A redox-responsive organogel based on a selenium-containing low molecular mass gelator

2020 ◽  
Vol 44 (1) ◽  
pp. 24-28 ◽  
Author(s):  
Haojie Zhang ◽  
Xiuping Lu ◽  
Zhao Chen ◽  
Jianzhong Jiang ◽  
Yukai Chen

A redox-responsive low molecular mass gelator (Chol-Se) with selenium as its redox-active center was designed and synthesized. Responsive transformation of Chol-Se in ethyl acetate between the gelation and solution was achieved.

2018 ◽  
Vol 54 (92) ◽  
pp. 12986-12989 ◽  
Author(s):  
Michael Harris ◽  
Jacek L. Kolanowski ◽  
Edward S. O’Neill ◽  
Céline Henoumont ◽  
Sophie Laurent ◽  
...  

A novel, reversible redox-active MRI probe, GdNR1, has been developed based on the biologically-inspired nicotinimidium redox switch.


1994 ◽  
Vol 39 (11-12) ◽  
pp. 663-667 ◽  
Author(s):  
R. A. Shalliker ◽  
P. E. Kavanagh ◽  
I. M. Russell

2017 ◽  
Vol 23 (59) ◽  
pp. 14860-14865 ◽  
Author(s):  
Shan She ◽  
Zehuan Huang ◽  
Panchao Yin ◽  
Aruuhan Bayaguud ◽  
Hongli Jia ◽  
...  

2008 ◽  
Vol 44 (3) ◽  
pp. 274-283 ◽  
Author(s):  
Brandon J. Reeder ◽  
Francesca Cutruzzola ◽  
Maria Giulia Bigotti ◽  
Robert C. Hider ◽  
Michael T. Wilson

2016 ◽  
Vol 52 (38) ◽  
pp. 6479-6481 ◽  
Author(s):  
Tomoki Ogoshi ◽  
Tomohiro Akutsu ◽  
Yasuo Shimada ◽  
Tada-aki Yamagishi

Pillar[5]arene with one benzoquinone formed weak complex with a guest, while pillar[5]arene containing one hydroquinone strongly captured the guest.


2008 ◽  
Vol 318 (2) ◽  
pp. 397-404 ◽  
Author(s):  
Jing Liu ◽  
Junlin Yan ◽  
Xuanwei Yuan ◽  
Kaiqiang Liu ◽  
Junxia Peng ◽  
...  

Molecules ◽  
2019 ◽  
Vol 24 (20) ◽  
pp. 3751 ◽  
Author(s):  
Tyler K. T. Smith ◽  
Zaina Kahiel ◽  
Nicholas D. LeBlond ◽  
Peyman Ghorbani ◽  
Eliya Farah ◽  
...  

Activation of the transcription factor liver X receptor (LXR) has beneficial effects on macrophage lipid metabolism and inflammation, making it a potential candidate for therapeutic targeting in cardiometabolic disease. While small molecule delivery via nanomedicine has promising applications for a number of chronic diseases, questions remain as to how nanoparticle formulation might be tailored to suit different tissue microenvironments and aid in drug delivery. In the current study, we aimed to compare the in vitro drug delivering capability of three nanoparticle (NP) formulations encapsulating the LXR activator, GW-3965. We observed little difference in the base characteristics of standard PLGA-PEG NP when compared to two redox-active polymeric NP formulations, which we called redox-responsive (RR)1 and RR2. Moreover, we also observed similar uptake of these NP into primary mouse macrophages. We used the transcript and protein expression of the cholesterol efflux protein and LXR target ATP-binding cassette A1 (ABCA1) as a readout of GW-3956-induced LXR activation. Following an initial acute uptake period that was meant to mimic circulating exposure in vivo, we determined that although the induction of transcript expression was similar between NPs, treatment with the redox-sensitive RR1 NPs resulted in a higher level of ABCA1 protein. Our results suggest that NP formulations responsive to cellular cues may be an effective tool for targeted and disease-specific drug release.


2007 ◽  
Vol 32 (10) ◽  
pp. 1640-1645 ◽  
Author(s):  
Rudy J. Castellani ◽  
Paula I. Moreira ◽  
Gang Liu ◽  
Jon Dobson ◽  
George Perry ◽  
...  

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