4.8 Article

X-ray-responsive polypeptide nanogel for concurrent chemoradiotherapy

期刊

JOURNAL OF CONTROLLED RELEASE
卷 332, 期 -, 页码 1-9

出版社

ELSEVIER
DOI: 10.1016/j.jconrel.2021.02.003

关键词

Polypeptide nanogel; Diselenide bond; X-ray-responsiveness; Chemoradiotherapy; Cancer therapy

资金

  1. National Natural Science Foundation of China [52073280, 52022095, 51973216, 81874224, 51873207, 81773232]
  2. National Key Research and Development Program of China [2016YFC0105106]
  3. Science and Technology Development Program of Shandong Province [2019GSF108092]
  4. Science Foundation of Shandong Province [ZR2017BEM048, ZR2019BH089]
  5. Academic Promotion Program of Shandong First Medical University [2019LJ004, 2020RC002]
  6. Taishan Scholar Construction Project [tsqn201909187]
  7. Youth Innovation Promotion Association of Chinese Academy of Sciences [2019230]

向作者/读者索取更多资源

An X-ray-responsive polypeptide nanogel was developed for on-demand delivery of chemotherapeutic agent triggered by radiotherapy to synergistically improve the efficacy of CCRT with reduced side effects. This smart nanogel provides a promising bridge between chemotherapy and radiotherapy, enhancing the potential application of CCRT in clinic.
Concurrent chemoradiotherapy (CCRT) is a standard treatment regimen for medically inoperable stage III nonsmall-cell lung carcinoma (NSCLC) owing to its superior prognostics compared with the sequential modality. Nevertheless, the current pattern of CCRT still fails to provide satisfactory survival outcome. Furthermore, CCRT is always accompanied by a higher risk of severe side effects, limiting the dose escalation. Herein, an X-rayresponsive polypeptide nanogel (PNG) was developed for on-demand delivery of chemotherapeutic agent triggered by radiotherapy to synergistically improve the efficacy of CCRT with reduced side effects. The smart PNG was formed by crosslinking methoxy poly(ethylene glycol)-block-poly(L-glutamic acid-co-?-2-chloroethyl-Lglutamate) (mPEG-b-P(LG-co-CELG)) with a diselenide (Se-Se) bond. The doxorubicin (DOX)-loaded polypeptide nanogel (PNG/DOX) exhibited accelerated drug release when exposed to X-ray irradiation as a result of Se-Se bond degradation. With prolonged circulation and enhanced intratumoral accumulation in vivo, PNG/DOX combined with X-ray irradiation exhibited better synergistic antitumor efficacy and fewer side effects toward human A549 lung carcinoma-bearing nude mice. The smart X-ray-responsive nanogel provides a promising bridge between chemotherapy and radiotherapy and enhances the potential application of CCRT in clinic.

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