Technical Considerations for Use of Oligonucleotide Solution API.


Journal

Nucleic acid therapeutics
ISSN: 2159-3345
Titre abrégé: Nucleic Acid Ther
Pays: United States
ID NLM: 101562758

Informations de publication

Date de publication:
08 2020
Historique:
pubmed: 8 5 2020
medline: 20 8 2021
entrez: 8 5 2020
Statut: ppublish

Résumé

The most common approach for the manufacture of oligonucleotides includes isolation of the active pharmaceutical ingredient (API) via lyophilization to provide a solid product, which is then dissolved to provide an aqueous formulation. It is well known from the development and manufacture of large molecules ("biologics") that API production does not always require isolation of solid API before drug product formulation, and this article provides technical considerations for the analogous use of oligonucleotide API in solution. The primary factor considered is solution stability, and additional factors such as viscosity, concentration, end-to-end manufacturing, microbiological control, packaging, and storage are also discussed. The technical considerations discussed in this article will aid the careful evaluation of the relative advantages and disadvantages of solution versus powder API for a given oligonucleotide drug substance.

Identifiants

pubmed: 32379529
doi: 10.1089/nat.2020.0846
pmc: PMC7415879
doi:

Substances chimiques

Oligonucleotides 0
Solutions 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

189-197

Références

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Auteurs

Jale Muslehiddinoglu (J)

Janssen, Beerse, Belgium.

Robert Simler (R)

Biogen, Cambridge, Massachusetts, USA.

Malcolm L Hill (ML)

GlaxoSmithKline, Stevenage, United Kingdom.

Claudia Mueller (C)

F. Hoffmann-La Roche Ltd., Basel, Switzerland.

John H A Amery (JHA)

Pfizer, Chesterfield, Missouri, USA.

Leigh Dixon (L)

AstraZeneca, Macclesfield, United Kingdom.

Anna Watson (A)

AstraZeneca, Macclesfield, United Kingdom.

Kirsten Storch (K)

F. Hoffmann-La Roche Ltd., Basel, Switzerland.

Cinzia Gazziola (C)

F. Hoffmann-La Roche Ltd., Basel, Switzerland.

Frank Gielen (F)

Janssen, Geel, Belgium.

Stefan Andreas Lange (SA)

Sanofi, Frankfurt, Germany.

Jeremy D Prail (JD)

GlaxoSmithKline, Worthing, United Kingdom.

Doug P Nesta (DP)

GlaxoSmithKline, King of Prussia, United Kingdom.

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Classifications MeSH