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Anti-tumor bioconjugates of hyaluronic acid or its derivatives obtained by indirect chemical complex formation and their use in the pharmaceutical field

机译:通过间接化学配合物形成获得的透明质酸或其衍生物的抗肿瘤生物缀合物及其在制药领域的用途

摘要

The present invention describes a new group of bioconjugates which can be obtained by means of indirect synthesis, via a molecular spacer, between hyaluronic acid and/or its derivatives and drugs with an antitumoral activity belonging to different groups, their preparation process and use in the oncological field. The new derivatives, in relation to the type of bond and Substitution degree, have different physico-chemical properties which improve their tolerability and efficiency and allow a more accurate modulation of the dosage, exploiting an active targeting mechanism.
机译:本发明描述了一组新的生物缀合物,其可以通过分子间隔子通过透明质酸和/或其衍生物与具有不同抗肿瘤活性的药物之间的间接合成而获得,它们的制备方法和用途肿瘤领域。与键的类型和取代度有关的新衍生物具有不同的理化性质,从而利用主动靶向机制提高了它们的耐受性和效率,并允许更精确地调节剂量。

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