下载PDF
{"title":"Fluorescence and surface-enhanced Raman study of 9-aminoacridine in relation to its aggregation and excimer emission in aqueous solution and on silver surface","authors":"A. Murza, S. Sánchez-Cortés, J. V. García-Ramos","doi":"10.1002/(SICI)1520-6343(1998)4:5<327::AID-BSPY4>3.0.CO;2-H","DOIUrl":null,"url":null,"abstract":"<p>Fluorescence spectroscopy and surface-enhanced Raman spectroscopy (SERS) have been applied to study the aggregation and excimer emission of 9-aminoacridine (9AA) and 9-aminoacridine hydrochloride (9AA-HCl) in aqueous solution and on silver colloids. The effect of the drug concentration, pH, and chloride concentration on these processes has been investigated. The excimer emission of 9AA is connected to the dimerization of this drug in solution: the formation of 9AA dimers is greatly favored when the drug is under the amino form at neutral and acidic pH, while at alkaline pH the imino 9AA form tends to form large-sized aggregates which cannot be excited to render excimer emission. 9AA is adsorbed on the silver surface under two different forms: strongly and weakly attached 9AA, each one corresponding to the different drug tautomers: imino and amino. The interaction of 9AA with silver induces a charge transfer from the adsorbate to the metal leading to a remarkable fluorescence quenching, a basicity decrease of the adsorbed drug and a considerable weakening of the dimer-excimer emission. Furthermore, an attribution of the main Raman features appearing in the SERS spectra has been proposed, providing marker bands for the imino and amino 9AA tautomers, and a mechanism for the molecular dimerization is also suggested. © 1998 John Wiley & Sons, Inc. Biospectroscopy 4: 327–339, 1998</p>","PeriodicalId":9037,"journal":{"name":"Biospectroscopy","volume":"4 5","pages":"327-339"},"PeriodicalIF":0.0000,"publicationDate":"1999-01-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/(SICI)1520-6343(1998)4:5<327::AID-BSPY4>3.0.CO;2-H","citationCount":"28","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biospectroscopy","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/%28SICI%291520-6343%281998%294%3A5%3C327%3A%3AAID-BSPY4%3E3.0.CO%3B2-H","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 28
引用
批量引用
Abstract
Fluorescence spectroscopy and surface-enhanced Raman spectroscopy (SERS) have been applied to study the aggregation and excimer emission of 9-aminoacridine (9AA) and 9-aminoacridine hydrochloride (9AA-HCl) in aqueous solution and on silver colloids. The effect of the drug concentration, pH, and chloride concentration on these processes has been investigated. The excimer emission of 9AA is connected to the dimerization of this drug in solution: the formation of 9AA dimers is greatly favored when the drug is under the amino form at neutral and acidic pH, while at alkaline pH the imino 9AA form tends to form large-sized aggregates which cannot be excited to render excimer emission. 9AA is adsorbed on the silver surface under two different forms: strongly and weakly attached 9AA, each one corresponding to the different drug tautomers: imino and amino. The interaction of 9AA with silver induces a charge transfer from the adsorbate to the metal leading to a remarkable fluorescence quenching, a basicity decrease of the adsorbed drug and a considerable weakening of the dimer-excimer emission. Furthermore, an attribution of the main Raman features appearing in the SERS spectra has been proposed, providing marker bands for the imino and amino 9AA tautomers, and a mechanism for the molecular dimerization is also suggested. © 1998 John Wiley & Sons, Inc. Biospectroscopy 4: 327–339, 1998
9-氨基吖啶在水溶液和银表面的聚集和准分子发射的荧光和表面增强拉曼研究
采用荧光光谱和表面增强拉曼光谱(SERS)研究了9-氨基吖啶(9AA)和9-氨基吖啶盐酸盐(9AA- hcl)在水溶液和银胶体上的聚集和准分子发射。考察了药物浓度、pH和氯化物浓度对这些过程的影响。9AA的准分子发射与药物在溶液中的二聚化有关:在中性和酸性pH下,药物处于氨基形式时,极大地有利于9AA二聚体的形成,而在碱性pH下,亚胺9AA形式倾向于形成大的聚集体,不能被激发以产生准分子发射。9AA以两种不同的形式吸附在银表面:强和弱附着9AA,每一种形式对应不同的药物互变异构体:亚氨基和氨基。9AA与银的相互作用诱导电荷从吸附物转移到金属,导致荧光猝灭,吸附药物的碱度降低,二聚体准分子发射明显减弱。此外,还提出了出现在SERS光谱中的主要拉曼特征的归属,为亚氨基和氨基9AA互变异构体提供了标记带,并提出了分子二聚化的机制。©1998 John Wiley &儿子,Inc。生物光谱学杂志,1998
本文章由计算机程序翻译,如有差异,请以英文原文为准。