ORGANOCHLORINE PESTICIDES LEVELS AND ASSOCIATED FACTORS IN THE POPULATION OF THE METROPOLITAN REGION OF SÃO PAULO - BRAZIL*

Similar documents
REPORT of ANALYSIS OF PESTICIDE RESIDUES. in SOFT DRINK SAMPLES sent by DIRECTORATE GENERAL OF HEALTH SERVICES, NEW DELHI to CFL, Mysore

GREENPEACE RESEARCH LABORATORIES

Off-line supercritical fluid extraction/gas chromatography-mass spectrometry analysis of pesticides in fish

RISK ASSESSMENT FOR HEALTH OF PESTICIDES FROM FOOD IN ROMANIA, 2002

Determination of multiple pesticide residues in animal foods using on-line gel permeation chromatography-gas chromatography/mass spectrometry

Intake of PCB from fatty foods

D. Cavagnino, A. Siviero, A. Mantegazza DANI Instruments, Italy V. Termopoli, P. Palma, G. Famiglini, A. Cappiello University of Urbino, Italy

GC-µECD Analysis and Confirmation of Contract Laboratory Protocol Pesticides in Olive Oil

HBM surveillance program for PCBs and heavy metals in the Czech Republic. Milena Černá, A. Krsková

3-Acetyldeoxynivalenol. 15-Acetyldeoxynivalenol

GC-MS DETERMINATION OF ORGANOCHLORINE PESTICIDES IN BOVINE MILK FROM TIRUCHIRAPPALLI, SOUTH INDIA- A PRELIMINARY ASSESSMENT

MALAYSIAN MALAYSIAN COCOA WORKSHOP ON THE SAFE USE OF PESTICIDES IN COCOA AND HARMONIZED

Uptake and Metabolism of Phthalate Esters by Edible Plants

German Environmental Survey (GerES) IV BPA in urine of German children

Evaluation of Exposure to Chemical Substances through Foods Exposure to Pesticides, Heavy Metals, Dioxins, Acrylamide and Food Additives in Japan

Determination of DDTs and Dicofol Residues in Vegetables by GC/MS and HPLC

Concentrations of Organochlorine Pesticides in Milk of Nicaraguan Mothers

Highly Repeatable Ultra Low Detection of Estradiol Using Triple Quadrupole GC/MS in NCI Mode

Validation Report 20

Children s exposure to DDT from different food categories

Analysis and Quantitation of Cocaine on Currency Using GC-MS/MS. No. GCMS No. SSI-GCMS-1501

IDENTIFICATION AND CONTROLOFRESIDUALSOLVENTS Identification and control of residual solvents EUROPEAN PHARMACOPOEIA 6.

Rapid Analysis of 37 FAMEs with the Agilent 8860 Gas Chromatograph

Long-Term Occupational Exposure to DDT*

Why use Signal-To-Noise as a Measure of MS Performance When it is Often Meaningless?

Analytical Summary Report

Automated Analysis and Quantitation of Fish Oil Supplements using the MIDI Sherlock Marine Oil Analysis Package

5.10 DIFENOCONAZOLE (224)

GC-MS/MS Analysis of Benzodiazepines Using Analyte Protectants

Determination and pharmacokinetics of manidipine in human plasma by HPLC/ESIMS

Increasing Extraction Efficiency of Wet Samples Using a Novel New Polymer During Accelerated Solvent Extraction

Pelagia Research Library

Secrets to Successful GC-MS/MS Pesticide Method Development

Analysis of Cannabinoids in Cannabis by UHPLC Using PDA Detection

Combination of Chemical Ionization (CI) and Low Energy Ionization (EI) Capabilities with High-Resolution Q-TOF GC/MS

Effective use of Pharmacopeia guidelines to reduce cost of chromatographic analysis for Fluticasone propionate

Certificate of Analysis

Advances in Environmental Biology

Application of the QuEChERS extraction method for the analysis of pyrethrin and pyrethroid pesticides in fin and non-fin fish.

