Literature DB >> 35516773

Greening the synthesis of peptide therapeutics: an industrial perspective.

Vincent Martin1, Peter H G Egelund1, Henrik Johansson1, Sebastian Thordal Le Quement1, Felix Wojcik1, Daniel Sejer Pedersen1.   

Abstract

Solid-phase peptide synthesis (SPPS) is generally the method of choice for the chemical synthesis of peptides, allowing routine synthesis of virtually any type of peptide sequence, including complex or cyclic peptide products. Importantly, SPPS can be automated and is scalable, which has led to its widespread adoption in the pharmaceutical industry, and a variety of marketed peptide-based drugs are now manufactured using this approach. However, SPPS-based synthetic strategies suffer from a negative environmental footprint mainly due to extensive solvent use. Moreover, most of the solvents used in peptide chemistry are classified as problematic by environmental agencies around the world and will soon need to be replaced, which in recent years has spurred a movement in academia and industry to make peptide synthesis greener. These efforts have been centred around solvent substitution, recycling and reduction, as well as exploring alternative synthetic methods. In this review, we focus on methods pertaining to solvent substitution and reduction with large-scale industrial production in mind, and further outline emerging technologies for peptide synthesis. Specifically, the technical requirements for large-scale manufacturing of peptide therapeutics are addressed. This journal is © The Royal Society of Chemistry.

Entities:  

Year:  2020        PMID: 35516773      PMCID: PMC9057961          DOI: 10.1039/d0ra07204d

Source DB:  PubMed          Journal:  RSC Adv        ISSN: 2046-2069            Impact factor:   4.036


  109 in total

Review 1.  Large-scale manufacture of peptide therapeutics by chemical synthesis.

Authors:  Brian L Bray
Journal:  Nat Rev Drug Discov       Date:  2003-07       Impact factor: 84.694

2.  Effect of residual water and microwave heating on the half-life of the reagents and reactive intermediates in peptide synthesis.

Authors:  A Pernille Tofteng; Søren L Pedersen; Dan Staerk; Knud J Jensen
Journal:  Chemistry       Date:  2012-06-13       Impact factor: 5.236

3.  Chemoselective amide ligations by decarboxylative condensations of N-alkylhydroxylamines and alpha-ketoacids.

Authors:  Jeffrey W Bode; Ryan M Fox; Kyle D Baucom
Journal:  Angew Chem Int Ed Engl       Date:  2006-02-13       Impact factor: 15.336

4.  The methylsulfonylethyloxycarbonyl group, a new and versatile amino protective function.

Authors:  G I Tesser; I C Balvert-Geers
Journal:  Int J Pept Protein Res       Date:  1975

5.  Hydrophobic benzyl amines as supports for liquid-phase C-terminal amidated peptide synthesis: application to the preparation of ABT-510.

Authors:  Emiko Matsumoto; Yuko Fujita; Yohei Okada; Esko I Kauppinen; Hidehiro Kamiya; Kazuhiro Chiba
Journal:  J Pept Sci       Date:  2015-07-22       Impact factor: 1.905

Review 6.  Polypept(o)ides: Hybrid Systems Based on Polypeptides and Polypeptoids.

Authors:  Kristina Klinker; Matthias Barz
Journal:  Macromol Rapid Commun       Date:  2015-09-23       Impact factor: 5.734

7.  Solid-phase peptide synthesis under continuous-flow conditions.

Authors:  T J Lukas; M B Prystowsky; B W Erickson
Journal:  Proc Natl Acad Sci U S A       Date:  1981-05       Impact factor: 11.205

8.  Leveraging the Knorr Pyrazole Synthesis for the Facile Generation of Thioester Surrogates for use in Native Chemical Ligation.

Authors:  Dillon T Flood; Jordi C J Hintzen; Michael J Bird; Philip A Cistrone; Jason S Chen; Philip E Dawson
Journal:  Angew Chem Int Ed Engl       Date:  2018-08-10       Impact factor: 15.336

9.  Kinetic mechanism of Staphylococcus aureus sortase SrtA.

Authors:  Xinyi Huang; Ann Aulabaugh; Weidong Ding; Bhupesh Kapoor; Lefa Alksne; Keiko Tabei; George Ellestad
Journal:  Biochemistry       Date:  2003-09-30       Impact factor: 3.162

10.  Accelerated microfluidic native chemical ligation at difficult amino acids toward cyclic peptides.

Authors:  Nathalie Ollivier; Thomas Toupy; Ruben C Hartkoorn; Rémi Desmet; Jean-Christophe M Monbaliu; Oleg Melnyk
Journal:  Nat Commun       Date:  2018-07-20       Impact factor: 14.919

View more
  1 in total

1.  Predicting the Success of Fmoc-Based Peptide Synthesis.

Authors:  Ilanit Gutman; Ron Gutman; John Sidney; Leila Chihab; Michele Mishto; Juliane Liepe; Anthony Chiem; Jason Greenbaum; Zhen Yan; Alessandro Sette; Zeynep Koşaloğlu-Yalçın; Bjoern Peters
Journal:  ACS Omega       Date:  2022-06-27
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.