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Drug Particle
Engineering |
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A number of factors
are creating interest in dry drug formulations. The growth in protein
and peptide drugs is forcing drug developers to deal with their in
vitro and in vivo stability limitations. Formulation these biological
as powder can solve both issues. Lyophilization is employed to
stabilize biologicals outside the cold chain. Inhalable powders
are replacing liquid inhaler drugs for many indications. Sustained release dry powder
formulations offer several possible benefits. Drugs that can be
released over an extended period hold the promise of less frequent
dosing. One goal of inhaled drug developers is a formulation that can
be taken once a day, reducing non-compliance related complications and
costs.
Some small molecules, such as Budsonide and Ketotifen, have been
prepared in freeze-dried liposomes to form a dry powder dispersion for
inhalation. The feasibility of lyophilization and milling for
preparation of protein-liposome dry powders for pulmonary delivery is
being explored. This report examines the benefits and opportunities of
drug powder engineering and formulation.
Publication: May 2007
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About Our
Reports |
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Our reports are carefully
researched and written to provide timely and insightful analysis of key
factors and developments shaping the commercial marketplace. The
focused nature of our publications is designed to allow readers to
identify emerging demand and growth opportunities in selected markets.
Numerous charts, tables
and graphs complement the text, with evaluations and assessments
of current and probable
future market developments, technology issues and business factors -
information necessary to compete effectively in the global marketplace. |
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