文献:Preparation and Characterization of Folate-Targeted Fe3O4 Nanoparticle Codelivering Cisplatin and TFPI-2 Plasmid DNA for Nasopharyngeal Carcinoma Therapy
作者:Juan Zhang, Huanhuan Weng, Xiangwan Miao, Quanming Li, Siqi Wang, Huifen Xie, Tao Liu, Minqiang Xie
文献链接:https://onlinelibrary.wiley.com/doi/full/10.1155/2017/2849801
摘要:
Our previous study has revealed that TFPI-2 is expressed at a low level in NPC cells and tissues [16]. As proof of concept we use FA as targeting molecules, which conjugated to amino-terminated polyethylene glycol (NH2-PEG-COOH) and polyethylenimine (PEI) to perform cationic polymers (FA-PEG-PEI) via amidation. Aldehyde sodium alginate modified Fe3O4 magnetic particles coated cisplatin (SPION-CDDP) was constructed with the above cationic polymer to obtain composite carriers (FA-PEG-PEI@SPION-CDDP), which then adsorbed TFPI-2 pDNA via electrostatic interaction to obtain the FA-targeted, CDDP, and TFPI-2-coated nanocomposites (FA-PEG-PEI@SPION-CDDP-TFPI-2). In vitro assays indicated that the novel compounds possessed excellent load-carrying capacity and drug stability and showed negligible cytotoxicity and enhanced targetability to FR positive (FR+) NPC HNE-1 cells.
研究表明,TFPI-2在鼻咽癌细胞和组织中的表达水平较低。作为概念验证,我们使用FA作为靶向分子,它与氨基封端的聚乙二醇(NH2-PEG-COOH)和聚乙烯亚胺(PEI)共轭,通过酰胺化形成阳离子聚合物(FA-PEG-PEI)。
用上述阳离子聚合物构建了醛-海藻酸钠改性的Fe3O4磁性粒子包覆顺铂(SPION-CDDP),以获得复合载体(FA-PEG-PEI@SPION-CDDP),然后通过静电相互作用吸附TFPI-2 pDNA,获得FA靶向、CDDP和TFPI-2涂覆的纳米复合材料(FA-PEG-PEI@SPION-CDDP-TFPI-2).体外试验表明,新化合物具有优异的承载能力和药物稳定性,对FR阳性(FR+)NPC HNE-1细胞的细胞毒性可以忽略不计,靶向性增强。
相关推荐:
OH-PEG-CH2COOtBu
S-Acetyl-PEG-OH
DA-PEG-OH
Br-PEG-OH
DBCO-PEG-OH
HZ-PEG-OH
Phthalimide-PEG-OH
PLL-PEG-OH
PLGA(10K)-PEG-OH
Silane-PEG-OH
以上文章内容来源各类期刊或文献,如有侵权请联系我们删除!