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马铃薯凝集素修饰的 PLGA 纳米粒经鼻腔给药的体内外评价。

Solanum tuberosum lectin-conjugated PLGA nanoparticles for nose-to-brain delivery: in vivo and in vitro evaluations.

机构信息

Department of Pharmaceutics, School of Pharmacy, Fudan University, Shanghai, People's Republic of China.

出版信息

J Drug Target. 2012 Feb;20(2):174-84. doi: 10.3109/1061186X.2011.622396. Epub 2011 Oct 12.

DOI:10.3109/1061186X.2011.622396
PMID:21992548
Abstract

Solanum tuberosum lectin (STL) conjugated poly (DL-lactic-co- glycolic acid) (PLGA) nanoparticle (STL-NP) was constructed in this paper as a novel biodegradable nose-to-brain drug delivery system. The in vitro uptake study showed markedly enhanced endocytosis of STL-NP compared to unmodified PLGA nanoparticles (NP) in Calu-3 cells and significant inhibition of uptake in the presence of inhibitor sugar (chitin hydrolysate). Following intranasal administration, coumarin-6 carried by STL-NP was rapidly absorbed into blood and brain. The AUC((0→12 h)) of coumarin-6 in blood, olfactory bulb, cerebrum and cerebellum were about 0.77-, 1.48-, 1.89- and 1.45-fold of those of NP, respectively (p < 0.05). STL-NP demonstrated 1.89-2.45 times (p < 0.01) higher brain targeting efficiency in different brain tissues than unmodified NP. Enhanced accumulation of STL-NP in the brain was also observed by near infrared fluorescence probe image following intranasal administration. The fluorescence signal of STL-NP appeared in olfactory bulb, cerebrum and brainstem early at 0.25 h. The signal in olfactory bulb decreased gradually after 2 h, while the obvious signal in brainstem, cerebrum and cerebellum lasted for more than 8 h. The STL-NP safety experiments showed mild cytotoxicity and negligible cilia irritation. These intriguing in vitro and in vivo results suggest that STL-NP might serve as a promising brain drug delivery system.

摘要

马铃薯凝集素(STL)修饰的聚(DL-乳酸-共- 乙醇酸)(PLGA)纳米粒(STL-NP)构建为一种新型的可生物降解的鼻内递药系统。体外摄取研究表明,与未经修饰的 PLGA 纳米粒(NP)相比,STL-NP 能够显著增强 Calu-3 细胞的内吞作用,并且在存在抑制剂糖(几丁质水解物)的情况下显著抑制摄取。经鼻内给予后,STL-NP 携带的香豆素-6 迅速被吸收到血液和脑中。血液、嗅球、大脑和小脑中的香豆素-6 的 AUC((0→12 h))分别约为 NP 的 0.77、1.48、1.89 和 1.45 倍(p < 0.05)。STL-NP 比未经修饰的 NP 具有更高的脑靶向效率,在不同脑区的脑靶向效率分别提高 1.89-2.45 倍(p < 0.01)。经鼻内给予后,通过近红外荧光探针成像也观察到 STL-NP 在脑中的蓄积增强。在 0.25 h 时,STL-NP 的荧光信号出现在嗅球、大脑和脑干中。2 h 后,嗅球中的信号逐渐减少,而脑干、大脑和小脑中的明显信号持续超过 8 h。STL-NP 的安全性实验显示出轻微的细胞毒性和可忽略的纤毛刺激。这些引人注目的体内外结果表明,STL-NP 可能作为一种有前途的脑内递药系统。

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