Manufacturing of Aspirin Tablets...step by Step Manufacturing of Aspirin Tablets...
Theory:
Aspirin is known as a salicylate and a nonsteroidal anti-inflammatory drug (NSAID) Direct compression or Dry granulation method is normally used in the preparation of aspirin tablets owing to its unstable nature and ability to undergo hydrolysis if made with wet granulation.
tablets are manufactured in various shape but weight,size and thickness of aspirin tablets are depend on amount of dose.
Uses of aspirin
Aspirin has been helpful for over an era for its pain-relieving, anti-inflammatory, and fever-reducing properties, and its status in modern medicine cannot be exaggerated. However, it is necessary to think that aspirin can have side effects, particularly in people with certain medical conditions or who are taking other medications. It is important to consult to a doctor before taking any medication, for safe use of medication.
Formula:
Ingredients Official
Formula Working Formula |
Asp 0.300g -- |
Starch Powder 5% 0.015g
-- |
Tale 2% 0.006g -- |
Calculate the working formula according to tablet count.
Step by Step Manufacturing of Aspirin Tablets
Requirements
Mortar and Pestle
Compression Machine
Sieve No 22, 44
• Weighing balance
Chemicals:
aspirin
Starch Powder
Talc
Procedure of aspirin tablets step by step :
Calculate the working formula depending on the number of
tablets to be manufactured. The details follow;
I . weighing
Granular acetylsalicylic acid weighed approximately greater
than the required quantity.
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manufacturing of syrup using steam jacketed kettle
II. screening :
weighed aspirin is
passed through 22/44 mesh sieves. collet the material retained on
44 as coarse granules. Collection of the material that passes through sieve no. 44
as fines.
Fifteen percent of the fines required are weighed. Five
percent of starch powder and 2% of ale powder are weighed.
III-Blending
Course granules, fines, arch powder, and sale powder are
blended thoroughly in a mortar with a pole in order uniformly distribute the
ingredients. The granules are now ready for compression.
A fraction of the lubricant is added during process and the rest is added after the tablets are compressed step.
IV-Compression
Three pockets of grades, each coining the practical weight
of one tablet are prepared. These are used to adjust the pressure of the
punches in order to get tablets of sufficient hardness. The remaining granules
are compressed to obtain Calculate percentage yield using the formula;
Percentage yield=
Actual Yield / Theoretical Yield
x 100
V-Packing:
Compressed tablets are placed in a wide-mouthed, tightly
closed container in a cool, dry place. The container is capped and cited.
The manufacturing of aspirin tablets are now completed and supply to health cares, drug stores and use under the doctor prescription.
Quality control
Throughout the manufacturing process, quality control tests are done to ensure the safety and efficacy of the end product. before the procedure start, it is important tested Raw materials for quality and purity, and any impurities or contaminants are removed.
During the synthesis of aspirin, reaction conditions are closely monitored to ensure that the reaction proceeds as expected and that the resulting product is of high purity. After synthesis, the aspirin is further purified to remove any remaining impurities.
Tablets are also tested to ensure that they meet specific quality standards, such as the amount of active ingredient per tablet and the rate of dissolution in the body. Any tablets that not approaches these standards are discarded.
Characteristics of aspirin tablets:
Colour -----------------white crystalline powder
Odor ------------------- no definite smell
Melting point --------- 138-140 c
Density of aspirin ----1.40gcm-3
solubility ------------- readly sobule in basic medium
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