About this blog

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On April 6th, 2011, Prof. Lucena launched @microextraction on Twitter. The main objective was to present a periodic digest of those research publications devoted to microextraction. This bibliographic update could be interesting to all those researchers interested in the role that extraction and microextraction techniques may play in the development of a competitive analytical methodology.

In March 2012, two new apps were launched almost simultaneously. On the one hand, the Facebook account tried to open a new communication network with people interested in (micro)extraction. On the other hand, this blog was developed as a new platform to highlight special contributions on the topic.

In January 2021, all the apps have been integrated into the "Affordable and Sustainable Sample Preparation" research group of the University of Córdoba. 

We want to open our blog to all researchers who want to spread their research in a simple way.

Welcome to microextraction

Popular posts from this blog

Gold coated magnetic beads for electrochemical detection

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This post summarizes an interesting article, recently accepted for publication in Analytical Chemistry, which presents an innovative use of magnetic beads. Researchers from the Osaka Prefecture University at Japan have proposed the synthesis of magnetic microbeads covered with a smooth gold layer that are used for the electrochemical detection of streptavidin (1). The synthesis, which is deeply described in the manuscript, consists of three well defined steps. First of all, the magnetic beads are introduced in a colloidal gold dispersion containing Au-nanoparticles (Au-NPs). Thanks to the opposite zeta potential of both materials (microbeads are negatively charged while Au-NPs present a positive charge), their assembly takes place by electrostatic interactions. However, the Au-NPs are not connected to each other and therefore the electrical resistance of the microbeads is too high. In a second step, the modified microbeads are dispersed in an aqueous medium containing HAuCl 4 as ...
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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...
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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...
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