Biomedical subjects

S Haam

Publications and source records attributed to S Haam.

11 recordsLinked to original sources

PubMed2006

Preparation of poly epsilon-caprolactone nanoparticles containing magnetite for magnetic drug carrier.

Magnetic poly epsilon-caprolactone (PCL) nanoparticles were prepared in a well shaped spherical form by the o/w emulsion method. The influence of some preparative variables on the size and surface property was investigated. Nanoparticles were smooth, well individualized and homogeneous in size. The presence of magnetite and its superparamagnetic characteristic were confirmed by transmission electron microscope (TEM), Fourier transform infrared spectroscopy (FT-IR) and vibrating sample magnetometer (VSM), respectively. The anti-cancer drug was encapsulated in the magnetic nanoparticle during preparation. A typical release behavior was observed for 30 days. In vitro experiment of magnetic susceptibility under external magnetic field demonstrated that the magnetic PCL nanoparticles have sufficient magnetic susceptibility for a potential magnetic drug carrier for targeted delivery.

Cisplatin↗

PubMed2006

Magnetic PECA nanoparticles as drug carriers for targeted delivery: synthesis and release characteristics.

Magnetic poly(ethyl-2-cyanoacrylate) (PECA) nanoparticles containing anti-cancer drugs (Cisplatin and Gemcitabine) were prepared by inter-facial polymerization. The spherical nanoparticles (d = 250 +/- 15 nm) with smooth surfaces and moderately uniform size distributions were obtained. The amount of magnetite encapsulated inside the polymer matrix was increased up to 14.26% (w/w) by controlling the initial weight ratio of monomer/magnetite. It was found that the amount of Cisplatin encapsulated in the magnetic nanoparticle is much higher than that of Gemcitabine because Cisplatin (hydrophobic) is highly soluble in the oil phase and encapsulated easier inside nanoparticles compared to Gemcitabine (hydrophilic). The presence of magnetite and its super-paramagnetic characteristic were confirmed by FTIR spectra and VSM. In-vitro experiments of drug release and magnetic mobility under external magnetic field demonstrated that magnetic poly(ethyl-2-cyanoacrylate) (PECA) nanoparticles can be a highly versatile magnetic drug carrier with sustained release behaviour and sufficient magnetic susceptibility.

Cyanoacrylates↗

PubMed2004

Ca-alginate microspheres encapsulated in chitosan beads.

Chitosan beads (CBs) incorporating Ca-alginate microspheres (CAMs), containing a drug, were prepared as an oral sustained delivery system. Stable and monodisperse Ca-alginate microspheres loaded with drug were obtained by a membrane emulsification method. The Ca-alginate microspheres were encapsulated in chitosan beads by the ionotropic gelation method with a polyelectrolyte complex reaction between two oppositely charged polyions. The surface and internal characteristics of the beads were improved by ionic cross-linking in tripolyphosphate (TPP) solution adjusted to pH 5.0. The release experiments were performed using lidocaine.HCl (cationic drug) and sodium salicylate (anionic drug) as model drugs. Initial release of drugs depended on the degree of swelling. Ca-alginate microspheres encapsulated in chitosan beads were superior to both drug-loaded CBs and CAMs beads for sustained release because they had a three-layer composition; a calcium alginate core bounded by an inter-phasic chitosan-alginate membrane, which itself was surrounded by a layer of chitosan-TPP.

Alginates↗

PubMed2004

Preparation of chitosan microspheres using membrane emulsification and its size modelling.

The chitosan microspheres were prepared by a membrane emulsification method with variations of the N2 gas pressure and the chitosan concentration. The pressure of N2 gas was varied within the range from 0.2 x 10(5) to 0.8 x 10(5) Pa at chitosan concentration 1.5 wt%. In addition, the concentration of chitosan was varied between 0.5 approximately 2.0 wt% at 0.4 x 10(5) Pa of N2 gas pressure. Using this method, it is possible to prepare stable emulsions with a very narrow droplet size distribution in comparison with conventional methods. The average size of the microspheres was dependent on the N2 gas pressure and the concentration, that is it was increased with the pressure and the concentration. The modelling of the size for the microspheres according to the concentration was carried out using Macleod's relation and Parkins & Brown equation. The former shows the relationship between density and surface tension and the latter demonstrates the correlation between the volume of the microspheres and the interfacial tension. The modelling results were in good agreement with the experimental data to predict the microspheres size with the variation of concentration.

Chitosan↗

PubMed2002

Biodegradation of toluene by a lab-scale biofilter inoculated with Pseudomonas putida DK-1.

The biodegradation of toluene by biofiltration inoculated with Pseudomonas putida DK-1 was investigated with variation of the several environmental parameters, such as temperature, bed length, gas flow rate and optimal humidity zone. The optimal temperature range to treat toluene gas was found to be 32-35 degrees C. Increasing the gas flow rate showed an inverse effect on the elimination capacity and the removal efficiency. The optimal gas flow rate was obtained at 65 ml min(-1) from the relation between the removal efficiency and the elimination capacity. The biodegradation rate of the toluene with respect to the bed lengths (3, 6, 9, 12 and 15 cm) increased up to 80 h but was then independent of the bed lengths after 80 h except for the 3 cm bed length. The elimination capacity was improved by about 70% compared with that reported in other literature and was also in agreement with theoretical models.

Air Movements↗

PubMed2001

Studies on the overall oxygen transfer rate and mixing time in pilot-scale surface aeration vessel.

