29 research outputs found
Instruments to assess secondhand smoke exposure in large cohorts of never smokers: The smoke scales
© 2014 The Authors. Published by PLOS. This is an open access article available under a Creative Commons licence.
The published version can be accessed at the following link on the publisher’s website: https://doi.org/10.1371/journal.pone.0085809The objectives of this study were to: (i) to develop questionnaires that can identify never-smoking children and adults experiencing increased exposure to secondhand smoke (SHS+), (ii) to determine their validity against hair nicotine, and (iii) assess their reliability. A sample of 191 children (85 males; 106 females; 7-18 years) and 95 adult (23 males; 72 females; 18- 62 years) never-smokers consented to hair nicotine analysis and answered a large number of questions assessing all sources of SHS. A randomly-selected 30% answered the questions again after 20-30 days. Prevalence of SHS+ in children and adults was 0.52±0.07 and 0.67±0.10, respectively (p16.5 and >16, respectively. Significant Kappa agreement (p0.05). Area under the curve and McNemar's Chi-square showed no pair-wise differences in sensitivity and specificity at the cutoff point between the two different days for SS-C and SS-A (p>0.05). We conclude that the SS-C and the SS-A represent valid, reliable, practical, and inexpensive instruments to identify children and adult never-smokers exposed to increased SHS. Future research should aim to further increase the validity of the two questionnaires. © 2014 Misailidi et al.Published versio
Airway epithelial cell exposure to distinct e-cigarette liquid flavorings reveals toxicity thresholds and activation of CFTR by the chocolate flavoring 2,5-dimethypyrazine
Biomonitoring of bisphenol A in hair of greek population
Objective: Bisphenol A (BPA) is considered as an endocrine-disruptor in which humans are exposed daily mainly by food-contact products, toys, recycled paper and drinking containers. In this study, we validated a method for the isolation and the detection of BPA in human head hair samples and estimated the burden of BPA in hair of Greek population. Methods: Hair samples were collected from 69 volunteers. The isolation of the BPA was performed by solid-liquid extraction with methanol and its determination by a liquid chromatography-mass spectrometry technique. Results: The limits of quantification (LOQ=9.7pgmg-1), the accuracy (92.6%), the precision (inter 15.3%, intra 13.0%), the ion suppression (<8.1%) and the recovery (88.3%) of the method were found satisfactory. Differences in the detection rates of the positive samples as well in detected levels of BPA between rural and urban population were observed. The 41.2% of the samples collected from urban population were positive whereas the positive samples from rural population were 14.8% (p=0.025). The mean concentration of the positive samples for the urban population was 64.1pgmg-1 (17.7-192.8pgmg-1), for the rural population 40.3pgmg-1 (13.1-72.8pgmg-1) and for the children 37.9pgmg-1 (13.1-72.8pgmg-1). Significant statistical differences (p=0.021) were observed though between urban and rural population only when negative samples were replaced with LOD/2 values. Conclusion: The proposed method was successfully applied for the determination of BPA in hair for the estimation of the population burden to BPA. © 2014 Elsevier Ltd
Development and application of LC-APCI-MS method for biomonitoring of animal and human exposure to imidacloprid
Imidacloprid (IMI) is a relatively new neuro-active neonicotinoid insecticide and nowadays one of the largest selling insecticides worldwide. In the present study a LC-APCI-MS based method was developed and validated for the quantification of imidacloprid and its main metabolite 6-chloronicotinic acid (6-CINA) in urine and hair specimens. The method was tested in biomonitoring of intentionally exposed animals and subsequently applied for biomonitoring of Cretan urban and rural population. The developed analytical method comprises two main steps of analytes isolation from specimen (solid-liquid extraction with methanol for hair, liquid-liquid extraction with methanol for urine) and subsequent instrumental analysis by LC-APCI-MS. The developed method was applied for the monitoring of IMI and 6-CINA in hair and urine of laboratory animals (rabbits) intentionally fed with insecticide at low or high doses (40 and 80 mg kg(-1) weight d(-1) respectively) for 24 weeks. The analytes were detected in the regularly acquired hair and urine specimens and their found levels were proportional to the feeding dose and time of exposure with the exception of slight decline of IMI levels in high dose fed rabbits after 24 weeks of feeding. This decline can be explained by the induction of IMI metabolizing enzymes by the substrate. After testing on animal models the method was applied for pilot biomonitoring of Crete urban (n = 26) and rural (n = 32) population. Rural but not urban population is exposed to IMI with 21 positive samples (65.6%) and found median concentration 0.03 ng mg(-1). Maximum concentration detected was 27 ng mg(-1). (C) 2013 Elsevier Ltd. All rights reserved
Imidacloprid and 6-chloronicotinic acid determination in blood serum of long-term exposed rabbits using LC-APCI-MS technique
Acute exposure to secondhand smoke is associated with endogenous lung acidosis and obstructive pulmonary disorder
Cardiotoxicity in rabbits after long-term nandrolone decanoate administration
