2019
DOI: 10.1016/j.inoche.2019.05.017
|View full text |Cite
|
Sign up to set email alerts
|

Organometallic binuclear Pd(II) complex: Synthesis, crystal structure and in-vitro antitumor activity study

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
3
0

Year Published

2021
2021
2024
2024

Publication Types

Select...
5
2

Relationship

1
6

Authors

Journals

citations
Cited by 9 publications
(3 citation statements)
references
References 21 publications
0
3
0
Order By: Relevance
“…As shown in Figure 4 C-E, the fluorescence intensity of tumors treated with DIR-labeled FCP/HA (referred to FCP-DIR/HA) was significantly higher than the tumors treated with DIR alone. This result suggested that HA contained nanoPDT was selectively taken up into tumor tissues, which was caused by the specific binding of HA and CD44 in the tumor tissue 27 , 31 . These results indicated that the HA-containing nanoPDT could help transport drugs to the tumor site in vivo .…”
Section: Resultsmentioning
confidence: 93%
See 1 more Smart Citation
“…As shown in Figure 4 C-E, the fluorescence intensity of tumors treated with DIR-labeled FCP/HA (referred to FCP-DIR/HA) was significantly higher than the tumors treated with DIR alone. This result suggested that HA contained nanoPDT was selectively taken up into tumor tissues, which was caused by the specific binding of HA and CD44 in the tumor tissue 27 , 31 . These results indicated that the HA-containing nanoPDT could help transport drugs to the tumor site in vivo .…”
Section: Resultsmentioning
confidence: 93%
“…Moreover, due to the switchability of the ligands, the acetic acid coordinated-FCP can form micelles with macromolecules containing carboxyl groups like HA 25 . Besides, HA is well-known to specifically bind to overexpressed CD44 on tumor cells 13 , 24 , facilitating an active targeting ability to tumors (Figure 1 C) 6 , 27 , 28 . Our results showed that the coordination between HA and FCP played a key role in the nanomicellar formation mechanism.…”
Section: Introductionmentioning
confidence: 99%
“…It is noteworthy that, in contrast to traditional chiral chemicals that possess one or more stereogenic centers, planar chiral molecules have seldom been studied as pesticides or human drugs. Obstacles might exist in the preparation of such planar chiral molecules. We have taken advantage of the organocatalytic methods that were previously developed in our group for the synthesis of the enantio-pure planar chiral molecules containing α-aminophosphonate structures …”
Section: Introductionmentioning
confidence: 99%