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Batch No.
Formulation Ingredients
Batch Size
MSA/tablet
Chitosan
Spray dried
MCC/tablet Colloidal
(mg)
(%w/v)
lactose /tablet
(% w/w)
silica
C1
C2
35
35
1
2
(% w/w)
10
10
_
_
(%w/w)
1
1
100
100
C3
35
10
100
C4
35
10
100
C5
35
10
100
C6
35
10
100
Hardness
(kg/cm2)
C1
Axial
Radial
Dia.
Dia.
(mm)
(mm)
2.020.03 4.010.03
% Weight
Variation
Friability
(%w/w)
4.40.38
Average
Weight
(mg)
44.721.10
C2
4.960.8
0.270.04
34.8730.12
91.2
951.1
2.040.06 4.020.05
4.20.41
44.591.92
4.951.1
0.350.05
33.9210.33
141.6
941.5
C3
2.030.05 4.030.08
4.90.26
44.891.47
4.981.2
0.320.08
34.7460.40
180.8
960.5
C4
2.050.02 4.020.04
4.30.48
43.942.01
4.880.7
0.400.01
33.8540.58
52.4
742.0
C5
2.010.01 4.040.02
4.10.22
44.241.84
4.911.6
0.420.07
33.9620.62
110.5
723.2
C6
2.020.04 4.050.01
4.00.56
44.672.42
4.971.9
0.450.09
34.2160.47
161.9
772.5
% Weight
Variation
% Weight
gain
5.070.2
10.661.02
5.020.5
11.710.09
C3
(1:1.25
)
4.920.4
9.461.66
Content
Disintegration
uniformity(mg)
time (mins)
%
yield
Table 3 Pharmacokinetic Parameters obtained after rat feeding of uncoated and coated
MSA tablet
Parameters
Tlag
0h
4h
Cmax
Tmax
AUC
20.37g/ml
2h
32.2 g/ml/h
19.87g/ml
12h
151.4 g/ml/h
Ka
0.1053h-1
2.588 h-1
AUMC
MRT
Ke
Tlast
58.4 g/ml/h
1.81h
0.9164 h-1
24h
1688 g/ml/h
11.17h
1.932 h-1
24h
Groups
I
II
III
IV
V
VI
TNBS treatment
(150mg/kg)
_
+
+
+
+
+
Dosage form
(MSA tablet)
_
_
Uncoated
Uncoated
Coated
Coated
Histopathological
Evaluation (Score)
0
5
4
3
2
0