Towards Matched Pairs of Porphyrin–ReI/99mTcI Conjugates that Combine Photodynamic Activity with Fluorescence and Radio Imaging. Issue 6 (23rd February 2014)
- Record Type:
- Journal Article
- Title:
- Towards Matched Pairs of Porphyrin–ReI/99mTcI Conjugates that Combine Photodynamic Activity with Fluorescence and Radio Imaging. Issue 6 (23rd February 2014)
- Main Title:
- Towards Matched Pairs of Porphyrin–ReI/99mTcI Conjugates that Combine Photodynamic Activity with Fluorescence and Radio Imaging
- Authors:
- Gianferrara, Teresa
Spagnul, Cinzia
Alberto, Roger
Gasser, Gilles
Ferrari, Stefano
Pierroz, Vanessa
Bergamo, Alberta
Alessio, Enzo - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>We recently prepared two novel water soluble porphyrins bearing a single peripheral chelator, either diethylenetriamine (<bold>1</bold>) or bipyridyl (<bold>2</bold>), tethered to one <italic>meso</italic> position. The preparation of their conjugates with a <italic>fac</italic>‐{<sup>99m</sup>Tc(CO)<sub>3</sub>}<sup>+</sup> fragment and the potential of these resulting conjugates as fluorescence and radio imaging tools were also described. In this work, we focused on the corresponding non‐radioactive analogues that bear the <italic>fac</italic>‐{Re(CO)<sub>3</sub>}<sup>+</sup> fragment (diethylenetriamine <bold>3</bold> and bipyridyl <bold>4</bold>). We report on the uptake, in vitro PDT activity, and cellular localization of Re<sup>I</sup> conjugates <bold>3</bold> and <bold>4</bold> in comparison to the parent porphyrins <bold>1</bold> and <bold>2</bold>. Compounds <bold>1</bold>–<bold>4</bold> have modest or negligible cytotoxicity in the dark against HeLa human cervical cancer cells but become remarkably cytotoxic after exposure to moderate doses of red visible light (590–700 nm). This phototoxicity was found to be directly proportional to the total light dose. Although the four compounds show distinct uptake patterns, they have comparable PDT activity. Confocal fluorescence measurements showed that porphyrin <bold>1</bold> and its Re<sup>I</sup> conjugate <bold>3</bold> have different cellular<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>We recently prepared two novel water soluble porphyrins bearing a single peripheral chelator, either diethylenetriamine (<bold>1</bold>) or bipyridyl (<bold>2</bold>), tethered to one <italic>meso</italic> position. The preparation of their conjugates with a <italic>fac</italic>‐{<sup>99m</sup>Tc(CO)<sub>3</sub>}<sup>+</sup> fragment and the potential of these resulting conjugates as fluorescence and radio imaging tools were also described. In this work, we focused on the corresponding non‐radioactive analogues that bear the <italic>fac</italic>‐{Re(CO)<sub>3</sub>}<sup>+</sup> fragment (diethylenetriamine <bold>3</bold> and bipyridyl <bold>4</bold>). We report on the uptake, in vitro PDT activity, and cellular localization of Re<sup>I</sup> conjugates <bold>3</bold> and <bold>4</bold> in comparison to the parent porphyrins <bold>1</bold> and <bold>2</bold>. Compounds <bold>1</bold>–<bold>4</bold> have modest or negligible cytotoxicity in the dark against HeLa human cervical cancer cells but become remarkably cytotoxic after exposure to moderate doses of red visible light (590–700 nm). This phototoxicity was found to be directly proportional to the total light dose. Although the four compounds show distinct uptake patterns, they have comparable PDT activity. Confocal fluorescence measurements showed that porphyrin <bold>1</bold> and its Re<sup>I</sup> conjugate <bold>3</bold> have different cellular localization patterns in HeLa cells.</p> </abstract> … (more)
- Is Part Of:
- ChemMedChem. Volume 9:Issue 6(2014:Jun.)
- Journal:
- ChemMedChem
- Issue:
- Volume 9:Issue 6(2014:Jun.)
- Issue Display:
- Volume 9, Issue 6 (2014)
- Year:
- 2014
- Volume:
- 9
- Issue:
- 6
- Issue Sort Value:
- 2014-0009-0006-0000
- Page Start:
- 1231
- Page End:
- 1237
- Publication Date:
- 2014-02-23
- Subjects:
- Pharmaceutical chemistry -- Periodicals
615.19005 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1860-7187 ↗
http://www3.interscience.wiley.com/cgi-bin/jhome/110485305 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cmdc.201300501 ↗
- Languages:
- English
- ISSNs:
- 1860-7179
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3172.254000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3440.xml