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            <subfield code="0">(orcid)0000-0003-0702-8260</subfield>
            <subfield code="a">Martín-Rapún, R.</subfield>
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            <subfield code="a">Targeted nanoparticles for the treatment of Alzheimer’s disease</subfield>
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        <datafield tag="260" ind1=" " ind2=" ">
            <subfield code="c">2017</subfield>
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            <subfield code="a">Access copy available to the general public</subfield>
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            <subfield code="a">Background: Alzheimer’s disease (AD) has a dramatic impact on society. The therapeutic targets are located in the central nervous system (CNS), which limits the efficacy of drugs systemically administered: the blood-brain barrier (BBB) selectively allows the permeation of just a few kinds of molecules from the systemic circulation to the CNS. On the other hand, local administration routes to CNS are highly invasive. Methods: In this article, we have reviewed therapeutic approaches against AD, which are based on nanoparticles targeted to the brain and to the pathological hallmarks of the disease. The existing literature has been classified according to the AD feature that is addressed. Results: Nanoparticles have been used for the targeted delivery of drugs aiming to reduce the AD symptoms or to reverse the course of the disease. For this task the multivalency of nanoparticles has allowed their functionalization with several kinds of targeting groups, to cross the BBB and to target the place of treatment. With this approach an increased drug bioavailability has been achieved in the CNS using intravenous administration in place of more invasive administration routes. Additionally, nanoparticles have also been used in the development of vaccines and therapeutic formulations for intranasal administration. Conclusion: Targeted nanoparticles have been proved useful to enhance the performance of therapies against AD in animal models. A better understanding of AD mechanisms will help the successful application of targeted nanoparticles for combined therapies.</subfield>
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            <subfield code="9">info:eu-repo/grantAgreement/ES/MINECO/RYC-2014-15512</subfield>
            <subfield code="9">info:eu-repo/grantAgreement/ES/MINECO/RYC-2013-12570</subfield>
            <subfield code="9">This project has received funding from the European Union’s Horizon 2020 research and innovation program under grant agreement No H2020 657566-CONFINES</subfield>
            <subfield code="9">info:eu-repo/grantAgreement/EC/H2020/657566/EU/Controlling Cell Fate through Smart Nanoheaters/CONFINES</subfield>
            <subfield code="9">info:eu-repo/grantAgreement/ES/DGA/E93</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">PHARMACOLOGY &amp; PHARMACY</subfield>
            <subfield code="b">114 / 261 = 0.437</subfield>
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            <subfield code="a">Pharmacology</subfield>
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            <subfield code="a">Drug Discovery</subfield>
            <subfield code="c">2017</subfield>
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            <subfield code="0">(orcid)0000-0001-6995-4302</subfield>
            <subfield code="a">de Matteis, L.</subfield>
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            <subfield code="a">Ambrosone, A.</subfield>
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            <subfield code="a">García-Embid, S.</subfield>
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            <subfield code="a">Gutiérrez, L.</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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            <subfield code="0">(orcid)0000-0003-1081-8482</subfield>
            <subfield code="a">de la Fuente, J.M.</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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            <subfield code="1">2009</subfield>
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            <subfield code="a">Universidad de Zaragoza</subfield>
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            <subfield code="t">Current pharmaceutical design</subfield>
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