Jeaneth M. Medina-Pérez, Melanie A. Zegarra-Zegarra, J. Villanueva-Salas, B. M. Salazar-Pinto, S. S. Flores-Calla, Angel G. Ramírez-Valverde, Hugo G. Jiménez-Pacheco, E. G. Gonzales-Condori
Lactobionic acid (LBA) is a polyhydroxy acid with attractive properties in the pharmaceutical, cosmetic, food, medical, and chemical industries, making it a versatile product with multiple applications, which supports the various studies aimed at its production by increasingly more simple, efficient, and environmentally friendly processes. For this reason, the purpose of this research was to synthesize gold nanoparticles (AuNPs) by a synthesis process using Myrciaria dubia (Camu camu) fruit extract. Subsequently, AuNPs were used to produce LBA from lactose. The results demonstrate that the Myrciaria dubia extract manages to synthesize AuNPs that were characterized by UV/vis spectrophotometry, energy-dispersive X-ray spectroscopy (EDX), and Zetasizer. LBA was quantified by FTIR-ATR spectroscopy and ion chromatography. The results showed that AuNPs succeeded in producing LBA from lactose showing the highest LBA production efficiency at a dose of 0.5 g/L and a temperature of 60°C. It has been shown that the AuNPs obtained by synthesis using the Myrciaria dubia extract efficiently catalyze the production of LBA from lactose, with a yield of 45.24%, which can be used to produce LBA for industrial or research purposes.
{"title":"Production of Lactobionic Acid Using Gold Nanoparticles Synthesized with Fruit Myrciaria dubia Extract","authors":"Jeaneth M. Medina-Pérez, Melanie A. Zegarra-Zegarra, J. Villanueva-Salas, B. M. Salazar-Pinto, S. S. Flores-Calla, Angel G. Ramírez-Valverde, Hugo G. Jiménez-Pacheco, E. G. Gonzales-Condori","doi":"10.1155/2023/5654802","DOIUrl":"https://doi.org/10.1155/2023/5654802","url":null,"abstract":"Lactobionic acid (LBA) is a polyhydroxy acid with attractive properties in the pharmaceutical, cosmetic, food, medical, and chemical industries, making it a versatile product with multiple applications, which supports the various studies aimed at its production by increasingly more simple, efficient, and environmentally friendly processes. For this reason, the purpose of this research was to synthesize gold nanoparticles (AuNPs) by a synthesis process using Myrciaria dubia (Camu camu) fruit extract. Subsequently, AuNPs were used to produce LBA from lactose. The results demonstrate that the Myrciaria dubia extract manages to synthesize AuNPs that were characterized by UV/vis spectrophotometry, energy-dispersive X-ray spectroscopy (EDX), and Zetasizer. LBA was quantified by FTIR-ATR spectroscopy and ion chromatography. The results showed that AuNPs succeeded in producing LBA from lactose showing the highest LBA production efficiency at a dose of 0.5 g/L and a temperature of 60°C. It has been shown that the AuNPs obtained by synthesis using the Myrciaria dubia extract efficiently catalyze the production of LBA from lactose, with a yield of 45.24%, which can be used to produce LBA for industrial or research purposes.","PeriodicalId":16378,"journal":{"name":"Journal of Nanotechnology","volume":"8 1","pages":""},"PeriodicalIF":4.2,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82742962","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
S. J. Beden, Hassan A. Dumboos, M. K. Ismael, Mohanad Kadhim Mejbel
Bismuth oxide (Bi2O3) has attracted considerable research interest in test thin films made utilizing the reactive plasma sputtering (RPS) technology-assisted annealing treatment, allowing the development of diverse BixOx thin films. SEM, phase X-ray diffraction patterns, UV-Vis spectrometers, and D.C. two-probes are used to identify the crystallographic structure and assess the films’ optical-electrical properties. The XRD examination showed that forming Bi2O3 films with an amorphous to multiphase crystalline structure for sputtering time of 40 min was due to soda glass substrate temperature at a range of 30–35°C. Thin films of Bi2O3 crystal structures improved with annealing heat treatment at 200, 300, 400, and 500°C. Yet the formation of crystalline phase (β-Bi2O3 with δ-Bi2O3) Bi2O3 nanostructures occurred at higher temperatures. SEM images showed transparent particles highly affected by annealing temperatures. The nanostructures were about 102–510 nm long, and the diameter was 50–100 nm. The Bi2O3 film optical band gaps and nanostructures ranged from 2.75 to 3.05 eV. The annealing temperature differences affected the crystallite sizes, optical band gaps, and surface roughness. The findings showed that these differences caused the phase transition in Bi2O3 structures. The electrical calculation revealed that the electrical conductivity improved with annealing temperatures of 150–250°C while declining with temperature (300–500)°C with typical semiconductor films.
