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首页> 外文期刊>Journal of drug delivery science and technology >Evaluation of the injection route of an anionic polymer for small interfering RNA delivery into the liver by sequential injection of anionic polymer and cationic lipoplex of small interfering RNA
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Evaluation of the injection route of an anionic polymer for small interfering RNA delivery into the liver by sequential injection of anionic polymer and cationic lipoplex of small interfering RNA

机译:通过依次注射小分子干扰RNA的阴离子聚合物和阳离子脂复合物,评估小分子干扰RNA进入肝脏的阴离子聚合物的注射途径

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摘要

Previously, we developed a novel small interfering RNA (siRNA) transfer method for the liver by sequential intravenous injection of an anionic polymer and cationic liposome/siRNA complex (cationic lipoplex). In this study, we examined the effects of the type of anionic polymer and injection route of the anionic polymer on the biodistribution of siRNA after sequential injection of anionic polymer and cationic lipoplexes. When cationic lipoplexes were injected intravenously into mice, siRNA largely accumulated in the lungs. In contrast, sequential injection of cationic lipoplex after intravenous injection of 1 mg chondroitin sulfate C and A (CS-C and CS-A) or polyaspartic acid decreased the accumulation of siRNA in the lungs and increased it in the liver, compared with injection of cationic lipoplex. Regarding the injection route of the anionic polymer, intramuscular, intraperitoneal, or subcutaneous injection of 10 mg CS-C before intravenous injection of cationic lipoplex resulted in siRNA accumulation mainly in the liver. Furthermore, the injection of cationic lipoplex of apolipoprotein B (ApoB) siRNA after intravenous or intramuscular injection of CS-C could suppress ApoB mRNA levels in the liver. Sequential injection of CS-C plus cationic lipoplex could deliver siRNA efficiently into the liver regardless of the injection route of CS-C. (C) 2016 Elsevier B.V. All rights reserved.
机译:以前,我们通过顺序静脉注射阴离子聚合物和阳离子脂质体/ siRNA复合物(阳离子脂质复合物),为肝脏开发了一种新颖的小干扰RNA(siRNA)转移方法。在这项研究中,我们检查了阴离子聚合物和阳离子脂质复合物顺序注射后,阴离子聚合物的类型和阴离子聚合物的注射途径对siRNA的生物分布的影响。当将阳离子脂质复合物静脉注射到小鼠体内时,siRNA大量积累在肺中。相反,静脉注射1 mg硫酸软骨素C和A(CS-C和CS-A)或聚天冬氨酸后,顺序注射阳离子脂质复合物,与注射s相比,减少了siRNA在肺中的积累并增加了在肝脏中的siRNA积累。阳离子脂复合物。关于阴离子聚合物的注射途径,在静脉内注射阳离子脂质复合物之前,肌肉内,腹膜内或皮下注射10mg CS-C导致siRNA主要在肝脏中积聚。此外,在静脉内或肌内注射CS-C后注射载脂蛋白B(ApoB)siRNA阳离子脂质复合物可抑制肝脏中ApoB mRNA的水平。无论CS-C的注射途径如何,连续注射CS-C加阳离子脂质复合物都可以将siRNA有效地传递到肝脏中。 (C)2016 Elsevier B.V.保留所有权利。

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