Drug Metabolism and Pharmacokinetics of Antisense Oligonucleotide Therapeutics: Typical Profiles, Evaluation Approaches, and Points to Consider Compared with Small Molecule Drugs.


Journal

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

Informations de publication

Date de publication:
04 2023
Historique:
medline: 5 4 2023
pubmed: 4 2 2023
entrez: 3 2 2023
Statut: ppublish

Résumé

Oligonucleotide therapeutics are attracting attention as a new treatment modality for a range of diseases that have been difficult to target using conventional approaches. Technical advances in chemical modification and drug delivery systems have led to the generation of compounds with excellent profiles as pharmaceuticals, and 16 oligonucleotide therapeutics have been marketed to date. There is a growing need to develop optimal and efficient approaches to evaluate drug metabolism and pharmacokinetics (DMPK) and drug-drug interactions (DDIs) of oligonucleotide therapeutics. The DMPK/DDI profiles of small molecule drugs are highly diverse depending on their structural and physicochemical characteristics, whereas oligonucleotide therapeutics share similar DMPK profiles within each chemistry type. Most importantly, the mechanisms and molecules involved in the distribution and metabolism of oligonucleotides differ from those of small molecules. In addition, there are considerations regarding experimental approaches in the evaluation of oligonucleotides, such as bioanalytical challenges, the use of radiolabeled tracers, materials for

Identifiants

pubmed: 36735616
doi: 10.1089/nat.2022.0054
pmc: PMC10066781
doi:

Substances chimiques

Oligonucleotides, Antisense 0
Pharmaceutical Preparations 0
Oligonucleotides 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

83-94

Auteurs

Hideo Takakusa (H)

Drug Metabolism & Pharmacokinetics Research Laboratories, Daiichi Sankyo Co., Ltd., Tokyo, Japan.

Norihiko Iwazaki (N)

Sohyaku. Innovative Research Division, Mitsubishi Tanabe Pharma Corp., Yokohama, Japan.

Makiya Nishikawa (M)

Faculty of Pharmaceutical Sciences, Tokyo University of Science, Noda, Japan.

Tokuyuki Yoshida (T)

Division of Molecular Target and Gene Therapy Products, National Institute of Health Sciences, Kawasaki, Japan.
Graduate School of Pharmaceutical Sciences, Osaka University, Suita, Japan.

Satoshi Obika (S)

Graduate School of Pharmaceutical Sciences, Osaka University, Suita, Japan.

Takao Inoue (T)

Division of Molecular Target and Gene Therapy Products, National Institute of Health Sciences, Kawasaki, Japan.
Graduate School of Pharmaceutical Sciences, Osaka University, Suita, Japan.

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Classifications MeSH