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   <subfield code="a">Controlled Delivery Systems: From Pharmaceuticals to Cells and Genes</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Elizabeth Balmayor, Helena Azevedo, Rui Reis]</subfield>
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   <subfield code="a">ABSTRACT: During the last few decades, a fair amount of scientific investigation has focused on developing novel and efficient drug delivery systems. According to different clinical needs, specific biopharmaceutical carriers have been proposed. Micro- and nanoparticulated systems, membranes and films, gels and even microelectronic chips have been successfully applied in order to deliver biopharmaceuticals via different anatomical routes. The ultimate goal is to deliver the potential drugs to target tissues, where regeneration or therapies (chemotherapy, antibiotics, and analgesics) are needed. Thereby, the bioactive molecule should be protected against environmental degradation. Delivery should be achieved in a dose- and time-correct manner. Drug delivery systems (DDS) have been conceived to provide improvements in drug administration such as ability to enhance the stability, absorption and therapeutic concentration of the molecules in combination with a long-term and controlled release of the drug. Moreover, the adverse effects related with some drugs can be reduced, and patient compliance could be improved. Recent advances in biotechnology, pharmaceutical sciences, molecular biology, polymer chemistry and nanotechnology are now opening up exciting possibilities in the field of DDS. However, it is also recognized that there are several key obstacles to overcome in bringing such approaches into routine clinical use. This review describes the present state-of-the-art DDS, with examples of current clinical applications, and the promises and challenges for the future in this innovative field.</subfield>
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   <subfield code="a">Springer Science+Business Media, LLC, 2011</subfield>
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   <subfield code="a">cell encapsulation</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">DDS routes of administration</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">gene therapy</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">growth factors</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">nanotechnology</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">regenerative medicine</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">BMP-2 : bone morphogenetic protein 2</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">BSA : bovine serum albumin</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">cDNA : complementary DNA</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">DDS : drug delivery systems</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">ECM : extracellular matrix</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">HEMA-MMA : Hydroxyethylmethacrylate- Methyl methacrylate</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">IGF-I : insulin-like growth factor 1</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">PC12 : cell line derived from a pheochromocytoma of the rat adrenal medulla</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">PDGF : platelet-derived growth factor</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">PLA-PEG : Polylactic acid-polyethylene glycol</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">PLGA-m-PEG : Poly(lactic-co-glycolic acid)-methoxy-polyethylene glycol</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">VEGF : vascular endothelial growth factor</subfield>
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   <subfield code="a">Balmayor</subfield>
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   <subfield code="u">3B's Research Group—Biomaterials, Biodegradables and Biomimetics Headquarters of the European Institute of Excellence on Tissue Engineering &amp; Regenerative Medicine, University of Minho, AvePark,, 4806-909, Guimarães, Taipas, Portugal</subfield>
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   <subfield code="u">Institute for Biotechnology and Bioengineering, PT Government Associated Laboratory, Guimarães, Portugal</subfield>
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   <subfield code="t">Pharmaceutical Research</subfield>
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