Exploiting Co-solubilization of Warfarin, Curcumin, and RhodamineB for Modulation of Energy Transfer: A Micelle FRET On/Off Switch

被引:17
作者
Bhat, Parvaiz Ahmad [2 ]
Chat, Oyais Ahmad [1 ]
Dar, Aijaz Ahmad [1 ]
机构
[1] Univ Kashmir, Dept Chem, Srinagar 190006, Jammu & Kashmir, India
[2] Govt Degree Coll Pulwama, Dept Higher Educ, Pulwama, Jammu & Kashmir, India
关键词
co-solubilization; fluorescence; FRET; micelles; surfactants; FEMTOSECOND SOLVATION DYNAMICS; PHOTOPHYSICAL PROPERTIES; IONIC LIQUID; TRIBLOCK COPOLYMER; ELECTRON-TRANSFER; DIKETO TAUTOMER; ATOM TRANSFER; TD-DFT; SURFACTANT; STABILIZATION;
D O I
10.1002/cphc.201600274
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Two new FRET pairs, warfarin (WF)-curcumin (CUR) and curcumin-rhodamineB (RhB), are explored by using surfactant-based self-assembled soft systems as scaffolds. The study is extended to design a two-step concurrent FRET system based on these three fluorophores, which is an important mechanism to devise artificial light-harvesting/antenna systems. Surfactant systems of varying nature (cationic, anionic, nonionic, and zwitterionic) are exploited to modulate the energy transfer in different FRET systems. Interestingly, micelle/water interfacial-charge-responsive FRET is observed owing to selective solubilization of the fluorophores during co-solubilization. The step-one FRET (WFCUR) is switched on in cationic and zwitterionic media but switched off in anionic/nonionic media, whereas the step-two FRET from CUR to RhB is switched on in anionic/nonionic and zwitterionic media. However, both the FRET steps (WFCURRhB) are observed to be active only in zwitterionic medium. Co-solubilized, appropriately mixed fluorophores having multistep FRET possibilities can be switched on/off selectively as and when required and energy efficiency can be tuned to an optimal level by varying the nature and geometry of the micellar scaffold. Thus, the two FRET pairs selectively acknowledge all types of media for their anticipated applications in biological systems, as structural tools, and for the development of artificial light-harvesting/antenna systems and lasers.
引用
收藏
页码:2360 / 2372
页数:13
相关论文
共 60 条
[1]  
Adhikari A, 2007, J PHYS CHEM B, V111, P12809, DOI [10.1021/jp075693l, 10.1021/jp0756931]
[2]   Excited-State Intramolecular Hydrogen Atom Transfer of Curcumin in Surfactant Micelles [J].
Adhikary, Ramkrishna ;
Carlson, Philip J. ;
Kee, Tak W. ;
Petrich, Jacob W. .
JOURNAL OF PHYSICAL CHEMISTRY B, 2010, 114 (08) :2997-3004
[3]  
Aggarwal BB, 2003, ANTICANCER RES, V23, P363
[4]  
Anderson JLR, 2014, CHEM SCI, V5, P507, DOI [10.1039/c3sc52019f, 10.1039/C3SC52019F]
[5]   An inhibitory effect of self-assembled soft systems on Fenton driven degradation of xanthene dye Rhodamine B [J].
Ashraf, Uzma ;
Chat, Oyais Ahmad ;
Dar, Aijaz Ahmad .
CHEMOSPHERE, 2014, 99 :199-206
[6]   ORIENTATIONAL BINDING OF SUBSTITUTED NAPHTHOATE COUNTERIONS TO THE TETRADECYLTRIMETHYLAMMONIUM BROMIDE MICELLAR INTERFACE [J].
BACHOFER, SJ ;
SIMONIS, U ;
NOWICKI, TA .
JOURNAL OF PHYSICAL CHEMISTRY, 1991, 95 (01) :480-488
[7]   Exploring the Photophysics of Curcumin in Zwitterionic Micellar System: An Approach to Control ESIPT Process in the Presence of Room Temperature Ionic Liquids (RTILs) and Anionic Surfactant [J].
Banerjee, Chiranjib ;
Ghosh, Surajit ;
Mandal, Sarthak ;
Kuchlyan, Jagannath ;
Kundu, Niloy ;
Sarkar, Nilmoni .
JOURNAL OF PHYSICAL CHEMISTRY B, 2014, 118 (13) :3669-3681
[8]   Effect of Surfactant Mixing on Partitioning of Model Hydrophobic Drug, Naproxen, between Aqueous and Micellar Phases [J].
Bhat, Parvaiz Ahmad ;
Rather, Ghulam Mohammad ;
Dar, Aijaz Ahmad .
JOURNAL OF PHYSICAL CHEMISTRY B, 2009, 113 (04) :997-1006
[9]   Structural Rearrangements and Interaction within HII Mesophase Induced by Cosolubilization of Vitamin E and Ascorbic Acid [J].
Bitan-Cherbakovsky, Liron ;
Yuli-Amar, Idit ;
Aserin, Abraham ;
Garti, Nissim .
LANGMUIR, 2009, 25 (22) :13106-13113
[10]   Supramolecular polymers [J].
Brunsveld, L ;
Folmer, BJB ;
Meijer, EW ;
Sijbesma, RP .
CHEMICAL REVIEWS, 2001, 101 (12) :4071-4097