What is sustain release tablet? Which Molecules are not suitable candidate for sustain release preparation?
Sustained-release
tablets, also known as extended-release tablets, are designed to release the
medication slowly over an extended period, typically over several hours or even
days. This gradual release of the active ingredient helps to maintain therapeutic
levels of the drug in the body, resulting in a more consistent and prolonged
effect.
There are several
factors to consider when selecting molecules for sustained release preparation,
and not all molecules are suitable for this purpose. Here are some factors that
may make a molecule unsuitable for sustained release preparation:
Small
molecules: Small molecules can be difficult to formulate for
sustained release, as they may diffuse too quickly out of the delivery system.
Highly
water-soluble molecules: Highly water-soluble molecules can
dissolve too quickly in the release medium and may be difficult to sustain the
release of.
Highly
lipophilic molecules: Highly lipophilic molecules tend to accumulate in the delivery system, which can result in a burst
release.
Molecules
with a short half-life: Molecules with a short half-life
may be difficult to sustain release as they may degrade too quickly.
Molecules
with high clearance rates:
Molecules with high
clearance rates can be difficult to sustain release as they may be rapidly
eliminated from the body.
Molecules
with narrow therapeutic windows: Molecules with narrow
therapeutic windows can be challenging to sustain release as maintaining a
constant concentration within the therapeutic range can be difficult.
Molecules
that are unstable or reactive: Molecules that are
unstable or reactive can degrade or react within the delivery system, leading
to a burst release.
Molecules that require
a specific environment: Molecules that require a specific environment, such as
a certain pH or temperature, may be difficult to sustain release in a different
environment.
In
summary, molecules that are small, highly water-soluble, or
lipophilic, have a short half-life, high clearance rates, narrow therapeutic
windows, are unstable or reactive or require a specific environment may not be
suitable candidates for sustained release preparation.
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