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Current
Analytical Chemistry
ISSN: 1573-4110

Current Analytical Chemistry
Volume 4, Number 2, April 2008
Contents

Recent Advances in Anthocyanin Analysis and Characterization
Pp. 75-101
Cara R. Welch, Qingli Wu and James E. Simon
[Abstract]
Biomedical Applications of Accelerator Mass Spectrometry
Pp. 102-110
Emily L.-C. Cheah and Hwee-Ling Koh
[Abstract]
Hydromorphone: Analytical Methodologies for its
Determination Pp. 111-126
Maansi G. Kumar and Senshang Lin
[Abstract]
Immobilised Metal Affinity Chromatography for
the Analysis of Proteins and Peptides Pp. 127-135
Gushinder Kaur-Atwal, Daniel J.Weston, Philip L.R. Bonner,
Philip S. Green and Colin S. Creaser
[Abstract]
Electrochemical Reduction of NAP on the Glassy Carbon Electrodes
Modified with aromatic diazonium salts Pp. 136-141
Murat Sadikoglu, Ali O. Solak, Muhammet Isiklan and Zeynel
Kiliç
[Abstract]
Experimental Design Techniques for Optimization
of Analytical Methods. Part II: Spectroscopic and Electroanalytica
Techniques Pp. 142-151
Federica Bianchi and Maria Careri
[Abstract]
Flow-Injection Chemiluminescence Analysis of
Lomefloxacin in Drugs and Biological Fluids Pp. 152-156
Liqing Li, Hanwen Sun and Xueyan Chen
[Abstract]
Pressurized Liquid Extraction of Contaminants
from Environmental Samples Pp. 157-167
Antonio Nieto, Francesc Borrull, Rosa M. Marcé
and Eva Pocurull
[Abstract]
Abstracts