{"title":"The Role of Annealing Treatment on Crystallographic, Optical, and Electrical Features of Bi2O3 Thin Films Prepared Using Reactive Plasma Sputtering Technology","authors":"S. J. Beden, Hassan A. Dumboos, M. K. Ismael, Mohanad Kadhim Mejbel","doi":"10.1155/2023/8638512","DOIUrl":"https://doi.org/10.1155/2023/8638512","url":null,"abstract":"Bismuth oxide (Bi2O3) has attracted considerable research interest in test thin films made utilizing the reactive plasma sputtering (RPS) technology-assisted annealing treatment, allowing the development of diverse BixOx thin films. SEM, phase X-ray diffraction patterns, UV-Vis spectrometers, and D.C. two-probes are used to identify the crystallographic structure and assess the films’ optical-electrical properties. The XRD examination showed that forming Bi2O3 films with an amorphous to multiphase crystalline structure for sputtering time of 40 min was due to soda glass substrate temperature at a range of 30–35°C. Thin films of Bi2O3 crystal structures improved with annealing heat treatment at 200, 300, 400, and 500°C. Yet the formation of crystalline phase (β-Bi2O3 with δ-Bi2O3) Bi2O3 nanostructures occurred at higher temperatures. SEM images showed transparent particles highly affected by annealing temperatures. The nanostructures were about 102–510 nm long, and the diameter was 50–100 nm. The Bi2O3 film optical band gaps and nanostructures ranged from 2.75 to 3.05 eV. The annealing temperature differences affected the crystallite sizes, optical band gaps, and surface roughness. The findings showed that these differences caused the phase transition in Bi2O3 structures. The electrical calculation revealed that the electrical conductivity improved with annealing temperatures of 150–250°C while declining with temperature (300–500)°C with typical semiconductor films.","PeriodicalId":16378,"journal":{"name":"Journal of Nanotechnology","volume":"299 1","pages":""},"PeriodicalIF":4.2,"publicationDate":"2023-06-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78330003","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Synthesis of cerium oxide (CeO2) nanoparticles (NPs) via biological approach has received a lot of interest to reduce the harmful effects of chemical synthesis. In the present study, Colocasia esculenta leaf extract facilitated the preparation of CeO2-NPs by using the sol-gel technique. The crystal structural of CeO2-NPs was proven by X-ray powder diffraction (XRD) investigation to be cubic with size of 2.94 nm according to Debye–Scherrer equation. As demonstrated in the transmission electron microscopy (TEM) image, CeO2-NPs have a spherical form with an average size of 2.04 nm which is almost consistent with a finding from XRD analysis. Energy dispersive X-ray (EDX) measurements exhibited high-intensity peaks attributed to Ce and oxygen and further proved the creation of CeO2-NPs. The Fourier transform infrared spectroscopy (FTIR) analysis revealed the presence of Ce-O stretching, indicating the formation of CeO2-NPs. Functional groups of O-H, C-O, and C=O peaks were found in a spectrum due to the phytochemical components that were responsible for reducing and stabilizing during the synthesis process of CeO2-NPs. The examined UV-visible spectra exhibited the absorbance peak at 213 nm. The synthesized NPs produced in this study were further investigated for mung bean seed germination, whereby the influence of grain germination and growth rate demonstrated the significant finding.
