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Journal ArticleDOI

Photophysical properties and intracellular imaging of water-soluble porphyrin dimers for two-photon excited photodynamic therapy

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TLDR
Analysis of the photophysical parameters and intracellular imaging data indicates that porphyrin dimers are promising candidates for one-photon and two- photon excited PDT.
Abstract
We have investigated the photophysical properties and intracellular behaviour of a series of hydrophilic conjugated porphyrin dimers. All the dimers exhibit intense linear absorption at 650–800 nm and high singlet oxygen quantum yields (0.5–0.9 in methanol), as required for an efficient sensitiser for photodynamic therapy (PDT). They also exhibit fluorescence at 700–800 nm, with fluorescence quantum yields of up to 0.13 in methanol, and show extremely large two-photon absorption maxima of 8,000–17,000 GM in the near-IR. The dimers aggregate in aqueous solution, but aggregation is reduced by binding to bovine serum albumin (BSA), as manifested by an increase in fluorescence intensity and a sharpening in the emission bands. This process can be regarded as a model for the interaction with proteins under physiological conditions. Confocal fluorescence microscopy of live cells was used to monitor the rate of cellular uptake, intracellular localisation and photostability. Porphyrin dimers with positively charged substituents partition into cells more efficiently than the negatively charged dimers. The photostability of these dimers, in living cells, is significantly better than that of the clinical photosensitiser verteporfin. Analysis of the photophysical parameters and intracellular imaging data indicates that these dimers are promising candidates for one-photon and two-photon excited PDT.

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Citations
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Imaging and photodynamic therapy: mechanisms, monitoring, and optimization.

TL;DR: The basic premise of this review is that a combination of imaging and PDT will provide improved research and therapeutic strategies.
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A review of NIR dyes in cancer targeting and imaging.

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NIR dyes for bioimaging applications

TL;DR: Examples of ongoing NIR fluorophore design strategies as well as their properties and anticipated applications relevant to the bioimaging are presented.
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Imaging intracellular viscosity of a single cell during photoinduced cell death

TL;DR: Insight is provided into the dynamics of diffusion in cells, which is pertinent to drug delivery, cell signalling and intracellular mass transport, and the effect of this viscosity increase is observed directly in the diffusion-dependent kinetics of the photosensitized formation and decay of a key cytotoxic agent.
Journal ArticleDOI

Conjugated porphyrin arrays: synthesis, properties and applications for functional materials.

TL;DR: This review aims to cover the multitude of synthetic methodologies that have been developed for the construction of conjugated porphyrin arrays as well as to summarise their structure-property relationships and use in various applications such as near infrared (NIR) dyes, nonlinear optical materials and electron-conducting molecular wires.
References
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Book

Photodynamic Therapy

C.J. Gomer
TL;DR: A comprehensive review of mechanisms of subcellular and tumor localization of photosensitizing agents, as well as of molecular, cellular, and tumor responses associated with photodynamic therapy, are discussed.
Journal ArticleDOI

Design of Organic Molecules with Large Two-Photon Absorption Cross Sections

TL;DR: The combination of large delta and high fluorescence quantum yield or triplet yield exhibited by molecules developed here offers potential for unprecedented brightness in two-photon fluorescent imaging or enhanced photosensitivity in two -photon sensitization, respectively.
Journal ArticleDOI

Photodynamic therapy: a new antimicrobial approach to infectious disease?

TL;DR: All the available evidence suggests that multi-antibiotic resistant strains are as easily killed by PDT as naive strains, and that bacteria will not readily develop resistance to PDT.
Journal ArticleDOI

Structural Basis of the Drug-Binding Specificity of Human Serum Albumin.

TL;DR: Crystallographic analysis of 17 different complexes of HSA with a wide variety of drugs and small-molecule toxins reveals the precise architecture of the two primary drug-binding sites on the protein, identifying residues that are key determinants of binding specificity and illuminating the capacity of both pockets for flexible accommodation.
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