Photophysical Study of Heteroatom-Doped Carbon Dots-MnO2-Based Nanosensor: Selective Detection of Glutathione in the Nanomolar Level.

Heteroatom doping on carbon dots (Cdots) has been developed as an efficient approach to modify its optical and electronic properties. The four different types of heteroatom-doped Cdots (undoped Cdots (u-Cdots, nitrogen-doped Cdots (N-Cdots), sulfur-doped Cdots (Cdots), nitrogen, sulfur codoped Cdots (N, S-Cdots)) have been synthesized through a simple heat treatment of 5 min. Among four different heteroatoms doped nanosensors, N, S-Cdots with MnO2 nanospheres (Mn NS) showed one of the best fluorescents "on-off-on" nanosensors for selective sensing of glutathione (GSH) and cell imaging. N, S-Cdots showed a high fluorescence quantum yield, good photostability, ionic strength, and pH stability. N, S-Cdots with Mn NS demonstrated extremely high fluorescence quenching efficiency and the maximum fluorescence recovery rate after adding GSH to the produced solution. The photophysical study of N, S-Cdots-Mn NS used as a sensor confirms the inner filter effect (IFE) quenching mechanism between them. The developed sensor has an 80 nM limit of detection (LOD) for GSH. The heteroatom-doped framework of Cdots plays a significant role in the sensitive detection of GSH. N, S-Cdots-Mn NS have good permeability, biocompatibility, and low toxicity, due to which it was used in the intracellular imaging of GSH in living cells. The prepared sensor is rapid, economical, less toxic, and highly applicable in diagnosing diseases.

Upcycling Waste: Citrus limon Peel-Derived Carbon Quantum Dots for Sensitive Detection of Tetracycline in the Nanomolar Range.

In this work, a sustainable method was developed for the production of water-soluble carbon quantum dots employing a green approach. The synthetic protocol was employed using the microwave pyrolysis technique, while lemon peel served as a carbon precursor. Fabrication of highly fluorescent lemon-peel-derived CQDs (LP-CQDs) having inherent nitrogen functionality was validated by X-ray photoelectron spectroscopy, FTIR, X-ray diffraction, Raman spectroscopic analysis, and TEM techniques. The average particle size of fabricated LP-CQDs was 4.46 nm. LP-CQDs yielded a remarkable quantum yield of 49.5%, which displayed excellent salinity, photostability, storage time, conditions, and pH stability. LP-CQDs displayed encouraging results for tetracycline (TC) detection using a PL turn-off approach. The sensitivity of LP-CQDs toward TC was seen in a nanomolar range having a detection limit of 50.4 nM. Method validation was comprehensively studied to ensure the precision of the nanosensor. A complete analysis of different photophysical parameters of LP-CQDs was performed with TC to gain a deeper understanding of the sensing mechanism. Fabricated LP-CQDs showed fluorescence quenching toward TC, elucidated by the inner filter effect (IFE) mechanism. The synthesized nanoprobe demonstrated a lesser detection limit with a broad linear range, enabling facile, cheap, environmentally friendly, and fast detection of TC. Practicality of the detection method was assessed through analysis of real samples, resulting in satisfactory recovery percentage and relative standard deviation with respect to the developed probes. Furthermore, LP-CQDs were used as fluorescent inks and to fabricate paper-based fluorescent strips. This study lays the door for the sensing platform of LP-CQDs toward detection of TC, which may impact the potential role of environmental sustainability.

Orange Pomace-Derived Fluorescent Carbon Quantum Dots: Detection of Dual Analytes in the Nanomolar Range.

