CHIRAL WOODPILE MORPHOLOGY OPTIMIZATION FOR PLASMONIC ENHANCED ENANTIOMERIC DETECTION IN PHARMACOLOGY QUALITY MANAGEMENT

Gautam Ramasamy, E. H. Khoo
{"title":"CHIRAL WOODPILE MORPHOLOGY OPTIMIZATION FOR PLASMONIC ENHANCED ENANTIOMERIC DETECTION IN PHARMACOLOGY QUALITY MANAGEMENT","authors":"Gautam Ramasamy, E. H. Khoo","doi":"10.20319/mijst.2019.52.0119","DOIUrl":null,"url":null,"abstract":"The majority of pharmaceuticals currently in circulation are chiral compounds; mostly sold as equimolar mixtures of two enantiomers. Albeit, they have identical chemical structures, the human body metabolizes each enantiomer by separate pathways due to their different handedness. Hence, one isomer may exhibit the intended pharmaceutical effect, whereas the other exists as an inactive impurity or, occasionally, may engender undesirable side-effects and toxicity, like in the Softenon disaster which caused circa one thousand congenital disabilities (International Union of Crystallography, 2016). Therefore, it is imperative to promote chiral separation and analysis of chiral drugs in pharmaceutical manufacture to eliminate the undesirable enantiomer (Nguyen, He, & Pham-Huy, 2006). Recently, plasmonic-enhanced metamaterials have been shown to amplify the subtle circular dichroic effects of chiral molecules by many orders of magnitude, making enantioselective assays more precise by amplifying the CD signal, enabling discrimination of nuanced spectral features, never seen before (Nguyen et al., 2006). This paper advances the sensitivity of CD spectroscopy by studying a newly designed chiral woodpile nanostructure that uses plasmon-generated superchiral near fields to enhance the dissymmetry of chiral molecules and magnify their chiroptical effects. Simulated to outperform gammadion arrays proposed by competitor papers by 1206 %, it empowers increased measurement precision in the assessment of enantiomeric excess in the quality management of drug manufacture, increasing safety. Furthermore, it may potentially lead to earlier detection of diseases such as HIV and other viruses. Lastly, for the first time, this paper proposes a revolutionary but intuitive mechanism to explain the generation of the superchiral near field of a plasmonic-enhanced nanostructure. Shown to corroborate with simulation, it provides a more profound understanding of the underlying mechanisms beyond just the ‘plasmon-plasmon coupling’ which preceding works have already discussed. This knowledge opens up new avenues to develop nanostructures with even stronger circular dichroic properties. Article DOI: https://dx.doi.org/10.20319/mijst.2019.52.0119 This work is licensed under the Creative Commons Attribution-Non-commercial 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc/4.0/ or send a letter to Creative Commons, PO Box 1866, Mountain View, CA 94042, USA.","PeriodicalId":411113,"journal":{"name":"MATTER: International Journal of Science and Technology","volume":"61 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"MATTER: International Journal of Science and Technology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.20319/mijst.2019.52.0119","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The majority of pharmaceuticals currently in circulation are chiral compounds; mostly sold as equimolar mixtures of two enantiomers. Albeit, they have identical chemical structures, the human body metabolizes each enantiomer by separate pathways due to their different handedness. Hence, one isomer may exhibit the intended pharmaceutical effect, whereas the other exists as an inactive impurity or, occasionally, may engender undesirable side-effects and toxicity, like in the Softenon disaster which caused circa one thousand congenital disabilities (International Union of Crystallography, 2016). Therefore, it is imperative to promote chiral separation and analysis of chiral drugs in pharmaceutical manufacture to eliminate the undesirable enantiomer (Nguyen, He, & Pham-Huy, 2006). Recently, plasmonic-enhanced metamaterials have been shown to amplify the subtle circular dichroic effects of chiral molecules by many orders of magnitude, making enantioselective assays more precise by amplifying the CD signal, enabling discrimination of nuanced spectral features, never seen before (Nguyen et al., 2006). This paper advances the sensitivity of CD spectroscopy by studying a newly designed chiral woodpile nanostructure that uses plasmon-generated superchiral near fields to enhance the dissymmetry of chiral molecules and magnify their chiroptical effects. Simulated to outperform gammadion arrays proposed by competitor papers by 1206 %, it empowers increased measurement precision in the assessment of enantiomeric excess in the quality management of drug manufacture, increasing safety. Furthermore, it may potentially lead to earlier detection of diseases such as HIV and other viruses. Lastly, for the first time, this paper proposes a revolutionary but intuitive mechanism to explain the generation of the superchiral near field of a plasmonic-enhanced nanostructure. Shown to corroborate with simulation, it provides a more profound understanding of the underlying mechanisms beyond just the ‘plasmon-plasmon coupling’ which preceding works have already discussed. This knowledge opens up new avenues to develop nanostructures with even stronger circular dichroic properties. Article DOI: https://dx.doi.org/10.20319/mijst.2019.52.0119 This work is licensed under the Creative Commons Attribution-Non-commercial 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc/4.0/ or send a letter to Creative Commons, PO Box 1866, Mountain View, CA 94042, USA.
药理学质量管理中等离子体增强对映体检测的手性木桩形貌优化
目前流通的大多数药物都是手性化合物;主要作为两种对映体的等摩尔混合物出售。尽管它们具有相同的化学结构,但由于它们的旋向性不同,人体通过不同的途径代谢每种对映体。因此,一种异构体可能表现出预期的药物效果,而另一种异构体作为非活性杂质存在,或者偶尔会产生不良的副作用和毒性,就像导致大约1000例先天性残疾的Softenon灾难一样(国际晶体学联盟,2016)。因此,必须促进手性药物的手性分离和分析,以消除不需要的对映体(Nguyen, He, & Pham-Huy, 2006)。最近,等离子体增强的超材料已被证明可以将手性分子的微妙的圆二色性效应放大许多个数量级,通过放大CD信号使对映选择性分析更加精确,从而能够区分细微的光谱特征,这是以前从未见过的(Nguyen et al., 2006)。本文通过研究一种新设计的手性木堆纳米结构,利用等离子体产生的超手性近场增强手性分子的不对称性,放大手性分子的手性效应,提高了CD光谱的灵敏度。模拟结果表明,该方法比竞争对手提出的伽玛仪阵列高出1206%,提高了药物生产质量管理中对映体过量评估的测量精度,提高了安全性。此外,它可能导致更早地发现艾滋病毒和其他病毒等疾病。最后,本文首次提出了一种革命性但直观的机制来解释等离子体增强纳米结构的超手性近场的产生。通过模拟证实,它提供了对潜在机制的更深刻的理解,而不仅仅是前面已经讨论过的“等离子体激元-等离子体激元耦合”。这一知识为开发具有更强圆二色性的纳米结构开辟了新的途径。文章DOI: https://dx.doi.org/10.20319/mijst.2019.52.0119本作品遵循知识共享署名-非商业4.0国际许可协议。要查看本许可协议的副本,请访问http://creativecommons.org/licenses/by-nc/4.0/或致函美国山景城CA 94042邮政信箱1866号创用cc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信