Conjugated Polymer Amplified Far‐Red/Near‐Infrared Fluorescence from Nanoparticles with Aggregation‐Induced Emission Characteristics for Targeted In Vivo Imaging. Issue 3 (26th November 2012)
- Record Type:
- Journal Article
- Title:
- Conjugated Polymer Amplified Far‐Red/Near‐Infrared Fluorescence from Nanoparticles with Aggregation‐Induced Emission Characteristics for Targeted In Vivo Imaging. Issue 3 (26th November 2012)
- Main Title:
- Conjugated Polymer Amplified Far‐Red/Near‐Infrared Fluorescence from Nanoparticles with Aggregation‐Induced Emission Characteristics for Targeted In Vivo Imaging
- Authors:
- Ding, Dan
Li, Kai
Qin, Wei
Zhan, Ruoyu
Hu, Yong
Liu, Jianzhao
Tang, Ben Zhong
Liu, Bin - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Fluorescence‐amplified far‐red/near‐infrared (FR/NIR) nanoparticles (NPs) are synthesized by co‐encapsulation of conjugated polymer donor (poly[9, 9‐bis(2‐(2‐(2‐methoxyethoxy)ethoxy)ethyl)fluorenyldivinylene]; PFV) and a fluorogen acceptor (2‐(2, 6‐bis((<italic>E</italic>)‐4‐(phenyl(4′‐(1, 2, 2‐triphenylvinyl)‐[1, 1′‐biphenyl]‐4‐yl)amino)styryl)‐4<italic>H</italic>‐pyran‐4‐ylidene)malononitrile; TPE‐TPA‐DCM) with aggregation‐induced emission (AIE) characteristics using biocompatible bovine serum albumin (BSA) as the encapsulation matrix. The good spectral overlap and close proximity between PFV and TPE‐TPA‐DCM in BSA NPs result in a 5.3‐fold amplified TPE‐TPA‐DCM emission signal via fluorescence resonance energy transfer (FRET). The obtained PFV/TPE‐TPA‐DCM co‐loaded BSA NPs are spherical in shape with a large Stokes shift of ∼223 nm and low cytotoxicity. The BSA matrix allows further functionalization with arginine‐glycine‐aspartic acid (RGD) peptide to yield fluorescent probes for specific recognition of integrin receptor‐overexpressed cancer cells. The advantage of PFV amplified FR/NIR signal from TPE‐TPA‐DCM is further demonstrated in cellular and in vivo imaging using HT‐29 colon cancer cells and a murine hepatoma H<sub>22</sub> tumor‐bearing mouse model, respectively. The high FR/NIR fluorescence and specific cancer targeting ability by RGD surface functionalization make the PFV/TPE‐TPA‐DCM<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Fluorescence‐amplified far‐red/near‐infrared (FR/NIR) nanoparticles (NPs) are synthesized by co‐encapsulation of conjugated polymer donor (poly[9, 9‐bis(2‐(2‐(2‐methoxyethoxy)ethoxy)ethyl)fluorenyldivinylene]; PFV) and a fluorogen acceptor (2‐(2, 6‐bis((<italic>E</italic>)‐4‐(phenyl(4′‐(1, 2, 2‐triphenylvinyl)‐[1, 1′‐biphenyl]‐4‐yl)amino)styryl)‐4<italic>H</italic>‐pyran‐4‐ylidene)malononitrile; TPE‐TPA‐DCM) with aggregation‐induced emission (AIE) characteristics using biocompatible bovine serum albumin (BSA) as the encapsulation matrix. The good spectral overlap and close proximity between PFV and TPE‐TPA‐DCM in BSA NPs result in a 5.3‐fold amplified TPE‐TPA‐DCM emission signal via fluorescence resonance energy transfer (FRET). The obtained PFV/TPE‐TPA‐DCM co‐loaded BSA NPs are spherical in shape with a large Stokes shift of ∼223 nm and low cytotoxicity. The BSA matrix allows further functionalization with arginine‐glycine‐aspartic acid (RGD) peptide to yield fluorescent probes for specific recognition of integrin receptor‐overexpressed cancer cells. The advantage of PFV amplified FR/NIR signal from TPE‐TPA‐DCM is further demonstrated in cellular and in vivo imaging using HT‐29 colon cancer cells and a murine hepatoma H<sub>22</sub> tumor‐bearing mouse model, respectively. The high FR/NIR fluorescence and specific cancer targeting ability by RGD surface functionalization make the PFV/TPE‐TPA‐DCM co‐loaded BSA‐RGD NPs a unique FR/NIR fluorescent probe for cellular imaging and in vivo tumor diagnosis in a high contrast and selective manner.</p> </abstract> … (more)
- Is Part Of:
- Advanced healthcare materials. Volume 2:Issue 3(2013:Mar.)
- Journal:
- Advanced healthcare materials
- Issue:
- Volume 2:Issue 3(2013:Mar.)
- Issue Display:
- Volume 2, Issue 3 (2013)
- Year:
- 2013
- Volume:
- 2
- Issue:
- 3
- Issue Sort Value:
- 2013-0002-0003-0000
- Page Start:
- 500
- Page End:
- 507
- Publication Date:
- 2012-11-26
- Subjects:
- Biomedical materials -- Periodicals
610.28 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2192-2659 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/adhm.201200243 ↗
- Languages:
- English
- ISSNs:
- 2192-2640
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0696.854650
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4211.xml