Green-emissive carbon quantum dots (CQDs) with exclusive chemosensing aspects were synthesized from orange pomace as a biomass-based precursor via a facile microwave method without using any chemicals. The synthesis of highly fluorescent CQDs with inherent nitrogen was confirmed through X-ray diffraction, X-ray photoelectron, Fourier transform infrared, Raman, and transmission electron microscopic techniques. The average size of the synthesized CQDs was found to be 7.5 nm. These fabricated CQDs displayed excellent photostability, water solubility, and outstanding fluorescent quantum yield, i.e., 54.26%. The synthesized CQDs showed promising results for the detection of Cr6+ ions and 4-nitrophenol (4-NP). The sensitivity of CQDs toward Cr6+ and 4-NP was found up to the nanomolar range with the limit of detection values of 59.6 and 14 nM, respectively. Several analytical performances were thoroughly studied for high precision of dual analytes of the proposed nanosensor. Various photophysical parameters of CQDs (quenching efficiency, binding constant, etc.) were analyzed in the presence of dual analytes to gain more insights into the sensing mechanism. The synthesized CQDs exhibited fluorescence quenching toward incrementing the quencher concentration, which was rationalized by the inner filter effect through time-correlated single-photon counting measurements. The CQDs fabricated in the current work exhibited a lower detection limit and a wide linear range through the simple, eco-friendly, and rapid detection of Cr6+ and 4-NP ions. To evaluate the feasibility of the detection approach, real sample analysis was conducted, demonstrating satisfactory recovery rates and relative standard deviations toward the developed probes. This research paves the way for developing CQDs with superior characteristics utilizing orange pomace (biowaste precursor).

Rice Husk-Derived Carbon Quantum Dots-Based Dual-Mode Nanoprobe for Selective and Sensitive Detection of Fe3+ and Fluoroquinolones.

Herein, eco-friendly, water-soluble, and fluorescent carbon quantum dots (CQDs) with an average size of 8.3 nm were synthesized from rice husk (RH) using the hydrothermal method, and the CQDs were labeled as rice husk CQDs (RH-CQDs). The composition and surface functionalities were studied using X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, and Raman spectroscopy. A study on the impact of pH and irradiation time on fluorescence affirmed the stability of RH-CQDs. The as-synthesized nanosensor has high selectivity and sensitivity for Fe3+ ions. Several photophysical studies were performed to investigate the interaction between RH-CQDs and Fe3+. Using the time-correlated single-photon technique, it is determined that the average lifetime value of RH-CQDs significantly decreases in the presence of Fe3+, which supports a dynamic quenching mechanism. The developed sensor exhibited excellent sensitivity with a detection limit in the nanomolar range (149 nM) with a wide linear range of 0-1300 nM for Fe3+ ions. The prepared nanosensor was also used to detect Fe3+ in a tablet supplement with high recoveries. Moreover, the RH-CQD nanoprobe was used to detect other analytes (fluoroquinolones) using the fluorescence enhancement technique. It showed high selectivity and sensitivity toward ofloxacin (OFX) and ciprofloxacin (CPX). The detection limits calculated were 150 nM and 127 nM with a linearity range of 50-1150 nM for OFX and CPX, respectively. The enhancement of the average lifetime value and quantum yield in the presence of OFX and CPX favors the increased fluorescence property of RH-CQDs through hydrogen bonding and charge transfer. In this work, the integration of two different mechanisms (fluorescence quenching and fluorescence enhancement) was followed to construct a single sensing platform for accurate quantification of dual-mode nanosensors for the detection of metal ions and fluoroquinolones by the excited-state electron transfer and hydrogen bonding mechanism, respectively. This strategy also stimulates the detection of more than one analyte.

Morphology Effect of One-Dimensional MnO2 Nanostructures on Heteroatom-Doped Carbon Dot-Based Biosensors for Selective Detection of Glutathione.

