Advances in the design of new types of inhaled medicines.

Aggregation Antibody Clinical trial Drug Inhalation Lung Lung retention Metabolism New modality Oligonucleotide PROTAC Peptide Protein Stability

Journal

Progress in medicinal chemistry
ISSN: 0079-6468
Titre abrégé: Prog Med Chem
Pays: Netherlands
ID NLM: 0376452

Informations de publication

Date de publication:
2022
Historique:
entrez: 26 6 2022
pubmed: 27 6 2022
medline: 29 6 2022
Statut: ppublish

Résumé

Inhalation of small molecule drugs has proven very efficacious for the treatment of respiratory diseases due to enhanced efficacy and a favourable therapeutic index compared with other dosing routes. It enables targeted delivery to the lung with rapid onset of therapeutic action, low systemic drug exposure, and thereby reduced systemic side effects. An increasing number of pharmaceutical companies and biotechs are investing in new modalities-for this review defined as therapeutic molecules with a molecular weight >800Da and therefore beyond usual inhaled small molecule drug-like space. However, our experience with inhaled administration of PROTACs, peptides, oligonucleotides (antisense oligonucleotides, siRNAs, miRs and antagomirs), diverse protein scaffolds, antibodies and antibody fragments is still limited. Investigating the retention and metabolism of these types of molecules in lung tissue and fluid will contribute to understanding which are best suited for inhalation. Nonetheless, the first such therapeutic molecules have already reached the clinic. This review will provide information on the physiology of healthy and diseased lungs and their capacity for drug metabolism. It will outline the stability, aggregation and immunogenicity aspects of new modalities, as well as recap on formulation and delivery aspects. It concludes by summarising clinical trial outcomes with inhaled new modalities based on information available at the end of 2021.

Identifiants

pubmed: 35753716
pii: S0079-6468(22)00001-7
doi: 10.1016/bs.pmch.2022.04.001
pii:
doi:

Substances chimiques

Peptides 0
Pharmaceutical Preparations 0
Proteins 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

93-162

Informations de copyright

Copyright © 2022 Elsevier B.V. All rights reserved.

Auteurs

Werngard Czechtizky (W)

Department of Medicinal Chemistry, Research and Early Development, Respiratory & Immunology, BioPharmaceuticals R&D, AstraZeneca, Mölndal, Sweden. Electronic address: werngard.czechtizky@astrazeneca.com.

Wu Su (W)

Department of Medicinal Chemistry, Research and Early Development, Respiratory & Immunology, BioPharmaceuticals R&D, AstraZeneca, Mölndal, Sweden.

Lena Ripa (L)

Department of Medicinal Chemistry, Research and Early Development, Respiratory & Immunology, BioPharmaceuticals R&D, AstraZeneca, Mölndal, Sweden.

Stefan Schiesser (S)

Department of Medicinal Chemistry, Research and Early Development, Respiratory & Immunology, BioPharmaceuticals R&D, AstraZeneca, Mölndal, Sweden.

Andreas Höijer (A)

Cardiovascular, Renal & Metabolism CMC Projects, Pharmaceutical Sciences, R&D, AstraZeneca, Gothenburg, Sweden.

Rhona J Cox (RJ)

Department of Medicinal Chemistry, Research and Early Development, Cardiovascular, Renal & Metabolism, BioPharmaceuticals R&D, AstraZeneca, Mölndal, Sweden.

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Classifications MeSH