Abuse of anabolic androgenic steroids is linked to a variety of cardiovascular complications. The aim of our study was to investigate the possible cardiovascular effects of nandrolone decanoate on young rabbits using echocardiography, histology and monitoring of telomerase activity, oxidative stress and biochemical markers. Fourteen rabbits were divided into three administration groups and the control group. Doses of 4. mg/kg and 10. mg/kg of nandrolone decanoate, given intramuscularly and subcutaneously, two days per week for six months were applied. A 4-months wash-out period followed. Focal fibrosis and inflammatory infiltrations of cardiac tissue were observed in the high dose groups. Thiobarbituric acid-reactive species (TBARS) levels were significantly increased in the high dose groups, while catalase activity decreased. Myocardial Performance Index (MPI) is the main echocardiographic index primarily affected by nandrolone administration in rabbits. Despite the preserved systolic performance, histological lesions observed associated with distorted MPI values, point to diastolic impairment of the thickened myocardium due to nandrolone treatment. Oxidative stress accumulates and telomerase activity in cardiac tissue rises. Subcutaneous administration seems to be more deleterious to the cardiovascular system, as oxidative stress, telomerase activity and biochemical markers do not appear to return into normal values in the wash-out period. © 2015 Elsevier Ireland Ltd
Достижения в области биомониторинга фосфорорганических и хлорорганических пестицидов
Organophosphorus (OPs) and organochlorine (OCs) pesticides are synthetic organic compounds used mainly in agriculture to manage pest problems. Human is occupationally and environmentally exposed to pesticides via inhalation, ingestion and skin absorption. When the pollutant enters human body it is rapidly metabolized to more toxic compounds than the parent compound. Their ability to interfere with biochemical and metabolic pathways in humans makes them compounds of high concern. Acute and chronic exposure has been linked with neurological, cardiovascular, birth effects and male infertility. Human exposure to pesticides is estimated by measuring their metabolites in biological tissues and fluids such as blood, urine, amniotic fluid and hair. In this review study advances on biomonitoring of pesticides are presented. Measured levels of pesticides in urine matrices, amniotic fluid, meconium and hair are presented in order to monitor the human burden and biomonitoring data between occupationally and environmentally exposed populations are being comparedФосфорорганические и хлорорганические пестициды – это синтетические органические соединения, используемые преимущественно в сельском хозяйстве для борьбы с вредителями. Люди подвергаются воздействию пестицидов в процессе профессиональной деятельности и при контакте с зараженной средой через их вдыхание, потребление с пищей и поглощение кожей. При попадании в организм человека поллютант быстро метаболизируется до более токсичных соединений, чем исходное вещество. Их способность взаимодействовать с биохимическими и метаболическими путями в человеческом организме делает их потенциально опасными соединениями. Обнаружена связь между острым и хроническим воздействием пестицидов и неврологическими и кардиоваскулярными эффектами, врожденными отклонениями и мужским бесплодием. Оценка воздействия пестицидов на организм человека проводится путем измерения их метаболитов в биологических тканях и жидкостях, таких как кровь, моча, амниотическая жидкость, а также в волосах. В данном обзоре представлены достижения в области биомониторинга пестицидов. Для оценки нагрузки на человека приведены измеренные уровни пестицидов в моче, амниотической жидкости, меконии и волосах. Проведено сравнение популяций, подвергшихся воздействию пестицидов в связи с производственной деятельностью и при контакте с окружающей средо
Evaluation of oxidative stress in long-term exposed rabbits to subtoxic levels of imidacloprid
Multicomponent Analysis of Replacement Liquids of Electronic Cigarettes Using Chromatographic Techniques
The electronic cigarette (e-cig) is an invention of the past few years and its popularity is rapidly growing all over the world. A rapid multicomponent analytical protocol for the analysis of the replacement liquids (e-liquids) of e-cig was developed using gas (GC) and liquid chromatography (LC)-mass spectrometry (MS). GC-MS-based methods were developed for the determination of the main humectants and polycyclic aromatic hydrocarbons (PAHs). For the determination and quantification of nicotine (NIC) and nitrosamines, appropriate LC-MS-based methods were developed. The approbated methods were applied for the analysis of 263 e-liquid samples obtained from the Greek market. The instruments response was linear; the limits of quantification ranged from 0.003 mu g/mL for three PAHs to 1.187 mu g/mL for glycerol. The precision was < 16% for all analytes, while the mean accuracy ranged from 99.1% for NIC to 106.6% for the flavor 2,5-dimethylpyrazine. The measured concentrations of NIC were correlated with the theoretical concentrations as reported by the manufacturers. An analog relation between the concentration of the glycerol and of propylene glycol was noticed. The frequency of detection of flavors ranged from 30.4% for the methyl cyclopentenolone to 5.3% for 3.4-dimethoxybenzaldehyde. Nitrosamines and PAHs were not detected in any sample. Because a similar analytical protocol was not available from the existing literature so far, our study offers the advantage of complete analytical methods for rapid and simultaneous multicomponent identification