Structural versatility of MnO2 nanostructures plays a significant role in biosensing applications. So, we have prepared simple and selective "turn-off-on" sensing probes for the detection of glutathione (GSH), based on nitrogen, sulfur codoped carbon dots (N, S-Cdots) and different morphologies of one-dimensional (1-D) MnO2 nanostructures. N, S-Cdots with a high fluorescence quantum yield (73.42%) were prepared by a green approach through high-temperature pyrolysis in just 5 min. The different morphologies of 1-D MnO2 nanostructures (nanowires with varying aspect ratios and nanorods) were synthesized through a hydrothermal method by varying the reaction period (8, 10, and 12 h). MnO2 nanowires prepared at 8 h showed a high specific surface area (34 m2 g-1) with a large aspect ratio. They showed significant fluorescence quenching, Stern-Volmer constants, and binding constants in the presence of N, S-Cdots. Further, ultraviolet-visible absorption, zeta potential, and time decay studies showed that the quenching mechanism of the developed sensing system was the inner filter effect, which was further confirmed by using the Parker equation. The N, S-Cdots-MnO2 nanowire (with a high aspect ratio) sensing system showed the best limit of detection, i.e., 28.5 µM for GSH. This fast, simple, eco-friendly, and cost-effective sensing system can be further used for real-time biosensing and bioimaging application.

Recent advances in heteroatom-doped graphene quantum dots for sensing applications.

Graphene quantum dots (GQDs) are carbon-based fluorescent nanomaterials having various applications due to attractive properties. But the low photoluminescence (PL) yield and monochromatic PL behavior of GQDs put limitations on their real-time applications. Therefore, heteroatom doping of GQDs is recognized as the best approach to modify the optical as well as electronic properties of GQDs by modifying their chemical composition and electronic structure. In this review, the new strategies for preparing the heteroatom (N, B, S, P) doped GQDs by using different precursors and methods are discussed in detail. The particle size, emission wavelength, PL emissive color, and quantum yield of recently developed heteroatom doped GQDs are reported in this article. The investigation of structure, crystalline nature, and composition of heteroatom doped GQDs by various characterization techniques such as high-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), Raman spectroscopy, Fourier transform infrared (FTIR) and X-ray photoelectron spectroscopy (XPS) are also described. The recent progress on the impact of mono or co-doping of heteroatoms on PL behavior, and optical, electrochemiluminescence (ECL), and electrochemical properties of GQDs is also surveyed. Further, heteroatom doped GQDs with attractive properties used in sensing of various metal ions, biomolecules, small organic molecules, etc. by using various techniques with different limits of detection are also summarized. This review provides progressive trends in the development of heteroatom doped GQDs and their various applications.

Morphology-Dependent Performance of MnO2 Nanostructure-Carbon Dot-Based Biosensors for the Detection of Glutathione.

Herein, we develop a facile, sensitive, and selective fluorescent nanosensor for the detection of glutathione (GSH). In this protocol, carbon dots (Cdots) with a fairly high quantum yield were synthesized by a microwave-assisted pyrolysis technique. Moreover, different shapes of the MnO2 nanostructure were also prepared by the hydrothermal technique. A comparative photophysical study of different morphology-dependent Cdots@MnO2 nanostructure-based biosensors was explored, which showed different results for the quenching values of ("turn-off") fluorescence intensity, quantum yields, electron transfer rate, and average lifetime. The structure, property, and performance of nanomaterials are interdependent. Therefore, the different shapes of MnO2, that is, nanoflowers (NFs), nanorods (NRs), and a mixture of NFs/NRs was prepared by the hydrothermal method owing to different specific surface areas (23-69 m2 g-1) which put the impact on their sensing activity. It was observed that the variation in the different photophysical parameters of fluorescent Cdots such as quantum yield (Φ), average lifetime values [τav (ns)], radiative (kr) rate constant, nonradiative (knr) rate constant, rate of electron transfer (kET), the efficiency of electron transfer (ΦEET), FRET efficiency (E), and Förster distance (R0) were dependent on the different shapes of the MnO2 nanostructure. These results indicate that the transfer of energy occurs between the Cdots and different shapes of MnO2 nanostructures based on fluorescence resonance energy transfer at different charge-transfer rates. The recovery rate ("turn-on") of fluorescence of Cdots with the addition of GSH was obtained best for the NF structure by conversion of MnO2 to Mn2+, and the limit of detection was obtained as ∼19 µM for GSH. The developed sensing probes were rapid, easy, cheap, and eco-friendly for the determination of GSH.

