4.6 Article

Enhancement of gold-nanocluster-mediated chemotherapeutic efficiency of cisplatin in lung cancer

期刊

JOURNAL OF MATERIALS CHEMISTRY B
卷 9, 期 24, 页码 4895-4905

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1tb00276g

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资金

  1. Strategic Priority Research Program of Chinese Academy of Sciences [XDB36000000]
  2. National Natural Science Foundation of China [51861135103, 21721002, 21773042, 21790394]
  3. Key Research Program of Frontier Sciences, Chinese Academy of Science [QYZDJ-SSW-SLH048]
  4. Beijing Obstetrics and Gynecology Hospital, Capital Medical University [FCYY202019]

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A novel delivery system for cisplatin was constructed using gold nanoclusters and PEGylated cationic peptide, which showed improved cellular uptake and enhanced chemotherapeutic efficiency against cisplatin-resistant lung cancer cells. In vivo assays confirmed the profound anti-tumor efficiency of the system, attributed to deep penetration and accumulation of the nanoscale cisplatin@GC-pKs via the enhanced permeability and retention (EPR) effect in tumor tissues, suggesting a potential treatment strategy for various cisplatin-resistant malignancies.
A novel delivery system for cisplatin was constructed based on electrostatics-mediated assemblies of gold nanoclusters and PEGylated cationic peptide (cisplatin@GC-pKs). Encapsulated cisplatin in the as-formed micelle like assemblies was observed to demonstrate improved cellar uptake and enhanced chemotherapeutic efficiency in the cisplatin-resistant lung cancer cells. In vivo assays further confirmed that cisplatin@GC-pKs had profound anti-tumor efficiency due to deep penetration and accumulation of nanoscale cisplatin@GC-pKs via the enhanced permeability and retention (EPR) effect at tumor tissues. The constructed cisplatin@GC-pKs in this work demonstrated enhanced anti-tumor activity for lung cancer therapy, as well as a potential treatment strategy for a variety of cisplatin-resistance related malignancies.

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