A polymeric prodrug for non-invasive, real-time reporting drug release based on “turn-on” fluorescent probes

2020 ◽  
Vol 154 ◽  
pp. 104649
Author(s):  
Xiaodan Zhao ◽  
Hengxin Lei ◽  
Yilong Cheng ◽  
Youshen Wu ◽  
Mingming Zhang ◽  
...  
2015 ◽  
Vol 51 (32) ◽  
pp. 6948-6951 ◽  
Author(s):  
Yanfeng Zhang ◽  
Qian Yin ◽  
Jonathan Yen ◽  
Joanne Li ◽  
Hanze Ying ◽  
...  

Anin vitroandin vivodrug-reporting system is developed for real-time monitoring of drug release via the analysis of the concurrently released near-infrared fluorescence dye.


2019 ◽  
Vol 18 (6) ◽  
pp. 1342-1349 ◽  
Author(s):  
Sumit Roy ◽  
Ashim Maity ◽  
Naren Mudi ◽  
Milan Shyamal ◽  
Ajay Misra

Rhodamine and its derivatives have been widely used in designing fluorescent ‘turn on’ cation sensors, while very few rhodamine based fluorescent probes have been reported to date for the detection of anions in water.


2014 ◽  
Vol 352 (1) ◽  
pp. 81-89 ◽  
Author(s):  
Shiran Ferber ◽  
Hemda Baabur-Cohen ◽  
Rachel Blau ◽  
Yana Epshtein ◽  
Einat Kisin-Finfer ◽  
...  

2020 ◽  
Vol 18 (1) ◽  
pp. 124-147
Author(s):  
Arjun Attri ◽  
Deepak Thakur ◽  
Taranpreet Kaur ◽  
Sebastian Sensale ◽  
Zhangli Peng ◽  
...  

2018 ◽  
Vol 6 (30) ◽  
pp. 4963-4971 ◽  
Author(s):  
Tia S. Jarvis ◽  
Felicia M. Roland ◽  
Kyle M. Dubiak ◽  
Paul W. Huber ◽  
Bradley D. Smith

Targeted solvatochromic probe enables non-invasive, time-lapse fluorescence imaging of cell death in cell culture and living frog embryo.


2021 ◽  
Author(s):  
Xue Tian ◽  
Lloyd C. Murfin ◽  
Luling Wu ◽  
Simon E. Lewis ◽  
Tony D. James

Small-molecule based fluorescent probes are increasingly important for the detection and imaging of biological signaling molecules due to their simplicity, high selectivity and sensitivity, whilst being non-invasive, and suitable for real-time analysis of living systems.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Howard Y. Park ◽  
Stephen D. Zoller ◽  
Vishal Hegde ◽  
William Sheppard ◽  
Zachary Burke ◽  
...  

AbstractImplant-associated infections are challenging to diagnose and treat. Fluorescent probes have been heralded as a technologic advancement that can improve our ability to non-invasively identify infecting organisms, as well as guide the inexact procedure of surgical debridement. This study’s purpose was to compare two fluorescent probes for their ability to localize Staphylococcus aureus biofilm infections on spinal implants utilizing noninvasive optical imaging, then assessing the broader applicability of the more successful probe in other infection animal models. This was followed by real-time, fluorescence image-guided surgery to facilitate debridement of infected tissue. The two probe candidates, a labelled antibiotic that targets peptidoglycan (Vanco-800CW), and the other, a labelled antibody targeting the immunodominant Staphylococcal antigen A (1D9-680), were injected into mice with spine implant infections. Mice were then imaged noninvasively with near infrared fluorescent imaging at wavelengths corresponding to the two probe candidates. Both probes localized to the infection, with the 1D9-680 probe showing greater fidelity over time. The 1D9-680 probe was then tested in mouse models of shoulder implant and allograft infection, demonstrating its broader applicability. Finally, an image-guided surgery system which superimposes fluorescent signals over analog, real-time, tissue images was employed to facilitate debridement of fluorescent-labelled bacteria.


2001 ◽  
Vol 7 (S2) ◽  
pp. 1012-1013
Author(s):  
Uyen Tram ◽  
William Sullivan

Embryonic development is a dynamic event and is best studied in live animals in real time. Much of our knowledge of the early events of embryogenesis, however, comes from immunofluourescent analysis of fixed embryos. While these studies provide an enormous amount of information about the organization of different structures during development, they can give only a static glimpse of a very dynamic event. More recently real-time fluorescent studies of living embryos have become much more routine and have given new insights to how different structures and organelles (chromosomes, centrosomes, cytoskeleton, etc.) are coordinately regulated. This is in large part due to the development of commercially available fluorescent probes, GFP technology, and newly developed sensitive fluorescent microscopes. For example, live confocal fluorescent analysis proved essential in determining the primary defect in mutations that disrupt early nuclear divisions in Drosophila melanogaster. For organisms in which GPF transgenics is not available, fluorescent probes that label DNA, microtubules, and actin are available for microinjection.


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