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Therapeutic use of novel pharmaceutical formulations containing antitumor drugs conjugated to hyaluronic acid in the treatment of tumors

机译:含有与透明质酸结合的抗肿瘤药物的新型药物制剂在肿瘤治疗中的治疗用途

摘要

The present invention describes the new use in the oncologic field of bioconjugates as differentiating agents obtained by the conjugation between hyaluronic acid (HA) and a chemotherapeutic product (identified hereafter with the trade-name ONCOFID®) among which, in particular, Irinotecan, Doxorubicin, Paclitaxel, Cis-platinum and 5-Fluorouracyl (5-FU) for treating primary tumors and metastasis. In particular, the biological behavior is described in terms of action mechanism, efficacy and tolerability of pharmaceutical preparations of derivative of ONCOFID® soluble in water. More specifically, the invention relates to the surprising biological and pharmacological effect demonstrated by formulations based on ONCOFID-S (HA-SN38 conjugates) and ONCOFID-D (HA-Doxorubicin conjugates) in promoting the differentiation of tumoral cells towards a untransformed phenotype, compared with the reference drug Irinotecan (or CPT11 whose active form is represented by SN38) and Doxorubicin.
机译:本发明描述了生物缀合物在肿瘤学领域中的新用途,所述生物缀合物是通过透明质酸(HA)和化学治疗产品(下文中以商品名ONCOFID?)缀合而获得的区分剂,其中特别是伊立替康,阿霉素,紫杉醇,顺铂和5-氟罗西汀(5-FU)用于治疗原发性肿瘤和转移。具体而言,根据水溶性的ONCOFID®衍生物的药物制剂的作用机理,功效和耐受性描述生物学行为。更具体地,本发明涉及通过基于ONCOFID-S(HA-SN38缀合物)和ONCOFID-D(HA-阿霉素缀合物)的制剂在促进肿瘤细胞向未转化表型的分化中所证明的令人惊讶的生物学和药理作用。与参考药物依立替康(或CPT11,其活性形式由SN38表示)和阿霉素。

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