METALS IN SOILS ADJACENT TO AVENUES OF HIGHLY DENSE TRAFFIC OF SÃO PAULO CITY, BRAZIL

PHOTOCATALYTIC DECONTAMINATION OF CHLORANTRANILIPROLE RESIDUES IN WATER USING ZnO NANOPARTICLES. DR. A. RAMESH, Ph.D, D.Sc.,

Cannabinoid Profiling and Quantitation in Hemp Extracts using the Agilent 1290 Infinity II/6230B LC/TOF system

Analysis of Omega 3 and Omega 6 FAMEs in Fish Oil and Animal Fat Using an Agilent J&W DB-FATWAX Ultra Inert GC Column

Screening by immunoassay and confirmation & quantitation by GC-MS of buprenorphine and norbuprenorphine in urine, whole blood and serum

Extraction of 11-nor-9-carboxy-tetrahydrocannabinol from Hydrolyzed Urine by ISOLUTE. SLE+ Prior to GC/MS Analysis

An Untargeted Exposure Study of Small Isolated Populations Using Atmospheric Gas Chromatography Coupled with High Resolution Mass Spectrometry

Analysis of several common. organic acids in tobacco leaf, snus, and moist snuff

Organophosphorus Pesticides Analysis Using an Agilent J&W DB-5ms Ultra Inert Capillary GC Column. Application Note. Environmental. Abstract.

Colonne Gascromatografiche

Rapidly Analyze a Wide Range of Glycol Ethers by GC-MS Using the New Rxi -1301Sil MS Column

Analysis of the fatty acids from Periploca sepium by GC-MS and GC-FID

Development and Validation of RP-HPLC Method for the Estimation of Gemigliptin

Column Chromatographic Isolation of Docosahexaenoic Acid from Fish Oil and its Assessment by Analytical Techniques

Toxicology Screening of Whole Blood Extracts Using GC/Triple Quadrupole/MS

Methods and Materials

SUPPLEMENTARY MATERIAL

Analysis of FAMEs Using Cold EI GC/MS for Enhanced Molecular Ion Selectivity

Keywords: aromatic plants, GC-MS chromatography, volatile oil

USP purity analysis of pravastatin sodium using the Agilent 1120 Compact LC

NUTRITIONAL COMPONENTS OF SUPERCRITICAL CARBON DIOXIDE EXTRACTED WHEAT GERM OIL

Fast Separation of EU and US EPA Regulated PAHs on Agilent J&W Select PAH GC Columns

S.C. Moldoveanu, A.G. Hudson, A. Harrison. R.J. Reynolds Tobacco Co.

Application Note. Small Molecule Pharmaceuticals. 2-Ethyl-2-phenylmalonamide Ethosuximide Primidone Carbamazepine. Carbamazepine-

[application note] Simultaneous detection and quantification of D 9 THC, 11-OH-D 9 T H C and D 9 THC-COOH in whole blood by GC tandem quadrupole MS

Trans Fat Determination in the Industrially Processed Edible Oils By Transmission FT-IR Spectroscopy By

Qualitative and quantitative determination of cannabinoid profiles and potency in CBD hemp oil using LC/UV and Mass Selective Detection

Application. Detection of Cannabinoids in Oral Fluid Using Inert Source GC/MS. Introduction. Authors. Abstract. Forensic Toxicology

1765 Toxic Effects CORE Profile - Blood/Urine

Determination of red blood cell fatty acid profiles in clinical research

Concentrations of persistent organic pollutants in the milk of New Zealand women

CORESTA RECOMMENDED METHOD NÄ 9

CORESTA Recommended Method No. 84

Lutein Esters from Tagetes Erecta

Fatty Acid Mass Spectrometry Protocol Updated 10/11/2007 By Daren Stephens

DETERMINATION OF CANNABINOIDS, THC AND THC-COOH, IN ORAL FLUID USING AN AGILENT 6490 TRIPLE QUADRUPOLE LC/MS

Separation of 54 PAHs on an Agilent J&W Select PAH GC Column

Chapter 2 Organochlorinated Contaminants in General Population of Argentina and Other Latin American Countries

