Cited by 151Advanced Drug Delivery SystemsDrug Solubulity and Delivery SystemsProteins in Food Systems

Challenges of peptide and protein drug delivery by oral route: Current strategies to improve the bioavailability

Verma, Saurabh, Goand, Umesh K., Husain, Athar, Katekar, Roshan A., Garg, Richa, Gayen, Jiaur R.·2021·Drug Development Research

Abstract

Advancement in biotechnology provided a notable expansion of peptide and protein therapeutics, used as antigens, vaccines, hormones. It has a prodigious potential to treat a broad spectrum of diseases such as cancer, metabolic disorders, bone disorders, and so forth. Protein and peptide therapeutics are administered parenterally due to their poor bioavailability and stability, restricting their use. Hence, research focuses on the oral delivery of peptides and proteins for the ease of self-administration. In the present review, we first address the main obstacles in the oral delivery system in addition to approaches used to enhance the stability and bioavailability of peptide/protein. We describe the physiochemical parameters of the peptides and proteins influencing bioavailability in the systemic circulation. It encounters, many barriers affecting its stability, such as poor cellular membrane permeability at the GIT site, enzymatic degradation (various proteases), and first-pass hepatic metabolism. Then describe the current approaches to overcome the challenges mentioned above by the use of absorption enhancers or carriers, structural modification, formulation and advance technology.

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Crossref · 10.1002/ddr.21832

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  • Gastrically irritating drugs (e.g., ketoprofen, ibuprofen, diclofenac) can cause gastric mucosal injury if released in the stomach, and acid-sensitive biotherapeutics (e.g., peptides and proteins such as insulin, calcitonin, and GLP-1 analogs) undergo rapid degradation in gastric acid and pepsin.

    “gastrically irritating drugs (e.g., ketoprofen, ibuprofen, diclofenac), which can cause gastric mucosal injury if released in the stomach, and for acid-sensitive biotherapeutics (e.g., peptides and proteins such as insulin, calcitonin, and GLP-1 analogs), which undergo rapid degradation in gastric acid and pepsin [58,59].”

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References 129 · Cited by 151

Authors
Verma, S., Goand, U. K., Husain, A., Katekar, R. A., Garg, R., & Gayen, J. R.
Affiliations
Central Drug Research Institute (IN)
Corresponding author
Gayen, Jiaur R.
Venue
Drug Development Research
Publisher
Wiley
Published
2021-05-14
Volume
82
Issue
7
Pages
927-944
ISSN
  • 0272-4391 (ISSN-L)
  • 1098-2299
OpenAlex
W3161474404
Cited by
151
References
129
Citations by year
2026: 33 · 2025: 41 · 2024: 37 · 2023: 26 · 2022: 12 · 2021: 1
FWCI
1.67
Type
journal article
Language
en
Open access
closed
Locations
  • Drug Development Research (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advanced Drug Delivery Systems
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Drug Solubulity and Delivery Systems
  • Life Sciences › Agricultural and Biological Sciences › Food Science › Proteins in Food Systems
Keywords
oral drug delivery, peptide therapeutics, therapeutic proteins, bioavailability enhancement, protein stability, proteolysis, hepatic first-pass metabolism, absorption enhancers, drug carriers, structural modification, drug formulation, self-administration
MeSH terms
Administration, Oral, Biological Availability, Peptides, Proteins, Drug Delivery Systems

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