2020
DOI: 10.1039/d0ra00104j
|View full text |Cite
|
Sign up to set email alerts
|

Design and evaluation of novel thrombin-based GLP-1 analogs with peptidic albumin binding domain for the controlled release of GLP-1

Abstract: Currently, the curative effects of polypeptide drugs are often restricted due to the short in vivo duration of action.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2022
2022
2022
2022

Publication Types

Select...
1

Relationship

0
1

Authors

Journals

citations
Cited by 1 publication
(1 citation statement)
references
References 38 publications
(44 reference statements)
0
1
0
Order By: Relevance
“… 59 Semaglutide forms a high-affinity non-covalent bond with plasma albumin (> 99%), enhancing drug stability. 49 , 60 , 61 Semaglutide distribution does not include crossing the blood-brain barrier. 62 The main elimination routes of semaglutide are thru the urine and feces.…”
Section: Methodsmentioning
confidence: 99%
“… 59 Semaglutide forms a high-affinity non-covalent bond with plasma albumin (> 99%), enhancing drug stability. 49 , 60 , 61 Semaglutide distribution does not include crossing the blood-brain barrier. 62 The main elimination routes of semaglutide are thru the urine and feces.…”
Section: Methodsmentioning
confidence: 99%