scholarly journals Reversibly Extracellular pH Controlled Cellular Uptake and Photothermal Therapy by PEGylated Mixed-Charge Gold Nanostars

Small ◽  
2015 ◽  
Vol 11 (15) ◽  
pp. 1801-1810 ◽  
Author(s):  
Shouju Wang ◽  
Zhaogang Teng ◽  
Peng Huang ◽  
Dingbin Liu ◽  
Ying Liu ◽  
...  
Small ◽  
2015 ◽  
Vol 11 (15) ◽  
pp. 1738-1738 ◽  
Author(s):  
Shouju Wang ◽  
Zhaogang Teng ◽  
Peng Huang ◽  
Dingbin Liu ◽  
Ying Liu ◽  
...  

2017 ◽  
Vol 2 (33) ◽  
pp. 10860-10864 ◽  
Author(s):  
Changshun Hou ◽  
Mengqi Wang ◽  
Liang Guo ◽  
Qingyan Jia ◽  
Jiechao Ge

2021 ◽  
Vol Volume 16 ◽  
pp. 5167-5183
Author(s):  
Jingyi Zhu ◽  
Junxing Yang ◽  
Lingzhou Zhao ◽  
Pingping Zhao ◽  
Jiqin Yang ◽  
...  

2016 ◽  
Vol 4 (23) ◽  
pp. 4216-4226 ◽  
Author(s):  
Du Li ◽  
Yongxing Zhang ◽  
Shihui Wen ◽  
Yang Song ◽  
Yueqin Tang ◽  
...  

A theranostic nanoplatform for in vivo CT imaging and enhanced PTT of tumors is reported.


2009 ◽  
Vol 27 (15_suppl) ◽  
pp. e13528-e13528
Author(s):  
R. Li ◽  
L. Xie ◽  
X. Li ◽  
Q. Liu ◽  
X. Qian ◽  
...  

e13528 Background: A number of studies have reported the superior antitumor effect of nanoparticles loading chemotherapeutics than the free agents, yet the underlying mechanism has not attract enough attention. The extracellular pH of cancer cells is lower than that of the intracellular pH. Due to this pH gradient, weakly basic drug will protonated extracellularly and display decreased intracellular concentration. In this study, we aimed to reveal a new mechanism of PEG-PCL nanoparticles, namely the reversion of physiological drug resistance. Methods: Tetradrine (Tet), an alkaloid isolated from traditional Chinese medicine, was incorporated into the diblock copolymer methoxy poly(ethylene glycol)-polycaprolactone (mPEG-PCL). In vitro cytotoxicity of free Tet and Tet-loaded nanoparticles at pH7.4 and pH6.8 was compared on four different cancer cell lines. Fluorescent particle cellular uptake study was also used. To evaluate the antitumor effect of the nanoparticles in a more complex model rather than monolayer cell culture, we used Histoculture Drug Resistance Assay (HDRA). The in vivo antitumor effect of the nanoparticles was also studied in ICR mice bearing H22 tumor with different in vivo pH values. Results: In vitro cytotoxicity study in four tumor cell lines showed that the cytotoxicity of free Tet decreased significantly (P<0.05) when the extracellular pH decreased from 7.4 to 6.8, while the cytotoxicity of Tet-loaded nanoparticles increased or didn’t change significantly. The possible mechanism may mainly be the endocytosis of nanoparticles, which was proven by fluorescent particle cellular uptake study. HDRA indicated better tissue penetration of nanoparticles over free Tet. As to in vivo study, the mice with in vivo tumor pH 6.8 and treated with Tet-loaded nanoparticles exhibited best tumor inhibit rate and mildest side effect, suggesting that the use of nanoparticles was more preferable than the manipulation of tumor pH by the use of basic water. Conclusions: Our study clearly demonstrated that the mPEG-PCL nanoparticles could overcome the drug resistance caused by low extracellular pH and enhance drug penetration in the tumor tissue, thus increasing the antitumor efficacy of weakly basic agents. No significant financial relationships to disclose.


2018 ◽  
Vol 39 (3) ◽  
pp. 280-286 ◽  
Author(s):  
吴 頔 WU Di ◽  
樊 淼 FAN Miao ◽  
张露云 ZHANG Lu-yun ◽  
邢晶晶 XING Jing-jing ◽  
吕树芳 LYU Shu-fang ◽  
...  

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