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Future Medicinal Chemistry | 2009

Manufacturing peptides as active pharmaceutical ingredients

Athanassios S. Galanis; Oleg Werbitzky; Fernando Albericio

BACKGROUND Today, there are more than 40 peptides on the pharmaceutical world market and more than 100 in several clinical phases. Although in the past the pharmaceutical industries had reduced their interest in peptides research, in recent decades, they have rekindled their interest in peptides as a result of contemporary novel technological accomplishments, strategic developments, advances in the areas of formulation and enhanced drug delivery technology of peptides. Thus, eight new peptide drugs that could previously have been characterized as difficult to prepare on the large scale required by industry, have entered the pharmaceutical market at the new millennium. DISCUSSION The manufacturing of most of these drugs has benefited from new technological advances. Traditional and most modern techniques have been applied to the manufacture of these new entries. CONCLUSION Recent accomplishments, together with the traditional benefits of peptides (high biological activity, high specificity and low toxicity), have led pharmaceutical companies to re-focus their attention on peptide-based agents. Therefore, several serious diseases can be treated using the potential next generation of peptide drugs.


Archive | 2015

CHAPTER 12:Manufacturing of Venom-Derived Therapeutic Peptides

Oleg Werbitzky; Matthieu Giraud

From the perspective of drug discovery, venoms represent a nearly unlimited and largely untapped source of new biologically active compounds, most of which are of peptidic and proteinic nature. As a result of the progress achieved in recent years in separation and characterization techniques, more and more interesting peptides of venom origin are likely to be identified and further developed into new drugs. A remarkable characteristic of these venom-derived peptide drugs is their large diversity in terms of structure. In this overview, taking advantage of this structural diversity, modern concepts of industrial peptide manufacturing will be presented using the examples of eptifibatide, ziconotide, exenatide and linaclotide. These real world examples will allow discussion of the different synthesis strategies used today in industrial manufacturing processes, including liquid phase peptide synthesis, stepwise solid phase peptide synthesis, and convergent solid phase peptide synthesis. Due to their structural complexity, peptides drugs are generally more expensive to manufacture compared with small-molecule drugs. When a peptide contains non-native amino acid residues or exotic modifications such as cyclic elements, chemical synthesis still remains the only viable route of manufacture. However, and this is another remarkable characteristic of venom-derived peptides, many of them have the necessary stability, potency, and selectivity for therapeutic applications without requiring modifications of their native amino acid sequence. For example, Exenatide and Ziconotide are simply synthetic versions of the native venom peptides without modification. This, in principle, opens up the opportunity for cheaper recombinant production methods, which will not be discussed here.


Archive | 2005

Method for solid phase peptide synthesis

Anne-Sophie Droz; Jasmine Schnidrig; Nicole Studer; Stephane Varray; Corinne Wenger; Oleg Werbitzky


Archive | 2007

METHOD FOR PEPTIDE SYNTHESIS

Matthieu Giraud; Fernando Albericio; Francesca Quattrini; Oleg Werbitzky; Katja Senn; Michaela Williner


Archive | 2008

PROCESS FOR THE PRODUCTION OF PRAMLINTIDE

Andreas Brunner; Oleg Werbitzky; Stephane Varray; Francesca Quattrini; Holger Hermann; Andrew Strong; Fernando Albericio; Judit Tulla-Puche; Yesica Garcia Ramos


Archive | 2007

Synthesis of glucagon-like peptide

Oleg Werbitzky; Stephane Varray; Matthieu Giraud; Carsten Meininghaus


Archive | 2005

S-Alkyl-Sulphenyl Protection Groups in Solid-Phase Synthesis

Stephane Varray; Oleg Werbitzky; Thomas Zeiter


Archive | 2005

Cyclization of a peptide

Francesca Quattrini; Stephane Varray; Oleg Werbitzky; Thomas Zeiter


Archive | 2005

On-resin peptide cyclization

Stephane Varray; Oleg Werbitzky; Thomas Zeiter


Archive | 2011

PROCÉDÉ DE PRODUCTION DE L'EXÉNATIDE ET D'UN ANALOGUE DE L'EXÉNATIDE

Marie-Hélène Brichard; Jeanne-Marie Cauvin; Christine Devijver; Anne-Sophie Droz; Pascal Gilles; Matthieu Giraud; Daniel Latassa; El Djouhar Rekai; Stephane Varray; Fernando Albericio; Marta Paradis Bas; Oleg Werbitzky

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Matthieu Giraud

Centre national de la recherche scientifique

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