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Development, Characterization, and Ex Vivo Assessment of Elastic Liposomes for Enhancing the Buccal Delivery of Insulinopen access

Authors
Bashyal, SantoshSeo, Jo-EunKeum, TaekwangNoh, GyubinLamichhane, ShrawaniLee, Sangkil
Issue Date
Apr-2021
Publisher
MDPI
Keywords
bile salts; elastic liposomes; porcine buccal tissues; buccal permeability; peptide delivery; buccal delivery
Citation
PHARMACEUTICS, v.13, no.4
Journal Title
PHARMACEUTICS
Volume
13
Number
4
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/69411
DOI
10.3390/pharmaceutics13040565
ISSN
1999-4923
1999-4923
Abstract
Buccal drug delivery is a suitable alternative to invasive routes of drug administration. The buccal administration of insulin for the management of diabetes has received substantial attention worldwide. The main aim of this study was to develop and characterize elastic liposomes and assess their permeability across porcine buccal tissues. Sodium-cholate-incorporated elastic liposomes (SC-EL) and sodium-glycodeoxycholate-incorporated elastic liposomes (SGDC-EL) were prepared using the thin-film hydration method. The prepared liposomes were characterized and their ex vivo permeability attributes were investigated. The distribution of the SC-EL and SGDC-EL across porcine buccal tissues was evaluated using confocal laser scanning microscopy (CLSM). The SGDC-EL were the most superior nanocarriers since they significantly enhanced the permeation of insulin across porcine buccal tissues, displaying a 4.33-fold increase in the permeability coefficient compared with the insulin solution. Compared with the SC-EL, the SGDC-EL were better at facilitating insulin permeability, with a 3.70-fold increase in the permeability coefficient across porcine buccal tissue. These findings were further corroborated based on bioimaging analysis using CLSM. SGDC-ELs showed the greatest fluorescence intensity in buccal tissues, as evidenced by the greater shift of fluorescence intensity toward the inner buccal tissue over time. The fluorescence intensity ranked as follows: SGDC-EL > SC-EL > FITC-insulin solution. Conclusively, this study highlighted the potential nanocarriers for enhancing the buccal permeability of insulin.
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