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Table 5 Evaluation of stability of OCNIG

From: Design and optimization of nano invasomal gel of Glibenclamide and Atenolol combination: in vitro and in vivo evaluation

S. No.

Characterization of OCNIG

Freshly prepared (initial)

After 3 months

25 ± 2 °C/65 ± 5%

40 ± 2 °C/75 ± 5% RH

Refrigerated condition (4 ± 2 °C)

1

Clarity

Clear, smooth and homogenous

Clear, smooth and homogenous

Clear, smooth and homogenous

Clear, smooth and homogenous

2

pH

6.8 ± 0.1

6.75 ± 0.1

6.78 ± 0.1

6.7 ± 0.2

3

Drug Content (%)

98.43 ± 0.023 (GLB)

97.89 ± 0.026 (ATN)

97.33 ± 0.012 (GLB)

97.21 ± 0.016 (ATN)

97.12 ± 0.01 (GLB)

97.01 ± 0.012 (ATN)

97.09 ± 0.02 (GLB)

96.21 ± 0.04 (ATN)

4

Entrapment Efficiency (%)

97.34 ± 0.034(GLB)

96.89 ± 0.015 (ATN)

97.04 ± 0.015 (GLB)

95.99 ± 0.025 (ATN)

97.34 ± 0.012 (GLB)

95.25 ± 0.055 (ATN)

96.04 ± 0.013 (GLB)

94.89 ± 0.04 (ATN)

5

Vesicle size (nm)

120.45 ± 3.87

120.08 ± 2.65

124.08 ± 2.65

130.08 ± 2.65