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GC–MS method for the determination of paraben preservatives in the human breast cancerous tissue
Institution:1. Department of Environmental Biotechnology, School of Environmental Sciences, Bharathidasan University, Tiruchirappalli-620024, India;2. National Institute of Advanced Industrial Science and Technology, 16-1 Onogawa, Tsukuba, Ibaraki-305-8569, Japan;1. Wenzhou Entry-Exit Inspection and Quarantine Bureau of P.R.C, Wenzhou 325027, China;2. Food Inspection Center of Shenzhen Entry-Exit Inspection and Quarantine, Shenzhen 518045, China;3. College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou 325035, China;1. Instituto de Investigación Biosanitaria (ibs. GRANADA), Hospitales Universitarios de Granada, Spain;2. Departamento de Química Analítica, Universidad de Granada, Granada, Spain;3. Fundación MEDINA, Centro de Excelencia en Investigación de Medicamentos Innovadores en Andalucía, Parque Tecnológico de Ciencias de la Salud, Armilla, Granada, Spain;4. CIBER en Epidemiología y Salud Pública (CIBERESP), Spain;5. Departamento de Radiología y Medicina Física, Universidad de Granada, Granada, Spain
Abstract:The general presumption that the preservative laden personal care products may be one of the causative agents for breast cancer, has remained a matter of controversy during this decade. Extensive studies have not been carried out to either prove or disprove the role of preservatives in breast cancer incidences. In this study we have developed a new method for the identification and quantification of the preservatives such as methyl paraben (MeP), ethyl paraben (EtP), propyl paraben (PrP) and butyl paraben (BuP) in breast tissue using Gas Chromatography and Mass Spectrometry (GC–MS). Tissue was extracted by using acetone:n-hexane mixture (1:1 v/v) and derivatized with N-Methyl-N-(trimethylsilyl) trifluoroacetamide (MSTFA). The extent of reaction time and the amount of MSTFA to attain greater derivatization were optimized. The developed method yielded good recovery (mean ± SD) of 99.8 ± 5.1, 96 ± 4.4, 107 ± 17 and 113 ± 13% with relative standard deviations (RSDs) of 5.1, 4.6, 15.6 and 13%, and the limits of detection (LOD) of 2.02, 1.05, 1.71 and 3.75 ng g 1 for MeP, EtP, PrP and BuP, respectively. The method was successfully validated for the determination of parabens including butyl paraben (log Kow = 3.57) in cancerous breast tissues; this could be a promising one for screening of breast tissues and also the environment for paraben residues. As far as our knowledge goes this is the first GC–MS method for the determination of parabens in human tissue.
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