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主体:环糊精与表面活性剂的主客体相互作用对光敏剂哈尔满原促旋光性的调制。

Modulation in prototropism of the photosensitizer Harmane by host:guest interactions between β-cyclodextrin and surfactants.

机构信息

Department of Chemistry, University of Calcutta, 92 A.P.C. Road, Calcutta 700 009, India.

出版信息

J Colloid Interface Sci. 2013 Dec 1;411:230-9. doi: 10.1016/j.jcis.2013.08.010. Epub 2013 Aug 29.

DOI:10.1016/j.jcis.2013.08.010
PMID:24060109
Abstract

The present contribution demonstrates the photophysics of a prospective cancer cell photosensitizer Harmane (HM) belonging to the family of β-carboline in mixed microheterogeneous environments of β-cyclodextrin (β-CD) and surfactants having varying surface charges using steady-state and time-resolved fluorescence spectroscopic techniques. The remarkable modulations in prototropic activities of the micelle-bound drug in the presence of β-CD evinces for disruption of the micellar structural integrity by β-CD. The results are meticulously discussed in relevance to the effect of a potential drug delivery vehicle (CD) on the membrane-mimetic micellar system. Further, application of an extrinsic fluorescence probe for monitoring such interactions is fraught by the possibilities of no less than three equilibria that can operate simultaneously viz., (i) surfactant-cyclodextrin, (ii) surfactant-fluorophore and (iii) cyclodextrin-fluorophore. This aspect highlights the enormous importance of the issue of suitability of the fluorescence probe to study such complicated systems and interaction phenomena. Also the varying interaction scenario of β-CD with the nature of the surfactant highlights the importance of precise knowledge of the strength and locus of drug binding in delineating such complex interactions. The results of the present investigation advocate for the potential applicability of the drug (HM) itself as a fluorescence reporter in study of such complex microheterogeneous interactions.

摘要

本研究以β-咔啉家族中的潜在癌细胞光敏剂哈尔满(HM)为模型,采用稳态和时间分辨荧光光谱技术,研究了其在具有不同表面电荷的β-环糊精(β-CD)和表面活性剂的混合微观异质环境中的光物理性质。在β-CD 存在下,胶束结合药物的质子转移活性发生显著变化,表明β-CD 破坏了胶束的结构完整性。结果与潜在药物输送载体(CD)对膜模拟胶束系统的影响进行了细致的讨论。此外,应用外源性荧光探针来监测这种相互作用存在不少于三种平衡同时作用的可能性,即:(i)表面活性剂-环糊精,(ii)表面活性剂-荧光团,(iii)环糊精-荧光团。这一方面突出了荧光探针适用于研究这种复杂体系和相互作用现象的重要性。此外,β-CD 与表面活性剂性质的相互作用变化情景强调了精确了解药物结合的强度和位置在描述这种复杂相互作用中的重要性。本研究的结果表明,该药物(HM)本身可能作为荧光报告基团,用于研究这种复杂的微观异质相互作用。

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