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Determination of lead in blood

O.A. Weber ; Institut za higijenu rada Zagreb
K. Voloder ; institut za higijenu rada Zagreb
V.B. Vouk ; Institut za higijenu rada Zagreb

Puni tekst: hrvatski, pdf (10 MB) str. 296-313 preuzimanja: 85* citiraj
APA 6th Edition
Weber, O.A., Voloder, K. i Vouk, V.B. (1952). Prilog određivanju malih količina olova u krvi. Arhiv za higijenu rada i toksikologiju, 3 (3), 296-313. Preuzeto s https://hrcak.srce.hr/187542
MLA 8th Edition
Weber, O.A., et al. "Prilog određivanju malih količina olova u krvi." Arhiv za higijenu rada i toksikologiju, vol. 3, br. 3, 1952, str. 296-313. https://hrcak.srce.hr/187542. Citirano 22.09.2020.
Chicago 17th Edition
Weber, O.A., K. Voloder i V.B. Vouk. "Prilog određivanju malih količina olova u krvi." Arhiv za higijenu rada i toksikologiju 3, br. 3 (1952): 296-313. https://hrcak.srce.hr/187542
Harvard
Weber, O.A., Voloder, K., i Vouk, V.B. (1952). 'Prilog određivanju malih količina olova u krvi', Arhiv za higijenu rada i toksikologiju, 3(3), str. 296-313. Preuzeto s: https://hrcak.srce.hr/187542 (Datum pristupa: 22.09.2020.)
Vancouver
Weber OA, Voloder K, Vouk VB. Prilog određivanju malih količina olova u krvi. Arh Hig Rada Toksikol. [Internet]. 1952 [pristupljeno 22.09.2020.];3(3):296-313. Dostupno na: https://hrcak.srce.hr/187542
IEEE
O.A. Weber, K. Voloder i V.B. Vouk, "Prilog određivanju malih količina olova u krvi", Arhiv za higijenu rada i toksikologiju, vol.3, br. 3, str. 296-313, 1952. [Online]. Dostupno na: https://hrcak.srce.hr/187542. [Citirano: 22.09.2020.]

Sažetak
A »mono-colour« dithizone method for determination of lead in blood is described. The main points in which the proposed method differs from the usual dithizone methods are the following:
(1) the extraction of lead with dithizone solution is performed at rather high pH values (10.5),
(2) the iron is removed after mincra lization of blood by means of a 2% aqueous cupferron solution.
The modification (I) increases the sensitivity of the method and at the same time dispenses with the necessity of washing lead-dithizonate solution to remove the excess dithizone before measuring the extinction. The cupferron extraction eliminates all the possible sources of error which are connected with the presence of iron. The statistical treatment of calibration curves showed that the proposed method is reliable, sensitive and precise. The standard error of a single determination is not more than ±7 µg for lead concentrations from 25 to 500 µg per 100 ml blood if the measurement of the optical density is performed with Beckman spectrophotometer at 520 mµ. If two parallel determinations arc made in each analysis the standard error may be reduced to ±5 µg.

Hrčak ID: 187542

URI
https://hrcak.srce.hr/187542

[hrvatski]

Posjeta: 157 *