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Multi-Drug/Gene NASH Therapy Delivery and Selective Hyperspectral NIR Imaging Using Chirality-Sorted Single-Walled Carbon Nanotubes

机译:多药物/基因NASH治疗传递和使用手性排序单壁碳纳米管的选择性高光谱NIR成像

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摘要

Single-walled carbon nanotubes (SWCNTs) can serve as drug delivery/biological imaging agents, as they exhibit intrinsic fluorescence in the near-infrared, allowing for deeper tissue imaging while providing therapeutic transport. In this work, CoMoCAT (Cobalt Molybdenum Catalyst) SWCNTs, chirality-sorted by aqueous two-phase extraction, are utilized for the first time to deliver a drug/gene combination therapy and image each therapeutic component separately via chirality-specific SWCNT fluorescence. Each of (7,5) and (7,6) sorted SWCNTs were non-covalently loaded with their specific payload: the PI3 kinase inhibitor targeting liver fibrosis or CCR5 siRNA targeting inflammatory pathways with the goal of addressing these processes in nonalcoholic steatohepatitis (NASH), ultimately to prevent its progression to hepatocellular carcinoma. PX-866-(7,5) SWCNTs and siRNA-(7,6) SWCNTs were each imaged via characteristic SWCNT emission at 1024/1120 nm in HepG2 and HeLa cells by hyperspectral fluorescence microscopy. Wavelength-resolved imaging verified the intracellular transport of each SWCNT chirality and drug release. The therapeutic efficacy of each formulation was further demonstrated by the dose-dependent cytotoxicity of SWCNT-bound PX-866 and >90% knockdown of CCR5 expression with SWCNT/siRNA transfection. This study verifies the feasibility of utilizing chirality-sorted SWCNTs for the delivery and component-specific imaging of combination therapies, also suggesting a novel nanotherapeutic approach for addressing the progressions of NASH to hepatocellular carcinoma.
机译:单壁碳纳米管(SWCNT)可以用作药物输送/生物显像剂,因为它们在近红外光中表现出固有的荧光,从而可以在提供治疗性转运的同时实现更深的组织显像。在这项工作中,首次通过水两相萃取手性分类的CoMoCAT(钴钼催化剂)SWCNT用于提供药物/基因联合治疗,并通过手性特异性SWCNT荧光分别对每种治疗成分进行成像。 (7,5)和(7,6)分类的SWCNT均非共价地装载了其特定的有效负载:靶向肝纤维化的PI3激酶抑制剂或靶向炎症途径的CCR5 siRNA,以解决非酒精性脂肪性肝炎(NASH)中的这些过程),最终防止其发展为肝细胞癌。 PX-866-(7,5)SWCNT和siRNA-(7,6)SWCNT分别通过高光谱荧光显微镜在HepG2和HeLa细胞中以1024/1120 nm的特征性SWCNT发射进行成像。波长分辨成像验证了每个SWCNT手性和药物释放的细胞内转运。通过SWCNT结合的PX-866的剂量依赖性细胞毒性和SWCNT / siRNA转染的CCR5表达的> 90%敲低进一步证明了每种制剂的治疗功效。这项研究验证了使用手性排序的SWCNTs进行联合疗法的递送和组分特异性成像的可行性,还提出了一种新颖的纳米疗法,用于解决NASH向肝细胞癌的进展。

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