Â
Compounding
Interpretation of Prescriptions
Prescription
is an order signed by a licensed medical practitioner directing the pharmacist
to compound and dispenses a medicament.
A complete
prescription includes the following:
1. Â
Prescriber’s
office information
2. Â
Date
of the prescription was written
3. Â
Name
of the patient and address
4. Â
Superscription:
contains the traditional symbol Rx meaning you take
5. Â
Inscription:
contains the list of ingredients and
their quantities
6. Â
Transcription:
contains the necessary directions to be labeled on the container for use by the
patient.
7. Â
Name of the prescriber or his initials
Labeling
The label
on dispensed medicine should provide the patient with all the information
necessary so that the medicine may be taken or used appropriately.
Information on the label includes:
1. Â
Patients
name
2. Â
Name and address of pharmacy
3. Â
Date
of dispensing
4. Â
Name,
strength and quantity of the preparation
5. Â
Direction
for use
6. Â
Storage
condition and shelf life ( expiry date)
7. Â
Cautionary
and advisory labels.
The
information on the labels of dispensed medicines should be accurate legible
intelligible adequate and relevant.
1. Â
Accurate: the label should be checked
immediately after writing and again prior to fixing to container.
2. Â
Legible:- theÂ
label should be type written or printed or written neatly with pen
3. Â
Intelligible: the information should be completely
unambiguous and arranged to avoid confusion. The terms should be readily
understandable by the lay person.
4. Â
Adequate and relevant: care should be take to avoid causing
confusion and anxiety. Too much information on the label may mean that none of
it is noted.
Note that the size of the label should be
related to the size of the container.
Formulation of liquid dosage forms
·       Â
Dosage
forms are the means by which drug molecules are delivered to sites of action
within the body.
Types of dosage forms
·       Â
Base
on the physical nature of the products dosage forms are classified into 3 groups
1. Â
Liquid dosage forms: - solution, suspension and emulsions.
2. Â
Semi –solid dosage forms: - ointments pastes, creams, jellies.
3. Â
Solid dosage forms: - powders, granules capsules,
tablets, suppositories etc.
Solutions
Solution
are homogenous liquid preparation
containing one or more dissolved ingredients and are used for a
variety of purposes as both internal and
external dosage forms.
1. Â
Solution taken orally:- mixtures, elixirs, syrups, linctuses
draughts
2. Â
Solution used in mouth and throat: - mouth washes and gargles, throat
paints, throat sprays.
3. Â
Solution instilled into body cavities: douches, enemas, eardrops, eyes,
drops, nasal drops, nasal sprays.
4. Â
Solution applied to body surface: collodions, liniments, lotion and
paints.
·       Â
In
addition to the active ingredient (medicaments), solutions also contain
vehicles and adjuncts.
·       Â
The
vehicle is the medium in which the ingredient of a  medicine are dissolved or dispersed for
solution this is the solvent. E.g.
water, aromatic waters, alcohol, glycerol, syrup, etc.
·       Â
Water
is the vehicle of choice for the majority of pharmaceutical solution. Because
water is generally available, relatively inexpensive, palatable and non- toxic
for oral use and non irritant for external use. It also acts as a solvent for a
wide range of substances.
·       Â
The
adjuncts are additives that are added to improve the quality of the
preparations. E.g. chemical stabilizers, colorants, flavorants, preservatives,
etc.
General procedure for
compounding
Performance
Criteria-Â
1. Wear personal protective (Gowon, Masks,
Glove, etc) & hand washing.
2. Clean work row material and
Ingredients
3. Collect row material and
equipments
4. Tare bottles
5. Correct calculation
6. Weighing technique use of
paper or watch glass
7. Measuring technique
8. Mixing /levigation of
technique
9. Packaging choice of
containerÂ
10. Labeling
11.
Clean work area.
Aromatic water
·       Â
Aromatic
waters are aqueous solutions usually saturated of volatile oils or other
volatile substances that are characterized by very low water solubilities. E.g.Â
Chloroform.
·       Â
Aromatic
waters are used externally as perfumes (e.g. Rose water) and internally as
flavoring agents (e.g. peppermint water, cinnamon water has been used as
carminative and chloroform water was used in expectorant preparations).
