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本文引用的文献

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Materials technology in drug eluting balloons: Current and future perspectives.药物洗脱球囊中的材料技术:现状与未来展望。
J Control Release. 2016 Oct 10;239:92-106. doi: 10.1016/j.jconrel.2016.08.018. Epub 2016 Aug 21.
2
Fluorescence imaging enabled poly(lactide-co-glycolide).荧光成像技术实现了聚(丙交酯-乙交酯)。
Acta Biomater. 2016 Jan;29:307-319. doi: 10.1016/j.actbio.2015.10.010. Epub 2015 Oct 20.
3
Dextran sulfate as a drug delivery platform for drug-coated balloons: Preparation, characterization, in vitro drug elution, and smooth muscle cell response.硫酸葡聚糖作为药物涂层球囊的药物递送平台:制备、表征、体外药物洗脱及平滑肌细胞反应。
J Biomed Mater Res B Appl Biomater. 2016 Oct;104(7):1416-30. doi: 10.1002/jbm.b.33494. Epub 2015 Jul 31.
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Polyacrylic acid polymers hydrogels intended to topical drug delivery: preparation and characterization.用于局部给药的聚丙烯酸聚合物水凝胶:制备与表征
Pharm Dev Technol. 2015 Jun;20(4):490-6. doi: 10.3109/10837450.2014.882941. Epub 2014 Feb 7.
5
Correlating coating characteristics with the performance of drug-coated balloons--a comparative in vitro investigation of own established hydrogel- and ionic liquid-based coating matrices.将涂层特性与药物涂层球囊性能相关联——对自行制备的水凝胶和离子液体基涂层基质的体外比较研究
PLoS One. 2015 Mar 3;10(3):e0116080. doi: 10.1371/journal.pone.0116080. eCollection 2015.
6
Mechanisms of tissue uptake and retention of paclitaxel-coated balloons: impact on neointimal proliferation and healing.紫杉醇涂层球囊的组织摄取和滞留机制:对新生内膜增殖和愈合的影响。
Open Heart. 2014 Aug 6;1(1):e000117. doi: 10.1136/openhrt-2014-000117. eCollection 2014.
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In situ re-endothelialization via multifunctional nanoscaffolds.通过多功能纳米支架实现原位再内皮化。
ACS Nano. 2014 Oct 28;8(10):10826-36. doi: 10.1021/nn504636n. Epub 2014 Sep 15.
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Polymeric nanoparticles for pulmonary protein and DNA delivery.聚合物纳米粒用于肺部蛋白和 DNA 的递送。
Acta Biomater. 2014 Jun;10(6):2643-52. doi: 10.1016/j.actbio.2014.01.033. Epub 2014 Feb 8.
9
Novel paclitaxel-coated angioplasty balloon catheter based on cetylpyridinium salicylate: preparation, characterization and simulated use in an in vitro vessel model.基于柳醇盐的新型紫杉醇涂层血管成形球囊导管:制备、表征和在体外血管模型中的模拟使用。
Mater Sci Eng C Mater Biol Appl. 2013 Oct;33(7):4244-50. doi: 10.1016/j.msec.2013.06.021. Epub 2013 Jun 26.
10
Emerging technologies: polymer-free phospholipid encapsulated sirolimus nanocarriers for the controlled release of drug from a stent-plus-balloon or a stand-alone balloon catheter.新兴技术:无聚合物磷脂包裹的西罗莫司纳米载体,用于从支架加球囊或单独球囊导管中控制药物释放。
EuroIntervention. 2013 May 20;9(1):148-56. doi: 10.4244/EIJV9I1A21.

载药球囊血管内成形术治疗心血管疾病。

Nanoparticle eluting-angioplasty balloons to treat cardiovascular diseases.

机构信息

Department of Bioengineering, University of Texas at Arlington, Arlington, TX, USA.

Department of Biomedical Engineering, Materials Research Institute, The Huck Institutes of the Life Sciences, Pennsylvania State University, University Park, PA, USA.

出版信息

Int J Pharm. 2019 Jan 10;554:212-223. doi: 10.1016/j.ijpharm.2018.11.011. Epub 2018 Nov 5.

DOI:10.1016/j.ijpharm.2018.11.011
PMID:30408532
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6489505/
Abstract

Nanoparticles (NPs) can be used to locally deliver anti-restenosis drugs when they are infused directly to the injured arteries after intervention procedures such as angioplasty. However, the efficacy of transferring NPs via infusion to the arterial wall is limited, at least partially, due to poor NP retention on the inner artery wall. To improve NP retention, angioplasty balloons coated with drug-loaded NPs were fabricated via either layer-by-layer (LbL) electrostatic coating or acrylic-based hydrogel (AAH) coating techniques. Three types of NPs, namely poly (lactide-co-glycolide) (PLGA), biodegradable photo-luminescent PLGA and urethane doped polyester were studied. The transfer efficacy of NPs from various coatings to the arterial wall were further evaluated to find the optimal coating conditions. The ex vivo NP transfer studies showed significantly more NPs being transferred to the rat arterial wall after the angioplasty procedure by the AAH coating (95% transfer efficiency) compared to that of the LbL technique (60%) and dip coating (20%) under flow conditions (10 dyn/cm). Our results suggest that the AAH coating of drug-loaded NPs on the angioplasty balloon could potentially provide superior retention of drug-loaded NPs onto the arterial wall for a better local delivery of drug-loaded NPs to effectively treat arterial diseases.

摘要

纳米颗粒 (NPs) 可在介入治疗(如血管成形术)后直接注入损伤的动脉内,用于局部递送抗再狭窄药物。然而,通过输注将 NPs 递送至动脉壁的效果有限,至少部分原因是 NP 在动脉内表面的保留率较差。为了提高 NP 的保留率,通过层层 (LbL) 静电涂层或基于丙烯酸的水凝胶 (AAH) 涂层技术制备了涂有载药 NPs 的血管成形术球囊。研究了三种 NPs,即聚(乳酸-共-乙醇酸)(PLGA)、可生物降解的光致发光 PLGA 和聚氨酯掺杂聚酯。进一步评估了从各种涂层向动脉壁转移 NPs 的效果,以找到最佳的涂层条件。在体外 NP 转移研究中,与 LbL 技术(60%)和浸涂(20%)相比,在流动条件(10 dyn/cm)下,AAH 涂层(95%的转移效率)可将更多的 NPs 转移到血管成形术后的大鼠动脉壁(10 dyn/cm)。我们的结果表明,在血管成形术球囊上涂覆载药 NPs 的 AAH 涂层可能会将载药 NPs 更好地保留在动脉壁上,从而更有效地将载药 NPs 局部递送至动脉壁,以有效治疗动脉疾病。