Self-delivery nanomedicine for chemotherapy sensitized photodynamic therapy

2021 ◽  
Author(s):  
Ling-Shan Liu ◽  
Xiang Zhou ◽  
Rongrong Zheng ◽  
Jia-Qi Huang ◽  
Ren-Jiang Kong ◽  
...  

A chlorine e6 (Ce6) and curcumain (Cur) based self-delivery nanomedicine (CeCu) is prepared for chemotherapy sensitized photodynamic therapy (PDT). The chemotherapeutic agent of Cur could inhibit the TrxR activity to...

2018 ◽  
Vol 1 (4) ◽  
pp. e00063 ◽  
Author(s):  
V.N. Prozorovskiy ◽  
L.V. Kostryukova ◽  
E.I. Korotkevich ◽  
T.I. Torkhovskaya ◽  
G.E. Morozevich ◽  
...  

The possibility of increased internalization of the photosensitizer chlorin e6 in tumor cells was investigatedusing soy phosphatidylcholine nanoparticles 20-30 nm with or without attached peptide containing Asn-Gly-Arg (NGR) motif was studied. This amino acid sequence exhibits affinity to aminopeptidase N (CD13), wich is overexpressed in a number of tumor cells and vessels. Nanoparticles with chlorin e6 were prepared with added of distearoylphosphatidylcholine (DSPE) conjugated through PEG with a hexapeptide containing the NGR sequence, and then were incubated with tumor cells НерG2 and MCF-7. Chlorin e6 accumulation in СD13-negative cells (MCF-7) did not depend on the presence of peptide NGR in nanoparticles. However, for НерG2 cells a twofold increase of chlorine e6 internalization was observed as compared with the same particles without NGR. Differences in the response of these two cell lines, differed in expression of aminopeptidase N (APN), suggest the possibility of this protein using for targeted delivery. The prospectivity of usage of phospholipids nanoparticles conjugated with targeting peptide for photodynamic therapy is discussed, taking into account possible variation of APN expression, inherent for many solid tumors.


2015 ◽  
Vol 12 (3) ◽  
pp. 369
Author(s):  
Pankaj Kumar Chaturvedi ◽  
Yong-Wan Kim ◽  
Sei Jun Han ◽  
Woong Shick Ahn

2010 ◽  
Vol 17 (3) ◽  
pp. 313-321 ◽  
Author(s):  
Kazuhiko Kasuya ◽  
Motohide Shimazu ◽  
Minako Suzuki ◽  
Yukari Kuroiwa ◽  
Jitsuo Usuda ◽  
...  

2017 ◽  
Vol 2 (2) ◽  
pp. 51-54
Author(s):  
Tuğba Kiriş Aydoğan ◽  
Saadet Akbulut ◽  
Bedia Çakmakoğlu ◽  
Elif Sinem Bireller ◽  
Haşim Özgür Tabakoğlu

Micromachines ◽  
2019 ◽  
Vol 10 (1) ◽  
pp. 60 ◽  
Author(s):  
Seemab Iqbal ◽  
Muhammad Fakhar-e-Alam ◽  
M. Atif ◽  
Nasar Ahmed ◽  
Aqrab -ul-Ahmad ◽  
...  

The current study is based on Zn/ZnO nanoparticles photodynamic therapy (PDT) mediated effects on healthy liver cells and cancerous cells. The synthesis of Zn/ZnO nanoparticles was accomplished using chemical and hydrothermal methods. The characterization of the synthesized nanoparticles was carried out using manifold techniques (e.g., transmission electron microscopy (TEM), X-ray diffraction (XRD), and energy dispersive X-ray spectroscopy (EDS)). In order to study the biotoxicity of the grown nanoparticles, they were applied individually and in conjunction with the third generation photosensitiser Fotolon (Chlorine e6) in the in vivo model of the normal liver of the Wister rat, and in the in vitro cancerous liver (HepG2) model both in the dark and under a variety of laser exposures (630 nm, Ultraviolet (UV) light). The localization of ZnO nanoparticles was observed by applying fluorescence spectroscopy on a 1 cm2 selected area of normal liver, whereas the in vitro cytotoxicity and reactive oxygen species (ROS) detection were carried out by calculating the loss in the cell viability of the hepatocellular model by applying a neutral red assay (NRA). Furthermore, a statistical analysis is carried out and it is ensured that the p value is less than 0.05. Thus, the current study has highlighted the potential for applying Zn/ZnO nanoparticles in photodynamic therapy that would lead to wider medical applications to improve the efficiency of cancer treatment and its biological aspect study.


Micromachines ◽  
2020 ◽  
Vol 11 (3) ◽  
pp. 262
Author(s):  
Seemab Iqbal ◽  
Muhammad Fakhar-e-Alam ◽  
M. Atif ◽  
Nasar Ahmed ◽  
Aqrab -ul-Ahmad ◽  
...  

In the published paper [...]


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