Carbazole‐Linked Near‐Infrared Aza‐BODIPY Dyes as Triplet Sensitizers and Photoacoustic Contrast Agents for Deep‐Tissue Imaging1. Issue 27 (18th April 2017)
- Record Type:
- Journal Article
- Title:
- Carbazole‐Linked Near‐Infrared Aza‐BODIPY Dyes as Triplet Sensitizers and Photoacoustic Contrast Agents for Deep‐Tissue Imaging1. Issue 27 (18th April 2017)
- Main Title:
- Carbazole‐Linked Near‐Infrared Aza‐BODIPY Dyes as Triplet Sensitizers and Photoacoustic Contrast Agents for Deep‐Tissue Imaging1
- Authors:
- Gawale, Yogesh
Adarsh, Nagappanpillai
Kalva, Sandeep Kumar
Joseph, Joshy
Pramanik, Manojit
Ramaiah, Danaboyina
Sekar, Nagaiyan - Abstract:
- Abstract: Four new N ‐ethylcarbazole‐linked aza‐boron‐dipyrromethene (aza‐BODIPY) dyes (8 a, b and9 a, b ) were synthesized and characterized. The presence of the N ‐ethylcarbazole moiety shifts their absorption and fluorescence spectra to the near‐infrared region, λ ≈650–730 nm, of the electromagnetic spectrum. These dyes possess strong molar absorptivity in the range of 3–4×10 4 m −1 cm −1 with low fluorescence quantum yields. The triplet excited state and singlet oxygen generation of these dyes were enhanced upon iodination at the core position. The core‐iodinated dyes9 a, b showed excellent triplet quantum yields of about 90 and 75 %, with singlet oxygen generation efficiency of about 70 and 60 % relative to that of the parent dyes. Derivatives8 a, b showed dual absorption profiles, in contrast to dyes9 a, b, which had the characteristic absorption band of aza‐BODIPY dyes. DFT calculations revealed that the electron density was spread over the iodine and dipyrromethene plane of9 a, b, whereas in8 a, b the electron density was distributed on the carbazole group and dipyrromethene plane of aza‐BODIPY. The uniqueness of these aza‐BODIPY systems is that they exhibit efficient triplet‐state quantum yields, high singlet oxygen generation yields, and good photostability. Furthermore, the photoacoustic (PA) characteristics of these aza‐BODIPY dyes was explored, and efficient PA signals for8 a were observed relative to blood serum with in vitro deep‐tissue imaging, therebyAbstract: Four new N ‐ethylcarbazole‐linked aza‐boron‐dipyrromethene (aza‐BODIPY) dyes (8 a, b and9 a, b ) were synthesized and characterized. The presence of the N ‐ethylcarbazole moiety shifts their absorption and fluorescence spectra to the near‐infrared region, λ ≈650–730 nm, of the electromagnetic spectrum. These dyes possess strong molar absorptivity in the range of 3–4×10 4 m −1 cm −1 with low fluorescence quantum yields. The triplet excited state and singlet oxygen generation of these dyes were enhanced upon iodination at the core position. The core‐iodinated dyes9 a, b showed excellent triplet quantum yields of about 90 and 75 %, with singlet oxygen generation efficiency of about 70 and 60 % relative to that of the parent dyes. Derivatives8 a, b showed dual absorption profiles, in contrast to dyes9 a, b, which had the characteristic absorption band of aza‐BODIPY dyes. DFT calculations revealed that the electron density was spread over the iodine and dipyrromethene plane of9 a, b, whereas in8 a, b the electron density was distributed on the carbazole group and dipyrromethene plane of aza‐BODIPY. The uniqueness of these aza‐BODIPY systems is that they exhibit efficient triplet‐state quantum yields, high singlet oxygen generation yields, and good photostability. Furthermore, the photoacoustic (PA) characteristics of these aza‐BODIPY dyes was explored, and efficient PA signals for8 a were observed relative to blood serum with in vitro deep‐tissue imaging, thereby confirming its use as a promising PA contrast agent. Abstract : Observation at depth : Carbazole‐linked aza‐boron‐dipyrromethene (aza‐BODIPY) dyes show favorable photophysical properties, as well as efficient triplet and singlet oxygen generation quantum yields. Furthermore, the efficient photoacoustic (PA) signals produced by these dyes makes them excellent candidates for photodynamic therapy and as contrast agents for photoacoustic imaging (see figure). … (more)
- Is Part Of:
- Chemistry. Volume 23:Issue 27(2017)
- Journal:
- Chemistry
- Issue:
- Volume 23:Issue 27(2017)
- Issue Display:
- Volume 23, Issue 27 (2017)
- Year:
- 2017
- Volume:
- 23
- Issue:
- 27
- Issue Sort Value:
- 2017-0023-0027-0000
- Page Start:
- 6570
- Page End:
- 6578
- Publication Date:
- 2017-04-18
- Subjects:
- dyes/pigments -- fluorescence -- imaging agents -- oxygen -- sensitizers
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3765 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chem.201605702 ↗
- Languages:
- English
- ISSNs:
- 0947-6539
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3168.860500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 2129.xml