Practical
1. Â
(a)
chloroform water BP. 88 |
||
Chloroform |
---------------- |
2.5 ml |
Water FBC to |
--------------- |
1000ml |
|
Send 100ml |
|
|
|
|
(b) double strength chloroform water
BP. 88Â |
||
Chloroform
|
---------------- |
5
ml |
Water
FBC to |
--------------- |
1000ml
|
|
Send
100ml |
|
Compounding: dissolve the
chloroform in Purified water by shaking.
1.  Peppermint water  |
||
Pepper
min oil |
--------------- |
0.2
ml |
Water
FBC to |
--------------- |
100ml
|
|
Send
50ml |
|
Compounding: dissolve the oil in purified water by
shaking
1. Â
Spirits
·       Â
Sprits also known as essences are
alcoholic or aqueous alcoholic solutions of volatile substances. Like the
aromatic water the active ingredients in the sprits may be a solid, liquid or
gas. The volatile substance in the majority of case is volatile oils.
·       Â
Some sprits are used internally for
their medical value a few medically by inhalation. But a large number are used
as flavoring agents.
·       Â
             Practical
Peppermint
spirit
Ingredient |
Master formula |
Peppermint oil |
100ml |
Ethanol (90%) |
1000ml |
Send
30 ml. |
Compounding:
dissolve the peppermint oil in ethanol. Add sufficient ethanol to produce the
final volume. If the solution is not clear shake with previously sterilized
talc and filter.
Action
and uses:
the spirit is an effective carminative. Also, mixed with other drugs or
preparation, it may be used as a flavor.
Ingredient |
Master formula |
Chloroform |
50ml |
Ethanol (90%) |
1000ml |
Send
40ml |
 Chloroform sprit
cmpoundiccompounding:
mix the chloroform with the ethanol.
·       Â
Uses
and actions: flavoring agent and preservative
           Â
 Â
Tinctures
·       Â
Tinctures are alcoholic or hydro
alcoholic solution of principles extracted from natural sources or of pure
chemical merely dissolved in these solvent systems an example of the latter
being iodine tincture.
·       Â
Tinctures vary widely in their method of preparation the strength
of their volatile ingredients their alcoholic content and their intended use
·       Â
Tinctures are prepared by a number of
processes: maceration (process M) percolation (process p) solution and
dilution.
 Iodine Tincture
Ingredient |
Master formula |
Iodine |
25gÂ
|
Potassium
iodide |
25g |
Purified
water |
25mg |
Ethanol (90%) to |
1000ml |
Send
50ml |
Compounding:
dissolve the potassium iodide and the iodide in the purified water and add
sufficient ethanol (90%) to produce 1000ml.
Actions
and uses:
antiseptic.
  Syrups
·       Â
Syrups are concentrated aqueous
solutions of sucrose other sugars or sweetening agents to which small
quantities of suitable polyhydric alcohols may be added to retard
crystallization or to increase theÂ
solubility of the other ingredients
·       Â
Syrups usually contain aromatic or
other  flavoring materials.
Practical
                                Â
  Simple syrup, USP |
|
Sucrose --------- 647.4 g |
Sucrose------- 850g |
Purified water to ------ 1000g |
Purified water to ----- 1000ml |
Send 50ml |
|
                   Methods of preparation
a.  Â
Hot
process: place the sucrose in dish, add the
water and dissolve the sucrose by heating on a water bath stirring
continuously. When dissolution of the sucrose is complete allow the solution
formed to cool and add sufficient boiling purified water to make up for that
lost by evaporation. Then strain the syrup while still warm to make up for that
lost by evaporation. Then strain the syrup while still warm though a fine
muslin supported in a funnel in to a bottle which is capable of nearly filling
and shake the bottle occasionally until the content is quite coil.
b. Â
 Cold process:
place the sucrose in a suitable percolator, the neck of which is nearly filled
with loosely packed cotton moistened after packing with a few drops of water.
Pour carefully about 450ml of purified water upon the sucrose and regulate the
outflow to a steady drip of percolate. Return the percolate if necessary until
all the sucrose has dissolved. Then wash the inside and the cotton with
sufficient purified water to bring the volume of the percolate to 100 ml and
mix.
c.  Â
Alternatively the sucrose may be
dissolved more rapidly in the proper amount of water by agitation in a
graduated bottle.
