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1.
Int J Mol Sci ; 24(13)2023 Jun 24.
Article in English | MEDLINE | ID: mdl-37445773

ABSTRACT

The design and engineering of antibacterial materials are key for preventing bacterial adherence and proliferation in biomedical and household instruments. Silver nanoparticles (AgNPs) and chitosan (CHI) are broad-spectrum antibacterial materials with different properties whose combined application is currently under optimization. This study proposes the formation of antibacterial films with AgNPs embedded in carboxymethylcellulose/chitosan multilayers by the layer-by-layer (LbL) method. The films were deposited onto nanoporous silicon (nPSi), an ideal platform for bioengineering applications due to its biocompatibility, biodegradability, and bioresorbability. We focused on two alternative multilayer deposition processes: cyclic dip coating (CDC) and cyclic spin coating (CSC). The physicochemical properties of the films were the subject of microscopic, microstructural, and surface-interface analyses. The antibacterial activity of each film was investigated against Escherichia coli (Gram-negative) and Staphylococcus aureus (Gram-positive) bacteria strains as model microorganisms. According to the findings, the CDC technique produced multilayer films with higher antibacterial activity for both bacteria compared to the CSC method. Bacteria adhesion inhibition was observed from only three cycles. The developed AgNPs-multilayer composite film offers advantageous antibacterial properties for biomedical applications.


Subject(s)
Chitosan , Metal Nanoparticles , Nanopores , Chitosan/chemistry , Silver/chemistry , Carboxymethylcellulose Sodium , Silicon , Layer-by-Layer Nanoparticles , Bacterial Adhesion , Metal Nanoparticles/chemistry , Anti-Bacterial Agents/pharmacology , Anti-Bacterial Agents/chemistry
2.
Int J Mol Sci ; 24(1)2022 Dec 28.
Article in English | MEDLINE | ID: mdl-36613959

ABSTRACT

Nanoparticles have proven to be biocompatible and suitable for many biomedical applications. Currently, hyperthermia cancer treatments based on Fe nanoparticle infusion excited by alternating magnetic fields are commonly used. In addition to this, MRI-based image-guided radiotherapy represents, nowadays, one of the most promising accurate radiotherapy modalities. Hence, assessing the feasibility of combining both techniques requires preliminary characterization of the corresponding dosimetry effects. The present work reports on a theoretical and numerical simulation feasibility study aimed at pointing out preliminary dosimetry issues. Spatial dose distributions incorporating magnetic nanoparticles in MRI-based image-guided radiotherapy have been obtained by Monte Carlo simulation approaches accounting for all relevant radiation interaction properties as well as charged particles coupling with strong external magnetic fields, which are representative of typical MRI-LINAC devices. Two main effects have been evidenced: local dose enhancement (up to 60% at local level) within the infused volume, and non-negligible changes in the dose distribution at the interfaces between different tissues, developing to over 70% for low-density anatomical cavities. Moreover, cellular uptakes up to 10% have been modeled by means of considering different Fe nanoparticle concentrations. A theoretical temperature-dependent model for the thermal enhancement ratio (TER) has been used to account for radiosensitization due to hyperthermia. The outcomes demonstrated the reliability of the Monte Carlo approach in accounting for strong magnetic fields and mass distributions from patient-specific anatomy CT scans to assess dose distributions in MRI-based image-guided radiotherapy combined with magnetic nanoparticles, while the hyperthermic radiosensitization provides further and synergic contributions.


Subject(s)
Hyperthermia, Induced , Nanoparticles , Neoplasms , Radiotherapy, Image-Guided , Humans , Reproducibility of Results , Radiometry/methods , Magnetic Resonance Imaging , Monte Carlo Method , Radiotherapy Dosage , Neoplasms/diagnostic imaging , Neoplasms/radiotherapy
3.
Phys Med ; 80: 363-372, 2020 Dec.
Article in English | MEDLINE | ID: mdl-33285337

ABSTRACT

The effects of low energy electrons in biological tissues have proved to lead to severe damages at the cellular and sub-cellular level. It is due to an increase in the relative biological effectiveness (RBE) of these electrons with a decrease in their penetration range. That is, lower the range higher will be its RBE.Therefore, accurate determination of low energy electron range becomes a key issue for radiation dosimetry. This work reports on in-water electron tracks evaluated at low kinetic energy (1-50 keV) using isotropic mono-energetic point source approach suitably implemented by different general-purpose Monte Carlo codes. For this aim, simulations were performed using PENELOPE, EGSnrc, MCNP6, FLUKA and Geant4-DNA Monte Carlo codes to obtain the particle range, R,R90,R50. Finally, evaluation of dose point kernel (DPK), as used for internal dosimetry, was carried out as an application example. Scaled dose point kernels (sDPK) were estimated for a range of mono-energetic low energy electron sources. The non-negligible differences among the calculated sDPK using different codes were obtained for energy electrons up to 5 keV. It was also observed that differences of in-water range for low-energy electrons, due to the different general-purpose Monte Carlo codes, affected the DPKs used for dosimetry by convolution approach. Finally, the 3D dosimetry was found to be almost not affected at macroscopic clinical scale, whereas non-negligible differences appeared at the microscopic level. Hence, a thorough validation of the used sDPKs have to be performed before they could be used in applications to derive any conclusions.


