Unreliability of the use of thyroglobulin concentration in postmortem blood samples in forensic diagnosis

2014 ◽  
Vol 16 (3) ◽  
pp. 164-167 ◽  
Author(s):  
Akira Hayakawa ◽  
Kotaro Matoba ◽  
Kie Horioka ◽  
Manabu Murakami ◽  
Koichi Terazawa
1997 ◽  
Vol 21 (7) ◽  
pp. 538-542 ◽  
Author(s):  
Michael Collins ◽  
Jenny Easson ◽  
Glyn Hansen ◽  
Allan Hodda ◽  
Keith Lewis

2018 ◽  
Vol 63 (6) ◽  
pp. 1875-1879 ◽  
Author(s):  
Marieke De Boeck ◽  
Wim Dehaen ◽  
Jan Tytgat ◽  
Eva Cuypers

2000 ◽  
Vol 24 (7) ◽  
pp. 572-578 ◽  
Author(s):  
G. W. Kunsman ◽  
C. L. Presses ◽  
P. Rodriguez

2005 ◽  
Vol 24 (4) ◽  
pp. 275-281 ◽  
Author(s):  
Vassiliki A. Boumba ◽  
Theodore Vougiouklakis

Numerous methods have been described in the literature for the determination of carboxyhemoglobin (COHb) in whole blood. The most popular and widely used have been (1) the spectrophotometric methods, which could be performed either by using a conventional spectrophotometer or by using specialized automated instruments known as CO-oximeters; (2) the gas chromatographic methods, with variable detection systems, which have been considered as the reference methods for every carbon monoxide analysis. The authors have critically reviewed previously reported comparative studies on these methods, considering statistical and analytical matters, in order to propose the best method for the determination of COHb in postmortem blood, that could be utilized in forensic toxicology laboratories where such analyses are limited in number (less than 20 per year). Criteria for evaluation have been accuracy, reliability, simplicity, time, and cost. The authors’ concluding statement has been that the manual spectrophotometric method could be the method of choice for COHb determination in postmortem blood samples. It is simple, rapid, and reliable and fulfills the forensically acceptable accuracy. It is performed by the use of a conventional spectrophotometer, which is considered a basic instrument in every analytical laboratory.


1990 ◽  
Vol 35 (6) ◽  
pp. 12967J ◽  
Author(s):  
Fumiyo Kusu ◽  
Taeko Tsuneta ◽  
Kiyoko Takamura

2013 ◽  
Vol 127 (6) ◽  
pp. 1101-1107 ◽  
Author(s):  
Verena Kiencke ◽  
Hilke Andresen-Streichert ◽  
Alexander Müller ◽  
Stefanie Iwersen-Bergmann

2014 ◽  
Vol 241 ◽  
pp. 173-177 ◽  
Author(s):  
Cora Wunder ◽  
Gerold F. Kauert ◽  
Stefan W. Toennes

Author(s):  
Camila Scheid ◽  
Sarah Eller ◽  
Anderson Luiz Oenning ◽  
Eduardo Carasek ◽  
Josias Merib ◽  
...  

Abstract Synthetic drugs for recreational purposes are in constant evolution, and their consumption promotes a significant increase in intoxication cases, resulting in damaging public health. The development of analytical methodologies to confirm the consumption of illicit drugs in biological matrices is required for the control of these substances. This work exploited the development of an extraction method based on homogenous liquid–liquid microextraction with switchable hydrophilicity solvent (SHS) as extraction phase for the determination of the synthetic drugs 3,4-methylenedioxymethamphetamine, 3,4-methylenedioxyamphetamine and N-methoxybenzyl-methoxyphenylethylamine derivates (25B, 25C and 25I) in postmortem blood, followed by liquid chromatography coupled to mass spectrometry in tandem. The optimized sample preparation conditions consisted of using 250 µL of ZnSO4 10% and 50 µL of NaOH 1 mol/L in the protein precipitation step; N,N-dimethylcyclohexylamine was used as SHS, 650 μL of a mixture of SHS:HCl 6 mol/L (1:1 v/v), 500 μL of whole blood, 500 μL of NaOH 10 mol/L and 1 min of extraction time. The proposed method was validated, providing determination coefficients higher than 0.99 for all analytes; limit of detection and limit of quantitation ranged from 0.1 to 10 ng/mL; intra-run precision from 2.16% to 9.19%; inter-run precision from 2.39% to 9.59%; bias from 93.57% to 115.71% and matrix effects from 28.94% to 51.54%. The developed method was successfully applied to four authentic postmortem blood samples from synthetic drugs users, and it was found to be reliable with good selectivity.


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