Marek Kozicki

Hydrogels made from chitosan and silver nitrate

This work describes a gelation of chitosan solution with silver nitrate. Above the critical concentration of chitosan (c*), continuous hydrogels of chitosan-silver can be formed. At lower concentrations, the formation of nano- and micro-hydrogels is discussed. The sol-gel analysis was performed to characterise the hydrogels swelling properties. Moreover, the following were employed: (i) mechanical testing of hydrogels, (ii) inductively coupled plasma-optical emission spectroscopy (ICP-OES) for the measurement of silver concentration, (iii) scanning electron microscopy (SEM) to examine the morphology of products obtained, and (iv) dynamic light scattering (DLS) and UV-vis spectrophotometry to examine products formed at low concentration of chitosan (c<c*). Some hydrogels were used for modification of cotton fabric in order to give it antimicrobial properties. The products obtained acted against Escherichia coli and Bacillus subtilis apart from the chitosan used that showed no such activity.

Facile and durable antimicrobial finishing of cotton textiles using a silver salt and UV light

In this study, we present facile antimicrobial finishing of cotton textiles. Screen printing was used for surface-finishing of cotton using a printing paste containing silver nitrate. UVC irradiation was applied to convert silver nitrate into a color product, thus also changing the color of the textiles. The color, its strength and stability of samples, depend on absorbed UVC energy and the formula of the printing paste. Scanning electron microscopy with the energy dispersive X-ray spectrometry revealed formation of silver particles on cotton threads; X-ray diffraction analysis and the time-of-flight secondary ion mass spectrometry did not provide clear information on these products. Microbiological studies revealed that the samples inhibited proliferation of Escherichia coli, Bacillus subtilis and Staphylococcus aureus. Washing fastness tests confirmed resistance of the samples to at least 50 washings. Additionally, the inhibition zones increased as the number of washing cycles increased, which is unique for such samples. This work also presents an approach to the design of antimicrobially finished workwear.

On the development of a VIPARnd radiotherapy 3D polymer gel dosimeter

This work presents an improvement of the VIPARnd (nd stands for normoxic, double, or VIP) polymer gel dosimeter. The gel composition was altered by increasing the concentration of the monomeric components, N-vinylpyrrolidone (NVP) and N,N-methylenebisacrylamide (MBA), in co-solvent solutions. The optimal composition (VIPARCT, where CT stands for computed tomography, or VIC) comprised: 17% NVP, 8% MBA, 12% t-BuOH, 7.5% gelatine, 0.007% ascorbic acid, 0.0008% CuSO4u2009u2009×u2009u20095H2O and 0.02% hydroquinone. The following characteristics of VIC were achieved: (i) linear dose range of 0.9_30 Gy, (ii) saturation for radiation doses of over 50 Gy, (iii) threshold dose of about 0.5 Gy, (iv) dose sensitivity of 0.171 Gy-1 s-1, which is roughly 2.2 times higher than that of VIP (for nuclear magnetic resonance measurements). It was also found that VIC is dose- rate-independent, and its dose response does not alter if the radiation source is changed from electrons to photons for external beam radiotherapy. The gel responded similarly to irradiation with small changes in radiation energy but was sensitive to larger energy changes. The VIC gel retained temporal stability from 20u2009h until at least 10 d after irradiation, whereas spatial stability was retained from 20u2009h until at least 6 d after irradiation. The scheme adopted for VIC manufacturing yields repeatable gels in terms of radiation dose response. The VIC was also shown to perform better than VIP using x-ray computed tomography as a readout method; the dose sensitivity of VIC (0.397 HU Gy-1) was 1.5 times higher than that of VIP. Also, the dose resolution of VIC was better than that of VIP in the whole dose range examined.

Ammonia gas sensors ink-jet printed on textile substrates

This work describes the fabrication of ammonia gas sensors on textile substrates by using the reactive inkjet printing for the deposition the polyaniline gas sensing layers. These layers were printed over vacuum deposited gold electrodes designed for the purposes of sensor conductivity analysis. The sensing properties such as sensing linearity, response and recovery times were studied in the range of ammonia gas concentrations from 15 to 100 ppm. The fabricated sensors showed a relevant increase in relative resistance from 0.30 to 14.4 times after exposing to ammonia gas at the concentrations of 15–100 ppm for 120 sec.