Encapsulation and release of non-fluorescent crystal violet confined in bile-salt aggregates.

In this work, the entrapment of non-fluorescent dye Crystal Violet (CV) in presence of bio-mimetic confined bile-salt aggregates has been studied. The photophysical characteristic properties of CV have been carried out by changing different kinds of hydrophilic head groups and hydrophobic skeletons of bile-salt aggregates (NaC, NaDC, NaTC and NaTGC). The main aim of this work is to modulate the solubility behaviour, fluorescence properties and elucidation of different kinds of non-covalent interaction of CV confined in bile-salt aggregates. To interpret the result, steady state absorption and fluorescence emission techniques have been employed. In aqueous buffer, the CV molecule is non-fluorescent in nature. The value of fluorescence quantum yield (Φ) is ∼10-4. It has been observed that CV confined in bile-salt aggregates becomes highly fluorescent in nature. The enhancement of 'Φ' value of CV in bile-salt aggregates is ∼1000 fold compared to that of aqueous buffer medium. It has also been observed that in the presence of different bile-salt aggregates, CV exhibits remarkable enhancement of absorption and fluorescence emission spectral behaviour. The ground state and the excited state binding constant values of CV in the presence of different bile-salt aggregates have been determined. Moreover, the release of the dye molecule from the confined bile-salt aggregates to the aqueous medium has been executed. It has been found that addition of a very minute concentration of KCl salt (100 nm) to the bile-salt aggregates leads to extreme modification of their photophysical properties of CV. The absorption, fluorescence intensity, fluorescence quantum yield, ground state and excited state binding constant values, partition coefficient and aggregation number of CV molecules entrapped in bile-salt aggregates significantly reduces by addition of KCl. This result clearly confirms that CV releases from the confined system to the aqueous medium.

Deciphering the interaction of solvents with dual emissive carbon dots: A photoluminescence study and its response for different metal ions.

Carbon-based fluorescent quantum dots exhibited tunable photoluminescence (PL) property which is mainly dependent on its excitation wavelength which is an important factor required for optoelectronic and sensing applications. Here, we have established a microwave-based synthesis of dual emissive carbon quantum dots (CDs) using mixed-acid (H3PO4 + H2SO4) and mono/disaccharides as carbon precursor. In aqueous medium, CDs showed dual emission peaks at 434 nm and 518 nm, which exhibited excitation independent fluorescence property with particle size in the range of 4-7 nm. Furthermore, its photophysical properties were explored in different solvents. The astonishing bathochromic shift was observed in its emission wavelengths with the decrease in polarity of the solvents. Moreover, the metal sensing efficacy of CDs was explored in these solvent systems. It exhibited utmost selectivity for Fe(III) ions in both the organic and aqueous medium with maximum and minimum detecting limit of 1 µM and 0.4 µM respectively. These experimental results were also validated through real samples (Ferric citrate tablets 200 mg) and it showed excellent metal ion sensing accuracy for CDs in different media. The fundamental motive of this work was to explain the role of the mixed acid for the development of dual emissive CDs using a single precursor. The solvatochromic and sensing properties of CDs were explored in various solvents, which could be useful for sensing applications.

Structural transition dynamics of biologically active flavins in alkylglucoside surfactants aggregates.

The photophysics and structural transition dynamics of a bio-active flavin lumichrome (LM) entrapped in two sugars based neutral surfactants were reported. Sugar-based surfactants, which were used for research purpose are potential environmentally friendly, green alternative amphiphilic surface active substance compared to other kinds of common surfactants. Here, two alkyl glucoside surfactants n-octyl-ß-D-glucopyranoside (OBG) and n-octyl-ß-D-thioglucopyranoside (OBTG) were used. This work is carried out by using steady-state absorption and fluorescence emission spectroscopy along with time-resolved fluorescence emission techniques. Photophysics of LM was modulated several folds in these two sugar-based neutral micelles. LM exhibits excitation and emission wavelength dependent fluorescence properties in these two sugars based neutral micelles. LM confined in the micellar environments exhibited structural transition dynamism, i.e. different kinds of conformers are equilibrated. Herein, different conformers of LM are identified and explained with the help of spectroscopic methods. From the fluorescence anisotropy measurement, it was found that the rotational relaxation time of LM in OBG micelle was more compared to that in OBTG micelle, which indicates that the LM molecule faced much more constrained environment in OBG micellar media.