Detection of Cannabinoids in Oral Fluid with the Agilent 7010 GC-MS/MS System

GPC Gel Permeation Chromatography

FLUNITRAZEPAM Latest Revision: January 24, 2006

ANALYSIS OF -HYDROXYBUTYRATE (GHB) AND -BUTYROLACTONE (GBL) IN LIQUIDS PERFORMED AT NATIONAL LABORATORY OF FORENSIC SCIENCE (SKL), SWEDEN

Rapid and Direct Analysis of Free Phytosterols by Reversed Phase HPLC with Electrochemical Detection

Family Smoking Prevention and Tobacco Control Act. Comments regarding crop protection agents

Determination of Gamma-Hydroxy-Butyrate (GHB) in Biological Samples

Pelagia Research Library

Research Article Persistent Organic Pollutants in Serum and Several Different Fat Compartments in Humans

Type Analysis of Citrus Essential Oils by Multidimensional Supercritical Fluid Chromatography/ Gas Chromatography

Fig.1. Denatonium benzoate (DB) chemical structure

Analele UniversităŃii din Oradea Fascicula: Ecotoxicologie, Zootehnie şi Tehnologii de Industrie Alimentară, 2010

Separation of 37 Fatty Acid Methyl Esters Utilizing a High-Efficiency 10 m Capillary GC Column with Optimization in Three Carrier Gases

Analysis of Cannabinoids in Hemp Seed Oils by HPLC Using PDA Detection

Analysis of Organic Acids and Alcohols Using the Agilent J&W DB-624UI Ultra Inert GC Column

Forensic Analysis of Blood Alcohol Concentration

Determination of Adulterants in Olive Oil Analysis of Waxes and Fatty Acid Methyl and Ethyl Esters with Capillary GC and Agilent OpenLAB Software

Martin Lommatzsch Gottfried-Hagener-Str. 60 D Köln. Report

HUMAN LIVER SLICE EXPERIMENT 1 Effects of Propylene Glycol on Ethylene Glycol Metabolism

Journal of Chemical and Pharmaceutical Research

Determination of Bath Salts (Pyrovalerone Analogs) in Biological Samples

Interested in conducting your own webinar?

Determination of β-hydroxybutyrate in Blood and Urine Using Gas Chromatography Mass Spectrometry

Transcription:

ORGANOCHLORINE PESTICIDES LEVELS AND ASSOCIATED FACTORS IN THE POPULATION OF THE METROPOLITAN REGION OF SÃO PAULO - BRAZIL* Nascimento FP 1, Kuno R 3, Cardeal de Oliveira MC 2** **, Lemes VRR 2, Kussumi TA 2, Nakano VE 2, Rocha SB 2, Kimura IA 2, Gouveia N 1 1. School of Medicine, University of São Paulo (USP). São Paulo, Brazil 2. Institute Adolfo Lutz (IAL), State Health Department of São Paulo. São Paulo, Brazil 3. Environmental Company of São Paulo State (CETESB). São Paulo, Brazil ** e-mail: celestecardeal@yahoo.com.br; moliveir@ial.sp.gov.br *This work is part of the Subproject Pilot of the First Brazilian Survey of Populations Exposed to Chemical Substances; Ministry of Health (CGVAM/SVS/MS), USP e IAL INTRODUCTION The former worldwide use of organochlorine pesticides is a Public Health concern given that the presence of high levels of these compounds in humans can lead to serious health problems. OBJECTIVES The study had as objective to evaluate exposure to persistent organochlorinated pesticide residues in the adult population from the Metropolitan Region of São Paulo (MRSP) and provide subsidies for realization of the First Brazilian Survey of Populations Exposed to Chemical Substances. This research aimed to evaluate 15 organochlorine pesticides in the serum of 547 blood donors and to investigate factors associated with the levels of these compounds. MATERIAL and METHODS Study group: Blood donors (N = 547) aged 18 to 65 from nine blood donation centers in the Metropolitan Region of Sao Paulo (MRSP) Analytical method: Hexachlorobenzene (HCB), hexachlorocyclohexane (HCH): α, β, γ and δ isomers, dieldrin, heptachlor, heptachlor epoxide, dodecachlor, o,p -DDT, p,p -DDT, o,p -DDD, p,p -DDD, o,p -DDE and p,p -DDE were determined by gas chromatography with μ-eletron capture detection, according Dale (1966) and EPA Manual(1981), with modifications. The mean recoveries at the limit of quantification level were in the range of 62-116% and the relative standard deviation for five replicate samples was 1.8-18.4%.

