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Application of Peptide-Based Prodrug Chemistry in Drug Development (Paperback, 2013 ed.)
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Application of Peptide-Based Prodrug Chemistry in Drug Development (Paperback, 2013 ed.)
Series: SpringerBriefs in Pharmaceutical Science & Drug Development
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Macromolecular (specifically peptide-based) drugs could potentially
be highly effective medicines. However they have a relatively short
duration of action and variable therapeutic index. An example of
such a peptide is Glucagon-like Peptide I which could potentially
be used as a revolutionary drug for diabetes. This is because it
stimulates insulin only when the blood glucose level is high
thereby reducing the risk of hypoglycemia (a significant
disadvantage of using insulin is that an insulin overdose is the
single most potent cause of life-threatening hypoglycemia). However
it's short duration of action (half-life of 2 minutes in plasma)
precludes its therapeutic use. In this volume, the use of novel
therapeutics like GLP1 as an alternative to tradition insulin-based
drugs in diabetes is described. Application of Peptide-Based
Prodrug Chemistry in Drug Development elucidates the traditional
concept of prodrugs as "specialized non-toxic protective groups
used in a transient manner to alter or to eliminate certain
limiting properties in the parent small molecule" (IUPAC
definition). It goes on to provide insight into how prodrugs of
peptides (with GLP1 as an example) could be appropriately used to
extend the biological half life, broaden the therapeutic index of
macromolecules and improve the pharmacodynamics of such drugs.
Author explains the logic behind designing peptide prodrugs,
synthetic procedures and bioassays to examine the conversion of the
prodrug to the drug under therapeutic conditions. The prodrugs
described slowly convert to the parent drug at physiological
conditions of 37C and pH 7.2 driven by their inherent chemical
instability without the need of any enzymatic cleavage. The
diketopiperazine and diketomorpholine (DKP and DMP) strategies for
prodrug conversion are demonstrated in detail with special emphasis
on the chemical flexibility that it offers to develop prodrugs with
variable time actions. This book will be of useful to chemists,
biochemists, medicinal chemists, biologists and people in the
medical profession (doctors). It may be used in undergraduate
classes but will certainly help post-graduate students and advanced
professionals. The author is grateful to Prof. Richard DiMarchi
(Standiford H. Cox Professor of Chemistry and the Linda & Jack
Gill Chair in Biomolecular Sciences at Indiana University) for
valuable suggestions. The foreword for the book has been written by
Prof. Jean Martinez, (Legion d'Honneur awarded by the French
Republic; Professor of Chemistry and Medicinal Chemistry of the
University of Montpellier, France; and Chairman of European Peptide
Society, 2002-2010).
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