{"title":"Synthesis of Green Cerium Oxide Nanoparticles Using Plant Waste from Colocasia esculenta for Seed Germination of Mung Bean (Vigna radiata)","authors":"Nor Monica Ahmad, Nor’ Aishah Hasan","doi":"10.1155/2023/9572025","DOIUrl":"https://doi.org/10.1155/2023/9572025","url":null,"abstract":"Synthesis of cerium oxide (CeO2) nanoparticles (NPs) via biological approach has received a lot of interest to reduce the harmful effects of chemical synthesis. In the present study, Colocasia esculenta leaf extract facilitated the preparation of CeO2-NPs by using the sol-gel technique. The crystal structural of CeO2-NPs was proven by X-ray powder diffraction (XRD) investigation to be cubic with size of 2.94 nm according to Debye–Scherrer equation. As demonstrated in the transmission electron microscopy (TEM) image, CeO2-NPs have a spherical form with an average size of 2.04 nm which is almost consistent with a finding from XRD analysis. Energy dispersive X-ray (EDX) measurements exhibited high-intensity peaks attributed to Ce and oxygen and further proved the creation of CeO2-NPs. The Fourier transform infrared spectroscopy (FTIR) analysis revealed the presence of Ce-O stretching, indicating the formation of CeO2-NPs. Functional groups of O-H, C-O, and C=O peaks were found in a spectrum due to the phytochemical components that were responsible for reducing and stabilizing during the synthesis process of CeO2-NPs. The examined UV-visible spectra exhibited the absorbance peak at 213 nm. The synthesized NPs produced in this study were further investigated for mung bean seed germination, whereby the influence of grain germination and growth rate demonstrated the significant finding.","PeriodicalId":16378,"journal":{"name":"Journal of Nanotechnology","volume":"362 1","pages":""},"PeriodicalIF":4.2,"publicationDate":"2023-05-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78977187","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A. A. Hussain, Haider Abdulelah, A. H. Amteghy, Raed A. Dheyab, Ban Hamdan AlMulla
Due to relatively low price and nontoxicity of photovoltaic (PV) systems, dye-sensitized solar cells (DSSCs) recently gained a lot of attention in terms of improving their performance and longevity. Because most of the major elements are impacted by their separate production and layering procedures, the substances in DSSCs are critical to achieving these goals. Methylene blue dye sensitizer-based solar cells were effectively constructed in this work, and DSSC performance was assessed. The morphologies of nanocrystalline CdS thin films were investigated by the FE-SEM machine, and then XRD patterns of 1 layer, 2 layers, and 3 layers of nanocrystalline CdS thin films were analyzed. The thicknesses of the prepared samples were about 391 nm, 457 nm, and 912 nm for 1, 2, and 3 layers of nanocrystalline CdS thin film, respectively. J-V characteristics of the multilayer CdS thin films have been studied under a 100 mW/cm2 sunlight source. The experimental results revealed that the highest power conversion efficiency of a 3 layer porous-nanowall CdS/MB device was about 0.47%.
{"title":"Effect of Multilayers CdS Nanocrystalline Thin Films on the Performance of Dye-Sensitized Solar Cells","authors":"A. A. Hussain, Haider Abdulelah, A. H. Amteghy, Raed A. Dheyab, Ban Hamdan AlMulla","doi":"10.1155/2023/7998917","DOIUrl":"https://doi.org/10.1155/2023/7998917","url":null,"abstract":"Due to relatively low price and nontoxicity of photovoltaic (PV) systems, dye-sensitized solar cells (DSSCs) recently gained a lot of attention in terms of improving their performance and longevity. Because most of the major elements are impacted by their separate production and layering procedures, the substances in DSSCs are critical to achieving these goals. Methylene blue dye sensitizer-based solar cells were effectively constructed in this work, and DSSC performance was assessed. The morphologies of nanocrystalline CdS thin films were investigated by the FE-SEM machine, and then XRD patterns of 1 layer, 2 layers, and 3 layers of nanocrystalline CdS thin films were analyzed. The thicknesses of the prepared samples were about 391 nm, 457 nm, and 912 nm for 1, 2, and 3 layers of nanocrystalline CdS thin film, respectively. J-V characteristics of the multilayer CdS thin films have been studied under a 100 mW/cm2 sunlight source. The experimental results revealed that the highest power conversion efficiency of a 3 layer porous-nanowall CdS/MB device was about 0.47%.","PeriodicalId":16378,"journal":{"name":"Journal of Nanotechnology","volume":"27 1","pages":""},"PeriodicalIF":4.2,"publicationDate":"2023-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78833992","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Valeriy A. Nebol’sin, E. Levchenko, V. Yuryev, N. Swaikat
In this paper, we focus on the thermodynamics of redox reactions occurring during the vapor-liquid-solid (VLS) growth of silicon nanowires (NWs) with the participation of liquid solutions of metal catalysts. The growth of NWs is difficult with the participation of Ti, Al, and Mg particles; this is because in this case, the drops of the metal catalyst are strongly oxidized and crystals either do not form at all or are characterized by instability in the direction of growth. However, the particles of Cu, Ni, and Fe give a much more stable growth of NWs. We have also established that if the oxide film of catalytic particles is formed by the basic metal oxides, then the silicon-NWs' growth slows down. In this work, we have concluded that only metals with a lower chemical affinity for O2 than Si are applicable as catalysts for the NWs' growth.
