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宝立达 - 自由基损伤防护。

PolyRad - Protection Against Free Radical Damage.

机构信息

Department of Biological Sciences, Missouri University of Science and Technology, Rolla, MO, 65409, USA.

Department of Chemical and Biochemical Engineering, Missouri University of Science and Technology, Rolla, MO, 65409, USA.

出版信息

Sci Rep. 2020 May 20;10(1):8335. doi: 10.1038/s41598-020-65247-y.

Abstract

The effects of elevated levels of radiation contribute to the instability of pharmaceutical formulations in space compared to those on earth. Existing technologies are ineffective at maintaining the therapeutic efficacies of drugs in space. Thus, there is an urgent need to develop novel space-hardy formulations for preserving the stability and efficacy of drug formulations. This work aims to develop a novel approach for the protection of space pharmaceutical drug molecules from the radiation-induced damage to help extend or at least preserve their structural integrity and potency. To achieve this, free radical scavenging antioxidant, Trolox was conjugated on the surface of poly-lactic-co-glycolic acid (PLGA) nanoparticles for the protection of a candidate drug, melatonin that is used as a sleep aid medication in International Space Station (ISS). Melatonin-PLGA-PLL-Trolox nanoparticle as named as PolyRad was synthesized employing single oil in water (o/w) emulsion solvent evaporation method. PolyRad is spherical in shape and has an average diameter of ~600 nm with a low polydispersity index of 0.2. PolyRad and free melatonin (control) were irradiated by UV light after being exposed to a strong oxidant, hydrogen peroxide (HO). Bare melatonin lost ~80% of the active structure of the drug following irradiation with UV light or treatment with HO. In contrast, PolyRad protected >80% of the active structure of melatonin. The ability of PolyRad to protect melatonin structure was also carried out using 0, 1, 5 and 10 Gy gamma radiation. Gamma irradiation showed >98% active structures of melatonin encapsulated in PolyRads. Drug release and effectiveness of melatonin using PolyRad were evaluated on human umbilical vein endothelial cells (HUVEC) in vitro. Non-irradiated PolyRad demonstrated maximum drug release of ~70% after 72 h, while UV-irradiated and HO-treated PolyRad showed a maximum drug release of ~85%. Cytotoxicity of melatonin was carried out using both live/dead and MTT assays. Melatonin, non-radiated PolyRad and irradiated PolyRad inhibited the viability of HUVEC in a dose-dependent manner. Cell viability of melatonin, PolyRad alone without melatonin (PolyRad carrier control), non-radiated PolyRad, and irradiated PolyRad were ~98, 87, 75 and 70%, respectively at a concentration [Formula: see text] 0.01 [Formula: see text] ([Formula: see text]). Taken together, PolyRad nanoparticle provides an attractive formulation platform for preventing damage to pharmaceutical drugs in potential space mission applications.

摘要

与地球上的情况相比,升高的辐射水平会影响药物制剂在太空中的稳定性。现有的技术无法有效维持药物在太空中的治疗效果。因此,迫切需要开发新型太空坚固制剂来保持药物制剂的稳定性和功效。本工作旨在开发一种新方法,以保护太空药物分子免受辐射诱导损伤,帮助延长或至少保持其结构完整性和效力。为了实现这一目标,自由基清除抗氧化剂 Trolox 被接枝到聚乳酸-共-羟基乙酸(PLGA)纳米粒子的表面,以保护候选药物褪黑素,褪黑素在国际空间站(ISS)中用作助眠药物。将褪黑素-PLGA-PLL-Trolox 纳米颗粒命名为 PolyRad,采用单油包水(o/w)乳液溶剂蒸发法合成。PolyRad 呈球形,平均直径约为 600nm,多分散指数低至 0.2。PolyRad 和游离褪黑素(对照)在暴露于强氧化剂过氧化氢(HO)后,用紫外线照射。在紫外线照射或用 HO 处理后,裸褪黑素失去了约 80%的药物活性结构。相比之下,PolyRad 保护了超过 80%的褪黑素的活性结构。还使用 0、1、5 和 10Gy 伽马射线对 PolyRad 保护褪黑素结构的能力进行了评估。伽马辐照显示,包封在 PolyRads 中的褪黑素的活性结构超过 98%。在体外用人脐静脉内皮细胞(HUVEC)评估了 PolyRad 中褪黑素的药物释放和有效性。未经辐照的 PolyRad 在 72 小时后显示最大药物释放约 70%,而经紫外线辐照和 HO 处理的 PolyRad 显示最大药物释放约 85%。使用活/死和 MTT 测定法进行了褪黑素的细胞毒性。褪黑素、未经辐照的 PolyRad 和辐照的 PolyRad 以剂量依赖性方式抑制 HUVEC 的活力。褪黑素、单独的 PolyRad 而没有褪黑素(PolyRad 载体对照)、未经辐照的 PolyRad 和辐照的 PolyRad 的细胞活力分别约为 98%、87%、75%和 70%,在浓度为[公式:见文本]0.01[公式:见文本]([公式:见文本])。综上所述,PolyRad 纳米颗粒为防止潜在太空任务应用中药物损伤提供了有吸引力的制剂平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/709b/7239908/e34a0c88b578/41598_2020_65247_Fig1_HTML.jpg

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