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通过等离子体聚合四甲基环四硅氧烷涂层屏障控制药物释放。

Controlled drug release through a plasma polymerized tetramethylcyclo-tetrasiloxane coating barrier.

机构信息

BioSurface Engineering Technologies (BioSET), Inc., 9430 Key West Avenue, Rockville, MD 20850, USA.

出版信息

J Biomater Sci Polym Ed. 2012;23(1-4):483-96. doi: 10.1163/092050610X552753. Epub 2011 Jan 28.

Abstract

A plasma polymerized tetramethylcyclo-tetrasiloxane (TMCTS) coating was deposited onto a metallic biomaterial, 316 stainless steel, to control the release rate of drugs, including daunomycin, rapamycin and NPC-15199 (N-(9-fluorenylmethoxy-carbonyl)-leucine), from the substrate surface. The plasma-state polymerized TMCTS thin film was deposited in a vacuum plasma reactor operated at a radio-frequency of 13.56 MHz, and was highly adhesive to the stainless steel, providing a smooth and hard coating layer for drugs coated on the substrate. To investigate the influence of plasma coating thickness on the drug diffusion profile, coatings were deposited at various time lengths from 20 s to 6 min, depending on the type of drug. Atomic force spectroscopy (AFM) was utilized to characterize coating thickness. Drug elution was measured using a spectrophotometer or high-performance liquid chromatography (HPLC) system. The experimental results indicate that plasma polymerized TMCTS can be used as an over-coating to control drug elution at the desired release rate. The drug-release rate was also found to be dependent on the molecular weight of the drug with plasma coating barrier on top of it. The in vitro cytotoxicity test result suggested that the TMCTS plasma coatings did not produce a cytotoxic response to mammalian cells. The non-cytotoxicity of TMCTS coating plus its high thrombo-resistance and biocompatibility are very beneficial to drug-eluting devices that contact blood.

摘要

一种等离子体聚合的四甲基环四硅氧烷 (TMCTS) 涂层被沉积在金属生物材料 316 不锈钢上,以控制药物(包括柔红霉素、雷帕霉素和 NPC-15199(N-(9-芴甲氧羰基)-亮氨酸))从基质表面的释放速率。等离子态聚合的 TMCTS 薄膜在射频为 13.56 MHz 的真空等离子体反应器中沉积,与不锈钢具有高附着力,为涂覆在基质上的药物提供了光滑而坚硬的涂层。为了研究等离子体涂层厚度对药物扩散分布的影响,根据药物的类型,将涂层沉积在从 20 秒到 6 分钟不等的各种时间长度上。原子力显微镜 (AFM) 用于表征涂层厚度。使用分光光度计或高效液相色谱 (HPLC) 系统测量药物洗脱。实验结果表明,等离子体聚合的 TMCTS 可用作包衣层,以控制所需释放速率的药物洗脱。还发现药物释放速率取决于其上有等离子体涂层阻挡层的药物的分子量。体外细胞毒性试验结果表明,TMCTS 等离子体涂层对哺乳动物细胞没有产生细胞毒性反应。TMCTS 涂层的非细胞毒性及其高抗血栓性和生物相容性对接触血液的药物洗脱装置非常有益。

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