Suppr超能文献

壳聚糖和三甲基壳聚糖修饰的聚(ε-己内酯)纳米颗粒作为DNA载体的制备与表征

Preparation and characterization of chitosan and trimethyl-chitosan-modified poly-(epsilon-caprolactone) nanoparticles as DNA carriers.

作者信息

Haas Jochen, Ravi Kumar M N V, Borchard Gerrit, Bakowsky Udo, Lehr Claus-Michael

机构信息

Department of Biopharmaceutics and Pharmaceutical Technology, Saarland University, Building 8.1, 66123 Saarbrücken, Germany.

出版信息

AAPS PharmSciTech. 2005 Aug 10;6(1):E22-30. doi: 10.1208/pt060106.

Abstract

The purpose of this research was to prepare poly-(epsilon-caprolactone) (PCL) particles by an emulsion-diffusion-evaporation method using a blend of poly-(vinyl alcohol) and chitosan derivatives as stabilizers. The chitosan derivatives used were chitosan hydrochloride and trimethyl chitosans (TMC) with varying degrees of quaternization. Particle characteristics-size, zeta potential, surface morphology, cytotoxicity, and transfection efficiency-were investigated. The developed method yields PCL nanoparticles in the size range of 250 to 300 nm with a positive surface charge (2.5 to 6.8 mV). The cytotoxicity was found to be moderate and virtually independent of the stabilizers' concentration with the exception of the highly quaternized TMC (degree of substitution 66%) being significantly more toxic. In immobilization experiments with gel electrophoresis, it could be shown that these cationic nanoparticles (NP) form stable complexes with DNA at a NP:DNA ratio of 3:1. These nanoplexes showed a significantly higher transfection efficiency on COS-1 cells than naked DNA.

摘要

本研究的目的是使用聚乙烯醇和壳聚糖衍生物的混合物作为稳定剂,通过乳液扩散蒸发法制备聚(ε-己内酯)(PCL)颗粒。所使用的壳聚糖衍生物为盐酸壳聚糖和不同季铵化程度的三甲基壳聚糖(TMC)。研究了颗粒特性——尺寸、zeta电位、表面形态、细胞毒性和转染效率。所开发的方法可产生尺寸范围为250至300nm且表面带正电荷(2.5至6.8mV)的PCL纳米颗粒。除了高度季铵化的TMC(取代度66%)毒性明显更大外,细胞毒性被发现为中等且几乎与稳定剂浓度无关。在凝胶电泳固定实验中,可以表明这些阳离子纳米颗粒(NP)在NP:DNA比例为3:1时与DNA形成稳定的复合物。这些纳米复合物在COS-1细胞上显示出比裸DNA显著更高的转染效率。

相似文献

2
Copolymers of epsilon-caprolactone and quaternized epsilon-caprolactone as gene carriers.
J Control Release. 2007 Mar 12;118(1):136-44. doi: 10.1016/j.jconrel.2006.12.005. Epub 2006 Dec 12.
3
Design and formulation of trimethylated chitosan-graft-poly(ε-caprolactone) nanoparticles used for gene delivery.
Carbohydr Polym. 2014 Jan 30;101:104-12. doi: 10.1016/j.carbpol.2013.09.053. Epub 2013 Sep 19.
4
Preparation and characterization of poly-epsilon-caprolactone nanoparticles containing griseofulvin.
Int J Pharm. 2005 Apr 27;294(1-2):261-7. doi: 10.1016/j.ijpharm.2005.01.020.
5
PEGylated quaternized copolymer/DNA complexes for gene delivery.
Int J Pharm. 2007 Nov 1;344(1-2):88-95. doi: 10.1016/j.ijpharm.2007.06.044. Epub 2007 Jul 3.
6
Chitosan N-betainates/DNA self-assembly nanoparticles for gene delivery: in vitro uptake and transfection efficiency.
Int J Pharm. 2009 Apr 17;371(1-2):156-62. doi: 10.1016/j.ijpharm.2008.12.012. Epub 2008 Dec 24.
7
Receptor-mediated gene delivery by folate-poly(ethylene glycol)-grafted-trimethyl chitosan in vitro.
J Drug Target. 2011 Sep;19(8):647-56. doi: 10.3109/1061186X.2010.525650. Epub 2010 Oct 22.
9
Trimethylated chitosans as non-viral gene delivery vectors: cytotoxicity and transfection efficiency.
J Control Release. 2005 Apr 18;103(3):643-53. doi: 10.1016/j.jconrel.2005.01.001.

引用本文的文献

1
Colloidal structure and proton conductivity of the gel within the electrosensory organs of cartilaginous fishes.
iScience. 2021 Aug 4;24(9):102947. doi: 10.1016/j.isci.2021.102947. eCollection 2021 Sep 24.
2
Carriers for the targeted delivery of aerosolized macromolecules for pulmonary pathologies.
Expert Opin Drug Deliv. 2018 Aug;15(8):821-834. doi: 10.1080/17425247.2018.1502267. Epub 2018 Jul 26.
6
Trimethyl chitosan and its applications in drug delivery.
J Mater Sci Mater Med. 2009 May;20(5):1057-79. doi: 10.1007/s10856-008-3659-z. Epub 2008 Dec 27.
7
Nanovehicular intracellular delivery systems.
J Pharm Sci. 2008 Sep;97(9):3518-90. doi: 10.1002/jps.21270.

本文引用的文献

1
Cationic poly(lactide-co-glycolide) nanoparticles as efficient in vivo gene transfection agents.
J Nanosci Nanotechnol. 2004 Nov;4(8):990-4. doi: 10.1166/jnn.2004.130.
3
Preparation and characterization of cationic PLGA nanospheres as DNA carriers.
Biomaterials. 2004 May;25(10):1771-7. doi: 10.1016/j.biomaterials.2003.08.069.
5
Dendriplexes and their characterisation.
Int J Pharm. 2003 Mar 18;254(1):17-21. doi: 10.1016/s0378-5173(02)00670-1.
6
Cell transfection in vitro and in vivo with nontoxic TAT peptide-liposome-DNA complexes.
Proc Natl Acad Sci U S A. 2003 Feb 18;100(4):1972-7. doi: 10.1073/pnas.0435906100. Epub 2003 Feb 5.
9
Prospects for cationic polymers in gene and oligonucleotide therapy against cancer.
Adv Drug Deliv Rev. 2002 Sep 13;54(5):715-58. doi: 10.1016/s0169-409x(02)00046-7.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验