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1.
Toxicol Lett ; 230(1): 10-8, 2014 Oct 01.
Article in English | MEDLINE | ID: mdl-25102025

ABSTRACT

Gold nanoparticles (GNPs) have considerable applications in biomedicine, such as in bio-sensing, bio-imaging, drug delivery and photothermal therapeutics. However, currently there are limited information regarding the impact of pregnancy on their biodistribution, elimination and toxicity. In this study, we investigated the biodistribution and potential toxic effects of different-sized GNPs (1.5, 4.5, 13, 30 and 70 nm in diameter) in non-pregnant and pregnant mice at different gestational ages (E5.5, 7.5, 9.5, 11.5 and 13.5). 5h after intravenous injection, GNPs exhibited size-dependent biodistribution profiles; however, regardless of size, no significant biodistribution changes were observed between non-pregnant and pregnant mice. Kinetic studies showed that 4.5 nm GNPs were primarily excreted through urine within 5h, whereas 30 nm GNPs had a more prolonged blood circulation time. No apparent toxic effects (e.g., increased mortality, altered behavior, reduced animal weight, abnormal organ morphology or reduced pregnancy duration) were observed with different-sized GNPs in pregnant mice. However, treatment with 30 nm GNPs induced mild emphysema-like changes in lungs of pregnant mice. These results indicated that the maternal biodistribution patterns of GNPs in pregnant mice depended on particle size, but not gestational age; organ-specific adverse effects may arise with treatment with some GNPs according to their size.


Subject(s)
Metal Nanoparticles , Organogold Compounds/pharmacokinetics , Animals , Dose-Response Relationship, Drug , Female , Gestational Age , Injections, Intravenous , Lung/drug effects , Lung/pathology , Metabolic Clearance Rate , Mice , Organogold Compounds/administration & dosage , Organogold Compounds/blood , Organogold Compounds/chemistry , Organogold Compounds/toxicity , Organogold Compounds/urine , Particle Size , Pregnancy , Pulmonary Emphysema/chemically induced , Pulmonary Emphysema/pathology , Risk Assessment , Tissue Distribution
2.
Chemosphere ; 85(3): 335-43, 2011 Oct.
Article in English | MEDLINE | ID: mdl-21767864

ABSTRACT

BACKGROUND: Environmental contaminants have recently been implicated in the pathogenesis of obesity. OBJECTIVE: To explore relations between persistent organic pollutants (POPs) and fat mass independently of body stature, using a cross-sectional design. METHODS: In the Prospective Study of the Vasculature in Uppsala Seniors (PIVUS), fat mass was determined in 70-year-old subjects (n=890) by dual-energy X-ray absorptiometry (DXA). The plasma levels of 21 POPs (including 16 PCB congeners, 3 OC pesticides, 1 BDE47, and 1 dioxin) were measured by high resolution chromatography coupled with high resolution mass spectrometry (HRGC/HRMS). RESULTS: Lipid-standardized plasma concentrations of octachlorodibenzo-p-dioxin (OCDD), the PCBs 74, 99, 105 and 118, and the pesticides HCB, TNK, and DDE were all positively related to fat mass (p=0.03-0.0001). Subjects in the fifth quintile for PCB 105 showed a mean fat mass that was 4.8 kg more than subjects in the first quintile. On the other hand, the PCBs 156, 157, 169, 170, 180, 189, 194, 206, and 209 were negatively related to fat mass (p=0.0001). For PCB 194, subjects in the fifth quintile showed a mean fat mass that was 10.8 kg less than subjects in the first quintile. Following adjustment for smoking, physical activity, education level, height, lean mass, and gender, these results remained significant (p=0.01-0.0001) except for the PCBs 74 and 99. For some PCBs, the associations vs. fat mass were more pronounced in women than in men. CONCLUSION: Plasma concentrations of some pesticides are positively related to fat mass, while divergent associations are seen for the PCBs. These results implicate a complex role of POPs in obesity.


