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          DSPE-PEG-NHS介導(dǎo)構(gòu)建PEI-PEG-DSPE復(fù)合物用于高效CpG遞送的免疫激活研究
          發(fā)布時(shí)間:2025-07-04     作者:kx   分享到:

          文獻(xiàn):脂質(zhì)聚乙烯亞胺結(jié)合物作為CpG寡脫氧核苷酸生物相容性載體對(duì)巨噬細(xì)胞的評(píng)價(jià)

          鏈接:https://link.springer.com/article/10.1007/s12257-020-0366-1

          作者:楊智媛,崔恩瑞,尤佳妍&穆慧靜 

          節(jié)選:

          摘要

          鑒于CpG寡脫氧核苷酸(CpG)具有強(qiáng)大的免疫刺激作用,開(kāi)發(fā)CpG載體是實(shí)現(xiàn)高效癌癥免疫*的先決條件。本研究將1,2-二硬脂酰-sn-甘油-3-磷酸乙醇胺-N-[羥基琥珀酰亞胺(聚乙二醇)] (DSPE-PEG-NHS) 與聚乙烯亞胺 (PEI) 偶聯(lián),開(kāi)發(fā)出一種PEI-PEG-DSPE偶聯(lián)物,可作為生物相容性的高效CpG載體。我們開(kāi)發(fā)了五種PEIPEG-DSPE偶聯(lián)物,每種偶聯(lián)物的PEI分子量不同,DSPEPEG的修飾程度也不同,均表現(xiàn)出顯著較低的細(xì)胞毒性。具體而言,與通過(guò)天然PEI遞送CpG相比,以摩爾比0.1遞送PEI (25 kDa)-PEG-DSPE和DSPE-PEG-NHS/(PEI的胺基)可導(dǎo)致RAW264.7細(xì)胞對(duì)CpG的吸收更高,這可能是由于存在疏水性脂質(zhì)部分。此外,PEI-PEG-DSPE/CpG復(fù)合物可誘導(dǎo)RAW264.7細(xì)胞顯著分泌細(xì)胞因子(TNF-α),其作用與PEI/CpG復(fù)合物相當(dāng)。因此,PEI-PEG-DSPE偶聯(lián)物可作為生物相容性的高效載體,將免疫刺激劑CpG遞送至巨噬細(xì)胞。

          Abstract

          Considering the potent immune stimulation by CpG oligodeoxynucleotides (CpGs), the development of CpG carriers is a prerequisite for efficient cancer immunotherapy. In this study, we conjugated 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-[hydroxyl succinimidyl (polyethylene glycol)] (DSPE-PEG-NHS) with polyethylenimine (PEI) to develop a PEI-PEG-DSPE conjugate that can serve as a biocompatible and efficient CpG carrier. Five types of PEIPEG-DSPE conjugates were developed, each with different molecular weights of PEI and different degrees of DSPEPEG modification, and all exhibited significantly lower cytotoxicity. In particular, compared to CpG delivery via natural PEI, delivery with PEI (25 kDa)-PEG-DSPE and DSPE-PEG-NHS/(amine groups of PEI) at a molar ratio of 0.1 resulted in a higher uptake of CpGs into RAW264.7 cells, probably because of the presence of a hydrophobic lipid moiety. In addition, PEI-PEG-DSPE/CpG complexes triggered significant cytokine secretion (TNF-α) from RAW264.7 cells, comparable to that triggered by PEI/CpG complexes. Thus, PEI-PEG-DSPE conjugates could serve as biocompatible and efficient carriers of the immune stimulator CpG to the macrophages.

          DSPE-PEG-NHS

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