Bi2S3–Tween 20 Nanodots Loading PI3K Inhibitor, LY294002, for Mild Photothermal Therapy of LoVo Cells In Vitro and In Vivo. Issue 22 (21st September 2018)

• Record Type: Journal Article
• Authors: Song, Li; Dong, Xinghua; Zhu, Shuang; Zhang, Chunfang; Yin, Wenyan; Zhang, Xiao; Liu, Xiangfeng; Gu, Zhanjun
• Is Part Of: Advanced healthcare materials. Volume 7:Issue 22(2018)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2018-09-21
• Subjects: Bi2S3–Tween 20 nanodots -- LY294002 -- mild photothermal therapy -- photothermal‐resistant -- PI3K inhibitors; Biomedical materials -- Periodicals; 610.28
• DOI: 10.1002/adhm.201800830
• Languages: English
• ISSNs: 2192-2640

Abstract

Abstract: Although various types of photothermal agents are developed for photothermal cancer therapy, relatively few photothermal agents exhibit high tumor inhibition rate under relatively mild conditions. Herein, a multifunctional Bi2 S3 –Tween 20 nanoplatform loaded with PI3K inhibitor LY294002 is designed as a novel photothermal agent for inhibitor and photothermal synergistic therapy of tumors under mild photothermal therapy conditions. The LY294002 of PI3K inhibitor, after being loaded by Bi2 S3 –Tween 20 nanodots, exhibits greatly increased drug utilization and reduced side effects on normal tissues. In vivo, Bi2 S3 –Tween 20@LY294002 upon near‐infrared 808 nm laser irradiation shows potent antitumor activity under relatively mild conditions (power density: 0.6 W cm −2 ). Moreover, the mechanism studies also demonstrate that Bi2 S3 –Tween 20@LY294002 potently kills LoVo cancer cells under low‐power near‐infrared light irradiation, by downregulating the expression of heat shock protein 70 (HSP70) so as to increase the sensitivity of tumor cell hyperthermia and activating BAX/BAK‐regulated mitochondrial apoptosis pathway. The results demonstrate that the newly synthesized multifunctional nanoplatform paves a new avenue for accurate therapy of photothermal‐resistant cancer. Abstract : The introduction of LY294002 into the multifunctional Bi2 S3 ‐based nanoplatform can effectively downregulate the expression of heat shock protein 70 and induce apoptosis in tumor cells, so as to achieve a good inhibitory effect on tumor cells under relatively mild conditions. The functionalized Bi2 S3 –Tween 20@LY294002 can be employed for CT/photoacoustic imaging for real‐time monitoring of therapeutic response.