Switchable PDT for reducing skin photosensitization by a NIR dye inducing self-assembled and photo-disassembled nanoparticles.

Biomaterials

State Key Laboratory of Pharmaceutical Biotechnology, Medical School of Nanjing University, Nanjing 210093, China; Institute of Drug R&D, Medical School of Nanjing University, Nanjing 210093, China; Jiangsu R&D Platform for Controlled & Targeted Drug Delivery, Nanjing University, Nanjing 210093, China; Jiangsu Key Laboratory for Nano Technology, Nanjing University, Nanjing 210093, China.

Published: November 2016

AI Article Synopsis

  • Photodynamic therapy (PDT) combines light and photosensitizers to kill tumor cells but faces limitations due to skin photosensitivity and distribution issues.
  • A new approach using a hydrophobic Near-infrared dye (IR-780 iodide) enables the creation of switchable PDT (Switch-PDT) agents that effectively control the PDT effect with light.
  • This strategy minimizes skin reactions in animal tests and achieves a 100% tumor inhibition rate, marking a significant advance in PDT applications.

Article Abstract

Photodynamic therapy (PDT) is the combination of light and photosensitizer (PS) to kill tumor cells, which has the potential to meet many currently unmet medical needs. However, the whole body distribution and activatability by sunlight of photosensitizers to induce skin photosensitivity have limited the extensive clinic application of PDT. Herein, a novel strategy is presented to overcome these limitations by using a hydrophobic Near-infared (NIR) dye IR-780 iodide (IR780) to induce the self-assembly of albumin-PS conjugates, as a switchable PDT (Switch-PDT) agent. The PDT effect of PS is effectively inhibited by IR780 and recovered by NIR light irradiation in vitro. This quench/recovery strategy dose not sacrifice the anti-tumor ability in vivo, and the combined PDT and PTT (photothermal) effect contributes a very effective tumor inhibition rate of 100%. More importantly, the PDT effect is significantly suppressed after intravenous administration in mice or subcutaneous administration in rabbits as exhibited by the negligible skin response, while traditional PDT agent arouses severe skin erythema and edema. To the best of our knowledge, the switchable PDT is the first time to be used to eradicate the skin photosensitization of PS in vivo.

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Source
http://dx.doi.org/10.1016/j.biomaterials.2016.08.037DOI Listing

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