1.0) Description: Visual
2.0) Average Weight: Check weight of 20 tablets at randomly and calculate the average weight by formula : wt of 20 tablets (gm) x 1000 / 20. found avg. wt in mg
3.0) Uniformity of weight:
Weigh 20 tablets selected at random and calculate the average weight. Not more than two of the individual weights deviate from the average weight by more than the percentage shown in table.
Tablets were weighed individually and the percentage of deviation of its weight from the average weight was determined for each tablet. Formula for calculate the percentage of deviation = (experimental weight – theoretical weight) x 100%
|Average weight of tablets||Percentage deviation|
|More than 80mg but Less than 250mg||7.5%|
|250 mg or More||5%|
4.0) Identification Test:
In the assay, the principal peak in the chromatogram obtained with the test solution corresponds to the peak in the chromatogram obtained with the reference solution.
The standard method used for tablet hardness testing is compression testing. The tablet is placed between two jaws that crush the tablet. The machine measures the force applied to the tablet and detects when it fractures. Although compressive force is applied to the tablet, along the diameter of the tablet at right angles to the applied force
6.0) Disintegration Time
Unless otherwise stated in the individual monograph, introduce one tablet into each tube and add a disc to each tube. The assembly is suspended in the liquid medium in a suitable vessel, preferably a 1-litre beaker. The volume of liquid is such that the wire mesh at its highest point is at least 15mm below the surface of the liquid, and at its lower point is at least 25mm above the bottom of the beaker. At no time should the top of the basket-rack assembly become submerged. There is a thermostatic arrangement for heating the liquid and maintaining the temperature at 37±2°.
If 1 or 2 tablets fail to disintegrate, repeat the test on 12 additional tablets; not less than 16 of the total of 18 tablets tested disintegrate.
If the tablets adhere to the disc and the preparation under examination fails to comply, repeat the test omitting the disc. The preparation complies with the test if all the tablets in the repeat test disintegrate.
7.0) Dimension of Tablet:
Length, breadth and thickness are determined by vernier in mm
Medium: 0.1M hydrochloric acid; 900ml
Time: 45 minutes
Limit: NLT 80 percent of the stated amount of Piroxicam in the medium.
Withdraw a suitable volume of the medium and filter. Measure the absorbance of the filtrate at the maximum at about 242nm. Calculate the content of Piroxicam in the medium from the absorbance obtained from a solution of known concentration of Piroxicam reference standard in the same medium.
9.0) Leak test:
The apparatus is used to test for the integrity of packed strips, blisters and Alu-Alu Blister pack containing tablets. Ensure apparatus bath is filled with purified water upto mark indicated and add 0.5% crystal violet solution in water. Samples are placed into the desiccators and the lid is placed in position. The pump starts to produce a vacuum 15inHg inside the desiccators and the vacuum is held for 1 minute. The sample remains at the required vacuum level for given time interval buzzer will sound after time is over and will cut off the vacuum pump. As the package is immersed in a colored dye solution the venting of the desiccators will allow any holes to be penetrated by the dye and the contents of the flexible packaging will also be stained with the same coloring material.
Examine all the strips for any leakage by opening the pockets manually. If anyone pocket shows evidence of leakage, reject the sample, stop the Blister / Strip machine and immediately take corrective action.
10.0) Assay: Determined by liquid chromatography.
Reference solution: A 0.005 per cent w/v solution of Piroxicam reference standard in 0.1 M methanolic HCl.
Test solution: Weigh and powder 20 tablets. Dissolve a quantity of powder containing about 50mg of Piroxicam in 100ml of 0.1M methanolic HCl. Further dilute 1.0ml of this solution to 100ml with same solvent.
Test preparation: Weigh and powder 20 tablets. Weigh sample containing 5mg of olanzapine in to 100ml volumetric flask. Add 10ml of mobile phase to dissolve the sample. Dilute this upto the mark. Filter and inject the sample.
- A stainless steel column 25cm X4.6mm, packed with octadecylsilane bonded to porous silica (5µm)
- Mobile Phase: A mixture of 45 volumes of methanol and 55 volumes of a buffer solution prepared by diluting a mixture of 7.72gm of anhydrous citric acid in 400ml of water and 5.3gm of sodium phosphate in 100ml of water to produce 1000ml with water.
- Flow rate: 1.2ml per minute,
- Spectropohtometer set at 254nm,
- Injection volume: 20µl
Inject the reference solution. The test is not valid unless the relative standard deviation for replicate injections is not more than 2 per cent.
Inject the reference solution and the test solution.
Calculate the content of Piroxicam.
Alternative method: (By UV spectrophotometer)
Reference solution:Weigh 25mg of Piroxicam reference standard in 50ml volumetric flask. Add 10ml of methanol and dissolve the standard. Dilute upto the mark with methanol. Dilute 1ml of this solution to 50ml in methanol.
Test preparation: Weigh and powder 20 tablets. Weigh sample containing 25mg of Piroxicam in to 100ml volumetric flask. Add 10ml of methanol to dissolve the sample. Dilute this upto the mark. Filter and dilute it further 2ml to 50ml in methanol.
Scan the solution by UV Spectrophotometer. It will give absorbance maxima at about 325nm. Note down the reading and calculate the content of Piroxicam in tablet.
Area of Test STD Wt.(mg) 1 100 50 Potency
—————–X————–X———X—————–X——–X———–X Average weight
Area of STD 50 50 Test Wt.(mg) 2 100
Acceptance criteria: 95.0%-105.0%
inHg: Inch of Mercury
RPM: Rounds per minute
E.coli: Escherichia coli
TAMC: Total aerobic microbial count
SCDA: Soyabean casein digest medium
TYMC: Total yeast and mold count
SDA: Sabourand dextrose agar
CFU: Colony forming unit
NaCl: Sodium Chloride