Bonding of doxorubicin to nanosilica and human serum albumin in various media.

Interaction of doxorubicin hydrochloride (DOX) (anti-cancer drug) with hydro-compacted nanosilica A-300 (cA-300) alone or cA-300/human serum albumin (HSA) at a small content of water (h = 0.4 g per gram of dry silica) in different dispersion media (air, chloroform, and chloroform/trifluoroacetic acid) was analyzed using low-temperature 1H NMR spectroscopy, NMR cryoporometry and quantum chemistry to elucidate specific changes in the interfacial layers. Initial (bulk density ρb ≈ 0.046 g/cm3) and hydro-compacted (ρb ≈ 0.051-0.265 g/cm3 as a function of the hydration degree) nanosilicas were analyzed using nitrogen adsorption-desorption, gelatin adsorption, small angle X-ray scattering (SAXS), TEM, and infrared (FTIR) spectroscopy. Equilibrium adsorption of DOX onto cA-300 and cA-300/HSA was analyzed using ultraviolet-visible light spectroscopy. Photon correlation spectroscopy was used to analyze the particle size distribution in aqueous suspensions with various contents of components. DOX more strongly bound to HSA than silica also affects structure of interfacial water layers that depends on dispersion media because chloroform as immiscible with water changes the water organization to enlarge water structures. In aqueous media, DOX alone remains mainly in the form of nano/microparticles (50 nm-2 µm in size). However, with the presence of cA-300, cA-300/HSA, and HSA alone DOX transforms into pure nano-sized structures. These effects are explained by effective bonding of DOX to HSA having good transport properties with respect to drug molecules/ions that exceed similar properties of nanosilica alone, but cA-300/HSA can be a more effective composite as a drug carrier.

Interfacial behavior of polar, weakly polar, and nonpolar compounds bound to activated carbons.

Detailed analysis of the interfacial behavior of water and weakly polar or nonpolar organics adsorbed alone or co-adsorbed onto activated carbons (AC) at different temperatures is a complex problem important for practical applications of adsorbents. Interaction of water, 1-decanol, and n-decane with AC possessing highly developed porosity (pore volume Vp≈1.4-2.3 cm(3)/g, specific surface area S(BET)≈1500-3500 m(2)/g) was studied over a broad temperature range using differential scanning calorimetry (DSC), thermoporometry, (1)H NMR spectroscopy, cryoporometry, and temperature-programmed desorption with mass-spectrometry control methods. Comparison of the pore size distributions (PSD) calculated using the DSC thermoporometry, NMR cryoporometry, and nitrogen adsorption isotherms allows us to determine localization of adsorbates in different pores, as well as changes in the PSD of AC due to freezing of adsorbates in pores. Theoretical calculations (using ab initio HF/6-31G(d,p), DFT B3LYP/6-31G(d,p), and PM7 methods) explain certain aspects of the interfacial behavior of water, decane, and decanol adsorbed onto AC that appear in the experimental data. Obtained results show strong temperature dependence (above and below the freezing point, Tf, of bulk liquids) of the interfacial behavior of adsorbates on the textural characteristics and hydrophilic/hydrophobic properties of AC and the adsorbate amounts that affect the distributions of adsorbates unfrozen at T

Complex investigations of structural and thermal properties of silica-titania adsorbents.

Mesoporous titanium-containing silicas with different Titania contents were investigated. The structural parameters of the materials were characterized by low-temperature adsorption/desorption of nitrogen and X-ray diffraction analysis. The thermodesorption of water using the quasi-isothermal thermogravimetry as well as the differential scanning calorimetry were used to characterize thermal and surface properties of these materials. The adsorbed water layers and the concentration of weakly and strongly bound water as well as the surface free energy on the adsorbent/water interfaces were calculated. It was stated that the increase of Titania content causes a gradual decrease of specific surface area and formation of biporous structure inside the tested materials. The water thermodesorption from the surface proceeds in two or three stages, which is connected mainly with pore distribution and TiO2 content. One can observe the increase of the total surface free energy (ΔGΣ) with the increasing TiO2 content, but the largest ΔGΣ value at the adsorbent/strongly bound water interface is exhibited by the adsorbent of intermediate content (30%) of TiO2. Freezing temperature of water contained in the pores of the studied materials is connected largely with their porous structure. Due to the well developed porous structure, the water freezing process is a multi-stage one.

Adsorption, NMR, and thermally stimulated depolarization current methods for comparative analysis of heterogeneous solid and soft materials.

Structural characterization of different silicas (ordered mesoporous silicas MCM-41, MCM-48, and SBA-15, amorphous silica gels Si-40, Si-60, and Si-100, and initial and wetted-dried fumed silica A-300) and bio-objects (fibrinogen solution, yeast cells, wheat seeds, and bone tissues) has been done using two versions of cryoporometry based on integral Gibbs-Thomson (IGT) equation for freezing point depression of pore liquids measured by 1H NMR spectroscopy (180-200 < T < 273 K) and thermally stimulated depolarization current (TSDC) method (90 < T < 273 K). The IGT equation was solved using a self-consisting regularization procedure including the maximum entropy principle applied to the distribution function of pore size (PSD). Comparison of the PSDs calculated by using the cryoporometry and nitrogen adsorption methods for the mentioned silicas demonstrates that IGT equation provides satisfactory fit which is better than that obtained with nonintegral Gibbs-Thomson (GT) equation (based on the GT equation) proposed by Aksnes and Kimtys. The NMR- and TSDC-cryoporometry methods applied to probe biosystems give clear pictures of changes in the structural characteristics caused, e.g., by hydration and swelling of wheat seeds and yeast cells, coagulation and interaction of fibrinogen with solid nanoparticles in the aqueous media, and human bone tissue disease.

