Professional Documents
Culture Documents
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1. WHAT IS THE REASON WHY WE NEED TO FORMULATE SUSPENSION?
- The reasons for the formulation of a pharmaceutical suspensionis when the drug is
insoluble in the delivery vehicle, to mask the bitter taste of the drug and to increase drug stability.
7. PASTE A PICTURE OF AN AEROSOL, LABEL ITS PARTS AND FUNCTION OF EACH PART.
Valve
Valve Cup
Propellant
Propellant/
product mixture
Dip tube
Pea
Aerosol valves leverage pressure between two fluids to force product through an atomizer,
creating a useful, fine mist. At rest, the high-pressure propellant pushes up on the stem and
mounting gasket, keeping the system sealed, while also pushing down on the product. The valve is
to regulate the flow of product concentrate from the container.
Propellants help to develop proper pressure within the container and expel the products in the
forms of vapor in the formulation of aerosols. When the propellant is a liquefied gas or a mixture of
liquefied gases, it can also serve as the solvent or vehicle for the product concentrate.
Propellant product/mixture are used in topical pharmaceutical aerosols because of their
environmental acceptance, low toxicity, and lack of reactivity. They are useful in three-phase (two-
layer) aerosol systems because they are immiscible with water and have a density less than 1.
Dip tube conveys the aerosol content from the container to the valve mechanism where it
is emitted as an aerosol spray. The dip tube includes a pliable tube main body and a tubular
weight fixed on the tube main body adjacent to the free end.
Pea is used to mix the paint when the can is shaken.
8. SEARCH THE TWO FILLING OPERATION OF AEROSOLS, STATE EACH PROCESS OF FILLING
Cold Fill process, both the product concentrate and the propellant must be cooled to temperatures
between 30°C to 60°C where they will remain liquefied. The cooling system may be a mixture of dry
ice and acetone or an elaborate refrigeration system.
Pressure Fill Process is carried out essentially at room temperature. The product concentrate is
placed in the container, the valve assembly is inserted and crimped into place, and then the
liquefied gas, under pressure, is added through the valve. The entrapped air in the package might
be ignored if it does not interfere with the stability of the product, or it may be evacuated prior to
or during filling. After the filling operation is complete, the valve is tested for proper function. This
spray testing also rids the dip tube of pure propellant prior to consumer use. Pressure filling is used
for most pharmaceutical aerosols. It has the advantage that there is less danger of moisture
contamination of the product and also less propellant is lost in the process.
9. PASTE A PICTURE OF METERED DOSE INHALER (MDI) AND LABEL ITS PARTS.
Canister
Drug/propellant
liquid mixture
Actuator
Metering valve
Actuator
nozzle
Actuator seat
10. ILLUSTRATE OR STATE THE PROCESS ON HOW TO USE METERED DOSE INHALER CORRECTLY
6While you are breathing in, press down on your inhaler one time to release the
medication.
9Repeat steps 3 to 8 until you have inhaled the number of puffs that your doctor
prescribed. Ask your doctor or pharmacist if you need to
wait between puffs of your medication.
10 Rinse your mouth thoroughly with water.