Dosage Form Design
Preformulation, choice of dosage form and the role of excipients.
Short notes and cheat sheetSubject guide
Dosage form design, physical pharmacy, formulation and stability.
Pharmaceutics explains how a drug becomes a medicine a patient can actually take. It runs through several professional years of the Pharm-D programme and is a staple of PPSC, FPSC and provincial pharmacist recruitment tests.
Exam questions reward understanding over recall: why a suspension settles, why a tablet fails a disintegration test, why a preservative is chosen for one formulation and not another. These pharmaceutics MCQs cover physical pharmacy, solid, liquid and sterile dosage forms, and stability.
What Pharmaceutics questions on PharmaPrep cover.
Preformulation, choice of dosage form and the role of excipients.
Short notes and cheat sheetGranulation, compression, coating, and quality tests such as disintegration, dissolution and friability.
Short notes and cheat sheetSuspensions, emulsions and colloids, including Stokes' law, HLB and flocculation.
Short notes and cheat sheetParenterals, ophthalmic preparations, isotonicity, pyrogens and sterilisation.
Short notes and cheat sheetNewtonian and non-Newtonian flow, particle size, flow properties and powder behaviour.
Short notes and cheat sheetDegradation kinetics, shelf life, accelerated stability testing and container choice.
Short notes and cheat sheetOriginal practice questions with answers and explanations.
Answer: B. A water-in-oil emulsion
Low HLB (roughly 3–6) emulsifiers are lipophilic and favour water-in-oil emulsions. Oil-in-water emulsions need hydrophilic emulsifiers with an HLB of roughly 8–18.
Answer: A. Independent of the initial concentration
For first-order degradation t90 = 0.105/k, which does not depend on the starting concentration. In zero-order degradation t90 = 0.1C0/k, so it rises with the initial concentration.
Answer: B. Friability test
The friability test tumbles tablets in a rotating drum and measures the weight lost to abrasion. Hardness testing measures breaking force, while disintegration and dissolution assess how the tablet releases the drug.
Disperse systems, tablet technology and quality control, sterile products, rheology and stability kinetics are the most frequently tested areas.
Yes. Expect questions on shelf life, isotonicity, Stokes' law and HLB, alongside conceptual questions on formulation.
Absorption, bioavailability and dosing calculations are grouped under Pharmacokinetics on PharmaPrep, so practise both subjects together.