Delivery of biologics: Topical administration.


Journal

Biomaterials
ISSN: 1878-5905
Titre abrégé: Biomaterials
Pays: Netherlands
ID NLM: 8100316

Informations de publication

Date de publication:
11 2023
Historique:
received: 14 07 2023
revised: 27 08 2023
accepted: 31 08 2023
medline: 6 11 2023
pubmed: 11 9 2023
entrez: 10 9 2023
Statut: ppublish

Résumé

Biologics are unaffordable to a large majority of the global population because of prohibitively expensive fermentation systems, purification and the requirement for cold chain for storage and transportation. Limitations of current production and delivery systems of biologics were evident during the recent pandemic when <2.5% of vaccines produced were available to low-income countries and ∼19 million doses were discarded in Africa due to lack of cold-chain infrastructure. Among FDA-approved biologics since 2015, >90% are delivered using invasive methods. While oral or topical drugs are highly preferred by patients because of their affordability and convenience, only two oral drugs have been approved by FDA since 2015. A newly launched oral biologic costs only ∼3% of the average cost of injectable biologics because of the simplified regulatory approval process by elimination of prohibitively expensive fermentation, purification, cold storage/transportation. In addition, the cost of developing a new biologic injectable product (∼$2.5 billion) has been dramatically reduced through oral or topical delivery. Topical delivery has the unique advantage of targeted delivery of high concentration protein drugs, without getting diluted in circulating blood. However, only very few topical drugs have been approved by the FDA. Therefore, this review highlights recent advances in oral or topical delivery of proteins at early or advanced stages of human clinical trials using chewing gums, patches or sprays, or nucleic acid drugs directly, or in combination with, nanoparticles and offers future directions.

Identifiants

pubmed: 37690380
pii: S0142-9612(23)00320-4
doi: 10.1016/j.biomaterials.2023.122312
pii:
doi:

Substances chimiques

Pharmaceutical Preparations 0
Proteins 0
Biological Products 0

Types de publication

Journal Article Review Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

122312

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL107904
Pays : United States

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Henry Daniell reports a relationship with PhylloPharma LLC that includes: equity or stocks. Henry Daniell has patent issued to University of Pennsylvania. All other authors declare no competing interests.

Auteurs

Rachel J Kulchar (RJ)

Department of Basic and Translational Sciences, School of Dental Medicine, University of Pennsylvania, Philadelphia PA, 19104, USA.

Rahul Singh (R)

Department of Basic and Translational Sciences, School of Dental Medicine, University of Pennsylvania, Philadelphia PA, 19104, USA.

Suwan Ding (S)

Department of Biomedical Engineering, Columbia University, New York City NY 10032, USA.

Elena Alexander (E)

Department of Biomedical Engineering, Columbia University, New York City NY 10032, USA.

Kam W Leong (KW)

Department of Biomedical Engineering, Columbia University, New York City NY 10032, USA.

Henry Daniell (H)

Department of Basic and Translational Sciences, School of Dental Medicine, University of Pennsylvania, Philadelphia PA, 19104, USA. Electronic address: hdaniell@upenn.edu.

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Classifications MeSH