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Physicochemical and Preclinical Evaluation of a Novel Buccal Measles Vaccine
Authors:Rikhav P Gala  Carmen Popescu  Gregory T Knipp  Robyn R McCain  Ruhi V Ubale  Richard Addo  Tuhin Bhowmik  Christopher D Kulczar  Martin J D’Souza
Institution:1.Vaccine Nanotechnology Laboratory, Department of Pharmaceutical Sciences,Mercer University,Atlanta,USA;2.Roquette America Inc,Geneva,USA;3.Department of Industrial and Physical Pharmacy, College of Pharmacy,Purdue University,West Lafayette,USA;4.Purdue Translational Pharmacology of Bindley Biosciences,Purdue University,West Lafayette,USA;5.Department of Pharmaceutical Sciences,Union University School of Pharmacy,Jackson,USA;6.Takeda Vaccine Business Unit,Bozeman,USA
Abstract:The aim of this study is to develop an orally disintegrating film (ODF) containing a microparticulate measles vaccine formulation for buccal delivery. The measles vaccine microparticles were made with biocompatible and biodegradable bovine serum albumin (BSA) and processed by spray drying. These vaccine microparticles were incorporated in the ODF, consisting of Lycoat RS720®, Neosorb P60W® and Tween 80. The yield of the microparticles was approximately 85–95%, w/w. The mean size of the vaccine microparticles was 3.65?±?1.89 μm and had a slightly negative surface charge of 32.65?±?2.4 mV. The vaccine particles were nontoxic to normal cells at high concentrations (500 μg/2.5?×?105 cells) of vaccine particles. There was a significant induction of innate immune response by vaccine microparticles which was observed in vitro when compared to blank microparticles (P?<?0.05). The vaccine microparticles also significantly increased the antigen presentation and co-stimulatory molecules expression on antigen presenting cells, which is a prerequisite for Th1 and Th2 immune responses. When the ODF vaccine formulation was dosed in juvenile pigs, significantly higher antibody titers were observed after week 2, with a significant increase at week 4 and plateauing through week 6 comparative to naïve predose titers. The results suggest that the ODF measles vaccine formulation is a viable dosage form alternative to noninvasive immunization that may increase patient compliance and commercial distribution.
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