Label-free detection of creatinine using nitrogen-passivated fluorescent carbon dots.

In the field of biochemistry and biosensing, the passivation of carbon dots using nitrogen dopants has attracted great attention, as this can control their photoluminescence (PL) properties and quantum yield. To date, in the fabrication of a sensing probe, the impact of the chemical composition of the passivating molecule remained unexplored. In this work, we chose a series of different nitrogen-rich precursors (such as urea, thiourea, cysteine, and glycine) and ascorbic acid to synthesize nitrogen-doped carbon dots (NCDs). A significant change in their surface states was obtained due to the evolution of variable contents of amino, pyridinic and pyrrolic nitrogen species, which is evident from X-ray photoelectron spectroscopy, and this leads to an increment in their PL quantum yields (PLQY ∼ 58%) and average lifetime values. Spectroscopic analysis revealed that a rise in the ratio of pyrrolic : amino groups on the surface of carbon dots cause a bathochromic shift and generate excitation-dependent properties of NCDs. Besides, these NCDs were used as fluorescence off-on sensing probes, where a PA-infested NCD solution was used to detect creatinine. Chiefly, fluorescence restoration was achieved due to the formation of Jaffe chromogen between creatinine and PA. However, all nitrogen-passivated carbon dot surfaces do not respond similarly towards creatinine and only non-amino-rich NCDs exhibit the maximum (50%) PL turn-on response. The PL turn-off-on methodology showed a satisfactory good linearity range between 0 and 150 µM with a detection limit of 0.021 nM for creatinine. Three input molecular logic gates were also designed based on the turn-off-on response of the NCDs@PA towards creatinine. Additionally, for analytical method validation, real-sample analysis was performed for creatinine, which showed good recoveries (93-102%) and verified that nitrogen passivation tailored the physicochemical properties and enhanced the sensing ability.

Drumstick (Moringa oleifera) Flower as an Antioxidant Dietary Fibre in Chicken Meat Nuggets.

The present work investigated the efficacy of Moringa flower (MF) extract to develop a functional chicken product. Three groups of cooked chicken nuggets-control (C), T1 (with 1% MF) and T2 (2% MF)-were elaborated and their physicochemical, nutritional, storage stability and sensory attributes were assessed during refrigerated storage at 4°C up to 20 days. In addition, MF extracts were characterised in terms of chemical composition, total phenolic content and its components using high-performance liquid chromatography with a diode-array detector (HPLC-DAD), dietary fibre and antioxidant capacity. MF contained high protein (17.87 ± 0.28 dry matter), dietary fibre (36.14 ± 0.77 dry matter) and total phenolics (18.34 ± 1.16 to 19.49 ± 1.35 mg gallic acid equivalent (GAE)/g dry matter) content. The treated nuggets (T1 and T2) had significantly enhanced cooking yield, emulsion stability, ash, protein, total phenolics and dietary fibre compared to control. Incorporation of MF extract at 2% not only significantly reduced the redness/increased the lightness, but also decreased the hardness, gumminess and chewiness of the product compared to control. Moreover, the addition of MF extract significantly improved the oxidative stability and odour scores by reducing lipid oxidation during storage time. Sensory attributes of nuggets were not affected by the addition of MF extract and the products remained stable and acceptable even on 15th day of storage. These results showed that MF extract could be considered as an effective natural functional ingredient for quality improvement and reducing lipid oxidation in cooked chicken nuggets.

