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Showing posts from 2014

Non-supported electrodriven liquid microextraction

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Today, we focus the attention on an interesting article recently published in Journal of Chromatography A by researchers from the University of Tasmania at Australia. As our readers well known, electrodriven liquid microextraction techniques present a high efficiency for the extraction of charged analytes. In those techniques, the analytes migrate from the sample to the acceptor phase as a consequence of the voltage gradient established between both phases. In the off-line modes, the involved phases are often physically separated by an organic phase or a polymeric membrane impregnated with an appropriate organic solvent. Our colleagues have proposed a novel configuration that permits the development of the extraction procedure without any physical barrier between phases (1). The device consists of a 20 µL micropipette (a microtube with length of 6.4 cm and inner diameter of 0.3 mm) where the acceptor phase is located. The upper part of the microtube is introduced into a syringe th

Graphene composite for the extraction of hydrophilic compounds

Every month, Analytical Methods journal publishes in its blog a list of hot articles that can be downloaded by free for a defined period of time. This is an interesting initiative that makes wider the impact of the journal providing free access to several articles. I usually read Analytical Methods blog for this reason (among others) and I strongly recommend it to our followers. In fact, this post is focused on one of the latest hot articles of this journal. Solid phase extraction is a consolidated sample preparation technique in any analytical laboratory. In spite of the wide variety of solids commercially available (e.g. silica-C18 and polymeric sorbents), the development of new ones capable of facing up the isolation and preconcentration of hydrophilic and ionic compounds would be desirable. For these compounds the performance of “conventional” sorbents is relatively low. Among the nanostructured solids, graphene and its derivative graphene oxide (GO) have been deeply stud

Bioanalysis Zone a vital tool for bioanalysts

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by Cameron Low, Digital Editor for Bioanalysis Zone As a reader of the Microextraction Tech blog, and as someone who possesses a keen interest in the bioanalytical field, it is a great honor to be able to write this post on Bioanalysis Zone . Bioanalysis Zone is brought to you by Future Science Group, the publishers of Bioanalysis, a prominent fortnightly, peer-reviewed journal. The site features the latest news relevant to those working within the bioanalytical field; articles from Bioanalysis; exclusive interviews and commentaries from opinion leaders working within academia and the pharmaceutical industry; exclusive webinars with a variety of experts; and a business directory. We also provide a forum for the community to discuss recent developments and pose any questions related to this fast moving field. Fabio Garofolo, Associate Editor of Bioanalysis, commented, “I truly believe that since bioanalytical science, techniques and regulations are evolving so fast, it is i

Returning to nature: use of pollen grains for solid phase extraction

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If you are interested in green analytical chemistry, this is an article for you. Researchers from the Wuhan University at China have recently proposed the use of pollen grains as sorbent in hydrophilic interaction solid phase extraction (1). These grains are characterized by a high superficial area (close to 20 m2/g), a high hydrophilic surface due to the presence of residual hydroxyl groups and particle size in the medium micrometer range. The selection of the proper variety of pollen to be used for analytical purposes is a critical issue according to the authors. They prefer pine pollen to bee pollen grains since the first one is more homogeneous from the chemical point of view and therefore it leads to more reproducible results. In addition, this type of pollen is available at higher amounts allowing the fabrication of many extraction cartridges for sample extraction. Figure 1. Pollen from a variety of common plants (Public domain image from wikipedia) Pollen grains cannot

Read all posts from November 2014

Working to Automate Micro-Extraction I am a regular reader of this blog, which I find relevant and interesting, so I am pleased to have this opportunity to introduce the Anatune blog to a wider audience and encourage more people to read it. Anatune is a company based in Cambridge, UK and we specialise in the automation of GC-MS sample preparation and injection. We provide upgrades to existing instruments, but best of all, we like to deliver complete, integrated systems where the sample preparation works seamlessly with GC-MS. ( Read more ) Stir bar sorptive dispersive microextraction mediated by magnetic nanoparticles We all are familiar with stir bar sorptive extraction (SBSE) and dispersive methodologies in this context. The advantages of both techniques are also well known and a deep research is being carried out to characterize new sorbent phases which improve the efficiency and open up the application field of these microextraction techniques. Research

Fabric phase sorptive extraction: a new generation green sample preparation strategy

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by Dr. Abuzar Kabir, International Forensic Research Institute, Department of Chemistry and Biochemistry, Florida International University, Miami, Florida, USA Fabric phase sorptive extraction (FPSE), the most recent member of the sorptive microextraction family, has innovatively incorporated both solid phase microextraction (SPME) and solid phase extraction (SPE) techniques into a single technology platform. FPSE utilizes permeable natural/synthetic fabrics e.g., cotton, polyester, fiber glass supports to chemically bind sol-gel hybrid inorganic-inorganic sorbents. A 5 cm2unit of coated fabric (2.5 cm x 2.0 cm) is typically used as the extraction media which can be inserted directly into the sample container. Extraction of the analytes is generally expedited by using a magnetic stir bar to diffuse the analyts into the sample matrix so that rapid mass transfer from the sample matrix to the extraction medium takes place.Once the mass transfer equilibrium between the FPSE media and

Microextraction in cancer research

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I have already arrived home after an interesting meeting in Madeira island regarding the HCV project dedicated to the study and characterization of human cancer volatome. The identification of biomarkers in several biological specimens is really essential since it will allow the development of analytical platforms for early detection of cancer or to study the disease progression. In this context, microextraction techniques can be used in two different scenarios. On the one hand, they can be used in the preliminary research to isolate potential candidates as biomarkers from several samples including urine or breath. On the other hand, once selected the appropriate candidates, microextraction techniques can be used to design screening and/or confirmation analytical methodologies for real-world tests. The HCV project involves research groups form different countries. The consortium includess researchers from the Madeira University at Portugal, the National Centre for Cell Science

Rotating Disk Sorptive Extraction

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by Prof. Dr. Pablo Richter, Department of Inorganic and Analytical Chemistry, Faculty of Chemical and Pharmaceutical Sciences, University of Chile. The modern trends in analytical chemistry promote efficiency and green technology in sample preparation. In this context, our research team developed a new technique in 2009 that is capable of extracting pollutants from liquid samples on a rotating PTFE disk with one surface coated with an extraction phase [1]. The disk has embedded a miniature magnetic rod, which allows rotation. We have termed this procedure rotating-disk sorptive extraction (RDSE). RDSE is currently available in two configurations. In the classic version (Figure 1), the extraction phase is a polymeric film adhered to one side of the PTFE disk (configuration 1). In this configuration, polydimethylsiloxane (PDMS), nylon and octadecyl (C18) have been used as the sorptive material for the extraction of low-polarity analytes (Log Kow between 3 and 7) [1-12]. However