Subject(s)
Absorptiometry, Photon , Adipose Tissue/chemistry , Environmental Pollutants/blood , Aged , Female , Gas Chromatography-Mass Spectrometry , Halogenated Diphenyl Ethers/blood , Humans , Male , Organogold Compounds/blood , Pesticides/blood , Polychlorinated Biphenyls/blood , Polychlorinated Dibenzodioxins/analogs & derivatives , Polychlorinated Dibenzodioxins/blood , Prospective Studies
3.
Biol Trace Elem Res ; 126(1-3): 56-64, 2008.
Article in English | MEDLINE | ID: mdl-18649049

ABSTRACT

Triethylphosphine gold-2,3,4,6-tetra-o-acetyl-L-thio-D-glucopyranoside (auranofin and sodium aurothiomalate; Myocrisin are two chemically different gold compounds used to treat rheumatoid arthritis. This study highlights the interaction, in vivo, of these drugs with erythrocyte membrane in patients with rheumatoid arthritis. Fifty-eight patients with definite or classical rheumatoid arthritis were included in this study and randomly allocated to three groups as 18 patients in the Myocrisin group, 20 patients in the auranofin group, and 20 patients in the placebo group. The drugs appeared to react, in vivo, in different ways. With Myocrisin, the level of gold in erythrocyte membrane was, initially, very high and decayed exponentially afterwards, whereas auranofin produced a constant high level up to 36 weeks. The erythrocyte membrane gold level in nonsmokers was higher than that in smokers in the auranofin group, and it decreased with an increase in the number of cigarettes smoked (r = 0.836 P < 0.01); no such correlation was observed in the Myocrisin group. In a changeover study, auranofin appeared to change the nature of erythrocyte membrane after reacting with it and rendering it incapable of picking up any gold from Myocrisin. In the case of auranofin, the hemolysate membrane gold level was found to correlate with clinical improvement.


Subject(s)
Arthritis, Rheumatoid/blood , Arthritis, Rheumatoid/drug therapy , Auranofin/therapeutic use , Erythrocyte Membrane/metabolism , Gold Sodium Thiomalate/therapeutic use , Organogold Compounds/blood , Adult , Aged , Auranofin/pharmacokinetics , Drug Interactions , Female , Gold Sodium Thiomalate/pharmacokinetics , Humans , Male , Middle Aged , Smoking
4.
Environ Health Perspect ; 115(6): 883-8, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17589595

ABSTRACT

BACKGROUND: Persistent organic pollutants (POPs) can influence the immune system, possibly increasing the risk of rheumatoid arthritis (RA). In addition, as metabolic change due to obesity has been proposed as one mechanism of osteoarthritis (OA), POPs stored in adipose tissue may be also associated with OA. OBJECTIVE: Our goal in this study was to examine associations of background exposure to POPs with arthritis among the general population. DESIGN: We investigated cross-sectional associations of serum POPs concentrations with the prevalence of self-reported arthritis in 1,721 adults >/= 20 years of age in the National Health and Nutrition Examination Survey 1999-2002. RESULTS: Among several POPs, dioxin-like polychlorinated biphenyls (PCBs) or nondioxin-like PCBs were positively associated with arthritis in women. After adjusting for possible confounders, odds ratios (ORs) were 1.0, 2.1, 3.5, and 2.9 across quartiles of dioxin-like PCBs (p for trend = 0.02). Corresponding figures for nondioxin-like PCBs were 1.0, 1.6, 2.6, and 2.5 (p for trend = 0.02). Organochlorine (OC) pesticides were also weakly associated with arthritis in women. For subtypes of arthritis, respectively, RA was more strongly associated with PCBs than was OA. The adjusted ORs for RA were 1.0, 7.6, 6.1, and 8.5 for dioxin-like PCBs (p for trend = 0.05), 1.0, 2.2, 4.4, and 5.4 for nondioxin-like PCBs (p for trend < 0.01), and 1.0, 2.8, 2.7, and 3.5 for OC pesticides (p for trend = 0.15). POPs in men did not show any clear relation with arthritis. CONCLUSIONS: The possibility that background exposure to PCBs may be involved in pathogenesis of arthritis, especially RA, in women should be investigated in prospective studies.


Subject(s)
Arthritis, Rheumatoid/blood , Arthritis, Rheumatoid/epidemiology , Environmental Pollutants/blood , Organogold Compounds/blood , Pesticides/blood , Polychlorinated Biphenyls/blood , Age Factors , Female , Humans , Male , Odds Ratio , Prevalence , Sex Factors , Socioeconomic Factors , United States/epidemiology
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