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1I–PH Group
#5
The use of a sand bath in heating mixtures is important as it helps conduct the heat evenly and
gradually to a reaction vessel. In this method, heat is indirect thus, less stirring is required and the
risk of glass apparatus cracking or breaking is reduced. Additionally, the duration of the reaction
and the possibility of side reactions due to changes in temperature is also reduced.
Surfactants typically contain both hydrophilic and lipophilic groups and each has an assigned HLB
value or number indicating the polarity of the substance. Below is a list of the type of activity of
surfactants and their assigned HLB values:
This method, also known as the 4:2:1 method, involves triturating 4 parts by volume of oil, 2 parts
of water, and 1 part of gum to form the primary emulsion. The mixture should be triturated until a
thick white cream with a ‘cracking’ sound is produced. Then, the remaining amount of water is
eventually added to form the final emulsion.
This method uses the same proportions of oil, water, and gum as in the continental method but
with a different order and technique of mixing. Gum and water are triturated first to form a
mucilage. Then, oil is added slowly and triturated to make the primary emulsion. Once formed,
the remaining amount of water is added to make the final emulsion. This method is more difficult
to perform but produces a more stable emulsion than the former.
This method is suitable for preparing emulsions of volatile oils or oleaginous substances of low
viscosity. It is a variation of the continental method that involves shaking one part of the gum and
four parts of oil together. Then, water is added, and the mixture is shaken thoroughly again to
form the primary emulsion. Once complete, more water is added to eventually achieve the final
volume.
D. Auxiliary Method
This method involves the use of hand homogenizers in increasing the quality of emulsions
prepared by either continental or English method. The pumping action of the apparatus forces the
emulsion through a very small orifice which reduces its dispersed droplet size to around 5 microns
or less. This method is less efficient for very thick emulsions and should not be used for emulsions
with high proportions of solid matter.
This method is employed in making calcium soap and soft soap. It may be prepared in a bottle or
mortar depending on whether the ingredients are soluble or not. For calcium soaps, oleic acid and
limewater are mixed at equal volumes to form a w/o emulsion.
F. Microemulsions
This method produces droplets ranging from 100 A to 1000 A in diameter. Microemulsions, both
o/w and w/o, are thermodynamically stable and formed spontaneously by agitating the oil and
water phases with carefully selected surfactants. The properties of the oil and surfactants often
dictate the type of emulsion produced.
3. What are the special labeling requirements for emulsion? Attach sample label of suspension
pharmaceutical products available in the market.
References:
Allen, L.V., Ansel, H.C. (2014). Ansel’s pharmaceutical dosage forms and drug delivery systems
(10th ed). Philadelphia, USA: Lippincott Williams & Wilkins.
Drugs.com. (n.d.). Cefaclor. Retrieved from https://www.drugs.com/pro/cefaclor.html
23 Pichay, Christian Paulo D. 1I–PH Group
#5
1. Enumerate examples of mixture preparation available in the market. Give their specific uses.
Cough Mixture: for the treatment of cough, stuffy nose, and sinus pain
Kaolin and Pectin Mixture: for the treatment of diarrhea
Magnesium Trisilicate Mixture: for the relief of indigestion, heartburn, and dyspepsia
Potassium Citrate Mixture: for the relief of cystitis and other mild urinary tract infections
2. Compare and contrast the advantages and disadvantages of mixture dosage forms.
ADVANTAGES DISADVANTAGES
Easy to administer May have incompatibilities with some ingredients
Suitable for insoluble/immiscible drugs Bulky to carry
Used for drugs causing stomach pain Less stable and more expensive
More bioavailable than solid dosage form Less soluble than solid dosage forms
3. Give information needed in labeling requirements for mixtures. Attach sample label of mixture
pharmaceutical products available in the market.
References:
Watsonss. (n.d.). Magtasil antacid mixture 200 ml. Retrieved from https://www.watsons.com.sg/
magtasil-antacid-mixture-200ml/p/BP_10664
Gels may be prepared in two ways. First is by freshly precipitating the disperse phase upon
reacting an inorganic agent to a gelatinous precipitate. For example, (NH 4)2SO4. Al2(SO4)3. 24 H2O +
4 Na2CO3 → (NH4)2CO3+ Al2(CO3)3+ 4 Na2SO4 + 24 H2O. And by directly hydrating the inorganic
material in water as in Al2(CO)3 + 3 H2O → 2 Al(OH)3 ↓ + 3 CO2 ↑.
3. Define and give examples of gelling agents. What are the factors to be considered in gel formulation?
Gelling agents provide structure, viscosity, and improved stability for aqueous solutions. It is
dissolved in a liquid as a colloid mixture to form an internal structure responsible for the gel
appearance of a solid matter. Common gelling agents include pectin, starch, tragacanth, acacia,
and xanthan gum.
Several factors are considered in gel formulation including the concentration and molecular
weight of gelling agent, solubility and affinity of gelling agent to the solvent, nature of the solvent,
pH of the solution, ionic strength of the solution, temperature, and humidity.
References:
Nabi, S.A.A., Sheraz, M.A., Ahmed, S., Mustaan, N. & Ahmad, I. (2016). Pharmaceutical gels: a
review. RADS-JPPS. 4 (1): 40 – 48. Retrieved from
http://www.jpps.juw.edu.pk/index.php/jpps/article/download/96/66
23 Pichay, Christian Paulo D. 1I–PH Group
#5
A good lotion should pour freely from its container and apply evenly over the affected area. It
should be able to dry quickly and provide a protective film that will not rub off easily. A good
lotion must also have an acceptable odor and color, maintain good physical and chemical stability,
and be free from contamination during storage.
3. What is the new important information you should know about Lindane Lotion? What prompted FDA
to make changes in labeling for Lindane Lotion?
Lindane Lotion may be poisonous when misused. It goes through the skin and may affect one’s
brain and nerves that may result to seizures or convulsions, “fits” or epilepsy, and in worse cases,
even death. Numerous reports of adverse events on its misuse and overuse prompted the FDA to
limit the product package size and include a medication guide and additional warnings on its label.
Reference:
The National Pediculosis Association. (2003). FDA issues health advisory regarding labeling
changes for lindane products. Retrieved from https://www.headlice.org/news/2003/fda-
lindane.htm
23 Pichay, Christian Paulo D. 1I–PH Group
#5
It has a faster rate of dissolution and oral absorption than solid dosage forms.
It is preferred for patients who have difficulty swallowing solid dosage forms.
It is suitable for drugs with very low solubility.
It increases the chemical stability of certain drugs.
It masks the unpleasant taste of some drugs.
It is used to achieve controlled/sustained drug release.
2. Define and differentiate the following terms from one another: dispersed phase and dispersing phase,
give examples.
The dispersed phase is a discontinuous phase composed of particles that are distributed into
another phase. The dispersing phase is the continuous medium or vehicle in which the disperse
phase is distributed throughout. The disperse phase is also known as the internal phase while the
dispersing phase is termed as the external phase. An example of a dispersed phase is the dust
particles in the air and an example of a dispersing phase is water in milk.
3. Give examples of official and commercial oral suspensions and their uses.
Acetaminophen Oral Suspension: for the treatment of mild to moderate pain and fever
Acyclovir Oral Suspension: for the treatment of infections caused by herpes viruses (e.g.
genital herpes, cold sores, shingles, chickenpox)
Albendazole Oral Suspension: for the treatment of certain infections caused by worms such
as pork tapeworm and dog tapeworm