4.6 Article

Evaluation of thermo-triggered drug release in intramuscular-transplanted tumors using thermosensitive polymer-modified liposomes and MRI

期刊

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.nano.2014.09.001

关键词

Drug targeting tumor therapeutics; Liposome; Thermo-sensitive polymer; MRI; Thermo-triggering

资金

  1. Research on Nano-Medicine from the Ministry of Health, Labor and Welfare of Japan
  2. Center of Innovation (COI) Program, Japan Science and Technology Agency (JST), Japan
  3. JSPS
  4. Ministry of Education, Culture, Sports, Science and Technology, Japan
  5. Grants-in-Aid for Scientific Research [26288063, 22107006, 26242049, 25750177] Funding Source: KAKEN

向作者/读者索取更多资源

Multi-modal thermo-sensitive polymer-modified liposomes (MTPLs) containing an anticancer drug, MR contrast agent, and fluorescent dye have been investigated as theranostic nanodevices that can be used to monitor drug delivery in cancer therapy. Here, we measured the physical characteristics of MTPLs, observed the dynamics of MTPLs in vivo, visualized heat-triggered drug release using MRI, and evaluated the treatment effects of the MTPLs with and without heating. In vitro experiments demonstrated that the MTPLs released drugs at temperatures above 41 degrees C. In vivo MTPLs accumulated in tumor tissue, with the accumulation maximized for 4-12 hours. MR signal in the tumor was significantly elevated after mild heating for 15 minutes, indicating release of the contrast agent from the MTPLs was facilitated by heat-triggering. Tumor size after treatment with MTPLs and heating was significantly smaller than those of the control groups. In conclusion, MTPLs with MRI are useful for low-invasive cancer theranostics. From the Clinical Editor: This team of investigators measured the physical characteristics of multi-modal thermo-sensitive polymer-modified liposomes, observed their dynamics in vivo, visualized drug release after heat-triggering using MRI, and evaluated the treatment effects of the MTPLs with and without heating, concluding that their approach may be useful in low-invasive cancer therapy. Crown Copyright (C) 2015 Published by Elsevier Inc. All rights reserved.

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