1 March 2005 Photodynamic Characterization and In Vitro Application of Methylene Blue-containing Nanoparticle Platforms
Wei Tang, Hao Xu, Raoul Kopelman, Martin A. Philbert
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This article presents the development and characterization of nanoparticles loaded with methylene blue (MB), which are designed to be administered to tumor cells externally and deliver singlet oxygen (1O2) for photodynamic therapy (PDT), i.e. cell kill via oxidative stress to the membrane. We demonstrated the encapsulation of MB, a photosensitizer (PS), in three types of sub-200 nm nanoparticles, composed of polyacrylamide, sol–gel silica and organically modified silicate (ORMOSIL), respectively. Induced by light irradiation, the entrapped MB generated 1O2, and the produced 1O2 was measured quantitatively with anthracene-9,10-dipropionic acid, disodium salt, to compare the effects of different matrices on 1O2 delivery. Among these three different kinds of nanoparticles, the polyacrylamide nanoparticles showed the most efficient delivery of 1O2, but its loading of MB was low. In contrast, the sol–gel nanoparticles had the best MB loading but the least efficient 1O2 delivery. In addition to investigating the matrix effects, a preliminary in vitro PDT study using the MB-loaded polyacrylamide nanoparticles was conducted on rat C6 glioma tumor cells with positive photodynamic results. The encapsulation of MB in nanoparticles should diminish the interaction of this PS with the biological milieu, thus facilitating its systemic administration. Furthermore, the concept of the drug-delivering nanoparticles has been extended to a new type of dynamic nanoplatform (DNP) that only delivers 1O2. This DNP could also be used as a targeted multifunctional platform for combined diagnostics and therapy of cancer.

Wei Tang, Hao Xu, Raoul Kopelman, and Martin A. Philbert "Photodynamic Characterization and In Vitro Application of Methylene Blue-containing Nanoparticle Platforms," Photochemistry and Photobiology 81(2), 242-249, (1 March 2005). https://doi.org/10.1562/2004-05-24-RA-176.1
Received: 22 October 2004; Accepted: 1 November 2004; Published: 1 March 2005

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