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Encapsulating a Hydrophilic Chemotherapeutic into Rod-like Nanoparticles of a Genetically Encoded Asymmetric Triblock Polypeptide Improves its Efficacy

机译:将亲水性化学疗法封装到遗传编码的不对称三嵌段多肽的棒状纳米粒子中提高其功效。

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摘要

Encapsulating hydrophilic chemotherapeutics into the core of polymeric nanoparticles can improve their therapeutic efficacy by increasing their plasma half-life, tumor accumulation and intracellular uptake, and by protecting them from premature degradation. To achieve these goals, we designed a recombinant asymmetric triblock polypeptide (ATBP) that self-assembles into rod-shaped nanoparticles, and which can be used to conjugate diverse hydrophilic molecules, including chemotherapeutics, into their core. These ATBPs consist of three segments: a biodegradable elastin-like polypeptide, a hydrophobic Tyrosine-rich segment, and a short Cysteine-rich segment, that spontaneously self-assemble into rod-shaped micelles. Covalent conjugation of a structurally diverse set of hydrophilic small molecules, including a hydrophilic chemotherapeutic —gemcitabine— to the Cysteine residues also leads to formation of nanoparticles over a range of ATBP concentrations. Gemcitabine-loaded ATBP nanoparticles have significantly better tumor regression compared to free drug in a murine cancer model. This simple strategy of encapsulation of hydrophilic small molecules by conjugation to an ATBP can be used to effectively deliver a range of water-soluble drugs and imaging agents in vivo.
机译:将亲水性化学疗法封装到聚合物纳米颗粒的核中可通过增加其血浆半衰期,肿瘤积累和细胞内摄取并保护其免于过早降解来提高其治疗功效。为了实现这些目标,我们设计了一种重组的不对称三嵌段多肽(ATBP),该多肽可自组装成棒状纳米颗粒,并可用于将包括化学治疗剂在内的各种亲水性分子缀合到其核心中。这些ATBPs由三个部分组成:可生物降解的弹性蛋白样多肽,疏水性富含酪氨酸的片段和短半胱氨酸富集的片段,它们自发地自组装成棒状胶束。结构多样的一组亲水性小分子(包括亲水性化疗药物吉西他滨)与半胱氨酸残基的共价缀合也导致在一定范围的ATBP浓度下形成纳米颗粒。与游离药物相比,吉非他滨负载的ATBP纳米颗粒在鼠癌模型中具有更好的肿瘤消退作用。通过与ATBP结合来封装亲水性小分子的这种简单策略可用于在体内有效地输送多种水溶性药物和显像剂。

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