An aerated vessel with Simcar type surface aerator was studied to estimate its significant performance characteristics i.e., oxygen transfer rate, mixing time and power consumption. The oxygen transfer and mixing characteristics were investigated with variations in the operating variables such as rotational speed, diameter, bottom clearance of impeller, liquid height and power consumption in single and dual impeller systems. The bottom clearance of the top impeller was found to affect largely the capacity of the impeller by varying the quantity of liquid loaded to it. It was also ensured that surface aeration caused a slight increase in mixing time compared to it under ungassed conditions. The dual impeller system was employed for the purpose of improving oxygen transfer and mixing at TH < 1 varying the types and the bottom clearance of thelower impeller. However, the oxygen transfer rate was independent of the lower impeller mainly depending on the capacity of the top impeller though mixing time was sharply reduced by the lower impeller. The effect of the bottom clearance of the lower impeller was related to the liquid flow pattern inside the vessel, which was presented by computational fluid dynamics (CFD). The oxygen transfer rate and the mixing time were correlated with power consumption within reliable error range.

Bioreactors↗

PubMed2001

Oxygen transfer characteristics in a pilot scale surface aeration vessel with Simcar aerator.

The volumetric mass transfer coefficient, KLa, was determined by dynamic method in a surface aerated pilot scale squared vessel up to 0.531 m3 equipped with Simcar type impeller. Through surface aeration, the oxygen transfer characteristics were investigated with the variations of operating variables such as stirring speed, impeller diameter, liquid height and power input per liquid volume (P0/V). It was seen from the results of different oxygen concentration absorption that the dynamic method might lead to errors in KLa when air was used for absorption. To provide reliable KLa values measured by dynamic, the KLa data using pure oxygen were used and confirmed with feeding steady-state method (FSM). As expected, KLa depends on P0/V, impeller size and liquid height. However, for Simcar type impeller, the KLa shows linear dependency on P0/V in contrast to majority of correlations reported in the literature which shows KLa variation of (P0/V)0.65 for disk type impeller. Moreover, it was interesting to find that the bubble behaviors inside the vessel computed by computational fluid dynamics (CFD) could explain qualitatively the KLa changes with operating variables. For the purpose of scale-up procedures, the empirical correlations for predicting KLa were developed within +/- 2% accuracy.

Adsorption↗

PubMed2000

Modeling of the Permeate Flux during Microfiltration of BSA-Adsorbed Microspheres in a Stirred Cell.

A study on the variation of the permeate flux was performed in a stirred cell charged with microspheres, to investigate the effects of the stirrer speeds (300, 400, and 600 rpm) and the BSA concentration (0.1, 0.2, 0.4, and 0.8 g/L) under constant pressure. The permeate flux increased over time before the saturation point, but it began to decrease after that point. An increase of the BSA concentration and the stirrer speed resulted in the rapid increase of the permeate flux. This is contrary to the observation of the conventional filtration experiments using a stirred cell. A resistance-in-series model was employed for the modeling of the permeate flux. The cake resistance (R(c), induced by the concentration polarization of microspheres) and the fouling resistance (R(f), induced by the adsorption of BSA inside the membrane pore) must be considered simultaneously for the modeling. These modeling results were in good agreement with the experimental data. These can be applied to the special system considering both R(c) and R(f) as well as the general filtration systems using a stirred cell. Copyright 2000 Academic Press.

Journal Article↗

PubMed1999

Quantification of cellular properties from external fields and resulting induced velocity: cellular hydrodynamic diameter.

An experimental technique is discussed in which the size distribution of a population of cells is determined by calculating each cell's settling velocity. The settling velocity is determined from microscopically obtained images which were recorded on SVHS tape. These images are then computer imaged and processed, and the cell's location and velocity are determined using a computer algorithm referred to as cell tracking velocimetry (CTV). Experimental data is presented comparing the distribution of human lymphocytes and a human breast cancer cell line, MCF-7, determined using a Coulter counter and the CTV approach.

Algorithms↗

PubMed1999

Quantification of cellular properties from external fields and resulting induced velocity: magnetic susceptibility.

An experimental technique is discussed in which the magnetic susceptibility of immunomagnetically labeled cells can be determined on a cell-by-cell basis. This technique is based on determining the magnetically induced velocity that an immunomagnetically labeled cell has in a well-defined magnetic energy gradient. This velocity is determined through the use of video recordings of microscopic images of cells moving in the magnetic energy gradient. These video images are then computer digitized and processed using a computer algorithm, cell tracking velocimetry, which allows larger numbers (>10(3)) of cells to be analyzed.

Cells, Cultured↗

PubMedDate not supplied

Preparation of regular sized Ca-alginate microspheres using membrane emulsification method.

Monodisperse Ca-alginate microspheres were prepared using the membrane emulsification method. Three ionic types of drugs (anionic, cationic and non-ionic) were incorporated into the microspheres, and the effects of sodium alginate concentration and the pressure applied during the dispersing process on the properties of the microspheres were examined. Monodisperse microspheres were obtained when the concentration of alginate solution was 2 wt% and the pressure applied was 0.4 x 10(5) Pa. The mean size of microspheres was approximately 4 microm. Lidocaine x HCl (cationic), sodium salicylate (anionic) and 4-acetamidophenol (non-ionic) were selected as ionic model drugs and included in the alginate microspheres. Lidocaine x HCl (cationic drug) release was more retarded than that of the anionic drug, because of the electrostatic attraction between the negative charge of the ionized carboxyl group in the alginate chain and the positive charge of the cationic drug. In acidic release medium, a slow release was observed due to the low swelling characteristic and the increased viscosity of alginate, regardless of ionic type of drug.

Acetaminophen↗