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新型米力农纳米制剂在心血管疾病中的应用:制备及体外特性研究。

Novel Milrinone Nanoformulation for Use in Cardiovascular Diseases: Preparation and in Vitro Characterization.

机构信息

Department of Biomedical Engineering , Biomedical Technology and Cell Therapy Research Laboratory , 3775 University Street , Montreal , QC H3A 2B4 , Canada.

Division of Experimental Medicine , 1001 Boulevard Decarie , Montréal , QC H4A 3J1 , Canada.

出版信息

Mol Pharm. 2018 Jul 2;15(7):2489-2502. doi: 10.1021/acs.molpharmaceut.7b00360. Epub 2018 Jun 8.

Abstract

Cardiovascular diseases are the leading causes of mortality across the globe. Over the years, various drug formulations and delivery methods have been tested for cardiac repair. Milrinone (MRN) is a widely known cardiac inotrope drug used for the treatment of congestive heart failure in patients, however, its efficacy is limited. This study is the first to report the design of a novel MRN-nanoformulation using human serum albumin nanoparticles (HSA-NPs). The HSA-NPs exhibit promising drug delivery characteristics, such as target specificity, nonimmunogenicity, biocompatibility, and enhanced bioavailability. This article describes a MRN-nanoformulation design for in vitro drug release, cellular uptake, biocompatibility, and other features. The MRN-nanoformulation was prepared by the ethanol desolvation technique and key parameters were optimized to obtain a desired particle size of 154.2 ± 5.8 nm, zeta potential of -29.5 ± 2.9 mV, and a drug encapsulation efficiency of 41.1 ± 1.7%. Molecular docking studies have revealed that MRN binds in the hydrophobic cavity of HSA, which has also been indicated by circular dichroism and enzyme-mediated drug release studies in the presence of trypsin, pepsin, proteinase K, protease, and cathepsin D. The intracellular uptake of fluorescently tagged MRN-HSA-NPs using HUVEC and H9c2 cells was evaluated by flow cytometry. The nanoparticle toxicity results indicated that MRN-HSA-NPs show significantly lower cytotoxicity and higher cell viability ( P < 0.0001) as compared to the MRN-lactate drug in HUVEC (61.6 ± 3.7% vs 36.2 ± 2.9%) and H9c2 (58.8 ± 5.7% vs 18.8 ± 4.9%) cells. These studies indicate that the novel MRN-nanoformulation offers better drug delivery procedures than currently used methods and has potential in treatment of congestive heart failure and other cardiovascular diseases.

摘要

心血管疾病是全球范围内导致死亡的主要原因。多年来,人们已经测试了各种药物制剂和给药方法来进行心脏修复。米力农(MRN)是一种广泛使用的心脏正性肌力药物,用于治疗充血性心力衰竭患者,但它的疗效有限。本研究首次报道了使用人血清白蛋白纳米粒(HSA-NPs)设计新型 MRN-纳米制剂。HSA-NPs 表现出有前途的药物递送特性,例如靶向特异性、非免疫原性、生物相容性和增强的生物利用度。本文描述了一种用于体外药物释放、细胞摄取、生物相容性和其他特性的 MRN-纳米制剂设计。MRN-纳米制剂通过乙醇去溶剂化技术制备,并对关键参数进行了优化,以获得理想的粒径为 154.2±5.8nm、zeta 电位为-29.5±2.9mV 和药物包封效率为 41.1±1.7%。分子对接研究表明,MRN 结合在 HSA 的疏水腔中,这也通过圆二色性和存在胰蛋白酶、胃蛋白酶、蛋白酶、蛋白酶 K 和组织蛋白酶 D 时的酶介导药物释放研究得到了证实。使用 HUVEC 和 H9c2 细胞通过流式细胞术评估荧光标记的 MRN-HSA-NPs 的细胞内摄取。纳米颗粒毒性结果表明,与 MRN-乳酸药物相比,MRN-HSA-NPs 在 HUVEC(61.6±3.7%比 36.2±2.9%)和 H9c2(58.8±5.7%比 18.8±4.9%)细胞中显示出显著更低的细胞毒性和更高的细胞活力(P<0.0001)。这些研究表明,新型 MRN-纳米制剂提供了比目前使用的方法更好的药物递送程序,并且在治疗充血性心力衰竭和其他心血管疾病方面具有潜力。

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