N.B
syrup made without heat is practically colorless while syrups made with heat
have pale amber color due to the levulose formed as a result of hydrolysis of
sucrose.
Ferrous
sulfate syrup USP
Ingredients |
Master formula |
Ferrous sulfate |
40g |
Citric acid hydrous |
2.1g |
Peppermint spirit |
2ml |
sucrose |
825g |
Purified water to |
1000ml |
Ft. syrup send 50ml |
|
Sig. Two 5 ml  |
|
Â
Formulation:
the peppermint spirit used as the source of flavor has a persisting effect
which makes the somewhat unpleasant ferruginous taste of the Fe2. Care must be
taken in preparing aqueous solution of ferrous salts since Fe2+ is readily
oxidized by dissolved oxygen to form Fe3+ which precipitates as basic ferric
salts discoloring the solution. Ferrous sulphate is dissolve in purified water
containing some sucrose which provides a reducing environment thereby in
inhibiting auto- oxidation. If all of the sucrose were added the solution would
be too viscous to allow perfect filtration. Citric acid is included in the
formulation to prevent discoloration of the syrup i.e. a change from a green to
a reddish brown tint it does this by preferentially chelating Fe3+.
Compounding:
dissolve the ferrous sulfide water and filter the solution until clear filtrate
and add purified water to make 1000 ml mix and filter if necessary through a
placed get of cotton.
Actions
and uses:
Heamatnic.
Iodine Solution (Lugols solution)
 Ingredients                   master
formula
   Iodine                                       50g
Potassium iodide                   Â
        100g
Water        up to                            1000ml
 Sent 100ml
Method:
Potassium iodide and Iodine are dissolved in small portion of
purified
Water by stirring & shaking till dissolve completely.
Sufficient Water is added to make the required volume
Use: Goiter Â
Compound iodine paint
(mand’l paint)
Ingredient |
Master formula |
Potassium Iodide   |
25.0g |
Iodine  |
12.5g |
Alcohol 90%Â |
40.01ml |
Water  |
25.0ml |
Peppermint Oil |
4.0ml |
Glycerol      to |
4.0ml |
Mitt. 40 ml. Sig store in cool place. Shake the bottle before use. Not to be swallowed in large quantities.  |
Compounding:
put the water into a 50ml conical measure. Dissolve the potassium iodide (it
dissolves very readily in water and need not be powdered). Add the iodine and
stir until complete dissolved. Although iodine is only slightly soluble n water
it is readily soluble in aqueous solution of iodine. In a small measure
dissolve the peppermint oil in the alcohol and transfer it to the iodine
solution and mix well. Make up to the volume with glycerol and mix toughly. If
the iodine solution is not well. Mixed
with the glycerol the preparation is streaky.
Note:
because of the high viscosity of the vehicle this preparation is best made
entirely in a measure. For the same reason an excess should be prepared since
it is impossible to transfer the entire contents of the measure to a bottle. A
glass or a counterbalanced watch glass and a vulcanite spatula must be used for
weighing the iodine
Actions
and used: Antiseptic in the treatment of
pharyngitis and tonstillis.
Suspension
    Suspension are disperse systems in which
finely divided drug practices (called the disperse phase) are distributed
thought out a vehicle (called
dispersion
medium o r continues phase) in which the drug exhibits a minimum degree of
solubility. It in include both powders in dry from to be place in suspension
and drugs suspended in liquid vehicles.
Suspension
can be classified in to coarse suspension in which the particles are large than
1um in diameter.
Major applications:
suspension dosage forms can be administered orally injected parentally
(intramuscularly or subcutaneously) or applied externally (topically) to the
skin eye ear etc.
The
physical properties of suspensions and their design depend upon the nature of
the dispersed phase the dispersion medium and the pharmaceutical adjuncts/additives.The
drug particles (dispersed phase) is suspension could be
o Â
Diffusible
solids
o Â
In
diffusible solids or
o Â
Poorly
wettable solids
Containers
and labeling
·       Â
Suspensions are generally packed in
well closed containers appropriate to the class of dispensed medicine be it
mixture lotion ear drop, enema etc.
·       Â
If the preparation is particularly
viscous a wide mouthed container may be used.
·       Â
Containers of suspensions should be of
suitable size to allow shaking of the products.