Host-guest interaction of 3-hydroxyflavone and 7-hydroxyflavone with cucurbit [7]uril: A spectroscopic and calorimetric approach.

The modulation of photophysical behaviour of small organic molecules in the presence of macrocycles is one of the most interesting areas of research. In this work we reported the interaction of two biologically active molecules 3-hydroxyflavone and 7-hydroxyflavone with macrocyclic host cucurbit [7]uril in aqueous medium. To investigate the change of photophysical properties of these two flavones, we have used steady state absorption, fluorescence, time resolved fluorescence emission spectroscopy and isothermal titration calorimetric technique. It is observed that on complexation with cucurbit [7]uril, the excited state proton transfer processes in both flavones have been facilitated. Isothermal titration calorimetric method was used in order to investigate the involvement of thermodynamic parameters in complexation between flavone with cucurbit [7]uril. The changes in thermodynamic properties due to the complexation of the flavones molecules with cucurbit [7]urils help to understand about the governing parameters involved in this complexation. The inclusion of flavone molecules inside the cavity of cucurbit [7]uril molecules was studied theoretically to decipher the molecular orientation of flavones in the presence of cucurbit [7]uril. The structure of HOMO and LUMO of the complexes between cucurbit [7]uril with flavones was reported. This study will be helpful to get the knowledge about the modulation of photophysical properties of the flavones molecules on addition of macrocyclic host cucurbit [7]uril. This study will be helpful for the use of cucurbit [7]uril as a potential drug delivery system.

Interaction of Biologically Active Flavins inside Bile Salt Aggregates: Molecular Level Investigation.

In this work we have studied the photophysics of biologically active flavin molecule lumichrome (LCM) in different bile-salt aggregates. With alteration of the functional groups of the bile salts, the photophysics of confined fluorophore is largely affected and shows difference in their spectral behavior. This study also reveals the selective prototropic species of LCM present in bile salt aggregates. In the presence of the bile salt aggregates, LCM molecule shows excitation and emission wavelength-dependent emission properties, indicating switch over of the structural change of different prototropic form of the LCM molecule. The observation of higher rotational relaxation time in NaDC aggregates compared to NaTC aggregates clearly reflects that NaDC aggregates are more rigid due to its greater hydrophobicity and large in size, which is capable to bind the guest molecule more into their nanoconfined medium. Moreover, due to less acidic nature, NaDC aggregates have more ability to accept hydrogen bond from the LCM molecule and show the selective formation of isoalloxazine N10 anion (A1 monoanionic form) of LCM.

Surfactants induced release of a red emitting dye from the nanocavity of a molecular container: A spectroscopic and calorimetric study.

Supramolecular interaction of a red emitting dye Nile blue A (NBA) with Cucurbit[7]uril (CB7) in aqueous solution was studied and the release of the dye from the hydrophobic cavity of CB7 was reported. To investigate the supramolecular host-guest complex formation and release of dye, we have used the steady state absorption, fluorescence and time resolved fluorescence emission spectroscopy, (1)H NMR spectroscopy and isothermal titration calorimetry (ITC). The spectral properties of NBA were changed in the presence of CB7. The change in spectral features of NBA in presence of CB7 indicates the formation of supramolecular host-guest complexes. By using the SED equation the diameter of the complex was estimated. The complex formation further affirmed by the (1)H NMR study. Upfield and downfield shifts of the protons of NBA was observed in both the aliphatic and aromatic region. From the ITC measurement, we have drawn up the forces involved for the complexation of NBA with CB7. We have studied the release of NBA from the hydrophobic cavity of CB7 by using ionic, neutral surfactants and ionic liquid with the help of spectroscopic and calorimetric techniques. It is observed that on addition of SDS and ionic liquid (

Alteration in DNA binding pattern of conformationally locked NC(O)N system: A spectroscopic investigation.

