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A laminated polymer film formulation for enteric delivery of live vaccine and probiotic bacteria.
de Barros, João M S; Scherer, Timothy; Charalampopoulos, Dimitrios; Khutoryanskiy, Vitaliy V; Edwards, Alexander D.
Afiliación
  • de Barros JMS; School of Pharmacy, University of Reading, Whiteknights, Reading RG6 6ADUK.
  • Scherer T; School of Pharmacy, University of Reading, Whiteknights, Reading RG6 6ADUK.
  • Charalampopoulos D; Food and Nutritional Sciences, University of Reading, Whiteknights, Reading RG6 6ADUK.
  • Khutoryanskiy VV; School of Pharmacy, University of Reading, Whiteknights, Reading RG6 6ADUK.
  • Edwards AD; School of Pharmacy, University of Reading, Whiteknights, Reading RG6 6ADUK. Electronic address: a.d.edwards@reading.ac.uk.
J Pharm Sci ; 103(7): 2022-2032, 2014 Jul.
Article en En | MEDLINE | ID: mdl-24801679
Live bacterial cells (LBCs) are administered orally as attenuated vaccines to deliver biopharmaceutical agents and as probiotics to improve gastrointestinal (GI) health. However, LBCs present unique formulation challenges and must survive GI antimicrobial defenses including gastric acid after administration. We present a simple new formulation concept, termed polymer film laminate (PFL). LBCs are ambient dried onto cast acid-resistant enteric polymer films that are then laminated together to produce a solid oral dosage form. LBC of a model live bacterial vaccine and a probiotic were dried directly onto a cast film of enteric polymer. The effectiveness at protecting dried cells in a simulated gastric fluid (SGF, pH 2.0) depended on the composition of enteric polymer film used, with a blend of ethylcellulose plus Eudragit L100 55 providing greater protection from acid than Eudragit alone. However, although PFL made from blended polymer films completely released low-molecular-weight dye into intestinal conditions (pH 7.0), they failed to release LBCs. In contrast, PFL made from Eudragit alone successfully protected dried probiotic or vaccine LBC from SGF for 2 h, and subsequently released all viable cells within 60 min of transfer into simulated intestinal fluid. Release kinetics could be controlled by modifying the lamination method.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Bifidobacterium / Portadores de Fármacos / Vacunas Bacterianas / Vacunas Atenuadas / Probióticos Idioma: En Revista: J Pharm Sci Año: 2014 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Bifidobacterium / Portadores de Fármacos / Vacunas Bacterianas / Vacunas Atenuadas / Probióticos Idioma: En Revista: J Pharm Sci Año: 2014 Tipo del documento: Article Pais de publicación: Estados Unidos