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.
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.
I. CREAMS
are homogenous,
semisolid preparation that is usually white and no greasy and has a water base.
Creams are intended for application to the skin or certain mucous membranes for
therapeutic or protective purposes. The term "cream" is most
frequently used to describe soft, cosmetically acceptable types of
preparations.
Example: Hydrocortisone cream, Ketoconazole
cream, etc
II. OINTMENTS
are
homogeneous, semi-solid and greasy preparations intended for external
application to the skin or mucous membranes for therapeutic or protective
purposes.
Example: Tetracycline ointment,
Bepanthene ointment, Nebanol ointment, etc
III. GELS
are usually
homogeneous, clear, semi-solid, jelly- like preparations that may be used for
topical medication. Gels are applied
to the skin or certain mucous membranes for therapeutic, or protective
purposes.
Example: Erythrogel, Metrogel,
Hiruscar, etc
IV. PASTES
are homogeneous,
semi-solid preparations containing high concentrations of insoluble powdered
substances (usually not less than 20%) dispersed in a suitable base. The pastes
are usually less greasy, more absorptive, and stiffer in consistency than
ointments because of the large quantity of powdered ingredients present. Pastes
adhere reasonably well to the skin and they are suited for application on and
around moist lesions.
Example: Orrepaste, Anagelsic and
anti-inflammatory containing dental paste, etc
V. PATCHED/PLASTERS
are
substances intended for external application made of such materials and of such
consistency as to adhere to the skin. Inner surface of the patch contacts skin
and allows
transdermal absorption of
lipid-soluble medicines. The total amount of medicine on the patch is very
large, but typically only a small fraction is absorbed.
Example: Dermal patches
VI. SUPPOSITORY
Semisolid
dosage forms to be inserted into body cavity-rectum or vagina, where medication
is melt at the body temperature which provides local or systemic effects.
Example: Kinal suppository, Poro suppository,
Flagyl suppository, etc References:
Essential Pharmacology for Health Occupations, 5TH EDITION, RUTH WOODRAW
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