively coupled plasma mass spectrometry for diagnostic studies.

Materials and Methods. From analytical point of view, biological fluids are difficult to analyze not only due to a very low content of the most determined microelements, but also due to their complex matrix composition. The most common noninvasive object of biomedia research is urine. Urine biological matrix due to renal filtration is free from plasma proteins, lipids and other compounds with large molecular mass that simplifies a sample preparation process. At the same time, the key problem in determining the elements in urine is its high salt composition (chlorides, sulfates and phosphates) resulting in a significant impact of matrix effect and beat interference. The use of octopole reaction/collision cell enables to minimize the matrix effect of urine salt composition and determine such complex elements as Cr, As, Se and V.

V, Cr, Mn, Ni, Cu, Zn, As, Se, Sr, Cd, Tl, Pb in

Results of microelement determination in percentage in regard to certified values in SeronormTM urine samples (n=12): y1 — minimal certified level (%); y2 — maximal certified level (%); y3 — detected (%)

urine samples were quantitatively determined on a quadrupole mass spectrometer with inductively coupled plasma Agilent 7500cx (Agilent Technologies, USA) with octopole reaction/collision cell. Helium was used as a reaction gas to determine all the elements. Helium flow rate of 5.0 ml/min was experimentally stated that enabled to reduce significantly the polyatomic overlay with saving a high sensitivity level. The capacity of high-frequency signal was 1,550 W. For sample administration we used a double-pass Scott-type spray chamber. The temperature of a spray chamber was 2.0°C. The sample feed rate in the spray chamber was 0.4 ml/min. The distance from a burner to a selecting cone was 9 mm. The detector rate was <100 ps per 1 ion. For tuning we used the solution of 7Li, 59Co, 89Y and 205Tl in 2% of HNO3 with the concentration of 1 pg/L for each element (Tuning Solution, USA). The ratio 140Ce16O+/140Ce+ was <1%, and for 140Ce2+/140Ce+ it being <3%. High purity liquid argon 99.99% (TU-2114-00500204760-99) was used. The maximum argon flow rate was 20 L/min, the pressure in the gas supply channel being 700±20 kPa, Tplasma=8,000-10,000 К. The analysis automation was provided by G3160B, Integrated autosampler (Germany). The solution containing 27 elements with concentration of 10 mg/L in 5% water solution of HNO3 (Multi-Element Calibration Standard-2A; Aligent Technologies, USA) was used as the main standard solution. To prepare calibration solutions and samples, we used especially pure HNO3 (Sigma-Aldrich, USA).

The concentrations of calibration solutions to determine Cd and Tl were 0.0; 0.1; 0.5; 1.0 pg/L; for Mn, Ni, Cr, V, Se, Cu: 0.0; 0.1; 0.5; 1.0; 5.0 pg/L; for As, Sr, Zn: 0.0; 1.0; 5.0; 10.0; 50.0 pg/L. The complex standard solution 209Bi, 73Ge, 115In, 6Li, 45Sc, 159Tb, 89Yc with concentration of 10 mg/L in 5% water solution of HNO3 (Internal Standard Mix; Aligent Technologies, USA) was used to prepare the internal standard (IS) solutions.

159Tb was used as an internal standard for Pb and Tl determination, 115In was used to determine Cd, and for other elements 72Ge was used due to the proximity of their ionization potentials and atomic mass. All solutions were diluted with deionized water with specific resistivity of 18.2 MOm-cm purified in the system Milli-Q Integral (Millipore SAS, France). A blank sample was prepared in the same manner as a work sample.

Ultrasonic cleaner Elmasonic S 100H (Germany) was used to prepare the glassware made of glass, Teflon, polypropylene for analysis. The dishes were incubated for 20 min in bidistilled water at 55°C, then for 20 min in an aqueous nitric acid solution (1:5) at 55°C followed by deionization in water for 20 min at 55°C.

To control the accuracy of the analysis results we used standard urine samples Seronorm™ urine (LOT 0511545; Sero AS, Norway). The preparation for the analysis of standard urine samples was similar to that of real samples. Control samples were analyzed after every fifth real sample.

