Challenges of peptide and protein drug delivery by oral route: Current strategies to improve the bioavailability
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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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].”
From Amidated Pectin/Nanocellulose Hybrid Cryogel System with a pH-Responsive Release Profile for Small Intestinal Delivery (2025) · cites this paper as [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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