Prodrug-Loaded Zirconium Carbide Nanosheets as a Novel Biophotonic Nanoplatform for Effective Treatment of Cancer.
Quan LiuZhongjian XieMeng QiuInseob ShimYunlong YangSisi XieQinhe YangDou WangShiyou ChenTaojian FanBo DingZiheng GuoDickson AdahXinhuang YaoYuhua ZhangHong WuZongze WuChaoying WeiHongzhong WangHyeong Seok KimQingshuang ZouQiaoting YanZhen CaiJong Seung KimLi-Ping LiuQizhen ZhangYihai CaoPublished in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2020)
Conventional chemotherapy and photothermal therapy (PTT) face many major challenges, including systemic toxicity, low bioavailability, ineffective tissue penetration, chemotherapy/hyperthermia-induced inflammation, and tumor angiogenesis. A versatile nanomedicine offers an exciting opportunity to circumvent the abovementioned limitations for their successful translation into clinical practice. Here, a promising biophotonic nanoplatform is developed based on the zirconium carbide (ZrC) nanosheet as a deep PTT-photosensitizer and on-demand designed anticancer prodrug SN38-Nif, which is released and activated by photothermia and tumor-overexpressed esterase. In vitro and in vivo experimental evidence shows the potent anticancer effects of the integrated ZrC@prodrug biophotonic nanoplatform by specifically targeting malignant cells, chemotherapy/hyperthermia-induced tumor inflammation, and angiogenesis. In mouse models, the ZrC@prodrug system markedly inhibits tumor recurrence, metastasis, inflammation and angiogenesis. The findings unravel a promising biophotonic strategy for precision treatment of cancer.
Keyphrases
- cancer therapy
- drug delivery
- drug release
- oxidative stress
- photodynamic therapy
- endothelial cells
- papillary thyroid
- high glucose
- diabetic rats
- clinical practice
- mouse model
- locally advanced
- wound healing
- squamous cell
- radiation therapy
- drug induced
- squamous cell carcinoma
- cell proliferation
- combination therapy
- endoplasmic reticulum stress