2023
DOI: 10.1039/d2bm01719a
|View full text |Cite
|
Sign up to set email alerts
|

QbD-based fabrication of transferrin-anchored nanocarriers for targeted drug delivery to macrophages and colon cells for mucosal inflammation healing

Abstract: Ulcerative colitis (UC) is a type of colon mucosal inflammation that attracts a plethora of immune cells. Colon drug targeting can be aided by exploiting overexpressed cell surface receptors which...

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
3
0

Year Published

2023
2023
2024
2024

Publication Types

Select...
6

Relationship

2
4

Authors

Journals

citations
Cited by 7 publications
(3 citation statements)
references
References 64 publications
0
3
0
Order By: Relevance
“…In the DSS-induced UC mouse model experiment, it demonstrated promising colon inflammation site-targeting potential based on tissue histopathological score, vascular integrity, and antioxidant levels. 132 Therefore, targeting TfR through drug delivery systems may be a promising active targeting therapy for IBD.…”
Section: Active Targeting-dependent Nps Drug Delivery Systemsmentioning
confidence: 99%
“…In the DSS-induced UC mouse model experiment, it demonstrated promising colon inflammation site-targeting potential based on tissue histopathological score, vascular integrity, and antioxidant levels. 132 Therefore, targeting TfR through drug delivery systems may be a promising active targeting therapy for IBD.…”
Section: Active Targeting-dependent Nps Drug Delivery Systemsmentioning
confidence: 99%
“…In the search for better therapy, the second generation of ligand bound nanocarriers have been developed that target with greater binding affinity to the specific intestinal immune cell or colon cell membrane receptor ( e.g. , CD71, CD301b/macrophage galactose type C-type lectin 2 (MGL2), folate, transferrin, or mannose receptors) [18] , [19] , [20] , [21] . However, it is not clear that ligand-anchored nanocarriers can survive the harsh conditions of the GIT and reach the colon without any dose dumping.…”
Section: Introductionmentioning
confidence: 99%
“…Similarly, we had already prepared QbD‐based d ‐galactose conjugated PLGA (Poly‐Lactic‐co‐Glycolic Acid) nanoparticles [ 26 ] and transferrin‐anchored PLGA nanocarriers. [ 27 ] Here, for the first time, n HA‐GLT NPs had been prepared using the QbD approach. The fabricated n HA‐GLT NPs had all the features of a nanosized carrier for Tofa, including targeted drug delivery, ease of penetration across the skin, sustained drug release, and improved localized effect.…”
Section: Introductionmentioning
confidence: 99%