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          DSPE-PEG-PEI介導(dǎo)的聯(lián)合遞藥系統(tǒng)在肝癌中的應(yīng)用研究
          發(fā)布時(shí)間:2025-06-23     作者:kx   分享到:

          DSPE-PEG-PEI介導(dǎo)的聯(lián)合遞藥系統(tǒng)在肝癌中的應(yīng)用研究

          鏈接:https://xueshu.baidu.com/usercenter/paper/show?paperid=13620650816s00y0k60q02j0k0742988&site=xueshu_se

          作者: G Tian,R Pan,B Zhang,M Qu,J Wu

          摘要:Combination therapy based on nano-sized drug delivery system has been developed as a promising strategy by combining two or more anti-tumor mechanisms. Here, we prepared liver-targeted nanoparticles (GH-DPP) composed of 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-polyethylene glycol-polyetherimide (DSPE-PEG-PEI) with Glycyrrhetinic acid-modified hyaluronic acid (GA-HA) for co-delivery of doxorubicin (DOX) and Bcl-2 siRNA. Particles size, zeta potential and morphology were determined for the drug-loaded GH-DPP nanoparticles (siRNA/DOX/GH-DPP). Cellular uptake and in vitro cytotoxicity were analyzed against HepG2 cells. In vivo bio-distribution and anti-tumor therapeutic effects of siRNA/DOX/GH-DPP were evaluated in H22-bearing mice. The results showed that siRNA/DOX/GH-DPP nanoparticles were nearly spherical and showed dose-dependent cytotoxicity against HepG2 cells. Compared to Glycyrrhetinic acid-free co-delivery system (siRNA/DOX/DPP) and GH-DPP nanoparticles for delivery of DOX or Bcl-2 siRNA alone, siRNA/DOX/GH-DPP nanoparticles could induce more cellular apoptosis, and showed higher anti-tumor effect. Herein GH-DPP nanoparticles could simultaneously deliver both chemotherapy drugs and siRNA into the tumor region, exhibiting great potential in anti-tumor therapy.

          譯文:

          通過結(jié)合兩種或多種**機(jī)制,已將基于納米級(jí)藥物遞送系統(tǒng)的聯(lián)合療法發(fā)展為一種有前途的策略。在這里,我們制備了肝靶向納米顆粒(GH-DPP),其由1,2-二硬脂酰-sn-甘油-3-磷酸乙醇胺-聚乙二醇-聚醚酰亞胺(DSPE-PEG-PEI)與甘草次酸修飾的透明質(zhì)酸(GA- HA)用于共同遞送阿霉素(DOX)和Bcl-2 siRNA。確定了載藥的GH-DPP納米顆粒(siRNA / DOX / GH-DPP)的粒徑,ζ電位和形態(tài)。分析了針對(duì)HepG2細(xì)胞的細(xì)胞攝取和體外細(xì)胞毒性。在荷H22小鼠中評(píng)估了siRNA / DOX / GH-DPP的體內(nèi)生物分布和***作用。結(jié)果表明,siRNA / DOX / GH-DPP納米顆粒接近球形,并且對(duì)HepG2細(xì)胞顯示出劑量依賴性的細(xì)胞毒性。與單獨(dú)使用DOG或Bcl-2 siRNA的無甘草次酸共遞送系統(tǒng)(siRNA / DOX / DPP)和GH-DPP納米顆粒相比,siRNA / DOX / GH-DPP納米顆?梢哉T導(dǎo)更多的細(xì)胞凋亡,并且顯示出更高的凋亡率。**作用。此處,GH-DPP納米顆?赏瑫r(shí)將化療藥物和siRNA送入*區(qū)域,在***中顯示出巨大的潛力。

          DOI:10.3389/fphar.2019.00004

          DSPE-PEG-PEI介導(dǎo)的聯(lián)合遞藥系統(tǒng)在肝癌中的應(yīng)用研究

          西安pg電子官方生物提供相關(guān)產(chǎn)品:

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