The Figure shows the results of microelements determined in percentage in relation to the certified values (n=12). The concentrations of Cr, Mn, Cu, As, Cd and Pb were found to be above 100%, the error detection being 1.5-7.0%. V, Ni, Zn, and Sr showed concentrations below 100%. The error of their determination was in the range from 2 to 7% and corresponded to the certified values. The contents of Se and Tl were found as 100% level.

The findings of investigations enable to elaborate the technique for simultaneous determination of 12 elements in urine (MUK 4.1.3230-14) [7]. The technique is different from the existing methodological guidelines 4.1.148303 [2] in that it has a proven procedure of sample preparation to minimize matrix effects, the selection of internal standards for each element being determined, the use of a collision/reaction cell with helium to correct polyatomic interferences. The Table shows the limits of determination (LOD) in undiluted urine.

The content of V, Cr, Mn, Ni, Cu, Zn, As, Se, Sr, Cd, Tl, Pb using the developed technique was determined in 57 urine samples of children from an industrial Russian region, their age being 3-7 years, among them there were 47% girls and 53% boys. The study groups included children with no congenital pathology, organic and infectious diseases of the central nervous system in their past history. Biomedical studies comply with the declaration of Helsinki (adopted in June, 1964 (Helsinki, Finland) and revised in October, 2000 (Edinburg, Scotland)). All legal representatives of children involved in the sampling gave their written informed consent to voluntary participation in the study.

Sampling of morning urine was performed in screw-capped sterile 125 ml polypropylene containers (FL Medical S.r.l., Italy). The urine samples were directly analyzed after diluting 1:10 with 1% solution of nitric acid: 4.45 ml of 1% water solution of HNO3 and 0.05 ml of the internal standard solution was added to 0.5 ml of urine.

The findings of urine samples were represented as arithmetic mean (АМ), median (Me), as well as the ranges of values in a group. The median appeared to be close to arithmetic mean only for Cu and Cd. For comparison the Table shows the known urinary findings of children in Canada (aged 6-11 years) [14], Southern Mexico (aged 6-11 years) [15] and Germany (aged 2-17 years) [16].

Results and Discussion. The content of elements in urine of children living on the observation area does not exceed the approved reference levels with the exception of vanadium and strontium exceeding the median 10 times as much. High strontium concentration in urine is associated with the proximity of to celestite ore deposit containing up to 20% of strontium sulfate. Vanadium content compared to that in Canadian children showed fivefold increase of median, manganese content was ten times as large, nickel and cuprum: twice as large, and plumbum three times as large. Arsenic and cadmium contents were higher in Canadian children. The contents of vanadium, chromium, manganese, cuprum, strontium, and lead according to the arithmetic mean exceeded those found in children in Germany. The content of chromium, manganese, nickel, zinc, arsenic and cadmium in the urine of children living in a mining district of Southern Mexico (inductively coupled plasma atomic emission spectroscopy method) exceeded the levels reported in our study.

The integrated assessment of the health status of children of the study group revealed that only 1.7% of the children could be referred to apparently healthy children. One third of preschool children had chronic pathology in the state of compensation and sub-compensation (31.1%). One in five children in the study group had the deviation from mean growth indices, 33.6% children had disharmonic physical development. Gastrointestinal diseases (half of the examined children) and nervous

system disorders (one in five children) were considered as the main diagnoses. Ultrasound findings of the liver, gallbladder and biliary tract of the children revealed the increase of the linear dimensions of the right lobe of the liver and reactive changes of hepatic parenchyma in one in eight children. Musculoskeletal diseases combined with high strontium level in urine prevailed in the structure of comorbidities. Musculoskeletal disorders were found in 62.9% children and were represented as postural disorders (84.6%) and accelerated bone maturation (27%).

Thus, according to the determination findings of toxic and essential elements in urine by ICP-MS using the developed technique, the present territory can be assessed as unfavorable ecologic hygienic situation.

Conclusion. The proposed easy method to determine the essential and toxic elements in urine using a mass spectrometer Agilent 7500cx with octopole collision/ reaction cell can be recommended for diagnostic and screening tests in clinical settings.

Study Funding and Conflicts of Interest. The study was not funded by any sources, and the authors have no conflicts of interest related to the present study.

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