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Oral Presentations (LDD, LPES, LNM, LPAT, LNT, LPPT, LPM)

S. Stummer,S. Salar-behzadi,Helmut Viernstein,Ronny Martien,Herbert Hoyer, G. Perera,Andreas Bernkop-Schnürch,Marjana Dürrigl, Ana Hafner,Jelena Filipović‐Grčić,Otto Glatter, Chandrashekar Kulkarni,Angela Chemelli, Xu-man Wang,Gerda Ratzinger, Melanie Wirth, Franz Gabor,Karmen Teskač,Jan Pelipenko, Slavomíra Doktorovová, Caroline Martins Lopes,Paula Martins-Lopes, R. Vangenechten, Ivo Backx,D. Brandl,Hanna Heimburg, Martin Dietzel, Markus Sommerfeld, A. Rinderhofer,T. Hörmann,Maurizio Iannuccelli, L. L. Simon,M. Schongut,F. Štěpánek, Konrad Hungerbuhler,Daniele Suzzi,Gregor Toschkoff, D. Machold,Stefan Radl, M. Gattringer, H. Steiner,Daniela Frascione,Matthias Saba-Lepek,Clemens Diwoky,Peter Opriessnig, Ralf Stollberger,Gunter Almer,Harald Mangge,Ruth Prassl,Jana Brüssler,Elena Eva Julianne Marxer, Abram Becker, R. Schubert, Ch. Nimsky,Udo Bakowsky, Radek Ambrus,A. Pomázi, Piroska Szabó-Révész, B. Looser,Asya Vaisman,Alain Blasco,Daniel M. Koller,Nikolaus Balak,Otto Scheibelhofer, J. Moor,G. Hörl,N. Heigl,Simon D. Fraser,Johannes G. Khinast, L. Marić,Irena Homšek,Claudia Meindl,Thomas R. Pieber,A. L. R. Souza,Tatiana Andreani,Slavomíra Doktorovová, A. J. Silva,Eliana B. Souto,Maria Palmira Daflon Gremião,Petra Kocbek,Karmen Teskač,M. E. Kreft,Gerd Leitinger,Ilse Letofsky-Papst, Laszloné Kürti, L. Kis,Szilvia Veszelka,Piroska Szabó-Révész,Mária A. Deli,F. Sinner,Eva Roblegg,Eleonore Fröhlich,Amber Zimmer, Astrid Falk,Fernando J. Muzzio,S. Baumgartner,Julijana Kristl,Biljana Govedarica,Stanko Srčič, A. Zupančič Valant, Urška Mikac,Ana Sepe, M. Smikalla, Nora Anna Urbanetz, I. Antal,Nikolett Kállai,Oliver Luhn, Jordi Mola,Ákos Ruszkai,Elijah Balogh, Dredán,Imre Klebovich, N. Neub, Swen Dietrich, D. Petrak,Mirco Köhler, Günter Eckardt,J. H. Finke,Jodi Schur,T. Gothsch, Stefanie Beinert, C. Lesche,Stephanus Büttgenbach, Alicja Kwade,Christel Charlotte Müller-Goymann, Nathan D. Evans, Salvatore Cascone,Felice De Santis, Gary A. Lamberti,Giuseppe Titomanlio,Anna Angela Barba

Scientia Pharmaceutica(2010)

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摘要
Probiotic microorganisms have been shown to provide specific health benefits when consumed as food supplements or as food components. The main problem of such products is the poor survival of the probiotic bacteria in the low pH of gastric fluid. However the use of synthetic excipients for enteric coating to prevent the exposure of microorganisms to gastric fluid is limited in food supplementary industry. Therefore the aim of this study was to develop an enteric coating formulation containing shellac as a natural polymer. Shellac possesses good resistance to gastric juice; the major disadvantage of this polymer is its low solubility in the intestinal fluid [1, 2]. Thus films containing different ratios of shellac and water-soluble polymers (sodium alginate, hydroxypropyl methylcellulose (HPMC) and polyvinylpyrrolidon (PVP)) or plasticizers (glycerol and glyceryl triacetate (GTA)) were prepared in order to analyse the films’ melting temperatures (Tm), the changes in enthalpy (ΔH), their capability of taking up water, and their solubility in different media. The release characteristics of the films were studied by loading pellets with Enterococcus faecium M74 and coating them with formulations containing different amounts of shellac and polymer or plasticized shellac. Using dissolution tests, performed according to USP XXXI paddle method, the resistance of the coatings to simulated gastric fluid (SGF, pH 1.2) and the release of cells in simulated intestinal fluid (SIF, pH 6.8) was investigated. The trials showed that an increasing amount of plasticizer results in a decrease of Tm and ΔH of the films whereat glycerol had a superior plasticization effect to GTA. The compatibility of films made of water-soluble polymers and shellac was also concentration dependent. HPMC and PVP showed superior compatibility with shellac compared to sodium alginate, since films containing shellac and more than 10% [w/w] sodium alginate tended to separate into two phases. In the end five formulations containing shellac and either 5% [w/w] glycerol, 10% [w/w] PVP, 20% [w/w] PVP, 10% [w/w] HPMC, or 5% [w/w] sodium alginate emerged as feasible for enteric coating purposes.
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