Enhanced luminescence and stability of TFMDSA nanoparticles polymer-induced aggregation for bioimaging.

J Mater Chem B

State Key Laboratory of Supramolecular Structure and Materials, Department of Chemistry, Jilin University, Qianjin Street No. 2699, Changchun, 130012, P. R. China.

Published: December 2024

AI Article Synopsis

  • Fluorescence imaging is crucial in life sciences, but creating stable and efficient nanomaterials for bioimaging is a challenge.
  • The researchers synthesized mPEG-PCL@TFMDSA and mPEG-PLLA@TFMDSA nanoparticles, improving luminescence efficiency through polymer-induced aggregation.
  • These nanoparticles showed great optical stability, low cytotoxicity, and better internalization by HeLa cells, indicating their potential as biofluorescent probes for cancer diagnosis and biomedical use.

Article Abstract

In recent years, fluorescence imaging has occupied a very important position in the life science and biomedical fields. However, achieving nanomaterials for bioimaging with both high fluorescence quantum efficiency and high stability remains a significant challenge. Herein, we synthesized mPEG-PCL@TFMDSA and mPEG-PLLA@TFMDSA nanoparticles using polymer-induced aggregation. This method significantly enhanced the luminescence efficiency of TFMDSA nanoparticles in solution, attributed to improved intermolecular interactions and restricted molecular vibrations. The resulting nanoparticles exhibited exceptional optical stability over a period of seven days and demonstrated low cytotoxicity towards HeLa cells, making them highly suitable for bioimaging applications. Cellular uptake studies indicated that these nanoparticles were more efficiently internalized by HeLa cells compared to their amorphous counterparts, likely due to their unique square morphology. Our findings highlight the potential of polymer-induced aggregation in enhancing the optical properties and stability of TFMDSA nanomaterials, suggesting their promise as biofluorescent probes for cancer diagnosis and other biomedical applications.

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Source
http://dx.doi.org/10.1039/d4tb01825gDOI Listing

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