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Barnabas Kállai-Szabó

Barnabas Kállai-Szabó
ViteCer Kft.

Ph.D.

About

41
Publications
12,254
Reads
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533
Citations
Additional affiliations
September 2019 - present
Cornexi Food Ltd.
Position
  • Head of Department
January 2016 - September 2019
ViteCer Kft.
Position
  • Technology and Product Developer
July 2014 - January 2016
Semmelweis University
Position
  • Research Associate
Description
  • -Pharmaceutical Technology (practice) -Pharmaceutical Technology (lectures) -Industrial Pharmaceutical Technology (lectures)
Education
September 2010 - May 2012
Semmelweis University
Field of study
  • Pharmaceutical Technology
September 2005 - June 2010
Eötvös Loránd University
Field of study
  • Chemistry

Publications

Publications (41)
Article
Full-text available
Today, in addition to many different physicochemical and pharmacological properties of the active ingredients and excipients, the developer of a pharmaceutical formulation must take into account several factors during the formulation process in order for the patient to cooperate to use the formulation accurately. One of the innovative solutions in...
Article
Full-text available
Most of the commercially available pharmaceutical products for oral administration route are marketed in the tablet dosage forms. However, compression of multiparticulate systems is a challenge for the pharmaceutical research and industry, especially if the individual unit is a coated particle, as the release of the active ingredient depends on the...
Article
The production of polymer microfibres and nanofibres using rotary jet spinning as platforms for drug delivery and tissue engineering applications has been explored. The aligned orientation of fibres and consequent improvement in the mechanical properties of the scaffold are essential in several pharmaceutical and biomedical applications, where elas...
Article
The aim of this study was to characterize the formation of emulsions by droplet size analysis and turbidimetry during reconstitution from a solid dosage form, namely from dry emulsion systems, which carry an oil phase for poorly soluble active ingredients. For the dry emulsion systems tablets were prepared either from oil-in-water systems using a f...
Article
Full-text available
Investigation of downstream processing of nanofibrous amorphous solid dispersions to generate tablet formulation is in a quite early phase. Development of high speed electrospinning opened up the possibility to study tableting of electrospun solid dispersions (containing polyvinylpyrrolidone-vinyl acetate and itraconazole [ITR] in this case). This...
Article
In this study, potassium chloride (KCl) containing matrix pellets were compressed into tablets using powder or pellet form of partially spray dried lactose as filler-binder excipient. The spatial distribution of potassium chloride pellets within the tablets was examined by non-destructive microfocus X-ray imaging (MFX) and image analysis technique....
Article
Batches of partially spray-dried lactose tablets with three different initial tensile strength (∼20N, ∼35N, ∼50N) were made. Changes along a 24hours long thermal treatment at 100°C in tensile strength, friability, individual mass, water content, disintegration time, average free volume and wetting properties were evaluated. Caffeine containing gast...
Article
Full-text available
Physical, chemical and microbiological stability of total parenteral nutrient (TPN) admixtures was studied as a function of storage time and temperature. Particle size analysis and zeta potential measurements were carried out to evaluate the possible changes in the kinetic stability of the emulsions as a function of storage time and temperature. Th...
Article
Physicochemical characterization of microfibers including powder X-ray diffraction, differential scanning calorimetry, attenuated total reflectance Fourier transform infrared spectroscopy, and positron annihilation spectroscopy were used to track the crystalline-amorphous transition of carvedilol during formulation and stability testing. The applie...
Article
Abstract The application of high-speed rotary spinning can offer a useful mean for either preparation of fibrous intermediate for conventional dosage forms or drug delivery systems. Polyvinylpyrrolidone (PVP) and poly(vinylpyrrolidone-vinylacetate) (PVP VA) micro- and nanofibers of different polymer concentrations and solvent ratios were prepared w...
Article
Solid dispersions of mebendazole were prepared in view of improving its extent and rate of dissolution. The solid dispersions were prepared by hot melt extrusion method using water soluble polymers and isomalt, polyethylene glycol and triethyl citrate as plasticizer. Solubility studies showed that solubility of solid dispersions, pure drug and phys...
Article
Full-text available
Water-soluble, nonionic cellulose-based fibers were prepared from aqueous hydroxypropyl cellulose gels of 5–13-μm diameter by using a high-speed rotary spinning technique. A combination of texture analysis and viscosity measurement was applied to determine the optimum concentration of hydroxypropyl cellulose gels for fiber formation. The examined c...
Article
Full-text available
During the last decade, the formulation of nanofibrous materials loaded with different drugs for biomedical applications has evoked considerable interest. The large specific surface area, the special micro- and macrostructure of fiber mats, the possibility for gradual release and site-specific local delivery of the active compounds lead to cytotoxi...
Article
Fiber-based dosage forms are potential alternatives of conventional dosage forms from the point of the improved extent and rate of drug dissolution. Rotary-spun polymer fibers and cast films were prepared and micronized in order to direct compress after homogenization with tabletting excipients. Particle size distribution of powder mixtures of micr...
Article
