Self emulsifying Drug Delivery System Preparation Evaluation Dr

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Self emulsifying Drug Delivery System : Preparation & Evaluation Dr Trapti Saxena

Self emulsifying Drug Delivery System : Preparation & Evaluation Dr Trapti Saxena

STEP 1: SCREENING OF EXCIPIENTS Solubility Studies ØDissolve excess amount of drug in each

STEP 1: SCREENING OF EXCIPIENTS Solubility Studies ØDissolve excess amount of drug in each of the solvents and put the samples in orbital shaker for 3 days. ØCentrifuge the equilibrated samples ØSuitably dilute the samples and analyze the solubility of drug. 2

STEP 2: TO FIND OUT CORRECT CMBINATION Pseudo Ternary Phase Diagram Study To find

STEP 2: TO FIND OUT CORRECT CMBINATION Pseudo Ternary Phase Diagram Study To find out the correct composition of oil, surfactant and cosurfactants 3

STEP 3: ADDITION OF DRUG üRequired amount of drug is loaded to SMEDDS. üGentle

STEP 3: ADDITION OF DRUG üRequired amount of drug is loaded to SMEDDS. üGentle stirring üSolidification using solid carrier : for solid SMEDDS 4

Evaluation of Self-microemulsifying System Self-emulsification Time Add SMEDDS to 20 m. L of water

Evaluation of Self-microemulsifying System Self-emulsification Time Add SMEDDS to 20 m. L of water and 300 m. L of 0. 1 N HCl Monitor the tendency to emulsify spontaneously and Final appearance 5

Evaluation of Self-microemulsifying System Precipitation Assessment Add SMEDDS to 300 m. L of 0.

Evaluation of Self-microemulsifying System Precipitation Assessment Add SMEDDS to 300 m. L of 0. 1 N HCl and water Store the Emulsion for 24 h and observe for phase separation and precipitation of the drug

Evaluation of Self-microemulsifying System Robustness to Dilution 50 X, 100 X and 1000 X

Evaluation of Self-microemulsifying System Robustness to Dilution 50 X, 100 X and 1000 X dilution of SMEDDS Emulsion - store for 24 h and observe for phase separation and precipitation of the drug 7

In vitro Drug Release Studies from Self-emulsifying Formulation • Pure drug and SMEDDS formulations

In vitro Drug Release Studies from Self-emulsifying Formulation • Pure drug and SMEDDS formulations - fill in hard gelatin capsules of size ‘ 0’ • Dissolution apparatus USP II is used • The samples is analyzed. 8

Droplet Size Analysis and Zeta Potential Measurement Determined by photon correlation spectroscopy using Malvern

Droplet Size Analysis and Zeta Potential Measurement Determined by photon correlation spectroscopy using Malvern Zetasizer at 25 °C. Disperse the formulation into 100 m. L of distilled water under gentle stirring Add 1 m. L aliquot into sample cell Monitor Light scattering at 90° to incident beam on samples 9

Evaluation of Self-microemulsifying System • Viscosity : by brookfield viscometer • Refractive index: by

Evaluation of Self-microemulsifying System • Viscosity : by brookfield viscometer • Refractive index: by refractometer and compared it with water (1. 333). • Percentage transmittance: measured at particular wavelength using Uv spectrophotometer. • Turbidimetric evaluation: by Nephelometer to monitor the growth of emulsification.