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Industrial Pharmacy-I
Course Code:BP502T
B.Pharm 5th Semester
Unit- II TABLETS
BY
Rajat Saxena
Assistant Professor
IFTM University, Moradabad
Tablets
• Tablets are solid dosage form usually prepared
with the aid of suitable pharmaceutical
excipients.
• They may vary in size, shape, weight, hardness,
thickness, disintegration and dissolution
characteristics.
• The oral route of drug administration is the
most important method of administering drugs
for systematic effect.
• Tablet is defined as a compressed solid
dosage form containing medicaments with or
without Excipients.
• According to the Indian Pharmacopoeia
Pharmaceutical tablets are solid, flat, unit
dosage form, prepared by compressing a drug
or a mixture of drugs, with or without
diluents
Tablets Ideal Properties
1. A tablet should be elegant and free of defects like
chips, cracks, discoloration, and contamination
2. Should be accurate & uniform in weight.
3. The size & shape should be reasonable for easy
administration
4. They have sufficient strength to withstand mechanical
shock during its production, packaging, shipping and
dispensing
5. The tablet must be able to release the medicinal
agents in a predictable and reproducible manner
Advantages
1. Easy to administration and dispense.
2. Accuracy in dose
3. Cost is lowest
4. Lightest and compact compared all dosage
forms
5. Easiest and cheapest to package and ship
6. Chemically and microbiologically stable
7. Sustained release product is possible by enteric
coating.
Disadvantages
1. Difficult to swallow in case of children and
unconscious patients
2. Hygroscopic drugs are not suitable for compressed
tablet
3. Drugs with low or poor water solubility, low
dissolution, may be difficult to formulate.
4. Cost of production may be increase because of
coating & encapsulation to remove bitter and
unpleasant taste.
5. Solids having irritant effects on GIT mucosa poses
problem for formulation into tablets.
Tablets Classification
Tablets ingested orally
• Compressed tablet
• Layered tablets
• Sustained release tablets
• Enteric coated tablets
• Sugar coated tablet
• Film coated tablet
• Chewable table
Tablets used in oral cavity
• Buccal tablet
• Sublingual tablet
• Troches or lozenges
• Dental cone
Tablets administered by other route
• Implantation tablet
• Vaginal tablet
Tablets used to prepare solution
• Effervescent tablet
• Hypodermic tablet
• Dispersible tablets
Tablet Manufacturing Process
. Active
Pharmaceuticals
Ingredients
Excipient
Mixing & Granulation
Lubricants Compression
Tablet Manufacturing Methods
Wet Granulation Dry Granulation
Direct Compression
Mixing Mixing
Sizing
Binder Solution Granulation
Mixing
Granulation/Drying Lubricants
Compression
Lubricants Compression
Compression
Tablet Excipients
In addition to active ingredients tablet contains
a number of inert materials known as additives
or excipients. These excipients are used for
various functions during tablets manufacturing
process.
Diluents Lubricants
Binders Glidants
Disintegrates Organoleptic agents
Diluents
Inert substances needed to increase the bulk when
quantity of medicaments is very small in each
tablet ( dose is low )
They make a tablet to a practical size for
compression.
Also provide improved cohesion, to permit use of
direct compression manufacturing.
Anhydous lactose, Dibasic ca-phosphate, Mannitol,
Sucrose/Dextrose, Starch
Binders
They are used for the cohesive qualities to the
powdered also called binders or granulators. They
provide
Cohesive strength after compression
Tablet remain intact after compression
Formulation of granules of desired hardness & size.
Starch paste -10-20 % solution
Acacia, tragacanth – Solution for 10-25% Conc.
Polyvinyl pyrrolidone (PVP)- 2% aqueous
Cellulose derivatives – Methyl cellulose, Hydroxy propyl
methyl cellulose, Hydroxy propyl cellulose
Disintegrates
Substance/mixture of substances added to facilitate a tablet
to break up or disintegrate when it contact in water in the
GIT after administration.
Starch derivative – Primogel and Explotab (1-8%)
Cellulose derivatives- Ac- Di-Sol (sodium carboxy methyl
cellulose)
Crosspovidone- cross-linked povidone (polymer)
Sodium starch glycolate- cross-linked starch
• Super- disintegrants
Swells up to ten fold within 30 seconds when contact water.
Examples: Crosscarmellose-cross-linked cellulose
Lubricants
To prevent adhesion of tablet materials to the
surface of dies and punches
Reduce inter-particle friction
Facilitate ejection of tablet from die cavity
Stearic acid,
Magnesium stearate,
Talc,
PEG (Polyethylene glycols),
Glidant
• They improve the flow properties of a powder
mixture by reducing the friction b/w particles
• Added in dry state just prior to compression
Corn Starch – 5-10% conc.,
Talc-5% conc.,
Silica derivative – Colloidal silicas such as
Cab-O-Sil, Syloid, Aerosil in 0.25- 3%
Organoleptic Agents
• Coloring Agents
• Flavoring gents
• Sweetening Agent
THANKU