吉西他滨
体内
胰腺癌
过氧化氢
化学
癌症研究
癌症
医学
内科学
生物
生物化学
生物技术
作者
Santanu Bhattacharya,Xun Gong,Enfeng Wang,Shamit K. Dutta,Joseph R. Caplette,Manki Son,Freddy T. Nguyen,Michael S. Strano,Debabrata Mukhopadhyay
标识
DOI:10.1158/0008-5472.c.6511301.v1
摘要
<div>Abstract<p>Pancreatic ductal adenocarcinoma (PDAC) is a highly desmoplastic cancer with limited treatment options. There is an urgent need for tools that monitor therapeutic responses in real time. Drugs such as gemcitabine and irinotecan elicit their therapeutic effect in cancer cells by producing hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>). In this study, specific DNA-wrapped single-walled carbon nanotubes (SWCNT), which precisely monitor H<sub>2</sub>O<sub>2</sub>, were used to determine the therapeutic response of PDAC cells <i>in vitro</i> and tumors <i>in vivo</i>. Drug therapeutic efficacy was evaluated <i>in vitro</i> by monitoring H<sub>2</sub>O<sub>2</sub> differences <i>in situ</i> using reversible alteration of Raman G-bands from the nanotubes. Implantation of the DNA–SWCNT probe inside the PDAC tumor resulted in approximately 50% reduction of Raman G-band intensity when treated with gemcitabine versus the pretreated tumor; the Raman G-band intensity reversed to its pretreatment level upon treatment withdrawal. In summary, using highly specific and sensitive DNA-SWCNT nanosensors, which can determine dynamic alteration of hydrogen peroxide in tumor, can evaluate the effectiveness of chemotherapeutics.</p>Significance:<p>A novel biosensor is used to detect intratumoral hydrogen peroxide, allowing real-time monitoring of responses to chemotherapeutic drugs.</p></div>
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