[Back to top]
Recent Advances in Anthocyanin Analysis and Characterization
Cara R. Welch, Qingli Wu and James E. Simon
Anthocyanins are a class of polyphenols responsible for
the orange, red, purple and blue colors of many fruits, vegetables,
grains, flowers and other plants. Consumption of anthocyanins
has been linked as protective agents against many chronic
diseases and possesses strong antioxidant properties leading
to a variety of health benefits. In this review, we examine
the advances in the chemical profiling of natural anthocyanins
in plant and biological matrices using various chromatographic
separations (HPLC and CE) coupled with different detection
systems (UV, MS and NMR). An overview of anthocyanin chemistry,
prevalence in plants, biosynthesis and metabolism, bioactivities
and health properties, sample preparation and phytochemical
investigations are discussed while the major focus examines
the comparative advantages and disadvantages of each analytical
technique.
[Back to top]
Biomedical Applications of Accelerator Mass Spectrometry
Emily L.-C. Cheah and Hwee-Ling Koh
Accelerator mass spectrometry (AMS) has emerged as an
important analytical tool in biomedical and pharmaceutical
research. Its sensitivity (up to attomole, 10-18
levels), precision, low sample requirements and the ability
to trace a biomarker over a prolonged period of time are valuable
attributes. Metabolomic, kinetic, toxicokinetic and dosimetric
studies of various chemical molecules, at environmental exposure
levels and physiologically relevant doses, using radioisotopes
(e.g. 14 C, 3H,
26 Al and 41Ca)
are possible. AMS has contributed significantly to the understanding
of DNA-adduct formation in carcinogenesis and is finding new
uses in the changing drug development paradigm where more
researchers are turning to biomarkers to predict functional
and clinical outcomes in patients. Microdosing and first-in-human
studies are also breakthroughs spearheaded by the innovative
use of AMS. Recent advances see AMS driven into fields of
phytochemical and nutritional research as well as clinical
diagnosis and disease state monitoring. As a result of the
high initial costs and forbidding size, developments in equipment
miniaturization and enhanced sample throughput seek to overcome
these barriers. AMS is expected to present new and exciting
opportunities in biomedical research as its breadth of applications
continues to expand. This article provides an insight into
the pharmaceutical and biomedical applications of AMS.
[Back to top]
Hydromorphone: Analytical Methodologies for its Determination
Maansi G. Kumar and Senshang Lin
Hydromorphone, a semi-synthetic derivative of morphine,
is being used in the treatment of moderate to severe cancer-related
and post-operative pain. It is also one of the most commonly
prescribed drug that is often abused. Hence, its detection
in biological samples and tissues is important for legal and
therapeutic reasons. The purpose of this review is to give
a brief description of the various non-chromatographic and
chromatographic analytical techniques, namely immunoassays,
thin layer chromatography, high performance liquid chromatography,
liquid chromatography/mass spectrometry, gas chromatography/mass
spectrometry and capillary electrochromatography, that have
been used by analysts to assay hydromorphone from the early
1970s to present. This review aims to help the analytical
community make efficient choices between various analytical
methodologies based on concrete parameters of reliability,
sensitivity, specificity, precision, accuracy, cost and potential
for automation.
[Back to top]
Immobilised Metal Affinity Chromatography for the Analysis
of Proteins and Peptides
Gushinder Kaur-Atwal, Daniel J.Weston, Philip L.R. Bonner,
Philip S. Green and Colin S. Creaser
Immobilised metal affinity chromatography (IMAC) has
become an established purification procedure for the selective
isolation of proteins, peptides and post-translationally modified
peptides, using a wide range of metal ions, including Cu(II),
Fe(III) and Ga(III). Recently, the potential of interfacing
capillary IMAC with mass spectrometry has been explored. This
article reviews the development and use of IMAC in protein/peptide
analysis, highlighting the benefits of capillary columns and
their application to IMAC based enrichment.
[Back to top]
Electrochemical Reduction of NAP on the Glassy Carbon Electrodes
Modified with aromatic diazonium salts
Murat Sadikoglu, Ali O. Solak, Muhammet Isiklan and Zeynel
Kiliç
The electrochemical reduction of 4-{[(IE)-(2-hydroxynaphthyl)
methylidene]amino}-1,5-dimethyl-2-phenyl-2,3-dihydro-1H-pyrazol-3-one
(NAP) was studied by using cyclic voltammetry in acetonitrile
media at a glassy carbon (GC) and modified GC electrodes.
The GC electrodes were grafted by electrochemical reduction
of diazonium salts of various organic molecules. GC surfaces
modified with anthraquinone, p-nitrophenyl, p-aminophenyl,
p-amino-N,N-dimethylphenyl and p-methoxyphenyl
radicals were used to investigate the reduction behaviors
of NAP. The effect of the modified glassy carbon electrodes
on the reduction of NAP was studied as being related to the
role of the electron donor or the electron acceptor groups
on the phenyl ring attached to the surface. The compound NAP
shows two reduction peaks in a cyclic voltammogram. These
peaks were observed at –2.1 V and –2.7 V on the
GC electrode surface. Also, the reduction peaks of NAP were
obtained for all the modified electrodes studied. The p-methoxyphenyl
modified GC electrode showed a significant increase in the
rate of electron transfer at the reduction of NAP. The kinetics
and the mechanism of the electrode process were simulated
and some parameters were calculated using BAS Digi-Sim®
software.
[Back to top]
Experimental Design Techniques for Optimization of Analytical
Methods. Part II: Spectroscopic and Electroanalytical Techniques
Federica Bianchi and Maria Careri
A review is presented on recent applications of experimental
design and optimization techniques for the analysis of compounds
of food, biomedical, toxicological and environmental concern.
The main features and the significant advantages of chemometric
approaches are discussed.
Examples related to the determination of substances like xenobiotics,
naturally occurring compounds and metals using different analytical
techniques like inductively coupled plasma (ICP) sources,
voltammetry and other techniques are provided in this Part.
The use of experimental design techniques for optimization
of extraction techniques is also emphasized.
This survey will attempt to cover the state-of-the-art from
2004 to 2006.
[Back to top]
Flow-Injection Chemiluminescence Analysis of Lomefloxacin
in Drugs and Biological Fluids
Liqing Li, Hanwen Sun and Xueyan Chen
A new method was developed for the determination of lomefloxacin
by using flow–injection chemiluminescence(CL) based
on the reaction of Ce(IV)–sodium thiosulfate–lomefloxacin–sulfuric
acid system. The CL conditions were investigated and optimized.
The CL intensity was correlated linearly with concentration
of lomefloxacin in the range of 1.0×10-
5 ~ 6.0×10-2
g L- 1. The determination
limit (3σ)
is 3×10- 6 g L-1.
The relative standard deviation is 1.9% for 11 measurements
of 2.0×10-4 g L-1
lomefloxacin. The method has been applied satisfactorily to
determine lomefloxacin in drugs, serum and urine with the
recovery of 97.0% ~ 104.5%. The CL mechanism of the system
was proposed.
[Back to top]
Pressurized Liquid Extraction of Contaminants from Environmental
Samples
Antonio Nieto, Francesc Borrull, Rosa M. Marcé
and Eva Pocurull
This review updates knowledge on pressurized liquid extraction
(PLE), a sample preparation technique that is increasingly
used to extract moderately volatile and non-volatile organic
pollutants from solid and semi-solid environmental matrices.
In environmental analyses, therefore, it is mainly been used
to analyse soils and sewage sludge, though it has also been
used, albeit to a lesser extent, to analyse air samples. As
interest in analysing contaminants in environmental solid
samples has increased in recent years, more extraction methods
are being developed.
This review is divided into two parts. In the first part we
discuss the main parameters affecting extraction, such as
solvent, extraction time, temperature, pressure, number of
cycles, flush volume and purge time. In the second part we
review recent applications of PLE in environmental analysis
and discuss the advantages of PLE over other extraction techniques
such as ultrasonic solvent extraction and microwave assisted
extraction.
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