2021
DOI: 10.1016/j.jconrel.2020.10.024
|View full text |Cite
|
Sign up to set email alerts
|

Design of a self-unfolding delivery concept for oral administration of macromolecules

Abstract: General rightsCopyright and moral rights for the publications made accessible in the public portal are retained by the authors and/or other copyright owners and it is a condition of accessing publications that users recognise and abide by the legal requirements associated with these rights. Users may download and print one copy of any publication from the public portal for the purpose of private study or research.  You may not further distribute the material or use it for any profit-making activity or commer… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

1
32
0

Year Published

2021
2021
2023
2023

Publication Types

Select...
10

Relationship

0
10

Authors

Journals

citations
Cited by 27 publications
(33 citation statements)
references
References 32 publications
1
32
0
Order By: Relevance
“…Photopolymerization of various monomers in the presence of photocatalytic doxorubicin hydrochloride proved an interesting method to prepare drug-loaded polymeric nanoparticles with higher polymerization rates and good doxorubicin encapsulation efficiency [ 41 ]. Protein nanoparticles were also prepared by various routes to easily entrap and release various anticancer drugs [ 43 ]. They are prepared within biological systems, require fewer production steps, and show high biocompatibility and biodegradability, as compared to synthetic polymers.…”
Section: Introductionmentioning
confidence: 99%
“…Photopolymerization of various monomers in the presence of photocatalytic doxorubicin hydrochloride proved an interesting method to prepare drug-loaded polymeric nanoparticles with higher polymerization rates and good doxorubicin encapsulation efficiency [ 41 ]. Protein nanoparticles were also prepared by various routes to easily entrap and release various anticancer drugs [ 43 ]. They are prepared within biological systems, require fewer production steps, and show high biocompatibility and biodegradability, as compared to synthetic polymers.…”
Section: Introductionmentioning
confidence: 99%
“…Indeed, this region has broadly been described for the increased chances of absorption if compared with the small bowel, in view of the relatively long transit time, the lower concentration of proteolytic enzymes in the lumen, the brush-border membrane and the higher responsiveness of the mucosa to permeation enhancers. More recently, systems able to develop a high surface in close contact with the small intestine epithelium, thus creating a local environment of high concentration and reducing the chance of macromolecule degradation into the lumen, have also been proposed [72]. However, besides entailing the development of broadly new drug-containing formulations, these approaches were generally characterized by reduced bioavailability compared with dosing via the parenteral routes.…”
Section: Goals Of Targeting Drug Release In the Upper Gi Tractmentioning
confidence: 99%
“…With the continuous development of nanotechnology, there are many countermeasures to improve the bioavailability of oral INS [ 7 , 8 ]. pH-responsive delivery systems are the most widely reported INS carriers for targeted delivery and controlled release [ 9 , 10 , 11 , 12 , 13 ].…”
Section: Introductionmentioning
confidence: 99%