The combined effect of permeation enhancement and proteolysis inhibition on the systemic exposure of orally administrated peptides: Salcaprozate sodium, soybean trypsin inhibitor, and teriparatide study in pigs
- PMID: 34704013
- PMCID: PMC8524144
- DOI: 10.1016/j.ijpx.2021.100097
The combined effect of permeation enhancement and proteolysis inhibition on the systemic exposure of orally administrated peptides: Salcaprozate sodium, soybean trypsin inhibitor, and teriparatide study in pigs
Abstract
Oral delivery of peptides and proteins is hindered by their rapid proteolysis in the gastrointestinal tract and their inability to permeate biological membranes. Various drug delivery approaches are being investigated and implemented to overcome these obstacles. In the discussed study conducted in pigs, an investigation was undertaken to assess the effect of combination of a permeation enhancer - salcaprozate sodium, and a proteolysis inhibitor - soybean trypsin inhibitor, on the systemic exposure of the peptide teriparatide, following intraduodenal administration. Results demonstrate that this combination achieves significantly higher Cmax and AUC (~10- and ~20-fold respectively) compared to each of these methodologies on their own. It was thus concluded that an appropriate combination of different technological approaches may considerably contribute to an efficient oral delivery of biological macromolecules.
Keywords: GIT, gastrointestinal tract; Oral delivery; PK, pharmacokinetics; PTH, parathyroid hormone; Permeation enhancer; Pharmacokinetics; SBTI, soybean trypsin inhibitor; SNAC; SNAC, salcaprozate sodium; Salcaprozate sodium; Soybean trypsin inhibitor; Teriparatide; hPTH(1–34), teriparatide.
© 2021 The Author(s).
Conflict of interest statement
None.
Figures



Similar articles
-
Intestinal Permeation Enhancers for Oral Delivery of Macromolecules: A Comparison between Salcaprozate Sodium (SNAC) and Sodium Caprate (C10).Pharmaceutics. 2019 Feb 13;11(2):78. doi: 10.3390/pharmaceutics11020078. Pharmaceutics. 2019. PMID: 30781867 Free PMC article. Review.
-
Gastrointestinal Permeation Enhancers for the Development of Oral Peptide Pharmaceuticals.Pharmaceuticals (Basel). 2022 Dec 19;15(12):1585. doi: 10.3390/ph15121585. Pharmaceuticals (Basel). 2022. PMID: 36559036 Free PMC article. Review.
-
Penetration Enhancement Strategies for Intradermal Delivery of Cromolyn Sodium.AAPS PharmSciTech. 2022 Jun 23;23(6):171. doi: 10.1208/s12249-022-02328-3. AAPS PharmSciTech. 2022. PMID: 35739411
-
Physical and barrier changes in gastrointestinal mucus induced by the permeation enhancer sodium 8-[(2-hydroxybenzoyl)amino]octanoate (SNAC).J Control Release. 2022 Dec;352:163-178. doi: 10.1016/j.jconrel.2022.09.034. Epub 2022 Oct 19. J Control Release. 2022. PMID: 36314534
-
Characterization of the physicochemical interactions between exenatide and two intestinal permeation enhancers: Sodium caprate (C10) and salcaprozate sodium (SNAC).Int J Pharm. 2022 Oct 15;626:122131. doi: 10.1016/j.ijpharm.2022.122131. Epub 2022 Aug 24. Int J Pharm. 2022. PMID: 36028084
Cited by
-
Self-assembled short peptides: Recent advances and strategies for potential pharmaceutical applications.Mater Today Bio. 2023 Apr 25;20:100644. doi: 10.1016/j.mtbio.2023.100644. eCollection 2023 Jun. Mater Today Bio. 2023. PMID: 37214549 Free PMC article. Review.
-
Interactions between Soybean Trypsin Inhibitor and Chitosan in an Aqueous Solution.Polymers (Basel). 2023 Mar 23;15(7):1594. doi: 10.3390/polym15071594. Polymers (Basel). 2023. PMID: 37050206 Free PMC article.
-
Insulin-Loaded Soybean Trypsin Inhibitor-Chitosan Nanoparticles: Preparation, Characterization, and Protective Effect Evaluation.Polymers (Basel). 2023 Jun 11;15(12):2648. doi: 10.3390/polym15122648. Polymers (Basel). 2023. PMID: 37376294 Free PMC article.
-
Identification of a Multi-Component Formulation for Intestinal Delivery of a GLP-1/Glucagon Co-agonist Peptide.Pharm Res. 2022 Oct;39(10):2555-2567. doi: 10.1007/s11095-022-03372-1. Epub 2022 Sep 1. Pharm Res. 2022. PMID: 36050547
-
Structure-based design of selective, orally available salt-inducible kinase inhibitors that stimulate bone formation in mice.Proc Natl Acad Sci U S A. 2022 Dec 13;119(50):e2214396119. doi: 10.1073/pnas.2214396119. Epub 2022 Dec 6. Proc Natl Acad Sci U S A. 2022. PMID: 36472957 Free PMC article.
References
-
- Aguirre T.A., Teijeiro-Osorio D., Rosa M., Coulter I.S., Alonso M.J., Brayden D.J. Current status of selected oral peptide technologies in advanced preclinical development and in clinical trials. Adv. Drug Deliv. Rev. 2016;106(Pt B):223–241. doi: 10.1016/j.addr.2016.02.004. https://www.ncbi.nlm.nih.gov/pubmed/26921819 - DOI - PubMed
-
- Alani A.W., Robinson J.R. Mechanistic understanding of oral drug absorption enhancement of cromolyn sodium by an amino acid derivative. Pharm. Res. 2008;25(1):48–54. doi: 10.1007/s11095-007-9438-6. https://www.ncbi.nlm.nih.gov/pubmed/17846867 - DOI - PubMed
-
- Animals, National Research Council (US) Committee for the Update of the Guide for the Care and Use of Laboratory . 2011. Guide for the Care and Use of Laboratory Animals.
-
- Birk Y. Trypsin and chymotrypsin inhibitors from soybeans. Methods Enzymol. 1976;45:700–707. doi: 10.1016/s0076-6879(76)45061-9. https://www.ncbi.nlm.nih.gov/pubmed/1034864 - DOI - PubMed
-
- Brayden D., Creed E., O’Connell A., Leipold H., Agarwal R., Leone-Bay A. Heparin absorption across the intestine: effects of sodium N-[8-(2-hydroxybenzoyl)amino]caprylate in rat in situ intestinal instillations and in Caco-2 monolayers. Pharm. Res. 1997;14(12):1772–1779. doi: 10.1023/a:1012192115828. https://www.ncbi.nlm.nih.gov/pubmed/9453067 - DOI - PubMed
LinkOut - more resources
Full Text Sources
Other Literature Sources