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Magnetic resonance (MR) imaging is advantageous because it concurrently provides anatomic, functional, and molecular information. MR molecular imaging can combine the high spatial resolution of this established clinical modality with molecular profiling in vivo. However, as a result of the intrinsically low sensitivity of MR imaging, high local concentrations of biological targets are required to generate discernable MR contrast. We hypothesize that the prostate-specific membrane antigen (PSMA), an attractive target for imaging and therapy of prostate cancer, could serve as a suitable biomarker for MR-based molecular imaging. We have synthesized three new high-affinity, low-molecular-weight GdIII-based PSMA-targeted contrast agents containing one to three GdIII chelates per molecule. We evaluated the relaxometric properties of these agents in solution, in prostate cancer cells, and in an in vivo experimental model to demonstrate the feasibility of PSMA-based MR molecular imaging. [ABSTRACT FROM AUTHOR]

Mitochondrial-targeting photosensitizers have been associated with effective photodynamic responses. However, most photosensitizers absorb light between 400 and 700 nm, where light penetration through tissues is limited. Two-photon excitation is a rational approach to improve light penetration through tissues. In this report, the two-photon photophysical properties of a porphyrin-rhodamine B conjugate (TPP-Rh), previously demonstrated to target the mitochondria, were evaluated. The properties studied included: two-photon absorption (TPA) cross sections ( σ2); resonance energy transfer (RET) kinetics and dynamics; and singlet oxygen generation. The conjugation of Rh B to TPP-OH approximately doubled the σ2 of TPP-Rh at 800 nm (40 ± 4 GM) compared with the parent porphyrin, TPP-OH (16 ± 4 GM). Furthermore, the rate of DPBF oxidation by singlet oxygen generated from TPP-Rh was twice as fast compared with that from TPP-OH (73 % versus 33% in 10 min) following two-photon excitation at 800 nm. In addition, a significantly stronger luminescence signal was detected from TPP-Rh, than from TPP-OH at 1270 nm, following two-photon excitation. This study indicates that conjugating photosensitizers to Rh B could provide greater TPA at the near-infrared range in addition to preferential mitochondrial accumulation for improved photodynamic responses. [ABSTRACT FROM AUTHOR]