Functional physico-chemical, ex vivo permeation and cell viability characterization of omeprazole loaded buccal films for paediatric drug delivery

被引:34
作者
Khan, Sajjad [1 ]
Trivedi, Vivek [1 ]
Boateng, Joshua [1 ]
机构
[1] Univ Greenwich Medway, Fac Sci & Engn, Dept Pharmaceut Chem & Environm Sci, Cent Ave, Chatham ME4 4TB, Kent, England
关键词
Permeation; Cell toxicity; Omeprazole; Metolose; Buccal films; Paediatric; FREEZE-DRIED WAFERS; IN-VITRO; ACID-SECRETION; MUCOSA; POLYMERS; SYSTEM; PERMEABILITY; FORMULATION; ABSORPTION; TISSUE;
D O I
10.1016/j.ijpharm.2016.01.045
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Buccal films were prepared from aqueous and ethanolic Metolose gels using the solvent casting approach (40 degrees C). The hydration (PBS and simulated saliva), mucoadhesion, physical stability (20 degrees C, 40 degrees C), in vitro drug (omeprazole) dissolution (PBS and simulated saliva), ex vivo permeation (pig buccal mucosa) in the presence of simulated saliva, ex vivo bioadhesion and cell viability using MTT of films were investigated. Hydration and mucoadhesion results showed that swelling capacity and adhesion was higher in the presence of PBS than simulated saliva (SS) due to differences in ionic strength. Omeprazole was more stable at 20 degrees C than 40 degrees C whilst omeprazole release reached a plateau within 1 h and faster in PBS than in SS. Fitting release data to kinetic models showed that Korsmeyer-Peppas equation best fit the dissolution data. Drug release in PBS was best described by zero order via non-Fickian diffusion but followed super case II transport in SS attributed to drug diffusion and polymer erosion. The amount of omeprazole permeating over 2 h was 275 ug/cm(2) whilst the formulations and starting materials showed cell viability values greater than 95%, confirming their safety for potential use in paediatric buccal delivery. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:217 / 226
页数:10
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