The limit of quantification (LOQ) was 0.02µg/dL for HCB, α-hch, γ-hch, and δ-hch; 0.04µg/dL for β-hch, heptachlor, dieldrin, and p,p -DDE; 0.08µg/dL for heptachlor epoxide, o,p -DDE, o,p -DDT, p,p -DDT, o,p -DDD, and p,p -DDD; and 0.16µg/dL for dodecachlor. Qualitative and quantitative analysis Identification and Quantification Confirmation Column Instrument Chromatographic conditions VF-5MS (5% phenyl 95% dimethylsiloxane) fusedsilica capillary column (30 m, 0.25 mm i.d., 0.25 μm film thickness) VF-35MS (35% phenyl 65% dimethylsiloxane) fusedsilica capillary column (30 m, 0.25 mm i.d., 0.25 μm film thickness GC Agilent 6890 CG Thermo Scientific Trace GC Ultra Injector temperature: 250 C, Detector µecd temperature: 310 C, Oven Temperature programmed for quantification: 60ºC (3min.), 20ºC/min to 200ºC, 3ºC/min, 280ºC, 290ºC (20min); Carrier gas N 2, Flow of 1mL/min, Mode and injection volume: splitless, 2μL. Injector temperature: 250 C, Detector: ECD, temperature: 310 C, Oven Temperature programmed for quantification: 60ºC (3min.), 10ºC/min, 220ºC, 3ºC/min., 280ºC; Carrier gas N 2, Flow of 1mL/min, Mode and injection volume: splitless, 2μL. RESULTS AND DISCUSSION The concentrations of the pesticide residues of heptachior, heptachior epoxide, diedrin, o,p -DDE, o,p DDT, o,p -DDD and Dodecachlor were below the LOQ for all sample analyzed and are not reported on table 1. All other compounds are shown on table 1.

Density Density Table 1 Serum concentrations of organochlorine compounds ( g/dl) on a group of blood donors from MRSP. HCB -HCH -HCH -HCN -HCH p.p - p.p -DDT DDE %>LOQ 0.18 0.74 10.70 0.18 0.37 31.18 0.74 Range 0.03 0.03 0.45 0.12 0.32 1.17 0.09 LOQ 0.02 0.02 0.04 0.02 0.02 0.04 0.08 LOQ = limit of qualification Only pesticide residues of β-hch and p,p -DDE were found in concentration levels above the limit of quantification, in a significant number of samples. The mean β-hch concentration was 0.028 μg/dl and mean p,p -DDE concentration was 0.045 μg/dl, figures 1 and 2 6 5 4 3 2 1 0 0.0 0.2 0.4 0.6 0.8 1.0 1.2 p.p -DDE ( g/dl) Figure 1 Distribution of samples above the LOQ for p,p -DDE residues 12 10 8 6 4 2 0 0.1 0.2 0.3 0.4 -HCH ( g/dl) Figure 2 Distribution of samples above the LOQ for -HCH residues

Table 2 Multiple regression linear for p,p -DDE residues results in serum of blood donors Variables Exp ( ) p-value Gender: Male (ref= 0.78 0.018 female) Color: non white 1.27 0.020 Worked with pesticides: 1.78 0.005 Yes Alcohol intake: yes 0.75 0.024 Water source (ref= piped) 0.019 Bottled 0.99 0.995 Alternative 2.03 0.008 Higher concentration levels of β-hch residues were mainly associated with past occupational exposure and diet, while p,p -DDE residues concentration levels were strongly associated with past exposure to pesticides and water sources. Gender had an important association with both compounds, females having higher residues concentration levels than males. Table 3 Multiple regression linear for -HCH results in serum of blood donors Variables Exp ( ) p-value Gender: Male (ref= female) 0.80 0.001 Previous contact with pesticides: Yes 1.29 0.004 Worked as a pesticide applicator in public health campaigns: Yes 2.27 0.001 Worked in capacitors or transformers companies: Yes 3.06 <0.001 Worked in chlorinated solvents industry: Yes 1.39 0.049 Income in minimum wages (ref= 1) 0.009 1 to 3 0.73 0.004 3 to 5 1.46 0.009 5 to10 0.95 0.772 Seafood consumption up to twice per week (ref = never) 1.18 0.020 Meat consumption (ref= never) 0.003 Up to twice per week 1.73 0.005 More than twice per week 0.99 0.943 Frequent beer consumption (ref= rarely) 0.32 0.001 CONCLUSION The data obtained represent significant contribution to the knowledge of organochlorine pesticides residues levels in adults of Metropolitan Area of São Paulo.

