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Lurtotecan liposome is a liposomal formulation of the topoisomerase I inhibitor lurtotecan. Lurtotecan is a synthetic camptothecin analog, structurally related to irinotecan and topotecan, designed to inhibit DNA replication in cancer cells by stabilizing the cleavable complex between topoisomerase I and DNA, leading to double-strand DNA breaks and cell death. The encapsulation of lurtotecan in a liposomal carrier aims to improve its pharmacokinetic profile, enhance tumor targeting via the enhanced permeability and retention (EPR) effect, reduce systemic toxicity compared to non-liposomal formulations, and potentially overcome drug resistance mechanisms. Lurtotecan liposome has been investigated primarily for oncological indications such as ovarian cancer and other solid tumors.
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