Proceedings of the 5th International Symposium on Applied Chemistry 2019 2019
DOI: 10.1063/1.5134595
|View full text |Cite
|
Sign up to set email alerts
|

Freeze-dried chitosan matrices for slow-release of acetogenins extracted from soursop (Annona muricata L.) leaves

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2

Citation Types

0
2
0

Year Published

2021
2021
2021
2021

Publication Types

Select...
1

Relationship

0
1

Authors

Journals

citations
Cited by 1 publication
(2 citation statements)
references
References 21 publications
0
2
0
Order By: Relevance
“…[14][15][16] A few researchers have reported the successful loading of AME extracts into drug delivery carriers to potentiate their cytotoxic effects through their sustained release to the target cells. [17][18][19] For instance, Aruan et al 17 incorporated AME leaf extracts into electrospun polyvinyl alcohol nanofiber scaffolds and demonstrated the cytotoxic effects of the released extracts on the growth of Staphylococcus aureus. Similar effects were exhibited by AME extracts loaded in liposomes and phytosmes 18 and freeze-dried matices.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…[14][15][16] A few researchers have reported the successful loading of AME extracts into drug delivery carriers to potentiate their cytotoxic effects through their sustained release to the target cells. [17][18][19] For instance, Aruan et al 17 incorporated AME leaf extracts into electrospun polyvinyl alcohol nanofiber scaffolds and demonstrated the cytotoxic effects of the released extracts on the growth of Staphylococcus aureus. Similar effects were exhibited by AME extracts loaded in liposomes and phytosmes 18 and freeze-dried matices.…”
Section: Introductionmentioning
confidence: 99%
“…Similar effects were exhibited by AME extracts loaded in liposomes and phytosmes 18 and freeze-dried matices. 19 However, these studies did not report on the release profiles and release kinetics of AME from the drug carriers, which are important for optimizing the drug delivery systems to facilitate the localized delivery of AME at desirable doses over longer durations to cancer cells. Hence, this work studied the release profiles and release kinetics of AME from different AME-eluting electrospun scaffold formulations.…”
Section: Introductionmentioning
confidence: 99%