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Preparation Pharmacokinetics Biodistribution Antitumor Efficacy and Safety of Lx2-32c-Containing Liposome

机译:含Lx2-32c脂质体的制备药代动力学生物分布抗肿瘤功效和安全性

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摘要

Lx2-32c is a novel taxane that has been demonstrated to have robust antitumor activity against different types of tumors including several paclitaxel-resistant neoplasms. Since the delivery vehicles for taxane, which include cremophor EL, are all associated with severe toxic effects, liposome-based Lx2-32c has been developed. In the present study, the pharmacokinetics, biodistribution, antitumor efficacy and safety characteristics of liposome-based Lx2-32c were explored and compared with those of cremophor-based Lx2-32c. The results showed that liposome-based Lx2-32c displayed similar antitumor effects to cremophor-based Lx2-32c, but with significantly lower bone marrow toxicity and cardiotoxicity, especially with regard to the low ratio of hypersensitivity reaction. In comparing these two delivery modalities, targeting was superior using the Lx2-32c liposome formulation; it achieved significantly higher uptake in tumor than in bone marrow and heart. Our data thus suggested that the Lx2-32c liposome was a novel alternative formulation with comparable antitumor efficacy and a superior safety profiles to cremophor-based Lx2-32c, which might be related to the improved pharmacokinetic and biodistribution characteristics. In conclusion, the Lx2-32c liposome could be a promising alternative formulation for further development.
机译:Lx2-32c是一种新型紫杉烷,已被证明对多种类型的肿瘤(包括几种耐紫杉醇的肿瘤)具有强大的抗肿瘤活性。由于紫杉烷的递送载体(包括cremophor EL)都具有严重的毒性作用,因此开发了基于脂质体的Lx2-32c。在本研究中,探索了基于脂质体的Lx2-32c的药代动力学,生物分布,抗肿瘤功效和安全性特征,并将其与基于cremophor的Lx2-32c进行了比较。结果表明,基于脂质体的Lx2-32c表现出与基于cremophor的Lx2-32c类似的抗肿瘤作用,但骨髓毒性和心脏毒性显着降低,特别是超敏反应率低。在比较这两种递送方式时,使用Lx2-32c脂质体制剂的靶向效果更好;它在肿瘤中的摄取显着高于骨髓和心脏。因此,我们的数据表明,Lx2-32c脂质体是一种新颖的替代制剂,具有与基于克列莫弗的Lx2-32c相当的抗肿瘤功效和更高的安全性,这可能与药代动力学和生物分布特性的改善有关。总之,Lx2-32c脂质体可能是有希望的替代制剂,可用于进一步开发。

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