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Enhanced Solubility and Percutaneous Permeability of Lornoxicam gel using Biosurfactant
The short term stability studies conducted for 3 months revealed that at room temperature (25oc±1oc and RH 40%) optimized formulation was stable without much variation in drug content, viscosity, pH, and in vitro drug release study. Biosurfactant have numerous uses in pharmaceuticals, for solubiliza...
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Published in: | Research journal of pharmacy and technology 2018-07, Vol.11 (7), p.2848-2854 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | The short term stability studies conducted for 3 months revealed that at room temperature (25oc±1oc and RH 40%) optimized formulation was stable without much variation in drug content, viscosity, pH, and in vitro drug release study. Biosurfactant have numerous uses in pharmaceuticals, for solubilization of lipophilic drugs in aqueous media, as components of emulsion or surfactant self-assembly vehicles for oral and transdermal drug delivery agents to improve drug absorption and as penetration enhancer, due to its very low critical micelle concentration (CMC). The final weight of gel was adjusted using phosphate buffer pH 6.8 stirred for 20 minutes and stored in airtight container at room temperature until further analysis. To know which mathematical model best fits the obtained release profile Skin irritation test: [10] Skin irritation test was performed in six male Wistar rats. |
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ISSN: | 0974-3618 0974-360X 0974-306X |
DOI: | 10.5958/0974-360X.2018.00525.5 |