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            <subfield code="a">10.2217/nnm-2017-0198</subfield>
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            <subfield code="2">sideral</subfield>
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            <subfield code="a">Schwinté, P.</subfield>
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            <subfield code="a">Anti-inflammatory effect of active nanofibrous polymeric membrane bearing nanocontainers of atorvastatin complexes</subfield>
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            <subfield code="c">2017</subfield>
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            <subfield code="a">Aim: We developed polymeric membranes for local administration of nonsoluble anti-inflammatory statin, as potential wound patch in rheumatic joint or periodontal lesions. Methods: Electrospun polycaprolactone membranes were fitted with polysaccharide-atorvastatin nanoreservoirs by using complexes with poly-aminocyclodextrin. Characterization methods are UV-Visible and X-ray photoelectron spectroscopy, molecular dynamics, scanning and transmission electron microscopy. In vitro, membranes were seeded with macrophages, and inflammatory cytokine expression were monitored. Results &amp;amp; conclusion: Stable inclusion complexes were formed in solution (1:1 stability constant 368 M- 1, -117.40 kJ mol- 1), with supramolecular globular organization (100 nm, substructure 30 nm). Nanoreservoir technology leads to homogeneous distribution of atorvastatin calcium trihydrate complexes in the membrane. Quantity embedded was estimated (70-90 µg in 30 µm × 6 mm membrane). Anti-inflammatory effect by cell contact-dependent release reached 60% inhibition for TNF-a and 80% for IL-6. The novelty resides in the double protection offered by the cyclodextrins as drug molecular chaperones, with further embedding into biodegradable nanoreservoirs. The strategy is versatile and can target other diseases.</subfield>
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            <subfield code="a">All rights reserved</subfield>
            <subfield code="u">http://www.europeana.eu/rights/rr-f/</subfield>
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            <subfield code="a">5.005</subfield>
            <subfield code="b">2017</subfield>
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            <subfield code="a">BIOTECHNOLOGY &amp; APPLIED MICROBIOLOGY</subfield>
            <subfield code="b">22 / 160 = 0.138</subfield>
            <subfield code="c">2017</subfield>
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            <subfield code="a">NANOSCIENCE &amp; NANOTECHNOLOGY</subfield>
            <subfield code="b">32 / 92 = 0.348</subfield>
            <subfield code="c">2017</subfield>
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            <subfield code="a">Bioengineering</subfield>
            <subfield code="c">2017</subfield>
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            <subfield code="a">Biomedical Engineering</subfield>
            <subfield code="c">2017</subfield>
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            <subfield code="a">Development</subfield>
            <subfield code="c">2017</subfield>
            <subfield code="d">Q1</subfield>
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            <subfield code="a">Materials Science (miscellaneous)</subfield>
            <subfield code="c">2017</subfield>
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            <subfield code="a">Medicine (miscellaneous)</subfield>
            <subfield code="c">2017</subfield>
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            <subfield code="a">Nanoscience and Nanotechnology</subfield>
            <subfield code="c">2017</subfield>
            <subfield code="d">Q2</subfield>
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        <datafield tag="700" ind1=" " ind2=" ">
            <subfield code="a">Mariotte, A.</subfield>
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            <subfield code="a">Anand, P.</subfield>
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            <subfield code="a">Keller, L.</subfield>
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            <subfield code="a">Idoux-Gillet, Y.</subfield>
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            <subfield code="a">Huck, O.</subfield>
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            <subfield code="a">Fioretti, F.</subfield>
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            <subfield code="a">Irusta, S.</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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            <subfield code="a">Benkirane-Jessel, N.</subfield>
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            <subfield code="a">Universidad de Zaragoza</subfield>
            <subfield code="b">Dpto. Ing.Quím.Tecnol.Med.Amb.</subfield>
            <subfield code="c">Área Ingeniería Química</subfield>
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            <subfield code="g">12, 23 (2017), 2651-2674</subfield>
            <subfield code="p">Nanomedicine</subfield>
            <subfield code="t">Nanomedicine</subfield>
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