Aptamer-functionalized nanoscale metal-organic frameworks for targeted photodynamic therapy.

Theranostics

Molecular Sciences and Biomedicine Laboratory, State Key Laboratory for Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Collaborative Innovation Center for Chemistry and Molecular Medicine, Hunan University, Changsha 410082, P. R. China.

Published: September 2019

AI Article Synopsis

  • A new targeted photodynamic therapy (PDT) approach using an aptamer-functionalized nanoscale metal-organic framework (NMOF) has shown promising results in cancer treatment.
  • This system combines an aptamer's strong binding capability with Zr-based frameworks and incorporates the photosensitizer TMPyP4 for effective cancer cell targeting.
  • In experiments with HeLa tumor models, the nanosystem led to a significant reduction in tumor cell viability (90% cell death) compared to control, demonstrating its potential for efficient cancer therapy.

Article Abstract

Photodynamic therapy (PDT) has been applied in clinical cancer treatment. Here we report an aptamer-functionalized nanoscale metal-organic framework for targeted PDT. Our nanosystem can be easily prepared and successfully used for targeted PDT with a significantly enhanced therapeutic efficacy and . By combining the strong binding ability between phosphate-terminated aptamers and Zr-based nanoscale metal-organic frameworks (Zr-NMOFs) and the intercalation of photosensitizer TMPyP4 within the G-quadruplex DNA structure, TMPyP4-G4-aptamer-NMOFs were prepared. The characteristics and photodynamic performance of TMPyP4-G4-aptamer-NMOFs were examined after preparation. Then, we studied their stability, specific recognition ability, and phototoxicity . For experiments, the nanosystem was intratumorally injected into a HeLa subcutaneous xenograft tumor mouse model. After irradiation on day 0, mice were further injected with the nanosystem on day 5 and were again subjected to laser irradiation for 30 min. Tumor volumes and body weights of all mice were measured by caliper every 2 days after the treatment. The nanosystem induced 90% cell death of targeted cells. In contrast, the control cells maintained about 40% cell viability at the same concentration of nanosystem. For the experiments, the nanosystem-treated group maintained more than 76% inhibition within the entire experimental period. We have demonstrated that our smart TMPyP4-G4-sgc8-NMOFs nanosystem can be used for targeted cancer therapy with high efficiency.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134922PMC
http://dx.doi.org/10.7150/thno.26768DOI Listing

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