dspe - mpeg2000修饰的靶向递送鬼臼毒素长循环脂质体:制备、表征和评价。

Langlang Zhang, Rongyu Li, Han Zhang, Xubin Suo, Bohong Guo
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引用次数: 0

摘要

目的:DSPE-mPEG2000是一种磷脂和聚乙二醇偶联物,用于各种生物医学应用,包括药物传递、基因转染和疫苗传递。由于DSPE-mPEG2000的亲疏水性,它可以作为药物载体,将药物包封在脂质体中,提高稳定性和疗效。方法:以DSPE-mPEG2000为修饰材料制备长循环鬼臼毒素脂质体(lc - ptoxo - lps),并对其药代动力学和抗癌活性进行评价。结果:Lc-PTOX-Lps包封率为87.11±1.77%,平均粒径为168.91±7.07 nm,多分散指数(PDI)为0.19±0.04,zeta电位为-24.37±0.36 mV。体外释放研究表明,Lc-PTOX-Lps具有明显的缓释作用。与正常脂质体相比,长循环脂质体表现出更好的稳定性,并表现出显著的缓释特征。药代动力学研究表明,Lc-PTOX-Lps的半衰期延长,体内清除率降低,生物利用度提高。此外,与PTOX相比,Lc-PTOX-Lps对MCF-7细胞具有更好的抗癌作用,对正常细胞的毒性较低。结论:lc - ptoxlp合成方法简单有效,是一种很有前景的抗癌药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DSPE-mPEG2000-Modified Podophyllotoxin Long-Circulating Liposomes for Targeted Delivery: Their Preparation, Characterization, and Evaluation.

Objective: DSPE-mPEG2000 is a phospholipid and polyethylene glycol conjugate used in various biomedical applications, including drug delivery, gene transfection, and vaccine delivery. Due to the hydrophilic and hydrophobic properties of DSPE-mPEG2000, it can serve as a drug carrier, encapsulating drugs in liposomes to enhance stability and efficacy.

Method: In this study, long-circulating podophyllotoxin liposomes (Lc-PTOX-Lps) were prepared using DSPE-mPEG2000 as a modifying material and evaluated for their pharmacokinetics and anticancer activity.

Result: Lc-PTOX-Lps had an encapsulation rate of 87.11±1.77%, an average particle size of 168.91±7.07 nm, a polydispersity index (PDI) of 0.19±0.04, and a zeta potential of -24.37±0.36 mV. In vitro release studies showed that Lc-PTOX-Lps exhibited a significant slow-release effect. The long-circulating liposomes demonstrated better stability compared to normal liposomes and exhibited a significant slow-release profile. Pharmacokinetic studies indicated that Lc-PTOX-Lps had a prolonged half-life, reduced in vivo clearance, and improved bioavailability. Additionally, Lc-PTOX-Lps exhibited better anticancer effects on MCF-7 cells and lower toxicity to normal cells compared to PTOX.

Conclusion: Lc-PTOX-Lps were synthesized using a simple and effective method, and Lc-PTOXLps are promising anticancer agents.

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