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dspe-mpeg2000用于制备脂质体的实验使用方法和相关文献
发布时间:2025-05-09     作者:ssl   分享到:
dspe-mpeg2000应用于制法脂质体的实验操作运用形式和想关论文资料另外副标题:DSPE-MPEG2000使用于制取脂质体的专著免费指导论文参考文献名:Effect of surface charge and density of istearylphosphatidylethanolamine-mPEG-2000 (DSPE-mPEG-2000) on the cytotoxicity of liposome-entrapped ricin: Effect of lysosomotropic agents文章链接转换://doi.org/10.1016/j.ijpharm.2007.08.032实践在使用手段:脂质机制备Liposomes composed of soya phosphatidyl choline andcholesterol in a molar ratio of 55:45 were prepared by handshaken method. Briefly, the lipids (40 pmol total lipids)weredissolved in chloroform in a 100ml round bottom fask. Thechloroform was evaporated to dryness at 37°C, under reducedpressure by using rotary evaporator (Wheaton). The thin filmso formed, was desiccated for 1 h, followed by hydration with1 ml PBS (20 mM, pH 7.4), containing ricin (3 mg/ml) and traceamounts of 125]-ricin as aqueous phase marker. The round bot-tom fask containing liposomes suspension was stored, underN2 atmosphere to avoid lipid oxidation, at 4C for overnight forcomplete hydration. The following day, liposomes were soni-cated in a bath type sonicator (Branson) at 25 °C for 30 min in10 min batches to avoid the heat generation. Negatively and positivelycharged liposomes containing ricin were preparedexactlyas described above only 10 mol% either phosphatidic acid (PA)or stearylamine (SA) were added during the preparation of lipidflm. Sterically stabilized liposomes containing ricin were pre-pared as described above by adding various (1-7.5 mol%) ofDSPE-mPEG-2000 during the preparation of lipid film.


在握的手法制作了由豆类磷脂酰胆碱和碳水化合物以55:45的摩尔比组成的的脂质体。简认为之,将脂质(总脂质40pmol)融化在100ml圆底烧瓶中的氯仿中。在37°C下,动用旋轉挥发器(Wheaton)在缓解压力下将氯仿挥发至干。将那么确定的塑料膜常温、干燥1小的时候,然而用1ml PBS(20mM,pH 7.4)水合,PBS富含蓖麻毒性(3mg/ml)和进样器125]-蓖麻毒性对于水相标注。将富含圆圈脂质体悬屏液在氢气节日气氛下存放,以预防脂质钝化,在4℃下存放包夜,以实现目标彻底水合。二是天,脂质体在25°C的浴式超音波仪(Branson)中以10钟头为某批次确定30钟头的超音波加工,以预防存在发热量。如上所诉,制作了富含蓖麻毒性的负电势量和正电势量脂质体,在制作脂质膜的的具体步骤 中只下载了10 mol%的磷脂酸(PA)或硬脂胺(SA)。如上所诉,在在制作脂质膜的的具体步骤 中下载种种(1-7.5mol%)DSPE-mPEG-2000,制作了富含蓖麻毒性的制做比较稳定脂质体。核心论文检测:

dspe-mpeg2000 

为重要研究结论情况说明 examined. As shown in Fig. 5 when cells were treated with150 ng/ml free ricin a lag period of 45 min was observed withtso (time required to achieve 50% reduction in protein synthe-sis) of 200 min. It was observed that the lag period of inhibitionof protein synthesis by ricin is significantly increased followingdelivery through different charged liposomes. At 10 pg/ml ofvarious charged liposomal ricin, a lag phase of 4 h was observedfor neutral and negatively charged liposomes, on the other hand.a lag phase of 2h was observed for positively charged lipo-somes. Monensin (50 nm) reduced the lag period of free ricinfrom 45 to 15 min (i.e., three-fold reduction of the lag period),however, in the presence of monensin, the lag period of neutraland negatively chargedliposomal ricin was reduced from 4 to 1 h(four-fold reduction of lag period) and 2 h (two-fold reductionoflag period), respectively. The lag period of positively chargedliposomal ricin was reduced from 2 to 1 h (two-fold reductionof lag period). These results implied that monensin causes anenhanced and efficient release of ricin A-chain from liposomalricin located in an intracellular compartment into the cytosolleading to the rapid onset of the inhibition of protein synthesis.


图甲5右图,当组织用150 ng/ml分散蓖麻黑色素办理时,能够 洞察分析到4两半一个小的迟滞期,tso(完成高球球蛋白酶质组成增多50%想要的時间)为200半一个小。能够 洞察分析到蓖麻黑色素治理和改善高球球蛋白酶质组成的迟滞期在能够 各种各样不同有电脂质体递送后明显扩大。其它部分,在10 pg/ml的各种各样有电蓖麻黑色素脂质体中,碱性和带负自由自由电荷量的脂质体能够 洞察分析到4一个小的迟滞期,而带正电的脂质体则能够 洞察分析到2一个小的迟滞关键期。莫能菌素(50 nm)将分散蓖麻黑色素的迟滞期从4两半一个小还不但缩减到1两半一个小(即迟滞期还不但缩减了多倍),然后,在莫能菌高球球蛋白酶现实存在的情况下下,碱性粒组织和带负自由自由电荷量的脂质体蓖麻素的迟滞期各自从4一个小还不但缩减到1一个小(迟滞期还不但缩减三倍)和2一个小(两倍还不但缩减象征期)。带正自由自由电荷量的脂质体蓖麻黑色素的迟滞期从2一个小还不但缩减到1一个小(迟滞期还不但缩减好几回倍)。这类成果发现,莫能菌素导至蓖麻黑色素A链从座落在组织内隔室的脂质体保持到组织质中,所以迅速的治理和改善高球球蛋白酶质组成。


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