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Pc1-d is an amphiphilic carbohydrate-based Zinc(ii)phthalocyanine (Zn(ii)Pc) derivative being investigated for its potential in photodynamic therapy (PDT). As a photosensitizer, it is designed to generate singlet oxygen upon light activation, which then leads to the destruction of target cells. Research indicates that structural modifications, such as the replacement of oxygen with sulfur in non-peripheral positions, can enhance its photophysical properties, including a bathochromic shift in maximum absorption for deeper tissue penetration, and influence its binding affinity to human serum albumin (HSA) and photodynamic activity against human cancer melanoma cells.
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