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FORMULATION AND EVALUATION OF PRONIOSOME BASED DRUG DELIVERY SYSTEM OF VALCYCLOVIR FOR IN-VITRO AND EX-VIVO PERFORMANCE ANALYSIS

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Figure

Table 2: Percentage of drug content, entrapment efficiency and particle size of Valcyclovir proniosome gel  Formulation Entrapment Particle Size
Fig. 3: FTIR of Span 20
Table 3: Release of Valcyclovir proniosome gel for the formulations F1 to F8 through cellopheone membrane
Fig.  9: Release of Valcyclovir proniosome gel for the formulations F1 to F8 through rat abdominal skin

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