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基于无载体低分子量肝素和十八烷基胺并具有白蛋白穿梭效应的纳米抗凝剂。

Nano-anticoagulant based on carrier-free low molecular weight heparin and octadecylamine with an albumin shuttling effect.

作者信息

Lee Jae-Hyeon, Lim Hansol, Ma Gaeun, Kweon Seho, Park Seong Jin, Seo Minho, Lee Jun-Hyuck, Yang Seong-Bin, Jeong Han-Gil, Park Jooho

机构信息

Department of Biomedical Chemistry, College of Biomedical and Health Science, Konkuk University, Seoul, Republic of Korea.

Department of Applied Life Science, BK21 Program, Konkuk University, Chungju, Republic of Korea.

出版信息

Nat Commun. 2024 Aug 8;15(1):6769. doi: 10.1038/s41467-024-50819-7.

Abstract

Low-molecular-weight heparin (LMWH), derived from unfractionated heparin (UFH), has enhanced anticoagulant efficacy, long duration of action, and extended half-life. Patients receiving LMWH for preventive therapies would strongly benefit from its long-term effects, however, achieving this is challenging. Here, we design and evaluate a nanoengineered LMWH and octadecylamine conjugate (LMHO) that can act for a long time while maintaining close to 97 ± 3% of LMWH activity via end-specific conjugation of the reducing end of LMWH. LMHO can self-assemble into nanoparticles with an average size of 105 ± 1.7 nm in water without any nanocarrier and can be combined with serum albumin, resulting in a lipid-based albumin shuttling effect. Such molecules can circulate in the bloodstream for 4-5 days. We corroborate the self-assembly capability of LMHO and its interaction with albumin through molecular dynamics (MD) simulations and transmission electron microscopy (TEM) analysis. This innovative approach to carrier-free polysaccharide delivery, enhanced by nanoengineered albumin shuttling, represents a promising platform to address limitations in conventional therapies.

摘要

低分子量肝素(LMWH)由普通肝素(UFH)衍生而来,具有增强的抗凝功效、较长的作用持续时间和延长的半衰期。接受LMWH预防性治疗的患者将从其长期效果中受益匪浅,然而,实现这一点具有挑战性。在此,我们设计并评估了一种纳米工程化的LMWH与十八烷基胺共轭物(LMHO),其可通过LMWH还原端的末端特异性共轭作用长时间发挥作用,同时保持接近97±3%的LMWH活性。LMHO在无任何纳米载体的情况下可在水中自组装成平均尺寸为105±1.7nm的纳米颗粒,并可与血清白蛋白结合,产生基于脂质的白蛋白穿梭效应。此类分子可在血液中循环4至5天。我们通过分子动力学(MD)模拟和透射电子显微镜(TEM)分析证实了LMHO的自组装能力及其与白蛋白的相互作用。这种通过纳米工程化白蛋白穿梭增强的无载体多糖递送创新方法,是解决传统疗法局限性的一个有前景的平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2b8/11310394/43ef0299f959/41467_2024_50819_Fig1_HTML.jpg

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