Drug substances and crude drugs are developed into
drug dosage forms in order to optimize stability, safety and effectiveness of
drug substances and to make them suitable for administration. According to the
consistence, they are classified as:
1.
Solid dosage forms
2.
Liquid dosage forms
3.
Semisolid dosage forms
4.
Aerosols
I.
SOLIDE DOSAGE FORMS
Solid
dosages, such as tablets, capsules,
have many advantages over other types: greater stability, less risk of chemical interaction between different medicaments, smaller bulk, accurate dosage, and ease of production.
have many advantages over other types: greater stability, less risk of chemical interaction between different medicaments, smaller bulk, accurate dosage, and ease of production.
1. Tablet
- Uncoated tablet
- Sugar coated tablet
- Sugar coated tablet
- Film coated tablet
- Modified release tablet: sustained release and delay release
- Effervescent tablet
- Chewable tablet
- Lozenge tablet
- Sublingual tablet
2. Capsule
- Hard gelatin capsule
- Soft gelatin capsule
- Modified release capsule: sustained release and delay release
3. Pill
4. Oral Powder
5. Granule
II. LIQUID DOSAGE FORMS
Liquid dosage forms are prepared by
dissolving the active ingredient(s) in an aqueous or nonaqueous solvent, by
suspending the drug in appropriate medium or by incorporating the drug
substance into one or two phases of an oil and water system. These forms can be
formulated for different routes of administration: oral use, introduction into
body cavities, or applied externally. Liquid drugs may also be administered
systemically by mouth or by injection throughout the body.
The oral liquid forms can be readily administered
to children or people unable to swallow tablets or capsules.
1. Syrup
2. Suspension
3. Emulsion
4. Elixir
5. Tincture
6. Eye, Ear, Nose Drops
7. Mouthwash solution
8. Enema
9. Douche solution
10. Liniment
11. Medications for injection
III.
SEMISOLID DOSAGE FORMS
Semisolid dosage forms are normally
presented in the form of creams, gels, ointments, pastes, suppository or patch.
They contain one or more active ingredients dissolved or uniformly dispersed in
a suitable base and any suitable excipients such as emulsifiers,
viscosity-increasing agents, antimicrobial agents, antioxidants, or stabilizing
agents. The choice of a base for semi-solid dosage forms depends on many
factors: the therapeutic effect desired, the nature of the active ingredient(s)
to be incorporated, the availability of the active ingredient(s) at the site of
action, the shelf-life of the finished product, and the environmental
conditions in which the product is intended to be administered. In many cases,
a compromise has to be made in order to achieve the required stability. For
example, drugs that hydrolyze rapidly are more stable in hydrophobic bases than
in water-containing bases, even though they may be more effective in the
latter.
The base should neither irritate
nor sensitize the skin, nor should it delay wound healing. It should be smooth,
inert, odorless, physically and chemically stable, and compatible with both the
skin and the active ingredient(s) to be incorporated. It should normally be of
such a consistency that it spreads and softens easily when stress is applied.
It may be necessary for a topical semi-solid
dosage form to be sterile, for example, when it is intended for use on large
open wounds or severely injured skin.
1. Cream
2. Ointment
3. Gel
4. Paste
5. Patch/Plaster
6. Suppository
IV.
AEROSOLS/GASES FORMS
Are heterogeneous systems
consisting of very finely subdivided liquid or solid particles dispersed in a
gas medium. The pressurized aerosol packages contain different propellants
(compressed gases) driving the drug in the form of mist or foam. They can be inhaled nasally or orally or
applied topically to dispense a variety of agents for systemic or topical
treatment.
Example: Salbutamol inhaler,
Nasonex nasal spray, Coplaster spray, Burnaid spray, etc
References: Essential Pharmacology for Health Occupations, 5TH EDITION, RUTH WOODRAW
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