2013
DOI: 10.1016/j.aca.2013.07.063
|View full text |Cite
|
Sign up to set email alerts
|

A new method for pH triggered curcumin release by applying poly(l-lysine) mediated nanoparticle-congregation

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

6
25
0

Year Published

2014
2014
2022
2022

Publication Types

Select...
6
2
1

Relationship

1
8

Authors

Journals

citations
Cited by 54 publications
(32 citation statements)
references
References 64 publications
6
25
0
Order By: Relevance
“…ca. 4 ppb (4 μg/L at pH = 7,3) [44]. Curcuminoids were the best extracted by CCMA-H 2 O (1:1:3), 0.355 ± 0.019 mg/g, which is in agreement with that reported by Euterpio et al [35] and Kwon and Chung [45].…”
Section: Hnuclear Overhauser Enhancement Spectroscopy (Noesy) It Revsupporting
confidence: 90%
“…ca. 4 ppb (4 μg/L at pH = 7,3) [44]. Curcuminoids were the best extracted by CCMA-H 2 O (1:1:3), 0.355 ± 0.019 mg/g, which is in agreement with that reported by Euterpio et al [35] and Kwon and Chung [45].…”
Section: Hnuclear Overhauser Enhancement Spectroscopy (Noesy) It Revsupporting
confidence: 90%
“…In Figure S6e–h, the condensed and/or fragmented nuclei are marked by arrows, providing the evidence of cell death33. Cur molecules were thus efficiently released from complexes distributed in cells because of the acidic environment (pH 5.0)31. Consequently, the graphene derivative-Cur complexes accumulated in cells may have enabled continuous Cur release in cancer cells, ensuring sufficient Cur accumulation in order to achieve adequate concentration to continually kill cancer cells14.…”
Section: Resultsmentioning
confidence: 96%
“…The concentration of the released Cur was determined by measuring free Cur. In particular, Cur molecules stacked on graphene derivatives remained stable in basic and near neutral buffers in which about ~9.8% to ~5% Cur was released from graphene derivatives at pH 7.5 or 9 in 24 h, respectively31. In sharp contrast, as much as ~85% of Cur was released from graphene derivatives after 24 h at ~pH 5 (Figure 4d) due to protonation and subsequent reduced interaction between Cur and graphene derivatives in acidic environments.…”
Section: Resultsmentioning
confidence: 98%
“…3B) obtained for the curcumin loaded CD-MOFs crystals dispersed in methanol is identical to that of curcumin in methanol, thus, the interaction between curcumin and the CD-MOFs crystals preserves the photo-physical properties of curcumin. Curcumin has been shown to be a good probe molecule to sense the local environment of heterogeneous systems (Gogoi & Sen Sarma, 2015;Patra & Sleem, 2013). The fluorescence spectra for curcumin encapsulated CD-MOFs and the supernatant washed off curcumin-loaded CD-MOFs were found to be similar and showed a negligible blue shift compared to curcumin in methanol.…”
Section: Spectroscopic Studymentioning
confidence: 96%