Figure 3. Fluorescence imaging of subcutaneous IGROV1 tumour-bearing mice, 10 min and 5 h after IV injection of the probes (dissolved in PBS 10 mm, pH 7.4, with 10 % DMSO, 10 % EtOH), at 10 nmol Cy5 per mouse. The images are acquired and presented with the same camera settings, with the fluorescence
Activatable probes for non-invasive small animal fluorescence imaging
✍ Scribed by Isabelle Texier; Jésus Razkin; Véronique Josserand; Didier Boturyn; Pascal Dumy; Jean-Luc Coll; Philippe Rizo
- Book ID
- 103856109
- Publisher
- Elsevier Science
- Year
- 2007
- Tongue
- English
- Weight
- 348 KB
- Volume
- 571
- Category
- Article
- ISSN
- 0168-9002
No coin nor oath required. For personal study only.
✦ Synopsis
Fluorescence tomography today appears as a complementary imaging modality for assessing molecular processes in small living animals. A new design of fluorescent activatable units for the imaging of cellular internalization of probes is proposed. Disulfide bridges are used as intracellular cleavable bounds for fluorescence activation. These units are not activated in blood, neither in vitro nor in mouse, but specifically in the presence of lysed cells or a chemical reducer. We therefore expect that the use of such activatable units, grafted to targeting moieties, will improve significantly the contrast of images obtained in the future.
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