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   <subfield code="a">Lyophilization of Protein-Loaded Polyelectrolyte Microcapsules</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Marie-Luce De Temmerman, Joanna Rejman, Johan Grooten, Thomas De Beer, Chris Vervaet, Jo Demeester, Stefaan De Smedt]</subfield>
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   <subfield code="a">ABSTRACT: Purpose: To evaluate if lyophilization can be used to obtain a dry formulation of polyelectrolyte microcapsules, which have emerged as a new class of microparticles for the encapsulation and delivery of biomacromolecules. Methods: Microcapsules composed of dextran sulfate and poly-L-arginine were obtained by coating CaCO3 microparticles by means of the layer-by-layer technique. Microcapsules were lyophilized using different stabilizers; intactness was checked by CLSM and SEM. Horseradish peroxidase was encapsulated as model enzyme and retained activity after freeze-drying was determined using a fluorescence assay. Ovalbumin was encapsulated as model antigen; immunogenicity after lyophilization was evaluated in vitro by a T-cell proliferation assay and in vivo by measuring the antibody titer in mice. Results: The results clearly demonstrate the necessity of using polyols in the formulation to prevent rupture of the microcapsules and to preserve the activity of encapsulated enzymes. Lyophilized microcapsules appeared as a promising adjuvant for antigen delivery, as both in vitro as in vivo assays showed higher immune activation compared to free antigen. Conclusions: Lyophilization is a promising strategy towards improved stability of protein-loaded microcapsules.</subfield>
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   <subfield code="a">Springer Science+Business Media, LLC, 2011</subfield>
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   <subfield code="a">drug delivery</subfield>
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   <subfield code="a">encapsulation</subfield>
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   <subfield code="a">layer-by-layer</subfield>
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   <subfield code="a">DEXS : dextran sulfate</subfield>
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