de Barros João M S, Scherer Timothy, Charalampopoulos Dimitrios, Khutoryanskiy Vitaliy V, Edwards Alexander D
School of Pharmacy, University of Reading, Whiteknights, Reading RG6 6ADUK.
Food and Nutritional Sciences, University of Reading, Whiteknights, Reading RG6 6ADUK.
J Pharm Sci. 2014 Jul;103(7):2022-2032. doi: 10.1002/jps.23997. Epub 2014 May 6.
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.
活细菌细胞(LBCs)作为减毒疫苗口服给药以递送生物药剂,并作为益生菌用于改善胃肠道(GI)健康。然而,LBCs存在独特的制剂挑战,给药后必须在胃肠道抗菌防御(包括胃酸)中存活下来。我们提出了一种简单的新制剂概念,称为聚合物薄膜层压板(PFL)。将LBCs在环境条件下干燥到浇铸的耐酸肠溶聚合物薄膜上,然后将这些薄膜层压在一起以制成固体口服剂型。将一种模型活细菌疫苗和一种益生菌的LBCs直接干燥到肠溶聚合物的浇铸薄膜上。在模拟胃液(SGF,pH 2.0)中保护干燥细胞的有效性取决于所用肠溶聚合物薄膜的组成,乙基纤维素与尤特奇L100 55的混合物比单独使用尤特奇能提供更好的抗酸保护。然而,尽管由混合聚合物薄膜制成的PFL在肠道条件(pH 7.0)下能完全释放低分子量染料,但它们未能释放LBCs。相比之下,仅由尤特奇制成的PFL成功地将干燥的益生菌或疫苗LBCs在SGF中保护2小时,随后在转移到模拟肠液后的60分钟内释放所有活细胞。释放动力学可以通过改变层压方法来控制。