Layered and coated pellets were formulated to control the release of the diclofenac sodium selected as model drug. A highly water soluble isomalt inert pellet core material was used to osmotically modulate the drug release through the swellable polyvinyl acetate coating layer. Image analysis was applied to determine the shape parameters and the swe...
Article
Full-text available
The application of nanoactive drugs and nanostructured drug delivery systems enables the increase of bioavailability of active agents of unfavorable physical and chemical characteristics, thus assuring the basis of the cost-effective therapy. Fiber formation procedures (high speed rotary/centrifugal spinning, blow/jet spinning, electrospinning, mel...
Article
In addition to the chemical composition the molecular architecture has a decisive impact on the formulation of polymeric drug delivery systems. An ideal buccal polymeric film or patch dosage form should be flexible, elastic, soft, yet adequately strong. The microstructural characteristics through the molecular ordering determine the mechanical prop...
Article
Sulfobuthylether-beta-cyclodextrin (SBECD) is a substituted derivative of a cyclic oligosaccharide containing seven glucopyranose units, which bear pH-independent negative charges because of sulfonate groups. This derivative has better solubility and toxicological characteristics than the unsubstituted beta-cyclodextrin, and the presence of sulfobu...
Article
The major objective of this study was to disclose the relationships between the physical quality attributes and supramolecular structure of novel composite pellet cores containing microcrystalline cellulose (MCC) and isomalt in different ratios. The novel composite pellet cores were manufactured by an extrusion/spheronisation process. The micro or...
Article
The application of nanoactive drugs and nanostructured drug delivery systems enables the increase of bioavailability of active agents of unfavorable physical and chemical characteristics, thus assuring the basis of the cost-effective therapy. Fiber formation procedures (high speed rotary/centrifugal spinning, blow/jet spinning, electrospinning, mel...
Article
Full-text available
The active pharmaceutical ingredient can be administered by several different routes. Although the oral route (per os) has been one of the most convenient and widely accepted delivery system for most drugs, it has number of disadvantages like the very low pH of the stomach, the high enzymatic activity, and extensive first-pass metabolism. Difficult...
Article
Full-text available
Beside the many advantages of intraarticular formulations (e.g., the systemic side effects are kept away), there is a big drawback. During the injections, there is the risk for infection therefore the number of injections in a year should be reduced. Also a long-term drug exposure should be achieved with an injection, and if it is possible, a combi...
Article
Real time positron annihilation lifetime spectroscopy was applied to study the transition from hydrogel to film in the case of two biopolymer gels (sodium alginate and Carbopol 71G) of various concentrations (3 %w/w and 0.1–1 %w/w). The transition from a polymer-in-water system to a water-in-polymer system was sensitively tracked by o-Ps lifetime v...
Article
Full-text available
TPN infusions are usually administered during a treatment period of 10-24 hours per day due to the metabolic capacity of the liver. During this time interval physicochemically stable TPN solution (emulsion) is needed for the treatment. The purpose of the present study was to examine how the kinetic stability features of ready-made total parenteral...
Article
Polyvinylalcohol (PVA) fiber web containing embedded bacteria was prepared by electrospinning technique. From the point of the complex functionality of such potential delivery systems, it will be of impact how bacteria can survive in such artificial biotopes. The present study suggests a possible fast method for the tracking of the viability of the...
Article
Full-text available
PALS is one of the most widely used "nuclear probe" techniques for the tracking of the structural characteristics of materials. The method is based on the matter-energy equivalence principle recognized by Einstein: the electrons and positrons as particle-antiparticle pairs disappear in mutual destruction of particles, they annihilate with high-ener...
Article
Full-text available
Different types of polymers are widely used in biomedical, pharmaceutical and cosmetic purposes. Their applications are curbed, if the polymers can not break down by the body or if the polymer itself is harmful or decompose to harmful material. Authors provide an overview of different types of pharmaceutical polymers of various sources, of the stru...
Article
Beside the many advantages of intraarticular formulations (e.g., the systemic side effects are kept away), there is a big drawback. During the injections, there is the risk for infection therefore the number of injections in a year should be reduced. Also a long-term drug exposure should be achieved with an injection, and if it is possible, a combi...
Article
Full-text available
Optimization of physical characteristics influencing the formation of electrospun poly(vinyl alcohol) (PVA) fibers designed for drug delivery system was performed. The viscosity and dynamic surface tension of solutions of PVA with different molecular weight were compared. The best circumstances for forming nanofibers, optimal for rapid drug release...
Article
Different types of Carbopols are frequently applied excipients of various dosage forms. Depending on the supramolecular structure, their water sorption behaviour could significantly differ. The purpose of the present study was to track the supramolecular changes of two types of Carbopol polymers (Carbopol 71G and Ultrez 10NF) alone and in their phy...
Article
Application of buccal dosage forms has several advantages. Buccal route can be used for systemic delivery because the mucosa has a rich blood supply and it is relatively permeable. This route of drug delivery is of special advantages, including the bypass of first pass effect and the avoidance of presystemic elimination within the GIT. Buccal deliv...

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