期刊
NANOSCALE HORIZONS
卷 7, 期 4, 页码 403-413出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1nh00632k
关键词
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资金
- Guangzhou Key Research and Development Program of China [202103000094]
- Guangdong Provincial Natural Science Foundation of China [2021A1515010605]
- Zhejiang Provincial Natural Science Foundation of China [LR19E030001]
- National Natural Science Foundation of China [51761145021]
This research proposes a new concept of contrary contrast-MRI (CC-MRI) and develops a tumor microenvironment dual responsive contrast agent that can provide contrary MRI signals between normal tissues and diseased tissues. This contrast agent significantly enhances the contrast between tumors and normal tissues, and also has tumor targetability and controlled chemotherapy release with reduced side effects.
Development of magnetic resonance imaging (MRI) contrast agents (CAs) is still one of the research hotspots due to the inherent limitations of T-1- or T-2-weighted CAs and T-1/T-2 dual-mode CAs. To dramatically enhance the MRI contrast between tumors and normal tissues, we propose a new concept of contrary contrast-MRI (CC-MRI), whose specific definition is that CC-MRI CAs present a positive or negative signal at normal tissues, but show contrary signals at diseased tissues. To realize CC-MRI of tumors, we designed and developed a tumor microenvironment (TME) dual responsive CA (i.e., SA-FeGdNP-DOX@mPEG), which is almost not responsive under normal physiological conditions, but highly responsive to the acidic and reductive TME. Our SA-FeGdNP-DOX@mPEG shows a negative MRI signal under normal physiological conditions due to the high r(2) value (336.9 mM(-1) s(-1)) and high r(2)/r(1) ratio (18.4), but switches to a positive MRI signal in the TME because of the high r(1) value (20.32 mM(-1) s(-1)) and low r(2)/r(1) ratio (7.2). Our TME dual responsive SA-FeGdNP-DOX@mPEG significantly enhanced the contrast of MR images between tumors and livers, and the Delta SNR difference reached 501%. In addition, our SA-FeGdNP-DOX2@mPEG2 with tumor targetability and controlled DOX release responding to the TME was also used for tumor-specific chemotherapy with reduced side effects.
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