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The aim of the study was to develop a proniosomal system for famotidine that could efficiently deliver entrapped drug over a prolonged period of time. The proniosomal system was formulated by selecting various ratios of Span 60 and cholesterol using a coacervation-phase separation method.
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This page is a summary of: Formulation and optimisation of famotidine proniosomes: anin vitroandex vivostudy, Journal of Experimental Nanoscience, April 2015, Taylor & Francis,
DOI: 10.1080/17458080.2015.1030711.
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