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Solution properties of a drug and its partitioning into lipid bilayers were studied for drug extraction using several different techniques, such as surface tension, zeta potential, ultra filtration and UV-Vis spectroscopy. From the surface tension study it was found that the presence of salt makes the drug molecules more surface-active. Zeta potential revealed the adsorption of the drug into the liposome bilayers to be governed mostly by electrostatic forces. The drug retention volume was expressed as a capacity factor, K, and that was normalized with respect to the amount of the immobilized phospholipids. The K-values for the positively charged drug on the liposomes decreased in the presence of phosphate buffer due to the presence of the oppositely charged ions. The above methods can thus be used to understand the mechanism of drug-membrane interaction and quantification of drug absorption into liposomes. 相似文献
3.
Somasundaran P Ananthapadmanabhan KP Deo P 《Journal of colloid and interface science》2005,290(2):357-363
Interactions of surfactants with solid substrates are important in the controlling of processes such as flotation, coating, flocculation and sedimentation. These interactions usually lead to adsorption on solids, but can also result in an exclusion of the reagents with dire consequences. In this work electrostatic exclusion of negatively charged dodecylbenzene sulfonate micelles from quartz/water, Bio-Sil/water and alumina/water interfaces has been investigated as a function of pH and ionic strength. Measurable negative adsorption of these surfactants from similarly charged solid/liquid interface was observed in the micellar region. In the case of porous samples with large surface area, comparison of pore size with the micelle size is necessary to avoid any erroneous conclusions regarding the role of electrostatic exclusion in a given system. A theoretical model for the electrostatic exclusion of micelles is developed and used to calculate the adsorption of negatively charged dodecylbenzene sulfonate on negatively charged quartz (pH 7), silica (Bio-Sil A, pH 3) and alumina (pH 11) in the micellar concentration region. The micellar exclusion values calculated using the model are in excellent agreement with the experimental results. 相似文献
4.
Deo P Deo N Somasundaran P Jockusch S Turro NJ 《The journal of physical chemistry. B》2005,109(44):20714-20718
Structural changes of pyrene-labeled and unlabeled poly(maleic acid/octyl vinyl ether) (PMAOVE) and poly(maleic acid/methyl vinyl ether) (PMAMVE) with changes in pH have been investigated in this study. The changes in the photophysical properties of pyrene are interpreted to investigate uncoiling or swelling of the polymeric chains with pH. The vibrational fine structure of the pyrene fluorescence (I(3)/I(1)) and the ratio between excimer and monomer fluorescence (I(e)/I(m)) of both pyrene-labeled and unlabeled PMAMVE and PMAOVE suggest that, at pH 4, the polymers are in the coiled form and PMAOVE forms hydrophobic nanodomains. An increase in pH ionizes a number of COOH groups on both PMAMVE and PMAOVE, which leads to the stretching or swelling of the polymers. 相似文献
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The oxidation and enhanced detection of traditionally 'non-electroactive' amino acids at a single-wall carbon nanotube (SWNT) surface and at a nickel hydroxide film electrochemically deposited and generated upon the SWNT layer is reported. Different CNT are compared, with Nafion-dispersed SWNT offering the most favorable layer for constant-potential amperometric detection. Factors affecting the oxidation process, including the pH or applied potential, are assessed. The response of the SWNT-Nafion coated electrode compares favorably with that of copper and nickel disk electrodes under flow injection analysis (FIA) conditions. The electrodeposition of nickel onto the SWNT-Nafion layer (Ni-CNT) led to a dramatic enhancement of the analytical response (vs. that observed at the SWNT or nickel electrodes alone). The oxidative process at the Ni(OH)(2) layer has been studied and the increase in sensitivity rationalized. In the presence of amino acid the Ni-CNT layer undergoes an electrocatalytic process in which the amino acid reduces the newly formed NiO(OH) species. Furthermore, the attractive response of both the CNT and Ni-CNT layers has allowed these electrodes to be used for constant-potential FIA of various amino acids and indicates great promise for monitoring chromatographic effluents. Once again an improved signal was observed at the Ni-CNT electrode compared to nickel deposited upon a bare glassy carbon electrode (Ni-GC). 相似文献
7.
Determination of organophosphate pesticides at a carbon nanotube/organophosphorus hydrolase electrochemical biosensor 总被引:7,自引:0,他引:7
Randhir Prakash Deo Joseph Wang Ines Block Ashok Mulchandani Kanchan A. Joshi Marek Trojanowicz Fritz Scholz Wilfred Chen Yuehe Lin 《Analytica chimica acta》2005,530(2):185-189
An amperometric biosensor for oganophosphorus (OP) pesticides based on a carbon nanotube (CNT)-modified transducer and an organophosphorus hydrolase (OPH) biocatalyst is described. A bilayer approach with the OPH layer atop of the CNT film was used for preparing the CNT/OPH biosensor. The CNT layer leads to a greatly improved anodic detection of the enzymatically generated p-nitrophenol product, including higher sensitivity and stability. The sensor performance was optimized with respect to the surface modification and operating conditions. Under the optimal conditions the biosensor was used to measure as low as 0.15 μM paraoxon and 0.8 μM methyl parathion with sensitivities of 25 and 6 nA/μM, respectively. 相似文献
8.
Complexes of CoII with N,N-bis-(3-carboxy-1-oxopropanyl)-1,2-ethylenediamine(L1), N,N-bis-(3-carboxy-1-oxopropanyl)-1,2-phenylenediamine(L2), N,N-bis-(2-carboxy-1-oxophenelenyl)-1,2-phenylenediamine(L3) and N,N-bis-(3-carboxy-1-oxoprop-2-enyl)-1,2-phenylenediamine(L4) have been prepared and characterized by elemental analysis, vibrational spectra, magnetic susceptibility measurements, electronic spectra and thermal studies. Stability constants of the complexes have been evaluated potentiometrically. Vibrational spectra indicate coordination of amide and carboxylate oxygens of the ligands along with two water molecules giving a MO6 weak field octahedral chromophore. Electronic spectra support octahedral geometry around CoII. The [Co(L1)-(H2O)2] · 2H2O complex has the maximum activation energy and [Co(L3)(H2O)2] complex has the minimum activation energy. The order of stability constants of the CoII complexes with various ligands is due to their -donor abilities. 相似文献
9.
Sreemoyee Mukherjee M. Manninen P. Singha Deo 《Physica E: Low-dimensional Systems and Nanostructures》2011,44(1):62-66
We start from microscopic approach to many body physics and show the analytical steps and approximations required to arrive at the concept of quantum capacitance. These approximations are valid only in the semi-classical limit and the quantum capacitance in that case is determined by Lindhard function. The effective capacitance is the geometrical capacitance and the quantum capacitance in series, and this too is established starting from a microscopic theory. 相似文献
10.
The ability of small particles to associate with DNA and to transport it to desired targets without being subjected to interferences can make them efficient vehicles for gene delivery. Keeping these requirements in mind, zwitterionic latex particles with two different functional tethers were chosen for studying their interaction with DNA as vehicle complexes. From adsorption and electrokinetic studies, it is evident that zwitterionic latex particles can have marked association with DNA. Moreover, DNA-latex complexation does not provoke undesired aggregation of latex particles. These characteristics are important for it to carry the DNA efficiently under changing media conditions. 相似文献