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基于热敏泊洛沙姆407凝胶的新型DNA制剂的心包内给药。

Intrapericardial administration of novel DNA formulations based on thermosensitive Poloxamer 407 gel.

作者信息

Roques C, Salmon A, Fiszman M Y, Fattal E, Fromes Y

机构信息

Institut de Myologie-Inserm U582, Groupe hospitalier Pitié-Salpêtrière 47, Boulevard de l'Hôpital, 75651 Paris, France.

出版信息

Int J Pharm. 2007 Mar 1;331(2):220-3. doi: 10.1016/j.ijpharm.2006.11.056. Epub 2006 Dec 1.

Abstract

Inherited cardiopathies are leading to life-threatening conditions such as heart failure. Moreover, treatments currently available fail in altering the cardiac phenotype. Thus, gene therapy appears as an attracting alternative to conventional treatments. However, gene delivery remains a major hurdle in achieving this goal. To obtain regional delivery of plasmid DNA, intrapericardial administration seems to be an interesting approach. In order to improve retention time at the site of injection, formulations based on a thermosensitive gel of Poloxamer 407 were assessed. Protection and condensation of plasmid DNA was initially performed through complexation with polyethyleneimine (PEI), a widely used polymer. Characterization of the size and zeta potential of the complexes suggested interactions between the polyplexes and the Poloxamer gel through significant increase of the size of the polyplexes and shielding of the surface charges. In vivo evaluation has highlighted the toxicity of PEI/DNA polyplexes toward the myocardium. However, feasibility of intrapericardial injection of Poloxamer based formulations as well as their very low toxicity has been established.

摘要

遗传性心脏病正导致诸如心力衰竭等危及生命的状况。此外,目前可用的治疗方法无法改变心脏表型。因此,基因治疗似乎是传统治疗方法的一个有吸引力的替代方案。然而,基因递送仍然是实现这一目标的主要障碍。为了实现质粒DNA的局部递送,心包内给药似乎是一种有趣的方法。为了延长在注射部位的保留时间,对基于泊洛沙姆407热敏凝胶的制剂进行了评估。质粒DNA的保护和浓缩最初是通过与广泛使用的聚合物聚乙烯亚胺(PEI)络合来实现的。复合物的大小和zeta电位的表征表明,通过复合物大小的显著增加和表面电荷的屏蔽,多聚体与泊洛沙姆凝胶之间存在相互作用。体内评估突出了PEI/DNA多聚体对心肌的毒性。然而,基于泊洛沙姆的制剂心包内注射的可行性及其极低的毒性已经得到证实。

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