TTC-Pluronic 3D radiochromic gel dosimetry of ionizing radiation

This work reports the first results obtained using a new 3D radiochromic gel dosimeter. The dosimeter is an aqueous physical gel matrix made of poly(ethylene oxide)-block-poly(propylene oxide)-block-poly(ethylene oxide) (Pluronic F-127, PEO-PPO-PEO) doped with a representative of tetrazolium salts, 2, 3, 5-triphenyltetrazolium chloride (TTC). There were several reasons for the choice of Pluronic as a gel forming substrate: (i) the high degree of transparency and colourlessness; (ii) the possibility of gel dosimeter preparation at both high and low temperatures due to the phase behaviour of Pluronic; (iii) the broad temperature range over which the TTC-Pluronic dosimeter is stable; and (iv) the non-toxicity of Pluronic. A reason for the choice of TTC was its ionising radiation-induced transformation to water-insoluble formazan, which was assumed to impact beneficially on the spatial stability of the dose distribution. If irradiated, the TTC-Pluronic gels become red but transparent in the irradiated part, while the non-irradiated part remains crystal clear. The best obtained composition is characterised byu2009u2009<4 Gy dose threshold, a dose sensitivity of 0.002u200931 (Gyu2009u2009×u2009u2009cm)-1, a large linear dose range ofu2009u2009>500 Gy and a dynamic dose response much greater than 500 Gy (7.5% TTC, 25% Pluronic F-127, 50 mmol dm-3 tetrakis). Temporal and spatial stability studies revealed that the TTC-Pluronic gels (7.5% TTC, 25% Pluronic F-127) were stable for more than one week. The addition of compounds boosting the gels dose performance caused deterioration of the gels temporal stability but did not impact the stability of the 3D dose distribution. The proposed method of preparation allows for the repeatable manufacture of the gels. There were no differences observed between gels irradiated fractionally and non-fractionally. The TTC-Pluronic dose response might be affected by the radiation source dose rate-this, however, requires further examination.

Tetrazolium salts-Pluronic F-127 gels for 3D radiotherapy dosimetry

This work is a follow-up study for a recently-proposed 3D radiochromic gel dosimeter that contains a tetrazolium salt and a physical gel matrix made of poly(ethylene oxide)-block-poly(propylene oxide)-block-poly(ethylene oxide) (Pluronic F-127). Several tetrazolium salts were examined in this work, including tetrazolium violet, blue tetrazolium chloride, nitro blue tetrazolium chloride (NBT), tetranitro blue tetrazolium chloride (tNBT) and thiazolyl blue tetrazolium bromide (TBTB). The salt-containing gel dosimeters were compared with the first Pluronic gel composition that contained 2,3,5-triphenyltetrazolium chloride (TTC) as the radiation-sensitive component (dose sensitivity of 0.0023 (Gy cm)-1). The Pluronic gels with NBT and tNBT outperformed the other gels, including the TTC-containing gel, with respect to their dose sensitivity and low dose-response. The NBT gels were found to have better stability over time than tNBT gels. Sensitization of the gels to ionizing radiation was examined by addition of tert-butyl alcohol and sodium formate. The best composition was 0.0818% NBT (1u2009mM), 25% Pluronic F-127 and 0.136u2009u2009×u2009u200910-2% sodium formate. This gel dosimeter was insensitive to changes in dose rate for photons of different energies. The mean dose sensitivity amounted to 0.0047u2009u2009±u2009u20090.1u2009u2009×u2009u200910-4 (Gy cm)-1. A diversion in the dose-response was observed for the gel irradiated with electrons. Additional characteristics of the NBT gel were a linear-dose range and a dynamic-dose range betweenu2009u2009<1 andu2009u2009⩾150 Gy and a dose threshold ofu2009u2009<1 Gy. The dose distribution registered for the NBT-Pluronic gel was stable after irradiation for over 7 d with no visible diffusion of the irradiated part, which is analogous to the original TTC-Pluronic gel.