Carbon-mineral adsorbents from waste materials: case study.

Waste bleaching earth from the food industry obtained in the process of fruit juice purification was utilized for preparation of carbon-mineral adsorbents. The waste material, containing 25.8 wt% C, was subjected to three kinds of treatment: (1) direct pyrolysis at 400 degrees C with a suitable temperature program; (2) preliminary hydrothermal modification (200 degrees C, 8 h, 15.3 atm) and then pyrolysis as in method 1; (3) preliminary thermal treatment (400 degrees C) and then chemical treatment (boiling in 3% solution Na(2)CO(3)), followed by heating at 400 degrees C (10 min). Moreover, the materials obtained by these methods were subjected to additional thermal treatment at 700 degrees C with a suitable temperature program. Both the morphology and the topography of carbon deposits and, in consequence, the porous structure of the obtained adsorbents depend on the method of their preparation. The additional thermal treatment of these samples at 700 degrees C makes it possible to obtain adsorbents of more thermally stable carbon deposits possessing better parameters of the porous structure. Carbon-mineral adsorbents of different specific surface areas (S(BET) from 17.6 to 153 m(2)/g) and pore volumes (from 0.035 to 0.093 cm(3)/g) were prepared. The mechanism of phenol and p-nitrophenol adsorption on the obtained adsorbents was discussed and their properties were compared with the suitable literature data.

Characterization of Titania/Silica Gel by Means of Low-Pressure Nitrogen Adsorption.

Adsorbents synthesized by grafting of titania onto mesoporous silica gel surfaces at different temperatures were studied by means of nitrogen adsorption-desorption and water desorption. The pore size distribution f(R(p)) of titania/silica gel depends on the titania concentration (C(TiO(2))) and the temperature of titania synthesis. Nonuniformity of TiO(2) phase is maximal at a low C(TiO(2)) value (3.2 wt.% anatase deposited at 473 K), and two peaks of the fractal dimension distribution f(D) are observed at such a concentration of titania, but at larger C(TiO(2)) values, only one f(D) peak is seen. More ordered filling of pores and adsorption sites by nitrogen, reflecting in the shape of adsorption energy distributions f(E) at different pressures of adsorbate, is observed for adsorbent with titania (rutile+anatase) grafted on silica gel at a higher temperature (673 K). Copyright 2000 Academic Press.

Carbon Dispersion and Morphology in Carbon-Mineral Adsorbents.

Carbon-mineral composite adsorbents prepared by deposition of carbon on various mineral supports have been studied extensively by a new textural approach. The evidence of significant influence of both organization of initial mineral support porous space and mobility of carbon precursors over the surface of mineral support on carbon localization has been obtained. Restricted mobility of carbon precursors leads to homogeneous distribution of carbon clusters over the support surface despite the presence of narrow mesopores in the structure of the support if the entire support surface is equiaccessible. Unrestricted mobility over the smooth surface of the mineral support without narrow mesopores leads to the similar resulting carbon distribution. However, unrestricted mobility of carbon precursors in densely packed porous materials seems to be the reason for carbon pulling and deposition in narrow mesopores. These peculiarities of carbon deposition influence the carbon/mineral (hydrophobic/hydrophilic) composition of the composite surface. Trapping of carbon in narrow mesopores leads to a decrease and, in contrast, homogeneous dispersion of carbon over the whole support surface leads to an increase in the part of the composite surface, which can be appropriated to carbon. Copyright 2000 Academic Press.

Effect of surface heterogeneity on adsorption on solid surfaces. Application of inverse gas chromatography in the studies of energetic heterogeneity of adsorbents.

The paper presents a literature review of the chromatographic methods used for investigations of the heterogeneity of solid surfaces. Special attention is paid to inverse gas chromatography (IGC). Quantitative characteristics of heterogeneity of real solid surfaces including extreme models on adsorption centre topography of the "patch-wise" and "random" types are described. Analytical and numerical methods used for calculating the adsorption energy distribution function as a quantitative measure of surface heterogeneity are presented. Special attention is paid to the condensation approximation as well as to other approximations based on this assumption. IGC is presented as a quick, precise and effective method to characterise physicochemical properties of different kinds of adsorbents. Advantages of IGC over traditional methods of gas and vapour adsorption are shown.

Surface Properties of Mesoporous Carbon-Silica Gel Adsorbents.

Carbon/silica (carbosil) samples prepared utilizing mesoporous silica gel (Si-60) modified by methylene chloride pyrolysis were studied by nitrogen adsorption, quasi-isothermal thermogravimetry, p-nitrophenol adsorption from aqueous solution, and (1)H NMR methods. The structural characteristics and other properties of carbosils depend markedly on the synthetic conditions and the amount of carbon deposited. The changes in the pore size distribution with increasing carbon concentration suggest grafting of carbon mainly in pores, leading to diminution of the mesopore radii. However, heating pure silica gel at the pyrolysis temperature of 550 degrees C leads to an increase in the pore radii. The quasi-isothermal thermogravimetry and (1)H NMR spectroscopy methods used to investigate the water layers on carbosils showed a significant capability of carbosils to adsorb water despite a relatively large content of the hydrophobic carbon deposit, which represents a nonuniform layer incompletely covering the oxide surface. Copyright 2000 Academic Press.