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Cellular and extracellular proteins near localized photosensitizer refers to the diverse set of biomolecules that serve as substrates for oxidation during Photodynamic Therapy (PDT). Photosensitizers are pharmacological agents that, upon excitation by specific light wavelengths, facilitate the production of reactive oxygen species (ROS), primarily singlet oxygen (Agostinis P, et al., 2011, CA Cancer J Clin) [1]. Because singlet oxygen has an extremely short half-life and a limited diffusion radius of approximately 10 to 20 nanometers, the damage is strictly confined to the proteins and structures in the immediate vicinity of the drug's localization (Moan J., 1990, J Photochem Photobiol B) [2]. This spatial restriction allows for high precision in destroying malignant cells or pathological vasculature while minimizing damage to surrounding healthy tissues (Castano AP, et al., 2004, Photodiagnosis Photodyn Ther) [3]. The specific proteins affected vary depending on whether the photosensitizer accumulates in the mitochondria, lysosomes, endoplasmic reticulum, or plasma membrane (Kessel D, et al., 2003, Photochem Photobiol) [4]. Consequently, this is a functional definition of the PDT effect zone rather than a single molecular entity, encompassing various enzymes, structural proteins, and signaling molecules whose degradation triggers cell death pathways (Robertson CA, et al., 2009, J Photochem Photobiol B) [5]. This approach is widely used in oncology for treating solid tumors and in ophthalmology for conditions like age-related macular degeneration.
Photosensitizers absorb light energy to produce reactive oxygen species, primarily singlet oxygen, which then cause localized oxidative damage to nearby proteins and lipids, leading to cell death and vascular shutdown.
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