·       Â
Labels for suspensions includes:
-Â Â Â Â Â
Shake well before use
-Â Â Â Â Â
Store in cool place(not refrigerator)
-Â Â Â Â Â
Also expiry dates for suspensions that
should be prepared recently is one month and if diluted two weeks.
Suspensions
containing diffusible solids
·       Â
Diffusible solid (also called
dispersible solids) are light and easily wettable solids. They readily mix with
water and on shaking diffuse evenly through the liquid for long enough for a
dose to be measured.(Ensure even distribution in each dose.)
·       Â
Examples of diffusible solids are
light kaolin magnesium trisilicate light magnesium carbonate and calcium
carbonate.
Practical
Pediatric
kaolin mixture, BP 1988
Ingredient
|
Master
formula |
Light
kaolin |
200g |
Amaranth
solution  |
10ml |
Benzoic
acid solution |
20ml |
Raspberry
syrup |
200ml |
Chloroform
water (D.S) |
500ml |
Water to |
1000ml |
M.S.A.
send 50ml. Sig. 1tsp
t.i.d. |
Formulation:
the kaolin should preferably be sterilized to remove any contaminating soil pathogens.
Kaolin
is a diffusible solid and therefore no additional suspending agent is required
although the raspberry syrup increases the viscosity of the vehicle.
Benzoic
acid solution and chloroform water act as preservatives. The raspberry syrup
provides a flavor and amaranth solution color which is attractive to children.
Compounding:
first tare the final container because if the syrup and a little of the
chloroform water. Add the amaranth solution and mix well.
If
the dye is added at a later stage in the preparation it will not penetrate in
to the powder and white specks will be visible in the final product. Dilute the
suspension until pourable and while specks will be visible in the final
product. Dilute the suspension until pourable and transfer to the bottle.
Although it is advisable to add volatile ingredients such as chloroform water
before making up to volume with water. Add the benzoic acid solution to the
bottle and make up to volume and shake thoroughly.
Storage and shelf
life:
unless the kaolin has been sterilized the preparation should be recently
prepared.
Container:
amber medicine bottle.
Advice for patients
when dispensed:
shake the bottle.
Maintain
fluid intake in diarrhea. If the product is counter prescribed the patient
should seek medical advice if the condition persists.
Actions
and uses:Â anti diarrhea mixture for children.
Magnesium
sulfate mixture
BP.88 (magnesium sulfate oral suspension)
Ingredient
|
Master
formula |
Scaled
quantities |
 Magnesium sulfate |
400 g |
|
light
magnesium carbonate |
50g |
|
Concentrated
peppermint emulsion |
25g |
|
Double strength chloroform water |
300ml |
|
Water FBC
sufficient to produce |
1000ml |
|
Mitt 50ml |
|
|
Sig. 10
ml t.i.d. shake the bottle before use |
Formulation:
magnesium sulfate mixture is a suspension containing 40% w/v magnesium sulfate
and 5%w/v of light magnesium carbonate. Both these solids act as laxatives by
preventing the normal absorption of water from the intestine with the result
that the bulky fluid contents distend the bowel active reflex peristalsis
excited and evacuation of the contents of the intestine occur. Active reflex
peristalsis excited and evacuation of the contents of the intestine occur.
Peppermint provides flavoring and act as a carminative and chloroform water
acts as flavoring preservative and vehicle light magnesium carbonate is a
diffusible solid and no extra thickening agent is required.
Compounding:Â first tare the final container and select a
mortar of sufficient size to allow for adequate mixing of the product. Mix the
magnesium sulfate and light magnesium carbonate in the mortar. This method is
to be preferred to making a separate solution of the magnesium sulfated which
is time consuming. Add enough vehicle to make a smooth paste and dilute with
the vehicle unit sufficiently pour able to transfer to the bottle. The volatile
peppermint emulsion should be added to the bottle before making up to final
volume.
The
mixture may also be prepared from a pre packed mix of the two powder ingredients
with the addition of the appropriate amount of peppermint emulsion and
chloroform water.
Storage and shelf
life:
the mixture should be recently prepared.
Container:
amber medicine bottle.
Advice
for patients when dispends:
shake the bottle
Actions
and uses:
 as laxative.
B.
