In vivo tumor diagnosis and photodynamic therapy via tumoral pH-responsive polymeric micelles

2010 ◽  
Vol 46 (31) ◽  
pp. 5668 ◽  
Author(s):  
Heebeom Koo ◽  
Hyejung Lee ◽  
Sojin Lee ◽  
Kyung Hyun Min ◽  
Min Sang Kim ◽  
...  
2007 ◽  
Vol 364-366 ◽  
pp. 1100-1104 ◽  
Author(s):  
Liang Zhong Xiang ◽  
Fei Fan Zhou

Photoacoustic imaging (also called optoacoustic or thermoacoustic imaging) can image vascularity clearly with simultaneous high contrast and high spatial resolution, and has the potential to be an application for tumor diagnosis and treatment monitoring. In a unique photoacoustic system, a single pulse laser beam was used as the light source for both cancer treatment and for concurrently generating ultrasound signals for photoacoustic imaging. The photoacoustic system was used to detect early tumor on the rat back, and the vascular structure around the tumor could be imaged clearly with optimal contrast. This system was also used to monitoring damage of the vascular structures before, during and after photodynamic therapy of tumor. This work demonstrates that photoacoustic imaging can potentially be used to guide photodynamic therapy and other phototherapies using vascular changes during treatment. Prospective application of photoacoustic imaging is to characterize and monitor the accumulation of gold nanoshells in vivo to guide nanoshell-based thermal tumor therapy.


Theranostics ◽  
2017 ◽  
Vol 7 (10) ◽  
pp. 2746-2756 ◽  
Author(s):  
Xingshu Li ◽  
Bi-Yuan Zheng ◽  
Mei-Rong Ke ◽  
Yongfan Zhang ◽  
Jian-Dong Huang ◽  
...  

2016 ◽  
Vol 4 (19) ◽  
pp. 3377-3386 ◽  
Author(s):  
Li Chen ◽  
Bizheng Chen ◽  
Xiaodong Liu ◽  
Yujie Xu ◽  
Lifen Zhang ◽  
...  

A self-assembled polymeric micelle from multifunctional amphiphilic copolymer with NIR and pH-sensitive groups can be used to monitor the dynamic process of its arriving at the tumor site in real time.


2001 ◽  
Vol 53 (2) ◽  
pp. 155-166 ◽  
Author(s):  
J. Taillefer ◽  
N. Brasseur ◽  
J. E. van Lier ◽  
V. Lenaerts ◽  
D. Le Garrec ◽  
...  

2019 ◽  
Vol 7 (1) ◽  
pp. 211-219 ◽  
Author(s):  
Ai-Lan Lin ◽  
Song-Zi Li ◽  
Cai-Hong Xu ◽  
Xing-Shu Li ◽  
Bi-Yuan Zheng ◽  
...  

A novel stellate mesoporous silica-based pH-responsive nanophotosensitizer can be localized and specifically activated at tumor site for cancer diagnosis and targeted PDT.


Cancers ◽  
2021 ◽  
Vol 14 (1) ◽  
pp. 5
Author(s):  
Rosa Iacobazzi ◽  
Ilaria Arduino ◽  
Roberta Di Fonte ◽  
Angela Lopedota ◽  
Simona Serratì ◽  
...  

Pancreatic ductal adenocarcinoma (PDAC) represents a great challenge to the successful delivery of the anticancer drugs. The intrinsic characteristics of the PDAC microenvironment and drugs resistance make it suitable for therapeutic approaches with stimulus-responsive drug delivery systems (DDSs), such as pH, within the tumor microenvironment (TME). Moreover, the high expression of uPAR in PDAC can be exploited for a drug receptor-mediated active targeting strategy. Here, a pH-responsive and uPAR-targeted Gemcitabine (Gem) DDS, consisting of polymeric micelles (Gem@TpHResMic), was formulated by microfluidic technique to obtain a preparation characterized by a narrow size distribution, good colloidal stability, and high drug-encapsulation efficiency (EE%). The Gem@TpHResMic was able to perform a controlled Gem release in an acidic environment and to selectively target uPAR-expressing tumor cells. The Gem@TpHResMic displayed relevant cellular internalization and greater antitumor properties than free Gem in 2D and 3D models of pancreatic cancer, by generating massive damage to DNA, in terms of H2AX phosphorylation and apoptosis induction. Further investigation into the physiological model of PDAC, obtained by a co-culture of tumor spheroids and cancer-associated fibroblast (CAF), highlighted that the micellar system enhanced the antitumor potential of Gem, and was demonstrated to overcome the TME-dependent drug resistance. In vivo investigation is warranted to consider this new DDS as a new approach to overcome drug resistance in PDAC.


2002 ◽  
Vol 10 (5) ◽  
pp. 429-437 ◽  
Author(s):  
D. Le Garrec ◽  
J. Taillefer ◽  
J.E. Van Lier ◽  
V. Lenaerts ◽  
J.-C. Leroux

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