Capsules V
Capsules V
Capsules:
Definition: capsules are solid dosage forms in which the
medication contained within gelatin shells. The medication may
be a powder, a liquid or a semisolid mass.
- Capsules are usually intended to be administered orally by
swallowing them whole. Occasionally, capsules may be
administered rectally or vaginally.
Advantages:
1- Neat and elegant in appearance.
2- Enclosing the medication within capsule shells provides a
tasteless, odourless means of administering medication.
Capsules (Cont.):
3- The ready solubility of gelatin at gastric pH provides rapid
release of medication in the stomach.
4- since hard gelatin capsules may be compounded by the
pharmacist, this dosage form offers physicians greater
flexibility in dosages and drug combinations than is available
with prefabricated medication.
Disadvantages:
1- Capsules are not suitable containers for liquids that dissolve
gelatin, such as aqueous or hydroalcoholic solutions.
2- Very soluble salts, such as bromides or iodides should not be
dispensed in capsules, as the rapid release of such materials
may cause gastric irritation.
Capsules (Cont.):
Raw materials:
1- Gelatin:
-It is the major component of the capsule. The reason for this is
that gelatin possesses five basic properties:
A- Non-toxic.
B- Soluble in biological fluids at body temperature.
C- It is a good film-forming material.
D- Solutions of high concentration, 40% w/v, are mobile at 50C.
E- A solution in water changes from a sol to a gel at temperatures
only a few degrees above ambient (Others require volatile
solvents or large quantities of heat).
Types of capsules:
1- Hard gelatin capsules:
- It consists of two pieces in the form
of cylinders: the shorter piece cap and
the longer piece body.
- The shells consist largely of gelatin,
sugar and water.
Manufacture:
The manufacturing machines consist of two parts, which are mirror
images of each other: on one half the capsule cap is made and on
the other the capsule body.
The moulds 'pins', are made of stainless steel and are mounted in
sets on metal strips, called 'bars'.
There are approximately 40000 mould pins per machine.
Capsule sizes:
SIZE
000
00
0
1
2
3
4
5
VOLUME (cm3)
1.37
0.95
0.68
0.50
0.37
0.30
0.21
0.13
typically filled with dry solids (powders, granules, pellets, tablets) and
semisolids.
Fixed oils and other liquids that do not dissolve gelatin may be filled into
hard gelatin capsules with a pipette or calibrated dropper, then capsules
are sealed by moisturizing the lower part of the caps with water.
Liquids may often be sorbed onto inert carrier powders to form dry
powders suitable for capsule filling.
The powder to be
encapsulated is placed
on a sheet of clean
paper or a glass or
porcelain plate.
The cap is replaced
and the filled capsule
is weighed using an
empty capsule of the
same size as a tare.
Capsules are delivered into the perforated capsule filling ring. The
ring is rotated on a turntable, and a vacuum pulls the bodies into
the lower half of the ring, leaving the caps in the upper half of the
ring.
The top & bottom halves of the filling ring are separated manually,
and the cap half of the ring is set aside.
The body half of the ring is then moved to another turntable where
it is rotated mechanically under a powder hopper.
The hopper contains an auger which feeds the powder into the
bodies.
When the capsule bodies are filled, the cap and body rings are
rejoined.
The hot gel mass is then supplied to the encapsulation machine through
heated transfer pipes by a casting method that forms two separate gelatin
ribbons (each approximately 150 mm wide).
During the casting process the gelatin passes through the sol-gel
transition and the thickness of each gel ribbon is controlled to 0.1 mm.
The two gel ribbons are then carried through rollers
to the rotary die
encapsulation tooling.
Capsules (Cont.):
Sustained release capsules:
- In general, a sustained release dosage form is consisting of two
parts:
1- an immediate release portion.
2- a sustained release portion which gradually release medicament.
The spansule is a hard gelatin capsule containing many coated
beads.
A-The medication is pan coated onto the surface of sugar starch
beads using non aqueous solution of the drug.
-
Capsules (Cont.):
C- The reminder (2/3 of the beads) are then pan coated with a fatty,
waxy material such as bees wax or cellulosic material such as
ethyl cellulose. Different portions of the beads receive different
thicknesses of coating.
- Sustained release capsules are suitable for antibiotics.
Advantage: Administration is more convenient, since a single dose
provides all-day or all-night medication.
Capsules (Cont.):
A- The drug is inactivated in the gastric fluids.
B- The drug is irritating to the gastric mucosa.
C- A high local concentration of the drug is desirable in the intestine ,
as in the case of anthelminitics.
- Materials used for enteric coating: shellac and cellulose acetate
phathalate.
Formulation factors affecting drug availability from capsules:
The overall dissolution rate of a drug from capsules may be
regarded as a function of several variables:
1- The dissolution rate of the shell.
2- The rate of penetration of the dissolution medium into the powder.
3- The rate at which the powder mass deaggregates.
Capsules (Cont.):
4- The amount and nature of adjuvant such as diluent, surfactant (if used).
5- drug particle size.
6- The composition and characteristics of the capsule shell.
Evaluation of commercial capsules:
1- content uniformity:
30 capsules are selected and 10 of these are assayed individually.
-
Capsules (Cont.):
2- Weight Uniformity :
- This test applies to all types of capsules and it is to be
done on 20 capsules.
Method:
1- Weigh an intact capsule.
2- Open the capsule without losing any part of the shell
and remove the contents as completely as possible.
3- Weigh the shell.
4- The weight of the contents is the difference between
the weighing.
5- Repeat the procedure with a further 19 capsules
selected at random.
6- Determine the average weight.
Capsules (Cont.):
Limit:
Not more than two of the individual weights deviate from
the average weight by more than the percentage
deviation shown in the table below, and none deviates
by more than twice that percentage.
Average
Weight
Capsule Content
Less than 300 mg
300 mg or more
of Percentage Deviation
10
7.5
Capsules (Cont.):
3- Disintegration:
The disintegration test determines whether tablets or capsules
disintegrate within a prescribed time when placed in a liquid
medium under the prescribed
experimental conditions.
Capsules (Cont.):
Method:
According to the B.P. and applies to hard and soft capsules.
1- Introduce one capsule into each tube and suspend the apparatus in
a beaker containing 600 ml water at 37 C.
If hard capsules float on the surface of the water, the discs may be
added.
2- Operate the apparatus for 30 minutes; remove the assembly from
the liquid.
3-The capsules pass the test if
Capsules (Cont.):
4- Dissolution:
The dissolution test is carried out using the dissolution apparatus
official in both the U.S.P. and N.F.
- The capsule is placed in a basket formed from 40-mesh stainless
steel fabric.
- A stirrer shaft is attached to the basket, and the basket is
immersed in the dissolution medium and caused to rotate at a
specified speed.
- The dissolution medium is held in a covered 1000 ml glass vessel
and maintained at 37C 0.5C by means of a suitable constanttemperature water bath.
- The stirrer speed and type of dissolution medium are specified in
the individual monograph.
-
Capsules (Cont.):