Suspensions containing in diffusible solids
In diffusible solids will not remain evenly
distributed in a vehicle long enough to ensure uniformity of dose. Examples
include chalk, zinc oxide, calamine aspirin and phenobarbitone.
The simplest way of correcting this problem is to
increase the viscosity of the formation of aggregates that settle rapids
The thickening agents used to stabilize
suspensions is substances that spontaneously from colloidal dispersions in
aqueous media because of their affinity to water. There are three major groups
of thickening agents:
1. Â
Polysaccharides include acacia,
tragacnath, methylcellulose, sodium alginate, microcrystalline cellulose sodium
carboxymethyl cellulose starch etc.
2. Â
Inorganic agents include bentonite
veegum hectorite aluminium hydroxide etc
3. Â
Synthetic agents include carboxyvinyl
polymer(carbomer) colloidal silicon dioxide etc.
Calamine Lotion B.P.
             Ingredients              master formula
Calamine                                15g       Â
Zinc Oxide                             5g
Bentonite                              3g
Sodium Citrate                    0.5g
Liquid phenol                       0.5g
Glycerin                                5ml
Purified Water   to              100ml
Procedure:
1)Â Â Â Â Â
Dissolve Sodium
Citrate in 35ml Purified Water
2)Â Â Â Â Â
Weigh Calamine,
Zinc Oxide and Bentonite & triturate it with Sodium. Citrate solution.
3)Â Â Â Â Â
Add Liquid
phenol, the Glycerin and sufficient quantity of water to make up the required
volume.
               4) Write Label
Â
Use:
Astringent & protective.
Compounding:
first tare the final container and select a large mortar. Mix the dry powers in
the mortar until evenly dispersed. It is important that the bentonite is well
distributed in the in diffusible powders. Use the calcium hydroxide solution to
make a smooth paste and to dilute the formed paste for transfer to the bottle.
Add the glycerol and liquid phenol to the bottle and make up to final
volume   with the vehicle.
Strong
and shelf life: the preparation is stable cool
storage is advised because of the volatile preservative.
Advice
for patients when dispensed: shake the bottle
for external use only. The lotion is applied to the skin as required and
allowed to dry. Action and uses: cooling lotion
useful for treating mild sunburn.
                                              OINTEMENTS
Ointments
are semisolid preparations intended for external application to the skin or
mucous membranes.
Ointments
may be medicated or non- medicated the later type being commonly referred to as
ointment bases and are used as such for their emollient or lubricant effect of
used as vehicles in preparation of medicated ointments.
·       Â
Hydrocarbon bases
·       Â
Absorption bases
·       Â
Water-miscible bases
·       Â
Water soluble bases
Preparation
 Ointments are not applied primary to irritated
areas it is an on broken wound rule that these preparations must contain
granular or gritty particles, which might cause further irritation regardless
of the condition of the skin. Ointments must be smooth and free from granular
or gritty particles.
Three
types of equipment are available for the preparation of ointments
1.    Â
Ointment slab and spatula
2.     Mortar
and pestle
3.    Â
Ointment fill
Two techniques are used
mixing ointments
Mixing by fusion
On
a small scale fusion is usually carried out in an evaporating basin a water
bath
Fusion
is necessary when waxes, hard paraffin, fatty alcohols, fatty acids or any hard
wax- like material is included in the formula.
Fusion
is used also when a medicament is soluble in the melted base
Mixing by trituration
This
method is applicable when the medicament is a solid insoluble in the bases or
liquid present in small amount
Trituration
may become out with an ointment tile and spatula or using a mortar and pestle
Packaging
Ointments
are dispensed in either ointment or collapsible tube. However ointments
prepared extemporaneously are usually packed in ointment jar.
Procedure
will be demonstrand
The
ointment should be packed and the top surface should be smoothed neatly.
Ointments
jars should be closed tightly when not in use particularly if the ointment
consisting water to prevent loss though operation.
Storage
Ointments
should be stored in a cool place to prevent softening and eventually
liquefiable in the base
Insoluble
medicament may settle to the bottom of the container if the ointment is permit
to liquefy.
