Visualization of the Plasmid DNA Delivery System by Complementary Fluorescence Labeling of Arginine-Rich Peptides.

IF 1.5 4区 医学 Q4 CHEMISTRY, MEDICINAL
Ayumi Imayoshi, Hidetomo Yokoo, Masashi Kawaguchi, Kazunori Tsubaki, Makoto Oba
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Abstract

Cell-penetrating peptides, such as arginine-rich peptides, encapsulate nucleic acid drugs and deliver them to intracellular compartments. Comprehensive tracking of drug delivery systems (DDSs) provides information about the behavior of the drug as well as the fate of the drug carrier after drug release, which is crucial for minimizing side effects. In this study, we labeled peptides designed to carry plasmid DNA with two types of dyes, traditional dye fluorescein and aggregation-induced emission (AIE) dye tetraphenylethylene, and subsequently tracked the DDS through the complementary ON and OFF fluorescence behaviors of the dyes. Traditional fluorescent dyes are susceptible to aggregation-caused quenching during bioimaging, a problem that is mitigated by using AIE dyes. However, by using both of these contrasting fluorescent labels, we were able to clearly visualize the DDS at different stages of its deployment, from drug transport and delivery to carrier dissociation and migration, demonstrating the feasibility of accurate DDS visualization by complementary fluorescence labeling.

通过对富精氨酸肽进行互补荧光标记实现质粒 DNA 运送系统的可视化。
细胞穿透肽,如富含精氨酸的肽,可以包裹核酸药物并将其输送到细胞内。对药物递送系统(DDS)的全面跟踪可提供有关药物行为以及药物释放后药物载体去向的信息,这对最大限度地减少副作用至关重要。在这项研究中,我们用两种染料(传统染料荧光素和聚集诱导发射(AIE)染料四苯乙烯)标记了设计用于携带质粒 DNA 的多肽,随后通过染料的互补 "开 "和 "关 "荧光行为来跟踪 DDS。传统的荧光染料在生物成像过程中容易受到聚集引起的淬灭影响,而使用 AIE 染料则可以缓解这一问题。不过,通过同时使用这两种对比鲜明的荧光标签,我们能够清晰地观察到 DDS 从药物运输和递送到载体解离和迁移等不同阶段的部署情况,证明了通过互补荧光标签准确观察 DDS 的可行性。
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来源期刊
CiteScore
3.20
自引率
5.90%
发文量
132
审稿时长
1.7 months
期刊介绍: The CPB covers various chemical topics in the pharmaceutical and health sciences fields dealing with biologically active compounds, natural products, and medicines, while BPB deals with a wide range of biological topics in the pharmaceutical and health sciences fields including scientific research from basic to clinical studies. For details of their respective scopes, please refer to the submission topic categories below. Topics: Organic chemistry In silico science Inorganic chemistry Pharmacognosy Health statistics Forensic science Biochemistry Pharmacology Pharmaceutical care and science Medicinal chemistry Analytical chemistry Physical pharmacy Natural product chemistry Toxicology Environmental science Molecular and cellular biology Biopharmacy and pharmacokinetics Pharmaceutical education Chemical biology Physical chemistry Pharmaceutical engineering Epidemiology Hygiene Regulatory science Immunology and microbiology Clinical pharmacy Miscellaneous.
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