Subject(s)
Electrons , Monte Carlo Method , Water , Computer Simulation , Radiometry , Relative Biological Effectiveness
4.
Appl Radiat Isot ; 151: 280-288, 2019 Sep.
Article in English | MEDLINE | ID: mdl-31229928

ABSTRACT

Different kinds of nanoparticles have been widely studied for biomedical purposes, including applications like dose enhancement in radiotherapy treatments and contrast agent in radiological studies. Recent work suggests that gold nanoparticles can be used as contrast agents in K-edge imaging and X-ray Fluorescence Computed Tomography, mainly due to their high K-edge energy value and good biocompatibility. However, the gold X-ray fluorescence (XRF) signal obtained in these procedures is relatively week when compared with Compton or bremsstrahlung radiation emitted in the surrounding tissues, mainly because it is not possible to achieve large gold nanoparticles concentrations within biological tissues added to the XRF is attenuated by other tissues when leaving the patient body. This work presents a feasibility study on implementation of FLUKA, PENELOPE and MCNP6 Monte Carlo codes to model the detection of gold XRF emitted by a small volume containing different gold concentrations and located at different depths in a tissue-equivalent phantom. Results indicate that there is good agreement between PENELOPE and FLUKA for gold Kα and Kß lines estimations when highly symmetric simulation scenario and kilovoltage X-ray beam were used, achieving differences lower than 2%; however, differences up to 6 times were observed between FLUKA and MCNP6 under the same conditions. In addition, remarkable differences were obtained when megavoltage X-ray beam was used, being up to 11 times between PENELOPE and FLUKA and up to 4 times between FLUKA and MCNP6 for gold Kα and Kß lines estimations. In this regard, a suitable normalization method was proposed and implemented to perform cross-comparisons of XRF estimations obtained from the Monte Carlo codes. By means of the proposed method, FLUKA, PENELOPE and MCNP6 can be successfully implemented to assess which configuration (gold concentration and target volume depth) leads to a better detection of gold XRF, despite differences in XRF estimation between the codes.


Subject(s)
Gold/chemistry , Monte Carlo Method , Tumor Burden , Biomarkers, Tumor/metabolism , Fluorescence , Humans , Metal Nanoparticles/chemistry , Neoplasms/metabolism , Neoplasms/radiotherapy , Phantoms, Imaging , Spectrometry, X-Ray Emission
5.
J Appl Clin Med Phys ; 17(4): 402-417, 2016 07 08.
Article in English | MEDLINE | ID: mdl-27455471

ABSTRACT

Fricke solution has a wide range of applications as radiation detector and dosimetry. It is particularly appreciated in terms of relevant comparative advantages, like tissue-equivalence when prepared in aqueous media like gel matrix, continuous mapping capability, independence of dose rate and incident direction, as well as linear dose response. This work presents the development and characterization of an improved Fricke gel system, based on modified chemical compositions, making possible its application in clinical radiology due to its improved sensitivity. Properties of standard Fricke gel dosimeter for high-dose levels are used as a starting point, and suitable chemical modifications are introduced and carefully investigated in order to attain high resolution for low-dose ranges, like those corresponding to radiology interventions. The developed Fricke gel radiation dosimeter system achieves the expected typical dose-dependency, showing linear response in the dose range from 20 up to 4000 mGy. Systematic investigations including several chemical compositions are carried out in order to obtain an adequate dosimeter response for low-dose levels. A suitable composition from among those studied is selected as a good candidate for low-dose-level radiation dosimetry consisting of a modified Fricke solution fixed to a gel matrix containing benzoic acid along with sulfuric acid, ferrous sulfate, Xylenol orange, and tridistilled water. Dosimeter samples are prepared in standard vials for in-phantom irradiation and further characterization by spectrophotometry measuring visible light transmission and absorbance before and after irradiation. Samples are irradiated using typical X-ray tubes for radiology and calibrated Farmer-type ionization chamber is used as reference to measure dose rates inside phantoms at vial locations. Once sensitive material composition is optimized, dose-response curves show significant improvement regarding overall sensitivity for low dose levels. The aim of this work consists of implementing the optimized gel dosimeter to perform direct measurements of absorbed dose in samples irradiated during microcomputed tomography scanning in order to preliminary assess dose levels for further scanning of small animals for further applications in veterinary and paleontology. As a first attempt, dose distributions were measured in water-equivalent phantoms having dimensions comparable to small animals, 100 to 1000 cm3, approximately. According to the obtained results, it is found that the proposed method shows satisfactory reliability and adequate performance for a promising gel dosimetry system.


Subject(s)
Phantoms, Imaging , Radiometry/instrumentation , Radiometry/methods , Ferrous Compounds , Humans , Radiation Dosage , Reproducibility of Results , Solutions , X-Ray Microtomography
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