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Preparation, Characterization, and Pharmacokinetic Study of a Novel Long-Acting Targeted Paclitaxel Liposome with Antitumor Activity

机译:一种具有抗肿瘤活性的新型长效靶向紫杉醇脂质体的制备,表征和药代动力学研究

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Background: Breast cancer is the leading cause of cancer death in women. Chemotherapy to inhibit the proliferation of cancer cells is considered to be the most important therapeutic strategy. The development of long-circulating PEG and targeting liposomes is a major advance in drug delivery. However, the techniques used in liposome preparation mainly involve conventional liposomes, which have a short half-life, high concentrations in the liver and spleen reticuloendothelial system, and no active targeting. Methods: Four kinds of paclitaxel liposomes were prepared and characterized by various analytical techniques. The long-term targeting effect of liposomes was verified by fluorescence detection methods in vivo and in vitro. Pharmacokinetic and acute toxicity tests were conducted in ICR mice to evaluate the safety of different paclitaxel preparations. The antitumor activity of ES-SSL-PTX was investigated in detail using in vitro and in vivo human breast cancer MCF-7 cell models. Results: ER-targeting liposomes had a particle size of 137.93± 1.22 nm and an acceptable encapsulation efficiency of 88.07± 1.25%. The liposome preparation is best stored at 4°C, and is stable for up to 48?hrs. Cytotoxicity test on MCF-7 cells demonstrated the stronger cytotoxic activity of liposomes in comparison to free paclitaxel. We used the near-infrared fluorescence imaging technique to confirm that ES-SSL-PTX was effectively targeted and could quickly and specifically identify the tumor site. Pharmacokinetics and acute toxicity in vivo experiments were carried out. The results showed that ES-SSL-PTX could significantly prolong the half-life of the drug, increase its circulation time in vivo, improve its bioavailability and reduce its toxicity and side effects. ES-SSL-PTX can significantly improve the pharmacokinetic properties of paclitaxel, avoid allergic reaction of the original solvent, increase antitumor efficacy?and reduce drug toxicity and side effects. Conclusion: ES-SSL-PTX has great potential for improving the treatment of breast cancer, thereby improving patient prognosis and quality of life.
机译:背景:乳腺癌是女性死亡的主要原因。化学疗法抑制癌细胞的增殖被认为是最重要的治疗策略。长循环栓和靶向脂质体的发展是药物递送的主要进步。然而,脂质体制剂中使用的技术主要涉及常规脂质体,其在肝脏和脾脏网状内皮系统中具有短的半衰期,高浓度,并且没有活性靶向。方法:制备四种紫杉醇脂质体,其特征在于各种分析技术。通过体内和体外荧光检测方法验证脂质体的长期靶向效果。药代动力学和急性毒性试验在ICR小鼠中进行,评价不同紫杉醇制剂的安全性。使用体外和体内人乳腺癌MCF-7细胞模型详细研究了ES-SSL-PTX的抗肿瘤活性。结果:ER靶向脂质体的粒度为137.93±1.22nm,可接受的封装效率为88.07±1.25%。脂质体制剂最佳地储存在4℃,并且稳定为高达48Ω。与游离紫杉醇相比,MCF-7细胞对MCF-7细胞的细胞毒性试验表明了脂质体的细胞毒性活性更强。我们使用近红外荧光成像技术来证实ES-SSL-PTX有效地靶向,并且可以快速,具体地鉴定肿瘤部位。进行了体内实验中的药代动力学和急性毒性。结果表明,ES-SSL-PTX可以显着延长药物的半衰期,增加其体内循环时间,提高其生物利用度,降低其毒性和副作用。 ES-SSL-PTX可以显着改善紫杉醇的药代动力学性质,避免原始溶剂的过敏反应,增加抗肿瘤功效?并降低药物毒性和副作用。结论:ES-SSL-PTX具有改善乳腺癌治疗的巨大潜力,从而提高患者预后和生活质量。

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