Detailed Information

Cited 29 time in webofscience Cited 34 time in scopus
Metadata Downloads

Development of an M cell targeted nanocomposite system for effective oral protein delivery: preparation, in vitro and in vivo characterizationopen access

Authors
Song, Jae GeunLee, Sang HoonHan, Hyo-Kyung
Issue Date
9-Jan-2021
Publisher
BMC
Keywords
Insulin; Oral delivery system; M cell targeting; Nano-carrier; Aminoclay
Citation
JOURNAL OF NANOBIOTECHNOLOGY, v.19, no.1
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF NANOBIOTECHNOLOGY
Volume
19
Number
1
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/5462
DOI
10.1186/s12951-020-00750-y
ISSN
1477-3155
1477-3155
Abstract
BackgroundThere is a strong need for non-invasive and patient-friendly delivery systems of protein drugs for long-term therapy. However, oral delivery of protein drugs is a big challenge due to many barriers including instability in the gastrointestinal (GI) tract and low permeability. To overcome the absorption barriers in GI tract and improve the patient compliance, this study aimed to develop an M cell targeted-nanocomposite delivery system of protein drugs.ResultsAn aminoclay-protein core complex (AC-Ins) was prepared by using insulin as a model protein and then sequentially coated with Ulex europaeus agglutinin 1 (UEA-1) for M-cell targeting and the pH sensitive polymer, Eudragit (R) L100 (EUAC-Ins). All nanoparticles were obtained with a high entrapment efficiency (>90%) and their structural characteristics were confirmed by Fourier transform-infrared spectroscopy, energy dispersive X-ray spectroscopy, and circular dichroism. Among the developed nanoparticles, EUAC-Ins effectively suppressed drug release at pH 1.2, while rapidly released drugs at pH 6.8 due to dissolution of the outer coating layer. The conformational stability of insulin entrapped in EUAC-Ins was well maintained in the presence of proteolytic enzymes. Compared to free insulin, EUAC-Ins increased the membrane transport of insulin by 4.4-fold in M cells. In parallel, oral administration of EUAC-Ins in mice enhanced insulin uptake by 4.1-fold in the intestinal Peyer's patches and 2.6-fold in intestinal epithelium tissues with normal villi, compared to free insulin. Orally administered EUAC-Ins decreased significantly the blood glucose level in diabetic mice, while the effect of oral insulin solution was negligible.ConclusionAn M cell targeted-ternary nanocomposite system obtained by dual coating of the aminoclay-protein core complex with UEA-1 and a pH dependent polymer is promising as an effective oral protein delivery carrier.
Files in This Item
There are no files associated with this item.
Appears in
Collections
College of Pharmacy > Department of Pharmacy > 1. Journal Articles

qrcode

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.

Related Researcher

Researcher Han, Hyo Kyung photo

Han, Hyo Kyung
College of Pharmacy (Department of Pharmacy)
Read more

Altmetrics

Total Views & Downloads

BROWSE