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Two-Step Delivery: Exploiting the Partition Coefficient Concept to Increase Intratumoral Paclitaxel Concentrations In vivo Using Responsive Nanoparticles

机译:分两步递送:利用分配系数概念提高使用响应性纳米粒子的体内肿瘤内紫杉醇浓度

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摘要

Drug dose, high local target tissue concentration, and prolonged duration of exposure are essential criteria in achieving optimal drug performance. However, systemically delivered drugs often fail to effectively address these factors with only fractions of the injected dose reaching the target tissue. This is especially evident in the treatment of peritoneal cancers, including mesothelioma, ovarian, and pancreatic cancer, which regularly employ regimens of intravenous and/or intraperitoneal chemotherapy (e.g., gemcitabine, cisplatin, pemetrexed, and paclitaxel) with limited results. Here, we show that a “two-step” nanoparticle (NP) delivery system may address this limitation. This two-step approach involves the separate administration of NP and drug where, first, the NP localizes to tumor. Second, subsequent administration of drug then rapidly concentrates into the NP already stationed within the target tissue. This two-step method results in a greater than 5-fold increase in intratumoral drug concentrations compared to conventional “drug-alone” administration. These results suggest that this unique two-step delivery may provide a novel method for increasing drug concentrations in target tissues.
机译:药物剂量,高局部靶组织浓度和延长暴露时间是获得最佳药物性能的必要标准。然而,全身性递送的药物常常不能有效地解决这些因素,仅注射剂量的一部分到达靶组织。这在腹膜癌(包括间皮瘤,卵巢癌和胰腺癌)的治疗中尤其明显,它们经常采用静脉和/或腹膜内化疗方案(例如吉西他滨,顺铂,培美曲塞和紫杉醇),但效果有限。在这里,我们表明“两步法”纳米颗粒(NP)输送系统可以解决这一局限性。这种两步法涉及将NP和药物分开给药,首先,NP定位于肿瘤。其次,随后的药物给药随后迅速集中到已经位于靶组织内的NP中。与传统的“单纯药物”给药相比,这种两步法可使肿瘤内药物浓度增加超过5倍。这些结果表明,这种独特的两步递送可以提供一种增加靶组织中药物浓度的新颖方法。

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