Excessive
heat or cold may cause an emulsion base to separate into two phases.
a.     Simple ointment BP
Ingredients
                           master Formula                   Reduced
Formula
Wool fat                                             50g
Hard paraffin                                     30g
Cetostearyl alcohol                            50g
Yellow or white soft paraffin            850g
           Send
25g
Formulation: simple ointment
is an absorption base prepared by fusion . yellow or white soft paraffin is chosen
according to the color of the finished product. In this case there is no dark
colored ingredient to be added. White soft paraffin should be used.
Compounding:
grate the hard paraffin and weigh out the ingredient for the base. place to
melt an evaporating dish on a water –bath. stir gently to aid melting and to
mix the ingredients. When homogenous, remove from the beat and continue to stri
gently until cold .
NB.
Weigh the wool fat and the soft paraffin using waxed papers to allow full
recovery of  the materials.
Storage: store in cool
places
Action and use: ointment base
emollient
a.     Sulfur ointment BP
Ingredients                                        master formula                                reduced formula
Precipitated
sulphur, finely sifted      100g
Simple
ointment                                 900g
                        Send 25 g
Formulation:
the BP directs that the simple ointment be prepared with white soft paraffin
ointment is adequate to ensure that 22.5g will be available (to compensate for
the manipulative  losses).
Compounding:
weigh out the amount of precipitate sulphur required and place it on the center
ointment tile, weigh the required amount of simple ointment (using a piece of
waxed paper) and place it on side of the tile Take a portion of the base (about
two to three times the weight of the powder) and levigate it with the sulphur
until there is no sign of any gritty particles (this can checked for by
spreading a thin layer on the tile). Gradually incorporate the reaming base in
geometrically and continue levigation until uniformly mixed. Finally, collect
the ointment to gather the center of the tile using the spatula and pack into
an ointment jar.
Storage and shelf life
: store in a cool place .
An
expire date of 4 weeks is appropriate.
 For External
use only.
Container:
wide – mounted amber jar with a grease proof paper disc
Advice for patient when
dispensed: the skin should be cleansed prior to
application and t ointment applied
sparingly to the affected area .
Action and uses:
mild antiseptic used in the treatment of acne and scabies.
a.     Whitfield’s Ointment
Ingredients                                        master formula                                reduced
formula
Benzoic
acid, in fine powder             60 g
Salicylic
Acid, in fine powder           30g
Emulsifying
ointment                                    910
g
                    Send 20gm
Compounding:
sift the medicament through separate 180µm sieves. Note that salicylic acid
very irritant to the respiratory tract and precautions should be taking to
avoid inhalation. Weigh the powders after sifting and mix them. Then place them
on an ointment tile and levigate with two or three times their weight of the
base until homogenous. Gradually incorporate the reaming base.
Storage shelf life:
store in a cool place.
Container:
wide – mouthed amber jar with a greaseproof paper disc.
Advice for patients
when dispensed: the ointment should be applied
sparingly to the affected area. Is should not be applied to the broken or inflamed
skin.                                              Actions and uses: topical anti fungal
preparation
                                  Pastes
Pastes
are ointment-like preparations intended for external application .most paste
differ from ointments in containing large amounts of finely powdered solids,
thus they are usually stiffer than ointments, less greasy and more absorptive.
They
are applied generously, either with a spatula or spread on lint or other
dressing and are not removed for long periods.
Compounding
and packaging
For
all practical purposes, pastes are prepared in the same manner as ointments
Pastes
are generally packed in glass ointment jars.Â
They are often too viscous for easy extrusion from tubes.
  Zinc
oxide paste. U.S.P
Ingredients                                        master formula                                 reduced
formula
Zinc
oxide, finely sifted                               250g
Starch,
finely sifted                                       250g
White
petrolatum                                           500g
           Send 20g
Compounding:
melt the base with a minimum of heat and sift the powders through separate 180
µm sieves. Mix the required weight of powders in a warm mortar. Triturate with
a little melted base until smooth, gradually adding the rest of the base and
until cooled.
NB.
The paste is much easier to manipulate in a warm mortar
Storage:
store in a cool place
Container:
wide – mouthed amber jar with grease proof paper disc.
Advice for patient when
dispensed: the paste should be spread thickly on
white lint and applied to the affected area.
Actions and uses:
absorbent, protectant and mild astringent used for variety of dermatological conditions
including eczema and psoriasis either alone or with additional medicaments.
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