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Spectrometric Study on the Interaction of Dodecyltrimethylammonium Bromide with Curcumin
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/jcc.21631openalex-snapshot
Density functional theory investigation of Cu(I)‐ and Cu(II)‐curcumin complexes
inferredcites →https://doi.org/10.1002/jnr.20025openalex-snapshot
Curcumin has potent anti‐amyloidogenic effects for Alzheimer's β‐amyloid fibrils in vitro
inferredcites →https://doi.org/10.1007/bf01027775openalex-snapshot
Studies on curcumin and curcuminoids
inferredcites →https://doi.org/10.1007/s10895-005-0025-0openalex-snapshot
The Sensitive Fluorimetric Method for the Determination of Curcumin Using the Enhancement of Mixed Micelle
inferredcites →https://doi.org/10.1016/0006-2952(76)90421-4openalex-snapshot
Antioxidant activity of curcumin and related compounds
inferredcites →https://doi.org/10.1016/0304-4157(78)90010-2openalex-snapshot
Fluidity parameters of lipid regions determined by fluorescence polarization
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2006.03.008openalex-snapshot
Effect of curcumin on protein glycosylation, lipid peroxidation, and oxygen radical generation in human red blood cells exposed to high glucose levels
inferredcites →https://doi.org/10.1016/j.ijpharm.2006.09.025openalex-snapshot
Curcumin–phospholipid complex: Preparation, therapeutic evaluation and pharmacokinetic study in rats
inferredcites →https://doi.org/10.1016/j.saa.2006.07.027openalex-snapshot
Investigation of the interaction between curcumin and nucleic acids in the presence of CTAB
inferredcites →https://doi.org/10.1016/s0006-291x(03)00030-5openalex-snapshot
Unique, pH-dependent biphasic band shape of the visible circular dichroism of curcumin–serum albumin complex
inferredcites →https://doi.org/10.1016/s0006-2952(98)00114-2openalex-snapshot
In Vivo Inhibition of Nitric Oxide Synthase Gene Expression by Curcumin, a Cancer Preventive Natural Product with Anti-Inflammatory Properties
inferredcites →https://doi.org/10.1016/s0014-5793(99)00114-3openalex-snapshot
Antitumor activity of curcumin is mediated through the induction of apoptosis in AK‐5 tumor cells
inferredcites →https://doi.org/10.1016/s0301-4622(99)00070-8openalex-snapshot
Free radical scavenging ability and antioxidant efficiency of curcumin and its substituted analogue
inferredcites →https://doi.org/10.1016/s0731-7085(96)02024-9openalex-snapshot
Stability of curcumin in buffer solutions and characterization of its degradation products
inferredcites →https://doi.org/10.1016/s0957-4166(03)00486-5openalex-snapshot
Molecular basis of the Cotton effects induced by the binding of curcumin to human serum albumin
inferredcites →https://doi.org/10.1016/s1359-0294(00)00020-0openalex-snapshot
Surfactant self-assembly objects as novel drug delivery vehicles
inferredcites →https://doi.org/10.1021/ac60304a041openalex-snapshot
Effects of halogens on o-phthaldialdehyde-histamine and spermidine fluorescence
inferredcites →https://doi.org/10.1021/ja809217uopenalex-snapshot
Determining the Effects of Lipophilic Drugs on Membrane Structure by Solid-State NMR Spectroscopy: The Case of the Antioxidant Curcumin
inferredcites →https://doi.org/10.1021/ja991446mopenalex-snapshot
H-Atom Transfer Is A Preferred Antioxidant Mechanism of Curcumin
inferredcites →https://doi.org/10.1021/jf102826qopenalex-snapshot
Interaction of Curcumin with β-Lactoglobulin—Stability, Spectroscopic Analysis, and Molecular Modeling of the Complex
inferredcites →https://doi.org/10.1021/jf9900837openalex-snapshot
Interaction of Curcumin with Phosphatidylcholine: A Spectrofluorometric Study
inferredcites →https://doi.org/10.1021/jp0450585openalex-snapshot
Salt Effect on the Complex Formation between Polyelectrolyte and Oppositely Charged Surfactant in Aqueous Solution
inferredcites →https://doi.org/10.1021/jp1096025openalex-snapshot
Cooperative Binding and Stabilization of the Medicinal Pigment Curcumin by Diamide Linked γ-Cyclodextrin Dimers: A Spectroscopic Characterization
inferredcites →https://doi.org/10.1021/jp807229copenalex-snapshot
Effect of Surfactant Mixing on Partitioning of Model Hydrophobic Drug, Naproxen, between Aqueous and Micellar Phases
inferredcites →https://doi.org/10.1021/jp9101527openalex-snapshot
Excited-State Intramolecular Hydrogen Atom Transfer of Curcumin in Surfactant Micelles
inferredcites →https://doi.org/10.1021/la800780wopenalex-snapshot
