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      Barrier Capacity of Human Placenta for Nanosized Materials

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          Abstract

          Background

          Humans have been exposed to fine and ultrafine particles throughout their history. Since the Industrial Revolution, sources, doses, and types of nanoparticles have changed dramatically. In the last decade, the rapidly developing field of nanotechnology has led to an increase of engineered nanoparticles with novel physical and chemical properties. Regardless of whether this exposure is unintended or not, a careful assessment of possible adverse effects is needed. A large number of projects have been carried out to assess the consequences of combustion-derived or engineered nanoparticle exposure on human health. In recent years there has been a growing concern about the possible health influence of exposure to air pollutants during pregnancy, hence an implicit concern about potential risk for nanoparticle exposure in utero. Previous work has not addressed the question of whether nanoparticles may cross the placenta.

          Objective

          In this study we investigated whether particles can cross the placental barrier and affect the fetus.

          Methods

          We used the ex vivo human placental perfusion model to investigate whether nanoparticles can cross this barrier and whether this process is size dependent. Fluorescently labeled polystyrene beads with diameters of 50, 80, 240, and 500 nm were chosen as model particles.

          Results

          We showed that fluorescent polystyrene particles with diameter up to 240 nm were taken up by the placenta and were able to cross the placental barrier without affecting the viability of the placental explant.

          Conclusions

          The findings suggest that nanomaterials have the potential for transplacental transfer and underscore the need for further nanotoxicologic studies on this important organ system.

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          Most cited references25

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          Regulated portals of entry into the cell.

          The plasma membrane is the interface between cells and their harsh environment. Uptake of nutrients and all communication among cells and between cells and their environment occurs through this interface. 'Endocytosis' encompasses several diverse mechanisms by which cells internalize macromolecules and particles into transport vesicles derived from the plasma membrane. It controls entry into the cell and has a crucial role in development, the immune response, neurotransmission, intercellular communication, signal transduction, and cellular and organismal homeostasis. As the complexity of molecular interactions governing endocytosis are revealed, it has become increasingly clear that it is tightly coordinated and coupled with overall cell physiology and thus, must be viewed in a broader context than simple vesicular trafficking.
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            Clinical applications of magnetic nanoparticles for hyperthermia.

            Magnetic fluids are increasingly used for clinical applications such as drug delivery, magnetic resonance imaging and magnetic fluid hyperthermia. The latter technique that has been developed as a cancer treatment for several decades comprises the injection of magnetic nanoparticles into tumors and their subsequent heating in an alternating magnetic field. Depending on the applied temperature and the duration of heating this treatment either results in direct tumor cell killing or makes the cells more susceptible to concomitant radio- or chemotherapy. Numerous groups are working in this field worldwide, but only one approach has been tested in clinical trials so far. Here, we summarize the clinical data gained in these studies on magnetic fluid induced hyperthermia.
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                Author and article information

                Journal
                Environ Health Perspect
                Environmental Health Perspectives
                National Institute of Environmental Health Sciences
                0091-6765
                1552-9924
                March 2010
                12 November 2009
                : 118
                : 3
                : 432-436
                Affiliations
                [1 ] Empa, Swiss Federal Laboratories for Material Testing and Research, Laboratory for Materials–Biology Interactions, St. Gallen, Switzerland
                [2 ] University Hospital Zurich, Department of Obstetrics, Zurich, Switzerland
                [3 ] Institute of Pathology, Cantonal Hospital, St. Gallen, Switzerland
                Author notes
                Address correspondence to P. Wick, Laboratory for Materials-Biology Interactions, Lerchenfeldstr. 5, 9014 St. Gallen, Switzerland. Telephone: 41-71-274-76-84. Fax: 41-71-274-76-94. E-mail: peter.wick@ 123456empa.ch
                [*]

                These authors contributed equally to this work.

                The authors declare they have no competing financial interests.

                Article
                ehp-118-432
                10.1289/ehp.0901200
                2854775
                20064770
                b4cff668-2f7d-472e-a93a-e45463de85f4
                This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original DOI.
                History
                : 14 July 2009
                : 12 November 2009
                Categories
                Research

                Public health
                nanoparticles,ex vivo perfusion,barrier tissue,nanotoxicity,human placenta
                Public health
                nanoparticles, ex vivo perfusion, barrier tissue, nanotoxicity, human placenta

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