4.6 Article

Ultra-thin metal-organic framework nanosheets for chemo-photodynamic synergistic therapy

期刊

JOURNAL OF MATERIALS CHEMISTRY B
卷 9, 期 20, 页码 4143-4153

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1tb00528f

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资金

  1. National Natural Science Foundation of China [21734002, 51825302, 52021004, 31700827]
  2. State Key Project of Research and Development [2016YFC1100300, 2017YFB0702603]

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The study successfully synthesized a pH-responsive drug delivery system with a two-dimensional structure from bottom to top, demonstrating high anti-tumor activity and excellent biocompatibility in cancer treatment.
Synergistic therapies, such as chemo-photodynamic therapy, have been growing fast because of their efficacy against cancers. Although metal-organic frameworks have been widely studied in the field of drug delivery, the metal-organic frameworks (MOFs) with a two-dimensional (2D) structure integrated by photosensitizers are rarely reported. However, chemo-photodynamic therapy still has limitations such as the inhibitory effect from intracellular glutathione (GSH). In this work, a simple bottom-up synthesis method was used to synthesize a pH-responsive drug delivery system with a 2D MOF structure. In particular, tetracarboxyporphyrin (TCPP) derivatives were coordinated with bivalent copper ions as organic bridging molecules in a polyvinylpyrrolidone (PVP) solution, and copper porphyrin MOFs (Cu-TCPP nanosheets) were synthesized by a hydrothermal method from bottom to top. DOX was loaded onto Cu-TCPP nanosheets by pi-pi stacking with a high drug loading rate of 33%. DOX@Cu-TCPP nanosheets showed pH-responsive DOX releasing behaviour and significant GSH scavenging ability. In addition, the evaluation of in vitro and in vivo treatment showed that DOX@Cu-TCPP nanosheets had high anti-tumor activity and excellent biocompatibility. Therefore, this study opens a new idea for the application of MOF nanosheets in tumor therapy and provides a supporting basis for the treatment of cancers by chemo-photodynamic synergistic therapy.

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