Evaluation of the hypoglycemic effect of exendin-4's new oral self-nanoemulsifying system in rats
dc.contributor.author | Celik Tekeli, Merve | |
dc.contributor.author | Celebi, Nevin | |
dc.contributor.author | Tekeli, M. Yasin | |
dc.contributor.author | Aktas, Yesim | |
dc.contributor.pubmedID | 33197556 | en_US |
dc.date.accessioned | 2022-09-08T11:04:53Z | |
dc.date.available | 2022-09-08T11:04:53Z | |
dc.date.issued | 2021 | |
dc.description.abstract | The objective of this study is to develop a new self-nanoemulsifying system containing exendin-4 with or without enzyme inhibitor chymostatin and to evaluate the effects of oral administration of exendin-4 and exendin-4/chymostatin loaded self nanoemulsifying system on plasma exendin-4, plasma insulin, blood glucose levels and to compare with the oral and subcutaneous administration of exendin-4 in non-diabetic and streptozotocin-induced type 2 diabetic rats. Exendin-4 and exendin-4/chymostatin loaded self-nanoemulsifying system containing ethyl oleate as the oil phase, Cremophor EL (R)/Labrasol (R) as the surfactants and propylene glycol as the co-solvent were prepared. The mean droplet size, polydispersity index, zeta potential and viscosity of exendin-4 loaded self-nanoemulsifying system were found as 24.28 +/- 0.43 nm, 0.17 +/- 0.01, -1.28 +/- 3.61 mV, 79.60 +/- 3.30 m.Pas, respectively. The mean droplet size, polydispersity index, zeta potential and viscosity of exendin-4/chymostatin loaded self-nanoemulsifying system were found as 20.25 +/- 0.35 nm, 0.11 +/- 0.02, -1.85 +/- 2.49 mV, 100.02 +/- 7.65 m.Pas, respectively according to our previous study. In the present study, we focused on long-term physical stability studies, pharmacokinetic studies and pharmacodynamic studies of prepared self-nanoemulsifying systems. According to the long-term physical stability data, exendin-4 and exendin-4/chymostatin loaded self-nanoemulsifying systems were found stable both at 5 degrees C +/- 3 degrees C and at 25 degrees C +/- 60% RH for 12 months. Exendin-4 and exendin-4/chymostatin loaded self-nanoemulsifying systems increased AUC and C-max values in non-diabetic rats compared to the oral exendin-4 solution. In diabetic rats, exendin-4/chymostatin loaded self nanoemulsifying systems increased C-max values compared to the exendin-4 solution. Exendin-4/chymostatin loaded self-nanoemulsifying system decreased inter-subject variability compared to commercial Byetta (R). At 30th minute after administration of exendin-4 loaded self-nanoemulsifying system, exendin-4/chymostatin loaded self nanoemulsifying system and Byetta (R), blood glucose levels decreased to 23%, 25%, 29%, respectively. It has been shown that pharmacodynamic response is close to Byetta (R) with exendin-4/chymostatin self-nanoemulsifying system oral administration. In conclusion, a self nanoemulsifying system was found to be a suitable carrier system, and the combination with enzyme inhibitor chymostatin is thought to be promising for oral delivery of exendin-4. | en_US |
dc.identifier.issn | 0928-0987 | en_US |
dc.identifier.scopus | 2-s2.0-85097049596 | en_US |
dc.identifier.uri | http://hdl.handle.net/11727/7600 | |
dc.identifier.volume | 158 | en_US |
dc.identifier.wos | 000653635200005 | en_US |
dc.language.iso | eng | en_US |
dc.relation.isversionof | 10.1016/j.ejps.2020.105644 | en_US |
dc.relation.journal | EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Exendin-4 | en_US |
dc.subject | Self-nanoemulsifying system | en_US |
dc.subject | Pharmacokinetics | en_US |
dc.subject | Pharmacodynamics | en_US |
dc.subject | Oral peptide delivery | en_US |
dc.title | Evaluation of the hypoglycemic effect of exendin-4's new oral self-nanoemulsifying system in rats | en_US |
dc.type | article | en_US |
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