2001
DOI: 10.1002/1522-2683(200111)22:19<4216::aid-elps4216>3.0.co;2-w
|View full text |Cite
|
Sign up to set email alerts
|

Advances of capillary electrophoresis in clinical and forensic analysis (1999-2000)

Abstract: In this paper, capillary electrophoresis in clinical and forensic analysis is reviewed on the basis of the literature of 1999, 2000 and the first papers in 2001. An overview of progress relevant examples for each major field of application, namely (i) analysis of drug seizures, explosives residues, gunshot residues and inks, (ii) monitoring of drugs, endogenous small molecules and ions in biofluids and tissues, (iii) general screening for serum proteins and analysis of specific proteins (carbohydrate deficient… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

0
39
0
4

Year Published

2002
2002
2020
2020

Publication Types

Select...
4
4

Relationship

2
6

Authors

Journals

citations
Cited by 89 publications
(43 citation statements)
references
References 316 publications
(283 reference statements)
0
39
0
4
Order By: Relevance
“…As pointed out by Ramsey et al, 23 ionic transport number mismatch during sweeping may play a role for the final stacked peaks. The other potential issue is the limited retention factor ( k ) of analytes in the micellar phase since the swept zone is controlled by Equation 4 ,24 (4) where l sweep and l inj are the lengths of the swept zone and the injected sample solution, respectively. When the interaction between the analyte and micelles is too weak, the analyte may 'leak' from the concentrated zone and flow through the detection window during the EKSI process.…”
Section: Theoretical Considerationmentioning
confidence: 99%
“…As pointed out by Ramsey et al, 23 ionic transport number mismatch during sweeping may play a role for the final stacked peaks. The other potential issue is the limited retention factor ( k ) of analytes in the micellar phase since the swept zone is controlled by Equation 4 ,24 (4) where l sweep and l inj are the lengths of the swept zone and the injected sample solution, respectively. When the interaction between the analyte and micelles is too weak, the analyte may 'leak' from the concentrated zone and flow through the detection window during the EKSI process.…”
Section: Theoretical Considerationmentioning
confidence: 99%
“…Among forensic drugs, phenethyla-mines by far represent the most important group of compounds for which chiral analysis may be of crucial importance. Although already reported in the past decade (for reviews see [6,27,28]), the use of CD CE for the chiral separation of amphetamines and congeners still attracts the attention of several researchers.…”
Section: Forensic Drugs and Poisonsmentioning
confidence: 99%
“…Although not new in the field of illicit drug analysis (see [6]), nonaqueous CE (NACE) has been used by Fang et al [36] for MDMA analysis in combination with fluorescence spectroscopy detection. A detection limit of 50 ng/mL for MDMA was reported.…”
Section: Forensic Drugs and Poisonsmentioning
confidence: 99%
See 1 more Smart Citation
“…All CE modes employ the same instrumentation; samples can be easily analyzed subsequently as diff erencing separation mechanisms. Generally, CE is a very promising tool for clinical analysis at the present time [14][15][16][17][18][19] and it could be a simple and less time-consuming alternative technique to HPLC and GC which are also based on diff erent separation mechanisms than CE. The selectivity of CE can be utilized for separation of complicated mixtures of target analytes (e.g.…”
Section: Introductionmentioning
confidence: 99%