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本文引用的文献

1
Nanoscale drug delivery systems and the blood-brain barrier.纳米级药物递送系统与血脑屏障。
Int J Nanomedicine. 2014 Feb 7;9:795-811. doi: 10.2147/IJN.S52236. eCollection 2014.
2
Current progress in gene delivery technology based on chemical methods and nano-carriers.基于化学方法和纳米载体的基因递送技术的当前进展。
Theranostics. 2014 Jan 15;4(3):240-55. doi: 10.7150/thno.6914. eCollection 2014.
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Development of a non-viral gene delivery vector based on the dynein light chain Rp3 and the TAT peptide.基于动力蛋白轻链 Rp3 和 TAT 肽的非病毒基因传递载体的开发。
J Biotechnol. 2014 Mar 10;173:10-8. doi: 10.1016/j.jbiotec.2014.01.001. Epub 2014 Jan 11.
4
Nanotechnology: emerging tools for biology and medicine.纳米技术:生物学和医学的新兴工具。
Genes Dev. 2013 Nov 15;27(22):2397-408. doi: 10.1101/gad.226837.113.
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Virus-like particle-based human vaccines: quality assessment based on structural and functional properties.基于病毒样颗粒的人用疫苗:基于结构和功能特性的质量评估。
Trends Biotechnol. 2013 Nov;31(11):654-63. doi: 10.1016/j.tibtech.2013.09.002. Epub 2013 Oct 11.
6
Availability of polymeric nanoparticles for specific enhanced and targeted drug delivery.用于特定增强和靶向药物递送的聚合物纳米颗粒的可用性。
Ther Deliv. 2013 Oct;4(10):1261-78. doi: 10.4155/tde.13.84.
7
Metallic nanoparticles and their medicinal potential. Part II: aluminosilicates, nanobiomagnets, quantum dots and cochleates.金属纳米颗粒及其医学潜力。第二部分:硅铝酸盐、纳米生物磁体、量子点和螺旋形脂质体。
Ther Deliv. 2013 Sep;4(9):1179-96. doi: 10.4155/tde.13.74.
8
Fabrication of nanoarchitectures templated by virus-based nanoparticles: strategies and applications.基于病毒纳米粒子模板的纳米结构的制造:策略与应用。
Small. 2014 Jan 29;10(2):230-45. doi: 10.1002/smll.201301393. Epub 2013 Sep 1.
9
gH625 is a viral derived peptide for effective delivery of intrinsically disordered proteins.gH625 是一种病毒衍生肽,可有效递呈天然无序蛋白。
Int J Nanomedicine. 2013;8:2555-65. doi: 10.2147/IJN.S44186. Epub 2013 Jul 22.
10
Nanoparticle- and liposome-carried drugs: new strategies for active targeting and drug delivery across blood-brain barrier.载药纳米粒和载药脂质体:血脑屏障主动靶向和药物递送的新策略。
Curr Drug Metab. 2013 Jul;14(6):625-40. doi: 10.2174/1389200211314060001.

利用病毒特性进行细胞内递送。

Exploitation of viral properties for intracellular delivery.

作者信息

Galdiero Stefania, Falanga Annarita, Vitiello Mariateresa, Grieco Paolo, Caraglia Michele, Morelli Giancarlo, Galdiero Massimiliano

机构信息

Department of Pharmacy, University of Naples "Federico II", Via Mezzocannone 16, and Via Domenico Montesano 49, 80100, Napoli, Italy; Centro Interuniversitario di Ricerca sui Peptidi Bioattivi, University of Naples "Federico II", Via Mezzocannone 16, 80134, Napoli, Italy; Istituto di Biostrutture e Bioimmagini - CNR, Via Mezzocannone 16, 80134, Napoli, Italy; DFM Scarl, Via Mezzocannone 16, 80134, Napoli, Italy.

出版信息

J Pept Sci. 2014 Jul;20(7):468-78. doi: 10.1002/psc.2649. Epub 2014 May 30.

DOI:10.1002/psc.2649
PMID:24889153
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7168031/
Abstract

Nanotechnology is an expanding area of study with potentially pivotal applications in a discipline as medicine where new biomedical active molecules or strategies are continuously developing. One of the principal drawbacks for the application of new therapies is the difficulty to cross membranes that represent the main physiological barrier in our body and in all living cells. Membranes are selectively permeable and allow the selective internalization of substances; generally, they form a highly impermeable barrier to most polar and charged molecules, and represent an obstacle for drug delivery, limiting absorption to specific routes and mechanisms. Viruses provide attracting suggestions for the development of targeted drug carriers as they have evolved naturally to deliver their genomes to host cells with high fidelity. A detailed understanding of virus structure and their mechanisms of entry into mammalian cells will facilitate the development and analysis of virus-based materials for medical applications.

摘要

纳米技术是一个不断扩展的研究领域,在医学等学科中具有潜在的关键应用,新的生物医学活性分子或策略正在该领域持续发展。新疗法应用的主要缺点之一是难以穿过细胞膜,细胞膜是我们身体和所有活细胞中的主要生理屏障。细胞膜具有选择性渗透性,允许物质选择性内化;一般来说,它们对大多数极性和带电分子形成高度不可渗透的屏障,并且是药物递送的障碍,将吸收限制在特定途径和机制。病毒为靶向药物载体的开发提供了诱人的思路,因为它们已经自然进化,能够将其基因组高保真地递送至宿主细胞。深入了解病毒结构及其进入哺乳动物细胞的机制将有助于开发和分析用于医学应用的基于病毒的材料。