References 1. Brasil, Ministério do Trabalho. Secretaria de Segurança e Saúde no Trabalho. Portaria nº 24 (NR-7), de 29/12/1994, D.O.U. de 30/12/94, Seção 1: 21278-280. 2. CETESB. Companhia de Tecnologia de Saneamento Ambiental - Relação de áreas contaminadas do Estado de São Paulo. Update in December 2012. http://www.cetesb.sp.gov.br/areas-contaminadas/relacoes-de-areascontaminadas/15-publicacoes. 3. CERNÁ M, SPĔVÁCKOVÁ V, BATÁRIOVÁ A, ET AL. Human biomonitoring system in the Czech Republic. Int J Hyg Environ Health. 2007; 210(3-4):495-9 4. CHARLIER JC, PLOMTEUX GJ. Determination of organochlorine pesticide residues in the blood of healthy individuals. Clin Chem Lab Med. 2002; 40 (4): 361-364. 5. CRUZ S, LINO C, SILVEIRA MI. Evaluation of organochlorine pesticide residues in human serum from an urban and two rural populations in Portugal. The Science of the Total Environment 2003; 317:23-35. 6. DALE, W.E., CURLEY, A. and CUETO, C., Hexane extractable chlorinated insecticides in human blood. Life Sciences, 5:47, 1966. In Manual of Analytical Methods for the Analysis of Pesticides in Human and Environmental Samples, Environmental and Protection Agency, 5A, (3), (a), rev. 1979. Manual of Analytical Quality Control for Pesticides and Related Compounds in Human and Environmental Samples, 2nd revision. 1981. Available at https://nepis.epa.gov/exe/zynet.exe/ nepis.epa.gov/exe/zypurl.cgi?dockey=30000en6.txt 7. KLAASSEM CD EDITOR. Casarett and Doull s Toxicology The Basic Science of Poisons, New York, 17th Ed., Mac Graw Hill Medical, 2007. 8. POPs - Persistent Organic Pollutants, 2001: Text of the Convention of POPs, Stockholm, Sweden,.22 May 2001. http://chmpps.int/the Convention/Overview/TextotheConvention/tabid./2232/Default.aspx. 9. TURCI R. ET AL. A simple and fast method for the determination of selected organohalogenated compounds in serum samples from the general population. Toxicology Letters, 192 (2010) 66-71. 10. ZHOU R, ZHU L, YANG K, CHEN Y. Distribution of organochlorine pesticides in surface water and sediments from Qiantang River, East China. Journal of Hazardous Materials A. 2006; 137: 68-75. 11. DO NASCIMENTO, F.P., KUNO, R., LEMES, V.R.R., NAKANO, V. E., ROCHA S. B., CARDEAL DE OLIVEIRA, M. C. KIMURA, I.A., GOUVEIA N. Organochlorine pesticides levels and associated factors in a group of blood donors in São Paulo. Environmental Monitoring and Assessment 2017 Aug; 189(8): 380

Acknowledgments The authors are thankful to Ministry of Health (Brazil) for funding this study, and Beneficent Association of Blood Donors(Colsan) for providing the blood samples Irani C. Silva and Valéria AC Diago, research trainees, Reinaldo A. Ribeiro, Ana LR de Faria, Kennia C. Waldhelm and Antonia L. Silva, IAL technical team; Rogério R. Prado, statistical analyzes and teams of sample collection and interviewers.