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Joint International Conference on Long-term Experiments ...

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MATERIALS AND METHODS<br />

The material c<strong>on</strong>sisted of 53 male lung cancer patients operated for the cancer, and of 39<br />

c<strong>on</strong>trol patients who died of n<strong>on</strong>-malignant diseases and were autopsied. Because<br />

pulm<strong>on</strong>ary emphysema is a good indicator for smoking, the c<strong>on</strong>trol material was collected<br />

to include cases with various degrees of emphysema. The smoking habits and occupati<strong>on</strong>al<br />

history were required from the patients or next of kin and from the hospital records (Table<br />

1). The severity of emphysema was graded in the radiographs of excised air-inflated lungs<br />

or lobes of lungs.<br />

Fresh lung tissue for analyses was taken from the (apico) posterior and anterior<br />

segment of the upper lobe and from the superior (apical) segment and basal part of the lower<br />

lobe. The samples, weighing 0.5-2 g, c<strong>on</strong>tained no pleural surface or cancer tissue. Ninety<br />

percent of the Cd analyses were made from the anterior segment and 80% of the Cr analyses<br />

from the (apico) posterior segment of the upper lobe. The samples were prepared under a<br />

laminar flow hood avoiding c<strong>on</strong>taminati<strong>on</strong>. The fresh, vacuum-dried samples were ashed in<br />

glass cups with a blank and NBS Bovine Liver (SRM 1577) c<strong>on</strong>trol for 48-72 h in a low<br />

temperature oxygen plasma asher (BIO-RAD Plasma Asher E 2000, 100-120 °C). The<br />

tissue residue was dissolved in a total of 3 ml of 50 % ethanol and transferred into a Tefl<strong>on</strong><br />

cup and dried at 80 °C for 24 h. The residue was digested in a mixture of 3 ml of<br />

c<strong>on</strong>centrated nitric acid and 0.2 ml of percloric acid. The soluti<strong>on</strong> was allowed to stand<br />

overnight and dry-heated at moderate temperature (100-150 °C) in a sand-bath. Finally the<br />

ash was diluted in 3-6 ml of high quality water. The Cd and Cr c<strong>on</strong>tents were de<strong>term</strong>ined <strong>on</strong><br />

a direct current plasma atomic emissi<strong>on</strong> spectrometer (DCP-AES) (SpectraSpan IIIB<br />

coupled with a Hewlett-Packard 85 data processor) not c<strong>on</strong>sidering speciati<strong>on</strong>. A standard<br />

additi<strong>on</strong> method was employed for Cr to eliminate matrix interference. The analytical<br />

characteristics are shown in Table 2.<br />

Table 2. Analytical characteristics<br />

Cd Cr______<br />

Accuracy<br />

NBS 1577 Bovine Liver 0.36 0.25<br />

(0.274 ±0.086) a (0.125±0.057) a<br />

Lan<strong>on</strong>orm-Metalle 2 0.028<br />

(0.021-0.030) b<br />

RSD (0.02 ppm) % 3.9 2.4<br />

Detecti<strong>on</strong> limit (ppm) 0.010 0.017<br />

_________________________________________________________<br />

RESULTS AND DISCUSSION<br />

Both the total pulm<strong>on</strong>ary Cd and Cr c<strong>on</strong>tent were higher in the lung cancer (Cd 3.0 ± 2.4<br />

and Cr 6.1 ± 4.2 µg/g dry weight) than in the c<strong>on</strong>trol patients (Cd 2.1 ± 1.9 and Cr 4.1 ± 4.0<br />

540

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