DOAJ Open Access 2012

Preparation and evaluation of cilnidipine microemulsion

Hemal Tandel Krunal Raval Anil Nayani Manish Upadhay

Abstrak

Cilnidipine, a calcium channel blocker having neuroprotective action and BCS Class II drug, hence formulating in Microemulsion will increase solubility, absorption and bioavailability. The formulation was prepared using titration method by tocotrienol, tween 20 and transcutol HP as oil, surfactant and co-surfactant and characterized for dilutability, dye solubility, assay (98.39±0.06), pH (6.6±1.5), Viscosity (98±1.0 cps) and Conductivity (0.2±0.09 μS/cm). The formulation was optimized on basis of percentage transmittance (99.269±0.23 at 700 nm), Globule size (13.31±4.3 nm) and zeta potential (-11.4±2.3 mV). Cilnidipine microemulsion was found to be stable for 3 months.

Penulis (4)

H

Hemal Tandel

K

Krunal Raval

A

Anil Nayani

M

Manish Upadhay

Format Sitasi

Tandel, H., Raval, K., Nayani, A., Upadhay, M. (2012). Preparation and evaluation of cilnidipine microemulsion. https://doi.org/10.4103/0975-7406.94162

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Informasi Jurnal
Tahun Terbit
2012
Sumber Database
DOAJ
DOI
10.4103/0975-7406.94162
Akses
Open Access ✓