PILOT-PLANT SCALE-UP CONSIDERATIONS FOR ORAL LIQUIDS
Oral liquids can be defined as homogenous liquid preparations, mainly contains an
emulsion, a suspension or a solution having one or more active ingredients in an
appropriate base, i.e. liquid. They are for oral administration. These preparations are
used either as such or after dilution. The main substances added in these preparations
are: Emulsifying agents, suspending agents, sweetening agents, flavouring agents,
stabilizing agents, thickening agents, etc. during pilot-plant scale-up each and every
material and equipment is tested in the same amount and with same characteristics as
to be used at large-scale production. This is a pourable dosage form which displays
Newtonian or Pseudoplastic flow behaviour. This dosage form remains conforms to
Steps in Liquid Manufacturing Process
a. Planning of material requirements
PILOT-PLANT SCALE-UP CONSIDERATIONS FOR SEMISOLIDS
Semisolid dosage forms are composed of mainly two phases, i.e. oil and water. One of
the phases is the continuous or external phase and the other one is dispersed or internal
phase. The active pharmaceutical ingredient is mainly dissolved in one phase and if it
is insoluble in one or both phases then a third phase is introduced. This is known as a
Various factors affect the physical property of the semisolid dosage form. Some of
ii. The interfacial tension between the phases
iii. The partition coefficient of an active ingredient in between the phases
v. The viscosity of both phases
vi. Nature of the third phase (if introduced)
The all factors mentioned above determined the release as well as other characteristics
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