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非病毒基因递送的障碍。

Barriers to nonviral gene delivery.

作者信息

Wiethoff Christopher M, Middaugh C Russell

机构信息

Department of Pharmaceutical Chemistry, The University of Kansas, 2095 Constant Avenue, Lawrence, Kansas 66047, USA.

出版信息

J Pharm Sci. 2003 Feb;92(2):203-17. doi: 10.1002/jps.10286.

Abstract

The use of various synthetic lipids and polymers to deliver DNA for gene therapy applications has been the subject of intense examination for the last 15 years. Our understanding of the processes involved in the delivery of DNA, although still limited, can be described in terms of specific physical and chemical barriers encountered along the delivery pathway. Successful engagement of this pathway involves avoiding inactivation in the extracellular compartment and initial favorable interactions with the cell surface. Internalization of the delivery system by endocytosis results in a poorly defined endosomal trafficking process which, if not escaped, leads to degradation of the therapeutic DNA in lysosomes. For the small fraction of material that is able to escape this vesicular trafficking pathway, the cytosol provides additional physical and metabolic barriers to further trafficking to the nucleus. Finally, nuclear uptake has been demonstrated to be a significant barrier to gene delivery. In this review, we outline in greater detail the various processes involved in each step and describe various formulation variables that have been explored to overcome these delivery barriers to nonviral gene delivery.

摘要

在过去15年里,使用各种合成脂质和聚合物递送用于基因治疗的DNA一直是深入研究的主题。我们对DNA递送过程的理解,尽管仍然有限,但可以根据递送途径中遇到的特定物理和化学屏障来描述。成功进入该途径涉及避免在细胞外区室失活以及与细胞表面最初的有利相互作用。通过内吞作用使递送系统内化会导致一个定义不明确的内体运输过程,如果不能逃脱,会导致治疗性DNA在溶酶体中降解。对于能够逃脱这种囊泡运输途径的一小部分物质,细胞质为进一步运输到细胞核提供了额外的物理和代谢屏障。最后,核摄取已被证明是基因递送的一个重大障碍。在这篇综述中,我们更详细地概述了每个步骤中涉及的各种过程,并描述了为克服这些非病毒基因递送的递送障碍而探索的各种制剂变量。

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