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Dive into the research topics where Freidoon Erdmann is active.

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Featured researches published by Freidoon Erdmann.


Forensic Science International | 2002

Simultaneous screening and detection of drugs in small blood samples and bloodstains.

H. Schutz; Jan Christoph Gotta; Freidoon Erdmann; Manfred Riße; G. Weiler

A gas chromatography-mass spectrometry (GC-MS) method is described for the screening and detection of morphine, codeine, cocaine, benzoylecgonine, methylecgonine, cocaethylene, delta-9-tetrahydrocannabinol (THC), 11-nor-9-carboxy-THC (THC-COOH), 11-hydroxy-THC (11-OH-THC), amphetamine, methamphetamine, 3,4-methylenedioxyamphetamine (MDA), 3,4-methylenedioxymetamphetamine (MDMA) and N-methyl-1-(3,4-methylenedioxyphenyl)-2-butanamine (MBDB) in small blood samples and bloodstains using solid phase SPE columns and a pipetting robot (Gilson Aspec XL). The detection limits are in the order of 1.62-4.10 ng/50 microl spot (amphetamines), 0.15-0.82 ng/50 microl spot (cannabinoids), 1.67-4.70 ng/50 microl spot (cocaine and derivatives) and 4.53-4.91 ng/50 microl spot (opiates) and the correlation factors are between 0.9957 and 0.9999. The method has proven useful in forensic cases with only small sample volumes or bloodstains.


Legal Medicine | 2003

Pitfalls of toxicological analysis

H. Schutz; Freidoon Erdmann; Verhoff Ma; G. Weiler

Pitfalls are a permanent risk in all fields of forensic- and clinical-toxicological analysis and are not only concerned with immunoassays, although they are at present mostly discussed with regard to this subject. There are risks inherent in the field of preanalysis (e.g. the sampling, transportation, storage und treatment of the samples immediately prior to analysis). Furthermore, various pitfalls during measurement itself are to be avoided in connection with derivatization, choice of analysis parameters, memory-effects and many other sources of error. Another important section concerns the pharmacokinetic and pharmacodynamic interpretation of analytical results. Many toxicokinetic (e.g. enzyme induction) and toxicodynamic factors (e.g. tolerance effects) must be considered with special regard to plausibility controls (e.g. constellation, longitudinal, transversal and trend monitoring).


Mikrochimica Acta | 1992

Retention-indices on OV-1 of approximately 170 commonly used pesticides

Freidoon Erdmann; Gertrud Rochholz; Harald Schütz

A screening program is reported for approximately 170 pesticides which are regularly encountered in toxicological analysis (organophosphates, carbamates, triazines, halogenated carbohydrates, phenoxycarbonic acid derivatives, and others). It is based on the retention index according to Kovats. Temperature dependence of the retention index and derivatization procedures are also studied.


Romanian Journal of Legal Medicine | 2017

Detection of drugs in paired maternal and umbilical cord blood samples

Florian Veit; Freidoon Erdmann; Christoph G. Birngruber; Reinhard Dettmeyer

Objectives. The consumption of drugs during pregnancy or delivery leads to pre and intranatal drug exposure of the fetus. The purpose of this study was to examine paired blood samples of the mother and the umbilical cord regarding drug


Journal of Analytical Toxicology | 2016

Automated GC–MS Determination of Δ9-Tetrahydrocannabinol, Cannabinol and Cannabidiol in Hair

Sonja Heinl; Oliver Lerch; Freidoon Erdmann

The determination of Δ(9)-tetrahydrocannabinol (THC), cannabinol (CBN) and cannabidiol (CBD) in hair is a major routine task in forensic laboratories worldwide. A comprehensively automated liquid-liquid extraction (LLE) method has been developed. The automation was carried out by an x-y-z sample robot equipped with modules capable of shaking, centrifugation and solvent evaporation. It comprises digestion of hair in sodium hydroxide solution, LLE, extract evaporation, reconstitution in silylation reagent, inlet derivatization and GC-MS analysis. Method validation guidelines of the Society for Toxicological and Forensic Chemistry were fulfilled. The limit of quantification (LOQ) was 0.01 ng/mg for THC, 0.06 ng/mg for CBN and 0.03 ng/mg for CBD. This is below the required LOQ for THC (0.02 ng/mg) in medical psychological assessments in Germany. Also it is far below the required LOQ of the Society of Hair Testing of 0.1 ng/mg for THC. Four-round robin tests were passed successfully and several post- and ante-mortem samples were analyzed. To date the method is routinely employed at the Institute of Legal Medicine in Giessen, Germany. To the best of our knowledge, this is the first publication on a comprehensively automated classical LLE workflow in the field of hair analysis.


Analytical and Bioanalytical Chemistry | 2011

Quantitative determination of 43 common drugs and drugs of abuse in human serum by HPLC-MS/MS

David M. Bassan; Freidoon Erdmann; Ralf Krüll


Analytical and Bioanalytical Chemistry | 2016

Development and validation of an automated liquid-liquid extraction GC/MS method for the determination of THC, 11-OH-THC, and free THC-carboxylic acid (THC-COOH) from blood serum.

Kirsten Purschke; Sonja Heinl; Oliver Lerch; Freidoon Erdmann; Florian Veit


Pharmazie in Unserer Zeit | 1993

Nachweis von Arznei- und anderen Fremdstoffen in Haaren†

Harald Schütz; Ahrens B; Freidoon Erdmann; Gertrud Rochholz


Archiv für Kriminologie | 2006

Investigations concerning the threshold value between endogenous and exogenous GHB (liquid ecstasy)

Freidoon Erdmann; Zandt D; Auch J; Harald Schütz; G. Weiler; Verhoff Ma


Archiv für Kriminologie | 1998

Analytical confirmation of error in false positive amphetamine immunoassays and results

Harald Schütz; Freidoon Erdmann; Magiera Es; Günter Weiler

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Marcel A. Verhoff

Goethe University Frankfurt

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