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Table 4 Kinetic parameters for dissolution data of different Meclizine HCl ER matrix pellets formulations according to various kinetic models

From: Lipids bearing extruded-spheronized pellets for extended release of poorly soluble antiemetic agent—Meclizine HCl

Codes

Zero order

First order

Higuchi model

Hixson-Crowell model

Baker and Lonsdale model

Jander’s equation model

Korsmeyer-Peppas model

MDT

DE6

R2

K0 (h-1)

R2

K1 (h-1)

R2

KH (h-1/2)

R2

KHC (h-1)

R2

KBL (h-1)

R2

KJ (h-1/2)

R2

KKP (h-n)

n

h

%

F1

0.917

16.152

0.937

1.992

0.972

45.274

0.977

1.142

0.974

0.197

0.925

0.504

0.986

0.507

0.490

1.724

N/A

F2

0.964

18.114

0.954

0.225

0.990

45.081

0.995

1.012

0.993

0.165

0.966

0.771

0.993

0.620

0.425

0.819

N/A

F3

0.987

29.600

0.961

3.243

1.000

64.028

0.988

1.756

0.983

0.256

0.961

1.028

1.000

0.724

0.451

0.687

N/A

F8

0.998

25.444

0.954

2.204

0.983

54.270

0.973

1.353

0.966

0.250

0.935

0.840

0.972

0.701

0.536

0.531

N/A

F9

0.991

12.015

0.809

1.515

0.973

40.471

0.921

0.461

0.866

0.116

0.830

0.608

0.985

0.323

0.575

1.343

N/A

F11

0.997

21.762

0.961

2.611

0.992

53.325

0.983

0.665

0.948

0.205

0.948

0.600

0.997

0.528

0.572

1.496

N/A

F12

0.992

5.237

0.981

0.136

0.982

22.473

0.991

0.124

0.939

0.016

0.944

0.222

0.991

0.185

0.556

4.884

29.676

F14

0.958

20.305

0.986

2.029

0.979

44.307

1.000

1.355

1.000

0.205

0.988

0.623

0.995

0.809

0.281

0.528

N/A

F15

0.988

17.162

0.852

1.342

0.980

41.982

0.921

0.948

0.911

0.139

0.861

0.485

0.978

0.692

0.323

0.921

N/A

F16

0.957

15.413

0.908

2.089

0.989

42.662

0.978

0.760

0.973

0.155

0.936

0.686

0.990

0.481

0.519

1.159

NA

F17

0.978

7.315

0.916

0.515

0.989

31.730

0.977

0.230

0.924

0.066

0.914

0.503

0.993

0.244

0.551

4.836

33.933

F18

0.974

7.697

0.957

0.404

0.979

33.287

0.989

0.235

0.947

0.041

0.930

0.416

0.978

0.215

0.597

4.832

33.698

F19

0.995

30.747

0.954

2.650

1.000

66.247

0.982

1.786

0.975

0.259

0.950

0.813

0.999

0.719

0.461

0.700

NA

F20

0.995

5.366

0.968

0.150

0.956

22.691

0.982

0.120

0.905

0.014

0.913

0.204

0.978

0.166

0.578

5.448

27.074

F22

0.887

17.594

0.663

3.561

0.841

46.653

0.740

0.748

0.682

0.356

0.654

1.950

0.905

0.472

0.533

1.921

NA

F23

0.967

14.414

0.796

2.389

0.966

42.713

0.907

0.606

0.872

0.195

0.832

1.206

0.963

2.389

0.501

1.855

NA

F24

0.990

24.496

0.966

2.309

1.000

52.932

0.990

1.546

0.987

0.230

0.963

0.706

1.000

0.777

0.345

0.604

NA

F25

0.960

14.995

0.874

1.205

0.971

37.046

0.933

0.858

0.929

0.128

0.886

0.442

0.973

0.723

0.273

0.816

NA

F26

0.950

13.089

0.908

0.635

0.987

36.336

0.978

0.701

0.979

0.103

0.940

0.315

0.992

0.637

0.316

1.023

NA

F27

0.875

16.587

0.966

2.049

0.937

42.169

0.988

0.962

0.993

0.115

0.985

0.377

0.953

0.559

0.517

0.728

NA

F28

0.991

7.284

0.842

0.937

0.959

30.910

0.927

0.201

0.802

0.109

0.839

0.310

0.984

0.166

0.696

6.008

26.679

F29

0.991

5.791

0.985

0.148

0.988

24.933

0.995

0.143

0.948

0.022

0.950

0.207

0.997

0.146

0.675

4.835

31.384

F30

1.000

36.837

1.000

5.368

1.000

62.856

1.000

3.197

1.000

0.479

1.000

1.176

1.000

0.987

0.298

0.343

N/A

F31

0.959

15.883

0.964

1.980

0.982

39.478

0.994

0.960

0.993

0.153

0.967

0.678

0.982

0.645

0.389

0.743

N/A

F32

0.965

9.731

0.820

2.149

0.993

31.476

0.938

0.448

0.929

0.163

0.880

0.539

0.995

0.508

0.371

1.724

N/A

  1. “R2 “is the regression coefficient; “K” is the release rate constant for respective models; “n” is the diffusion exponent; “MDT” is the mean dissolution time, “DE” is the dissolution efficiency at 6 h. N/A indicates that DE is not calculated as 90% drug released before 6 h. F4, F5, F6, F7, F10, F13 and F21 released 90% drug within 2 h