2015
DOI: 10.1016/j.drudis.2015.03.002
|View full text |Cite
|
Sign up to set email alerts
|

The design of pH-sensitive chitosan-based formulations for gastrointestinal delivery

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

1
45
0

Year Published

2016
2016
2024
2024

Publication Types

Select...
6
4

Relationship

0
10

Authors

Journals

citations
Cited by 131 publications
(46 citation statements)
references
References 61 publications
1
45
0
Order By: Relevance
“…3. Chitosan used as a polymer for microparticles becomes soluble under low pH condition due to protonation of amino group that leads to increase the release of drug at lower pH [18]; it was reported that microspheres almost released all entrapped drug at pH 1.2, however, nearly 70% of the drug was released over 3 h at pH 3.0 [18]. These results are in agreement with the current study showing that increase in pH leads to slower release of the drug.…”
Section: In-vitro Drug Releasesupporting
confidence: 92%
“…3. Chitosan used as a polymer for microparticles becomes soluble under low pH condition due to protonation of amino group that leads to increase the release of drug at lower pH [18]; it was reported that microspheres almost released all entrapped drug at pH 1.2, however, nearly 70% of the drug was released over 3 h at pH 3.0 [18]. These results are in agreement with the current study showing that increase in pH leads to slower release of the drug.…”
Section: In-vitro Drug Releasesupporting
confidence: 92%
“…Furthermore, the SA layer could have prevented the gastric degradation of CH, because the positive charges from CH reduced solubility at low pH. However, at around neutral pH, a higher amount of negative charges sequester positive CH charges, resulting in dissolution of the CH/SA complex and increase in the release of Zn 2+ in the middle enteric region [19]. ZnO/CA and ZnO/CAT showed good release of Zn 2+ in SEF, triggered by the change in the pH.…”
Section: Discussionmentioning
confidence: 99%
“…Since the microenvironment of the atherosclerotic plaque is mildly acidic [26], drug delivery systems sensitive to changes in pH in lesions are designed to improve the targeted delivery of drugs, thereby enhancing drug efficacy [34]. To investigate the pH sensitivity of RAP@PFN1-CD-MNPs, hydrolysis of these NPs was studied under various pH conditions.…”
Section: In Vitro Drug Release Studiesmentioning
confidence: 99%