Novel nanomedicine with a chemical-exchange saturation transfer effect for breast cancer treatment in vivo

被引:18
|
作者
Jia, Yanlong [1 ]
Wang, Chaochao [2 ]
Zheng, Jiehua [3 ]
Lin, Guisen [1 ]
Ni, Dalong [4 ,5 ]
Shen, Zhiwei [1 ]
Huang, Baoxuan [2 ]
Li, Yan [1 ]
Guan, Jitian [1 ]
Hong, Weida [3 ]
Chen, Yuanfeng [1 ]
Wu, Renhua [1 ]
机构
[1] Shantou Univ, Coll Med, Dept Radiol, Affiliated Hosp 2, Shantou 515041, Peoples R China
[2] East China Univ Sci & Technol, Sch Chem & Mol Engn, Shanghai Key Lab Adv Polymer Mat, 130 Meilong Rd, Shanghai 200237, Peoples R China
[3] Shantou Univ, Affiliated Hosp 2, Dept Gen Surg, Coll Med, Shantou 515041, Peoples R China
[4] Univ Wisconsin Madison, Dept Radiol, Madison, WI 53705 USA
[5] Univ Wisconsin Madison, Dept Med Phys, Madison, WI 53705 USA
基金
中国国家自然科学基金;
关键词
Breast cancer; Magnetic resonance imaging; Chemical exchange saturation transfer; Doxorubicin; Nanomedicine; ENHANCED PERMEABILITY; COPOLYMER MICELLES; CONTRAST AGENTS; CEST-MRI; DELIVERY; CHEMOTHERAPY; NANOPARTICLES; DESIGN; ENZYME;
D O I
10.1186/s12951-019-0557-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background Nanomedicine is a promising new approach to cancer treatment that avoids the disadvantages of traditional chemotherapy and improves therapeutic indices. However, the lack of a real-time visualization imaging technology to monitor drug distribution greatly limits its clinical application. Image-tracked drug delivery is of great clinical interest; it is useful for identifying those patients for whom the therapy is more likely to be beneficial. This paper discusses a novel nanomedicine that displays features of nanoparticles and facilitates functional magnetic resonance imaging but is challenging to prepare. Results To achieve this goal, we synthesized an acylamino-containing amphiphilic block copolymer (polyethylene glycol-polyacrylamide-polyacetonitrile, PEG-b-P(AM-co-AN)) by reversible addition-fragmentation chain transfer (RAFT) polymerization. The PEG-b-P(AM-co-AN) has chemical exchange saturation transfer (CEST) effects, which enable the use of CEST imaging for monitoring nanocarrier accumulation and providing molecular information of pathological tissues. Based on PEG-b-P(AM-co-AN), a new nanomedicine PEG-PAM-PAN@DOX was constructed by nano-precipitation. The self-assembling nature of PEG-PAM-PAN@DOX made the synthesis effective, straightforward, and biocompatible. In vitro studies demonstrate decreased cytotoxicity of PEG-PAM-PAN@DOX compared to free doxorubicin (half-maximal inhibitory concentration (IC50), mean similar to 0.62 mu g/mL vs. similar to 5 mu g/mL), and the nanomedicine more efficiently entered the cytoplasm and nucleus of cancer cells to kill them. Further, in vivo animal experiments showed that the nanomedicine developed was not only effective against breast cancer, but also displayed an excellent sensitive CEST effect for monitoring drug accumulation (at about 0.5 ppm) in tumor areas. The CEST signal of post-injection 2 h was significantly higher than that of pre-injection (2.17 +/- 0.88% vs. 0. 09 +/- 0.75%, p < 0.01). Conclusions The nanomedicine with CEST imaging reflects the characterization of tumors and therapeutic functions has great potential medical applications.
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页数:14
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