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pH-sensitive niosomes: Effects on cytotoxicity and on inflammation and pain in murine models

机译:pH敏感的脂质体:对小鼠模型的细胞毒性以及炎症和疼痛的影响

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摘要

pH-sensitive nonionic surfactant vesicles (niosomes) by polysorbate-20 (Tween-20) or polysorbate-20 derivatized by glycine (added as pH sensitive agent), were developed to deliver Ibuprofen (IBU) and Lidocaine (LID). For the physical-chemical characterization of vesicles (mean size, size distribution, zeta potential, vesicle morphology, bilayer properties and stability) dynamic light scattering (DLS), small angle X-ray scattering and fluorescence studies were performed. Potential cytotoxicity was evaluated on immortalized human keratinocyte cells (HaCaT) and on immortalized mouse fibroblasts Balb/3T3. In vivo antinociceptive activity (formalin test) and anti-inflammatory activity tests (paw edema induced by zymosan) in murine models were performed on drug-loaded niosomes. pH-sensitive niosomes were stable in the presence of 0 and 10% fetal bovine serum, non-cytotoxic and able to modify IBU or LID pharmacological activity in vivo. The synthesis of stimuli responsive surfactant, as an alternative to add pH-sensitive molecules to niosomes, could represent a promising delivery strategy for anesthetic and anti-inflammatory drugs.
机译:开发了通过聚山梨酯20(Tween-20)或甘氨酸衍生化的聚山梨酯20(作为pH敏感剂)对pH敏感的非离子表面活性剂囊泡(脂质体),以递送布洛芬(IBU)和利多卡因(LID)。为了对囊泡进行物理化学表征(平均大小,大小分布,ζ电势,囊泡形态,双层性质和稳定性),进行了动态光散射(DLS),小角度X射线散射和荧光研究。在永生化的人角质形成细胞(HaCaT)和永生化的小鼠成纤维细胞Balb / 3T3上评估了潜在的细胞毒性。在载有药物的脂质体上进行了鼠模型中的体内抗伤害感受活性(福尔马林试验)和抗炎活性试验(由酵母聚糖诱导的爪水肿)。 pH敏感的脂质体在0%和10%的胎牛血清存在下稳定,无细胞毒性,并能够在体内改变IBU或LID药理活性。刺激响应性表面活性剂的合成,作为将pH敏感分子添加到脂质体中的替代方法,可能代表麻醉药和消炎药的一种有前途的递送策略。

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