Encapsulation of Curcumin in Cationic Micelles Suppresses Alkaline Hydrolysis
inferredcites →https://doi.org/10.1021/la801636uopenalex-snapshot
Modulation of Drug Transport Properties by Multicomponent Diffusion in Surfactant Aqueous Solutions
inferredcites →https://doi.org/10.1021/la903772eopenalex-snapshot
The Role of Charge in the Surfactant-Assisted Stabilization of the Natural Product Curcumin
inferredcites →https://doi.org/10.1021/mp700113ropenalex-snapshot
Bioavailability of Curcumin: Problems and Promises
inferredcites →https://doi.org/10.1039/b409724fopenalex-snapshot
Circular dichroism spectroscopic studies reveal pH dependent binding of curcumin in the minor groove of natural and synthetic nucleic acids
inferredcites →https://doi.org/10.1111/j.1365-2621.2003.tb05699.xopenalex-snapshot
Effects of Light, Oxygen, and pH on the Absorbance of 2,2‐Diphenyl‐1‐picrylhydrazyl
inferredcites →https://doi.org/10.1529/biophysj.107.126888openalex-snapshot
Membrane-Thinning Effect of Curcumin
inferredcites →https://doi.org/10.1562/0031-8655(2003)0770597psoboc2.0.co2openalex-snapshot
Photophysical Studies on Binding of Curcumin to Bovine Serum Albumin¶
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Shift of acid–base equilibrium of curcumin in its complexes with gemini surfactant hexamethylene-1,6-bis-(dodecyldimethyl ammonium bromide)
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Core–shell microcapsules of solid lipid nanoparticles and mesoporous silica for enhanced oral delivery of curcumin
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The mechanism of encapsulating curcumin into oleosomes (Lipid Droplets)
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Spectroscopic study on the interaction of curcumin with single chain and gemini surfactants
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Spectrometric study on the binding of curcumin with AOT: Effect of micelle-to-vesicle transition
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Effects of length and unsaturation of the alkyl chain on the hydrophobic binding of curcumin with Tween micelles
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Solubilization of α-tocopherol and curcumin by polyoxyethylene alkyl ether surfactants: Effect of alkyl chain structure
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Soluble soybean polysaccharide/gelatin active edible films incorporated with curcumin for oil packaging
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Bioactive pH-sensitive nanoemulsion in melanoma cell lines
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Interaction of bisdemethoxycurcumin with cationic (cetyltrimethylammonium) + nonionic (Tween 20/Tween 60) mixed surfactants: Thermodynamic study and functional improvement
inferred← citeshttps://doi.org/10.1016/j.jlumin.2013.06.032openalex-snapshot
Picosecond spectral relaxation of curcumin excited state in toluene–alcohol mixtures
inferred← citeshttps://doi.org/10.1016/j.jlumin.2013.08.060openalex-snapshot
Photophysics of Curcumin excited state in toluene-polar solvent mixtures: Role of H-bonding properties of the polar solvent
inferred← citeshttps://doi.org/10.1016/j.jphotobiol.2012.06.004openalex-snapshot
Role of curcumin on the determination of the critical micellar concentration by absorbance, fluorescence and fluorescence anisotropy techniques
inferred← citeshttps://doi.org/10.1016/j.jphotobiol.2016.03.004openalex-snapshot
Stability of curcumin in different solvent and solution media: UV–visible and steady-state fluorescence spectral study
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Mesoporous silica particles based on complex micelles of poorly water-soluble compounds. One simple step to multidrug carriers
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Protonation of acridine orange in dye-surfactant ion pair micelles
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Stabilization of diketo tautomer of curcumin by premicellar cationic surfactants: A spectroscopic, tensiometric and TD-DFT study
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Curcumin nanoemulsion as a biocompatible medium to study the metal ion imbalance in a biological system
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Molecular dynamics simulation studies on the concentration-dependent interaction of dodecyltrimethylammonium bromide with curcumin
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