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Table 3 In vitro drug release kinetic study of the API from the various tenofovir and maraviroc bigel formulations

From: Development and evaluation of mucoadhesive bigel containing tenofovir and maraviroc for HIV prophylaxis

In vitro drug release kinetic study for maraviroc

 

Zero order

First order

Higuchi

Korsmeyer-Peppas

Formulation

r2

k0

r2

k1

r2

k2

r2

k3

 BG A

0.938

4.176

0.8323

0.0928

0.9702

28.22

0.9473

4.117

 BG B

0.9355

3.8941

0.8529

0.0931

0.9662

26.30

0.9575

3.825

 BG C

0.9179

4.309

0.8604

0.1166

0.9439

29.04

0.9502

1.834

 BG D

0.776

3.833

0.7253

0.0912

0.8343

26.39

0.8538

4.077

In vitro drug release kinetic study for tenofovir

 

Zero order

First order

Higuchi

Korsmeyer-Peppas

Formulation

r2

k0

r2

k1

Formulation

r2

k0

r2

 BG A

0.8412

4.0938

0.6362

0.0764

0.9000

28.14

0.8159

4.89

 BG B

0.6979

2.7713

0.5532

0.0636

0.7781

19.45

0.7875

5.40

 BG C

0.5171

2.1370

0.4575

0.056

0.6020

15.32

0.6882

5.84

 BG D

0.6552

2.7074

0.5404

0.0653

0.7374

19.08

0.7859

4.74