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可生物降解树枝状聚-L-赖氨酸在小分子干扰RNA递送系统中的应用。

Application of biodegradable dendrigraft poly-l-lysine to a small interfering RNA delivery system.

作者信息

Kodama Yukinobu, Kuramoto Haruka, Mieda Yukari, Muro Takahiro, Nakagawa Hiroo, Kurosaki Tomoaki, Sakaguchi Miako, Nakamura Tadahiro, Kitahara Takashi, Sasaki Hitoshi

机构信息

a Department of Hospital Pharmacy , Nagasaki University Hospital , Nagasaki , Japan.

b Institute of Tropical Medicine, Nagasaki University , Nagasaki , Japan.

出版信息

J Drug Target. 2017 Jan;25(1):49-57. doi: 10.1080/1061186X.2016.1184670. Epub 2016 May 16.

Abstract

Dendrigraft poly-l-lysine (DGL), including its central core, consists entirely of lysine, hence it is completely biodegradable. We applied DGL in a small interfering RNA (siRNA) delivery system. Binary complexes with siRNA and DGL had particle sizes of 23-73 nm and ζ-potentials of 34-42 mV. The siRNA-DGL complexes showed significant silencing effects in a mouse colon carcinoma cell line expressing luciferase (Colon26/Luc cells). The siRNA-DGL complexes induced slight cytotoxicity and hematological toxicity at a high charge ratio of DGL to siRNA, probably because of their cationic charges. Therefore, we recharged the siRNA-DGL complexes with γ-polyglutamic acid (γ-PGA), a biodegradable anionic compound, which was reported to reduce the cytotoxicity of cationic complexes. The ternary complexes showed particle sizes of 35-47 nm at a charge ratio of greater than 14 to siRNA with negative charges. Strong silencing effects of the ternary complexes were observed in Colon26/Luc cells without cytotoxicity or hematological toxicity. The cellular uptake and degradation of the binary and ternary complexes were confirmed by fluorescence microscopy. The ternary complexes suppressed luciferase activity in the tumor after direct injection into the tumors of mice bearing Colon26/Luc cells. Thus, a potentially important siRNA delivery system was constructed using biodegradable DGL.

摘要

树枝状聚-L-赖氨酸(DGL),包括其核心部分,完全由赖氨酸组成,因此它是完全可生物降解的。我们将DGL应用于小干扰RNA(siRNA)递送系统。与siRNA形成的二元复合物和DGL的粒径为23 - 73纳米,ζ电位为34 - 42毫伏。siRNA - DGL复合物在表达荧光素酶的小鼠结肠癌细胞系(Colon26/Luc细胞)中显示出显著的沉默效果。在DGL与siRNA电荷比高时,siRNA - DGL复合物诱导轻微的细胞毒性和血液学毒性,可能是由于它们的阳离子电荷。因此,我们用γ-聚谷氨酸(γ-PGA)对siRNA - DGL复合物进行再电荷处理,γ-PGA是一种可生物降解的阴离子化合物,据报道它能降低阳离子复合物的细胞毒性。三元复合物在与siRNA电荷比大于14且带负电荷时,粒径为35 - 47纳米。在Colon26/Luc细胞中观察到三元复合物有强烈的沉默效果,且无细胞毒性或血液学毒性。通过荧光显微镜证实了二元和三元复合物的细胞摄取和降解情况。将三元复合物直接注射到携带Colon26/Luc细胞的小鼠肿瘤中后,它抑制了肿瘤中的荧光素酶活性。因此,利用可生物降解的DGL构建了一个潜在重要的siRNA递送系统。

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