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Avidin-biotin technology to synthesize multi-arm nano-construct for drug delivery.用于药物递送的抗生物素蛋白-生物素技术合成多臂纳米结构。
MethodsX. 2020 Apr 22;7:100882. doi: 10.1016/j.mex.2020.100882. eCollection 2020.
2
A potent peptide-steroid conjugate accumulates in cartilage and reverses arthritis without evidence of systemic corticosteroid exposure.一种强效的肽-甾体缀合物在软骨中积累,并逆转关节炎,而没有全身皮质类固醇暴露的证据。
Sci Transl Med. 2020 Mar 4;12(533). doi: 10.1126/scitranslmed.aay1041.
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Multi-arm Avidin nano-construct for intra-cartilage delivery of small molecule drugs.用于小分子药物软骨内递送的多臂抗生物素蛋白纳米构建体。
J Control Release. 2020 Feb;318:109-123. doi: 10.1016/j.jconrel.2019.12.020. Epub 2019 Dec 13.
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Interleukin-1 receptor antagonist (IL-1Ra) is more effective in suppressing cytokine-induced catabolism in cartilage-synovium co-culture than in cartilage monoculture.白细胞介素-1 受体拮抗剂 (IL-1Ra) 在抑制软骨-滑膜共培养中细胞因子诱导的软骨分解代谢方面比在软骨单核培养中更有效。
Arthritis Res Ther. 2019 Nov 13;21(1):238. doi: 10.1186/s13075-019-2003-y.
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Direct Nucleus-Targeted Drug Delivery Using Cascade pH /Photo Dual-Sensitive Polymeric Nanocarrier for Cancer Therapy.利用级联 pH/光双敏感聚合物纳米载体进行靶向细胞核的药物传递用于癌症治疗。
Small. 2019 Sep;15(36):e1902022. doi: 10.1002/smll.201902022. Epub 2019 Jul 18.
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Efficacy and Safety of AM-111 in the Treatment of Acute Unilateral Sudden Deafness-A Double-blind, Randomized, Placebo-controlled Phase 3 Study.AM-111 治疗急性单侧突发性耳聋的疗效和安全性:一项双盲、随机、安慰剂对照的 3 期研究。
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Cell-penetrating peptide sequence and modification dependent uptake and subcellular distribution of green florescent protein in different cell lines.穿膜肽序列和修饰依赖性对不同细胞系中绿色荧光蛋白的摄取和亚细胞分布。
Sci Rep. 2019 Apr 18;9(1):6298. doi: 10.1038/s41598-019-42456-8.
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Improving cellular uptake of therapeutic entities through interaction with components of cell membrane.通过与细胞膜成分相互作用提高治疗实体的细胞摄取。
Drug Deliv. 2019 Dec;26(1):328-342. doi: 10.1080/10717544.2019.1582730.
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New Cell-Penetrating Peptide (KRP) with Multiple Physicochemical Properties Endows Doxorubicin with Tumor Targeting and Improves Its Therapeutic Index.新型细胞穿透肽(KRP)具有多种物理化学性质,赋予多柔比星肿瘤靶向性并提高其治疗指数。
ACS Appl Mater Interfaces. 2019 Jan 16;11(2):2448-2458. doi: 10.1021/acsami.8b21027. Epub 2019 Jan 3.
10
Cartilage penetrating cationic peptide carriers for applications in drug delivery to avascular negatively charged tissues.用于向无血管负电荷组织递药的穿透软骨阳离子肽载体。
Acta Biomater. 2019 Jul 15;93:258-269. doi: 10.1016/j.actbio.2018.12.004. Epub 2018 Dec 6.

用于药物递送的生物电:阳离子疗法的前景。

Bioelectricity for Drug Delivery: The Promise of Cationic Therapeutics.

作者信息

Young Cameron C, Vedadghavami Armin, Bajpayee Ambika G

机构信息

Department of Chemical Engineering, Northeastern University, Boston, Massachusetts, USA.

Department of Bioengineering, Northeastern University, Boston, Massachusetts, USA.

出版信息

Bioelectricity. 2020 Jun 17;2(2):68-81. doi: 10.1089/bioe.2020.0012. Epub 2020 May 21.

DOI:10.1089/bioe.2020.0012
PMID:32803148
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7313641/
Abstract

Biological systems overwhelmingly comprise charged entities generating electrical activity that can have significant impact on biological structure and function. This intrinsic bio-electrical activity can also be harnessed for overcoming the tissue matrix and cell membrane barriers, which have been outstanding challenges for targeted drug delivery, by using rationally designed cationic carriers. The weak and reversible long-range electrostatic interactions with fixed negatively charged groups facilitate electro-diffusive transport of cationic therapeutics through full-tissue thickness to effectively reach intra-tissue, cellular, and intracellular target sites. This article presents a perspective on the promise of using rationally designed cationic biomaterials in targeted drug delivery, the underlying charge-based mechanisms, and bio-transport phenomena while addressing outstanding concerns around toxicity and methods to mitigate them. We also discuss electrically charged drugs that are currently being evaluated in clinical trials and identify areas of further development that have the potential to usher in new treatments.

摘要

生物系统绝大多数由产生电活动的带电实体组成,这些电活动会对生物结构和功能产生重大影响。这种内在的生物电活动还可以通过使用合理设计的阳离子载体来克服组织基质和细胞膜屏障,而这些屏障一直是靶向药物递送面临的突出挑战。与固定的带负电荷基团之间微弱且可逆的远程静电相互作用,有助于阳离子治疗药物通过全组织厚度进行电扩散运输,从而有效到达组织内、细胞内和细胞内的靶点。本文阐述了在靶向药物递送中使用合理设计的阳离子生物材料的前景、潜在的基于电荷的机制以及生物转运现象,同时解决了围绕毒性及其缓解方法的突出问题。我们还讨论了目前正在临床试验中评估的带电药物,并确定了有可能带来新治疗方法的进一步发展领域。