Evidence map›Paper›PMID 38508870›Full record

ReviewThe Journal of organic chemistry2024

Process Mass Intensity (PMI): A Holistic Analysis of Current Peptide Manufacturing Processes Informs Sustainability in Peptide Synthesis.

Ivy Kekessie, Katarzyna Wegner, Isamir Martinez, Michael E Kopach, Timothy D White, Janine K Tom, Martin N Kenworthy, Fabrice Gallou, John Lopez, Stefan G Koenig and 11 more

Open access · bronzeAbstract readReview
In one paragraph

Review in The Journal of organic chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
24.3field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 97 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors at 11 institutions in 4 countries.

Ivy KekessieEarly Discovery Biochemistry - Peptide Therapeutics, Genentech, Inc., A Member of the Roche Group, 1 DNA Way, South San Francisco, California 94080, United States.ORCID 0009-0000-2844-9051
Katarzyna WegnerActive Pharmaceutical Ingredient Development, Ipsen Manufacturing Ireland Ltd., Blanchardstown Industrial Park, Dublin 15, Ireland.
Isamir MartinezGreen Chemistry Institute, American Chemical Society, 1155 16th St North West, Washington, District of Columbia, 20036, United States.
Michael E KopachSynthetic Molecule Design and Development, Eli Lilly and Company, Indianapolis, Indiana 46285, United States.ORCID 0000-0002-3590-702X
Timothy D WhiteSynthetic Molecule Design and Development, Eli Lilly and Company, Indianapolis, Indiana 46285, United States.
Janine K TomDrug Substance Technologies, Amgen, Inc., 1 Amgen Center Drive, Thousand Oaks, California 91320, United States.ORCID 0000-0002-3531-8751
Martin N KenworthyChemical Development, Pharmaceutical Technology & Development, Operations, AstraZeneca, Macclesfield, SK10 2NA, United Kingdom.
Fabrice GallouChemical & Analytical Development, Novartis Pharma AG, 4056 Basel, Switzerland.ORCID 0000-0001-8996-6079
John LopezChemical & Analytical Development, Novartis Pharma AG, 4056 Basel, Switzerland.ORCID 0000-0002-0551-6511
Stefan G KoenigSmall Molecule Pharmaceutical Sciences, Genentech, Inc., A Member of the Roche Group, 1 DNA Way, South San Francisco, California 94080, United States.ORCID 0000-0002-1878-614X
Philippa R PayneOutsourced Manufacturing, Pharmaceutical Development & Manufacturing, Gilead Alberta ULC, 1021 Hayter Rd NW, Edmonton, T6S 1A1, Canada.
Stefan EisslerBachem AG, Hauptstrasse 144, 4416 Bubendorf, Switzerland.
Balasubramanian ArumugamChemical Macromolecule Division, Asymchem Life Science (Tianjin) Co., Ltd., 71 Seventh Avenue, TEDA Tianjin 300457, China.
Changfeng LiChemical Macromolecule Division, Asymchem Life Science (Tianjin) Co., Ltd., 71 Seventh Avenue, TEDA Tianjin 300457, China.
Subha MukherjeeChemical Process Development, Bristol Myers Squibb, New Brunswick, New Jersey 08903, United States.ORCID 0000-0002-9359-990X
Albert Isidro-LlobetGSK, Gunnels Wood Road, Stevenage, Hertfordshire SG1 2NY, U.K.ORCID 0000-0001-9108-5916
Olivier Ludemann-HombourgerPolyPeptide Laboratories France SAS, 7 Rue de Boulogne, 67100 Strasbourg, France.
Paul RichardsonChemistry, Pfizer, 10578 Science Center Drive (CB6), San Diego, California 09121, United States.ORCID 0000-0002-3700-8749
Jörg KittelmannCMC API Development, Novo Allé, 2880 Bagsværd, Denmark.
Daniel Sejer PedersenChemical Development, Novo Allé, CMC API Development, 2880 Bagsværd, Denmark.ORCID 0000-0003-3926-7047
Leendert J van den BosEnzyTag B.V, Daelderweg 9, 6361HK, Nuth, Netherlands.
Eli Lilly (United States) · USNovartis (Switzerland) · CHRoche (United States) · USAge UK · GBAmerican Chemical Society · USAmgen (United States) · USAstraZeneca (United Kingdom) · GBBachem (Switzerland) · CHBristol-Myers Squibb (United States) · USIpsen (Ireland) · IEPfizer (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Small molecule therapeutics represent the majority of the FDA-approved drugs. Yet, many attractive targets are poorly tractable by small molecules, generating a need for new therapeutic modalities. Due to their biocompatibility profile and structural versatility, peptide-based therapeutics are a possible solution. Additionally, in the past two decades, advances in peptide design, delivery, formulation, and devices have occurred, making therapeutic peptides an attractive modality. However, peptide manufacturing is often limited to solid-phase peptide synthesis (SPPS), liquid phase peptide synthesis (LPPS), and to a lesser extent hybrid SPPS/LPPS, with SPPS emerging as a predominant platform technology for peptide synthesis. SPPS involves the use of excess solvents and reagents which negatively impact the environment, thus highlighting the need for newer technologies to reduce the environmental footprint. Herein, fourteen American Chemical Society Green Chemistry Institute Pharmaceutical Roundtable (ACS GCIPR) member companies with peptide-based therapeutics in their portfolio have compiled Process Mass Intensity (PMI) metrics to help inform the sustainability efforts in peptide synthesis. This includes PMI assessment on 40 synthetic peptide processes at various development stages in pharma, classified according to the development phase. This is the most comprehensive assessment of synthetic peptide environmental metrics to date. The synthetic peptide manufacturing process was divided into stages (synthesis, purification, isolation) to determine their respective PMI. On average, solid-phase peptide synthesis (SPPS) (PMI ≈ 13,000) does not compare favorably with other modalities such as small molecules (PMI median 168-308) and biopharmaceuticals (PMI ≈ 8300). Thus, the high PMI for peptide synthesis warrants more environmentally friendly processes in peptide manufacturing.

Indexed as

PeptidesSolid-Phase Synthesis TechniquesChemistry Techniques, SyntheticSolventsPeptidesSolvents

Identifiers

PMID38508870
PMCPMC11002941
OpenAlexW4393022591

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.