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Depth Profiling of 4-Acetamindophenol-Doped Poly(lactic acid) Films Using Cluster Secondary Ion Mass Spectrometry

机译:簇二次离子质谱法深度分析4-乙胺基苯酚掺杂的聚乳酸薄膜

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摘要

The feasibility of using cluster secondary ion mass spectrometry for depth profiling of drug delivery systems is explored. The behavior of various biodegradable polymer films under dynamic SF_(5)~(+) primary ion bombardment was investigated, including several films doped with model drugs. The SF_(5)~(+) depth profiles obtained from these biodegradable polymer films showed very little degradation in secondary ion signal as a function of increasing primary ion dose, and it was discovered that the characteristic ion signals for the polymers remained constant for ion doses up to ~5×10~(15) ions/cm~(2). These results suggest that the polyester structure of the biodegradable polymers studied here allows for a greater ability to depth profile due to ease of main chain scission. Attempts were also made to depth profile through a series of poly(lactic acid) (PLA) films containing varying concentrations of the drug 4-acetamidophenol. The depth profiles obtained from these films show very little decrease in both the 4-acetamidophenol molecular ion and PLA fragment ion signals as a function of increasing SF_(5)~(+) primary ion dose. Similar results were obtained with theophylline-doped PLA films. These results show that, in some drug delivery devices, it is possible to monitor the distribution of a drug as a function of depth by using cluster primary ion beams.
机译:探索了使用簇二次离子质谱仪对药物输送系统进行深度分析的可行性。研究了在动态SF_(5)〜(+)一次离子轰击下各种可生物降解的聚合物薄膜的行为,包括几种掺有模型药物的薄膜。从这些可生物降解的聚合物薄膜获得的SF_(5)〜(+)深度分布图显示,随着增加一次离子剂量,二次离子信号几乎没有降解,并且发现聚合物的特征离子信号对于离子保持恒定。剂量高达〜5×10〜(15)离子/ cm〜(2)。这些结果表明,由于容易进行主链断裂,本文研究的生物可降解聚合物的聚酯结构具有更大的深度分布能力。还尝试通过一系列含有不同浓度的药物4-对乙酰氨基苯酚的聚乳酸(PLA)薄膜进行深度剖析。从这些薄膜获得的深度图显示,4-乙酰氨基酚分子离子和PLA碎片离子信号几乎都没有随SF_(5)〜(+)初级离子剂量的增加而降低。用茶碱掺杂的PLA膜获得了相似的结果。这些结果表明,在某些药物输送装置中,可以通过使用簇一次离子束来监测药物随深度的分布。

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