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Verteporfin-loaded poly(ethylene glycol)-poly(beta-amino ester)- poly(ethylene glycol) triblock micelles for cancer therapy

机译:负载Verteporfin的聚(乙二醇)-聚(β-氨基酯)-聚(乙二醇)三嵌段胶束用于癌症治疗

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摘要

Amphiphilic polymers can be used to form micelles to deliver water-insoluble drugs. A biodegradable poly(ethylene glycol) (PEG)-poly(beta-amino ester) (PBAE)-PEG triblock copolymer was developed that is useful for drug delivery. It was shown to successfully encapsulate and pH-dependently release a water-insoluble, small molecule anti-cancer drug, verteporfin. PEG-PBAE-PEG micelle morphology was also controlled through variations to the hydrophobicity of the central PBAE block of the copolymer in order to evade macrophage uptake. Spherical micelles were 50 nm in diameter, while filamentous micelles were 31 nm in width with an average aspect ratio of 20. When delivered to RAW 264.7 mouse macrophages, filamentous micelles exhibited a 89% drop in cellular uptake percentage and a 5.6-fold drop in normalized geometric mean cellular uptake compared to spherical micelles. This demonstrates the potential of high aspect ratio, anisotropic shaped PEG-PBAE-PEG micelles to evade macrophage-mediated clearance. Both spherical and filamentous micelles also showed therapeutic efficacy in human triple-negative breast cancer and small cell lung cancer cells without requiring photodynamic therapy to achieve an anti-cancer effect. Both spherical and filamentous micelles were more effective in killing lung cancer cells than breast cancer cells at equivalent verteporfin concentrations, while spherical micelles were shown to be more effective than filamentous micelles against both cancer cells. Spherical and filamentous micelles at 5 and 10 μM respective verteporfin concentration resulted in 100% cell killing of lung cancer cells, but both micelles required a higher verteporfin concentration of 20 μM to kill breast cancer cells at the levels of 80% and 50% respectively. This work demonstrates the potential of PEG-PBAE-PEG as a biodegradable, anisotropic drug delivery system as well as the in vitro use of verteporfin-loaded micelles for cancer therapy.
机译:两亲性聚合物可用于形成胶束以递送水不溶性药物。开发了可生物降解的聚(乙二醇)(PEG)-聚(β-氨基酯)(PBAE)-PEG三嵌段共聚物,可用于药物递送。它被证明可以成功地封装并依赖pH释放水不溶性小分子抗癌药物韦替泊芬。 PEG-PBAE-PEG胶束形态也通过改变共聚物中心PBAE嵌段的疏水性来控制,以逃避巨噬细胞的摄取。球形胶束的直径为50 nm,而丝状胶束的宽度为31 nm,平均长径比为20。当递送至RAW 264.7小鼠巨噬细胞时,丝状胶束的细胞摄取百分比下降89%,而胶束微滴下降5.6倍。与球形胶束相比,归一化的几何平均细胞摄取量。这证明了高纵横比的各向异性形状的PEG-PBAE-PEG胶束有可能逃避巨噬细胞介导的清除。球形和丝状胶束在人三阴性乳腺癌和小细胞肺癌细胞中也显示出治疗功效,而无需光动力疗法来达到抗癌作用。在等效维替泊芬浓度下,球形和丝状胶束都比乳腺癌细胞更有效地杀死肺癌细胞,而球形胶束对两个癌细胞都比丝状胶束更有效。分别为5和10μM的Verteporfin浓度的球形和丝状胶束导致100%的肺癌细胞被细胞杀死,但是两个胶束都需要更高的20μM的Verteporfin浓度才能分别杀死80%和50%的乳腺癌细胞。这项工作证明了PEG-PBAE-PEG作为可生物降解的各向异性药物递送系统的潜力,以及在体外使用负载维替泊芬的胶束进行癌症治疗的潜力。

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