The binding mode of a conformationally locked NC(O)N planar system with deoxyribonucleic acid (DNA) is investigated using various spectroscopic and enzymatic assays. Compound 1 and its four different salts (comp. 2-5) were prepared for this purpose. They showed certain changes in their respective DNA-compound complex at ground state and excited state as measured by UV-vis and fluorescence emission spectra. The Stern-Volmer quenching constant (KSV) for the neutral species (1) is found 8545 M(-1), whereas, for its salts 2, 3, 4 and 5 the quenching constants were 33510 M(-1), 11352 M(-1), 19693 M(-1) and 27270 M(-1) respectively. Nevertheless, the binding constant values remain comparable in neutral and salt forms except for 5. To elucidate the reason we took their CD spectra and ran a topoisomerase I (Topo I) assay. These experimental data revel the fact that compound 1 (neutral form) binds at the minor groove of DNA, whereas, its salt (2) has an extended intercalating property.

Supramolecular interaction of a cancer cell photosensitizer in the nanocavity of cucurbit[7]uril: A spectroscopic and calorimetric study.

The interaction of small biologically active molecules in the nanocavity of supramolecular host is very interesting and thriving research area. In the presence of supramolecular host the absorption and emission properties of small biologically active molecules were modulated several folds compared to bulk solution. In this study we have investigated the supramolecular interaction of a cancer cell photosensitizer molecule harmane in the presence of cucurbit[7]uril (CB7) as host in aqueous buffer solution (pH∼7.2). We have used steady state absorption, emission and time resolved fluorescence spectroscopy techniques. The thermodynamics of the binding between harmane in the nanochannel of CB7 were studied by using isothermal titration calorimetry (ITC) method. The emission properties of harmane are modulated several fold in the presence of CB7. ITC study indicates that the complexation between harmane and CB7 are enthalpically favourable.

Photophysics and Rotational Dynamics of a Hydrophilic Molecule in a Room Temperature Ionic Liquid.

We have studied the photophysics and rotational diffusion of hydrophilic solute 7-(N, N'-diethylamino)coumarin-3-carboxylic acid (7-DCCA) in a room temperature ionic liquid methyltrioctylammonium bis(trifluoromethylsulfonyl) imide ([N1888 ][NTf2 ]). Comparison of activation energies of viscous flow and nonradiative decay shows that the photophysical properties of 7-DCCA are not guided by the bulk viscosity of the medium but are dependent on the specific solute solvent interaction and structural heterogeneity of the medium. The rotational relaxation behaviour of 7-DCCA in [N1888 ][NTf2] shows significant deviation from the Stokes Einstein Debye hydrodynamic model of rotational diffusion. This is indicative of the influence of specific solute solvent interaction on the rotational relaxation behaviour of 7-DCCA. Comparison of activation energy of rotational relaxation with activation energy of viscous flow clearly reinforces our assumption that the structural heterogeneity of the medium and specific solute solvent interaction plays a dominant role on the rotational diffusion instead of bulk viscosity.

Interaction of the nonsteroidal anti-inflammatory drug indomethacin with micelles and its release.

In this study, we have reported the binding interaction and photophysics of a nonsteroidal anti-inflammatory drug (NSAID) indomethacin (IMC) in the presence of different micelles. We have used several spectroscopic techniques such as UV-vis absorption, steady state fluorescence and time-resolved fluorescence emission spectroscopy. The spectral properties of IMC were modulated in the presence of micelles compared to that in neat water. The weak emitting drug molecule (IMC) becomes highly fluorescent after binding with the micelles. The fluorescence quantum yield and fluorescence lifetime increase in the presence of micelles compared to those in neat water. The isothermal titration calorimetry (ITC) method was used to study the binding interaction of IMC with different micelles. The thermodynamic parameters and the nature of binding between IMC and different micelles have been estimated. Moreover, addition of KCl salt in the respective micelles releases IMC molecule from the micelles to the aqueous medium. This study will help elicidate the binding behavior of IMC in the presence of different micelles for possible use as potential drug delivery systems.