tablets using 8mm punch in multi punch tablet compression
machine (Dhiman Industries, India).
Optimization of Polyvinylpyrrolidone (PVP K-30) or Microcrystalline
Cellulose (Avicel PH-102) as Binder along with
Optimized Concentration of Superdisintegrant. Tablets were
prepared by direct compression technique.The composition
of fast disintegrating tablet is shown in Table 2. Weighed
quantity of Cetirizine Hydrochloride with optimized concentration
of Sodium Starch Glycolate along with different
concentration of binders (PVP K-30,MCC) along with excipients
was mixed in geometric progression in a dry and clean
mortar. Then the blend was passed through sieve number
60 for direct compression. The powder blend was then
compressed into tablets using 8mm punch in multi punch
tablet compression machine (Dhiman Industries, India).
2.3. Final Formulation of Cetirizine Hydrochloride Fast Disintegrating
Tablets by Direct CompressionMethod. Fast disintegrating
tablets of Cetirizine Hydrochloride were prepared by
direct compression method according to the formula given
in Table 3. Weighed quantities of Cetirizine Hydrochloride
along with optimized concentration of superdisintegrant
and binder along with excipients were mixed in geometric
progression in a dry and clean mortar. Then the blend was
passed through sieve no. 60 for direct compression. The
powder blend was then compressed into tablets using 8mm
punch in multi punch tablet compression machine. These
fabricated tablets were evaluated.
2.4. Evaluation Parameters
2.4.1. Weight Variation. Twenty tablets were selected,
weighed on digital weighting balance (Ohaus, USA) and
average weight was determined. Then individual tablets were
weighed and the individual weight was compared with an
average weight as given in Table 4 [9].
2.4.2. Thickness. Thickness of tablets was determined using
Vernier Caliper (Indian caliper industries, Ambala, India).
tablets using 8mm punch in multi punch tablet compression
machine (Dhiman Industries, India).
Optimization of Polyvinylpyrrolidone (PVP K-30) or Microcrystalline
Cellulose (Avicel PH-102) as Binder along with
Optimized Concentration of Superdisintegrant. Tablets were
prepared by direct compression technique.The composition
of fast disintegrating tablet is shown in Table 2. Weighed
quantity of Cetirizine Hydrochloride with optimized concentration
of Sodium Starch Glycolate along with different
concentration of binders (PVP K-30,MCC) along with excipients
was mixed in geometric progression in a dry and clean
mortar. Then the blend was passed through sieve number
60 for direct compression. The powder blend was then
compressed into tablets using 8mm punch in multi punch
tablet compression machine (Dhiman Industries, India).
2.3. Final Formulation of Cetirizine Hydrochloride Fast Disintegrating
Tablets by Direct CompressionMethod. Fast disintegrating
tablets of Cetirizine Hydrochloride were prepared by
direct compression method according to the formula given
in Table 3. Weighed quantities of Cetirizine Hydrochloride
along with optimized concentration of superdisintegrant
and binder along with excipients were mixed in geometric
progression in a dry and clean mortar. Then the blend was
passed through sieve no. 60 for direct compression. The
powder blend was then compressed into tablets using 8mm
punch in multi punch tablet compression machine. These
fabricated tablets were evaluated.
2.4. Evaluation Parameters
2.4.1. Weight Variation. Twenty tablets were selected,
weighed on digital weighting balance (Ohaus, USA) and
average weight was determined. Then individual tablets were
weighed and the individual weight was compared with an
average weight as given in Table 4 [9].
2.4.2. Thickness. Thickness of tablets was determined using
Vernier Caliper (Indian caliper industries, Ambala, India).
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