Β‐Ionic Conjugated Chlorin‐Type Photosensitizers Based on Porpholactone: Synthesis, Photophysical Properties, and Photodynamic Activity. Issue 1 (22nd December 2014)
- Record Type:
- Journal Article
- Title:
- Β‐Ionic Conjugated Chlorin‐Type Photosensitizers Based on Porpholactone: Synthesis, Photophysical Properties, and Photodynamic Activity. Issue 1 (22nd December 2014)
- Main Title:
- Β‐Ionic Conjugated Chlorin‐Type Photosensitizers Based on Porpholactone: Synthesis, Photophysical Properties, and Photodynamic Activity
- Authors:
- Ke, Xian‐Sheng
Tang, Juan
Chen, Juan‐Juan
Zhou, Zheng‐Yang
Zhang, Jun‐Long - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Porpholactones and their derivatives have attracted increasing attention for their promising application as photosensitizers. Reduction of the β‐lactone moiety in porpholactone to β‐hemiacetal, named porpholactol, allows the synthesis of chlorin‐type photosensitizers with enhanced near‐infrared absorption as well as β functionalization of water‐soluble conjugates. By employing β‐hydrophilic conjugates terminated by different ionic groups, such as neutral (<bold>ZnL<sub>1</sub></bold>), anionic (<bold>ZnL<sub>2</sub></bold>), zwitterionic (<bold>ZnL<sub>3</sub></bold>), and cationic (<bold>ZnL<sub>4–6</sub></bold>) groups, a series of photosensitizers (<bold>ZnL<sub>1–6</sub></bold>) were synthesized and characterized, and their photophysical properties were studied, including magnetic circular dichroism measurement. The terminal ionic groups on β conjugates influence significantly the cellular uptake of <bold>ZnL<sub>1–6</sub></bold> in the order <bold>ZnL<sub>4–6</sub></bold> (positive charge)&gt;<bold>ZnL<sub>1–3</sub></bold> (negative charge or neutral). Importantly, the photocytotoxicity of <bold>ZnL<sub>1–6</sub></bold> against cancer cells showed IC<sub>50</sub> values down to the sub‐micromolar range and exhibited the same trend as their cellular uptake, clearly revealing the relationship of β‐ionic conjugates, cellular uptake, and intracellular photodynamic therapy (PDT) activity. Furthermore,<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Porpholactones and their derivatives have attracted increasing attention for their promising application as photosensitizers. Reduction of the β‐lactone moiety in porpholactone to β‐hemiacetal, named porpholactol, allows the synthesis of chlorin‐type photosensitizers with enhanced near‐infrared absorption as well as β functionalization of water‐soluble conjugates. By employing β‐hydrophilic conjugates terminated by different ionic groups, such as neutral (<bold>ZnL<sub>1</sub></bold>), anionic (<bold>ZnL<sub>2</sub></bold>), zwitterionic (<bold>ZnL<sub>3</sub></bold>), and cationic (<bold>ZnL<sub>4–6</sub></bold>) groups, a series of photosensitizers (<bold>ZnL<sub>1–6</sub></bold>) were synthesized and characterized, and their photophysical properties were studied, including magnetic circular dichroism measurement. The terminal ionic groups on β conjugates influence significantly the cellular uptake of <bold>ZnL<sub>1–6</sub></bold> in the order <bold>ZnL<sub>4–6</sub></bold> (positive charge)&gt;<bold>ZnL<sub>1–3</sub></bold> (negative charge or neutral). Importantly, the photocytotoxicity of <bold>ZnL<sub>1–6</sub></bold> against cancer cells showed IC<sub>50</sub> values down to the sub‐micromolar range and exhibited the same trend as their cellular uptake, clearly revealing the relationship of β‐ionic conjugates, cellular uptake, and intracellular photodynamic therapy (PDT) activity. Furthermore, using <bold>ZnL<sub>4</sub></bold> as an example, mechanistic studies, such as cell imaging experiments and Western blot analysis for the PDT process, indicate that <bold>ZnL<sub>4</sub></bold> exerts photodynamic activity through apoptosis, which is highly associated with lysosome disruption, mitochondria depolarization, and nuclei condensation.</p> </abstract> … (more)
- Is Part Of:
- ChemPlusChem. Volume 80:Issue 1(2015:Jan.)
- Journal:
- ChemPlusChem
- Issue:
- Volume 80:Issue 1(2015:Jan.)
- Issue Display:
- Volume 80, Issue 1 (2015)
- Year:
- 2015
- Volume:
- 80
- Issue:
- 1
- Issue Sort Value:
- 2015-0080-0001-0000
- Page Start:
- 237
- Page End:
- 252
- Publication Date:
- 2014-12-22
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2192-6506 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cplu.201402356 ↗
- Languages:
- English
- ISSNs:
- 2192-6506
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4358.xml