DSPE-PEG-COOH用于制备DSPE-PEG-DOX的相关文献(含合成路线)
DSPE-PEG-COOH用于制备DSPE-PEG-DOX的相关文献(含合成路线)
专著名: Peptide Engraftment on PEGylated Nanoliposomes for Bone Specific Delivery of PTH (1-34) in Osteoporosis我们:Taewon Hwang 1, Hee Dong Han, Chung Kil Song, Hasoo Seong, Jung Hyun Kim, Xiaoyuan Chen, Byung Cheol Shin绪论:治癌口服药的肉瘤特女性朋友递送是口服药设计方式中 中要面临的大部分试炼之四。在仅仅论述中,各位可以按照将新制成的DSPE-PEG2000-DOX(DPD)对于脂质组成成分掺杂脂质体中光催化原理了阿霉素(DOX)偶联脂质体(DCL),并测试测试了其身体内部抗肉瘤催化活化。可以按照酰胺键将DOX偶联到DSPE-PEG2000-COOH上制成了DPD,并可以按照(1)H-NMR数据具体分析确定了所有DPD的催化的结构。可以按照塑料薄膜浇铸水范法光催化原理了脂质体面积为130nm的DCL。普鲁士蓝染色癌细胞膜术数据具体分析核实,DCL的癌细胞膜摄取量清晰要高于传统艺术的脂质体。DCL对小鼠B16F10黑灰着色剂瘤荷瘤小鼠的抗肉瘤催化活化是因为,DCL比传统艺术的脂质体更有效率地抑止肉瘤生长发育,这有机会是考虑到DOX介导的内吞方式中 。实验使用方法:
Synthesis ofConjugate (SDSSD-DSPE)A lipid-PEG-peptide combination that may subsequently be added to liposomes forbone targeting was developed, SDSSD was conjugated to DSPE-PEG2000-C00H usingcarbodiimide chemistry, based on the previously described method by Wang et al. withmodi fications [32. Briefly, DSPE-PEG2000-COOH was dissolved in 0.1 M MES bufferat pH 6.0 and stirred at 2-8 °C for 10 min. Then, EDC.HCl and NHS (20 equivalentseach) were added to the reaction mixture and stirred for 60 min at 2-8 °C. A 7.4 pHadjustment was made to the reaction mixture, Finally, SDSSD, previously dissolved inMilli-Q water, was added to the reaction mixture and stirred overnight. The resultantmixture was dialyzed using a 2KD dialysis membrane for 48 h to remove unconjugatedSDSSD. Purifield SDSSD-DSPE (conjugate) was freeze-dried and characterized by'H-NMRMaldi-TOF, and a Scanning Electron Microscope (SEM) followed by Energy Dispersive。
反应结构路线
重要检测:
文献核磁
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制造厂:郑州pg电子娱乐游戏app 动物科技有限的总部有限的总部
应用领域:科研项目
情形:气体/粉状/饱和溶液
主产地:昆明
贴心警醒:未经许可科技,不用在人身体工作!
相关的品牌:
DSPE-PEG-α-Syn(α-突触核蛋清移除肽)DSPE-PEG-TrkB(精神有营养细胞肾上腺素受体过于兴奋肽)DSPE-PEG-GABA(γ-氨基丁酸多巴胺受体缓解肽)DSPE-PEG-5-HT(5-羟色胺蛋白激酶靶点)DSPE-PEG-AMPA(谷氨酸肾上腺素受体自动调节肽)DSPE-PEG-BMP-2(骨底部形态发生蛋白质模拟训练肽)DSPE-PEG-VEGF(微血管内皮发芽细胞因子模拟训练肽)DSPE-PEG-FGF2(成植物纤维血细胞植物的生长分子靶向疗法)DSPE-PEG-EPO(促红组织细胞导出素虚拟肽)