{"title":"Thermodynamics of Silicon Nanowire Growth under Unintended Oxidation of Catalytic Particles","authors":"Valeriy A. Nebol’sin, E. Levchenko, V. Yuryev, N. Swaikat","doi":"10.1155/2023/3485793","DOIUrl":"https://doi.org/10.1155/2023/3485793","url":null,"abstract":"In this paper, we focus on the thermodynamics of redox reactions occurring during the vapor-liquid-solid (VLS) growth of silicon nanowires (NWs) with the participation of liquid solutions of metal catalysts. The growth of NWs is difficult with the participation of Ti, Al, and Mg particles; this is because in this case, the drops of the metal catalyst are strongly oxidized and crystals either do not form at all or are characterized by instability in the direction of growth. However, the particles of Cu, Ni, and Fe give a much more stable growth of NWs. We have also established that if the oxide film of catalytic particles is formed by the basic metal oxides, then the silicon-NWs' growth slows down. In this work, we have concluded that only metals with a lower chemical affinity for O2 than Si are applicable as catalysts for the NWs' growth.","PeriodicalId":16378,"journal":{"name":"Journal of Nanotechnology","volume":"47 1","pages":""},"PeriodicalIF":4.2,"publicationDate":"2023-05-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88582538","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
T. Kantaria, Tengiz Kantaria, P. Heiduschka, N. Eter, D. Tugushi, R. Katsarava
Ophthalmic drug delivery for treating various eye diseases still remains a challenge in ophthalmology. One perspective way of overcoming this problem is to use nanoscale biodegradable drug carriers that are able to safely deliver pharmaceuticals directly to the locus of disease and maintain a therapeutic concentration of drug for a long time. The goal of the present study was the preparation of drug- (dexamethasone-, DEX-) loaded pseudo-protein nanoparticles (NPs) and investigation of drug encapsulation efficiency and drug release kinetics. DEX-loaded pseudo-protein NPs (DEX-NPs) were successfully prepared by the nanoprecipitation method. DEX-NPs were characterized by size (average diameter, AD), size distribution (polydispersity index, PDI), and surface charge (zeta-potential, ZP) using the dynamic light scattering technique. DEX encapsulation characteristics were determined using the UV-spectrophotometric method, and kinetics of DEX release from DEX-NPs was studied according to the dialysis method in PBS at 37°C. The obtained results showed that size of DEX-NPs varies within 143.6–164.1 nm depending on DEX content during the preparation. DEX incorporation characteristics were determined—encapsulation efficiency (EE) and actual drug loading (DL) were high enough and reached 55.1 and 10.2%, respectively. The kinetics of DEX release from DEX-NPs showed a typical biphasic release pattern—an initial rapid (burst) release and further much more continuous slow release. Based on the obtained data, we can conclude that the elaborated DEX-NPs have potential for the application in ophthalmology as ocular drug delivery nanocarriers.
{"title":"Dexamethasone-Loaded Pseudo-Protein Nanoparticles for Ocular Drug Delivery: Evaluation of Drug Encapsulation Efficiency and Drug Release","authors":"T. Kantaria, Tengiz Kantaria, P. Heiduschka, N. Eter, D. Tugushi, R. Katsarava","doi":"10.1155/2023/8827248","DOIUrl":"https://doi.org/10.1155/2023/8827248","url":null,"abstract":"Ophthalmic drug delivery for treating various eye diseases still remains a challenge in ophthalmology. One perspective way of overcoming this problem is to use nanoscale biodegradable drug carriers that are able to safely deliver pharmaceuticals directly to the locus of disease and maintain a therapeutic concentration of drug for a long time. The goal of the present study was the preparation of drug- (dexamethasone-, DEX-) loaded pseudo-protein nanoparticles (NPs) and investigation of drug encapsulation efficiency and drug release kinetics. DEX-loaded pseudo-protein NPs (DEX-NPs) were successfully prepared by the nanoprecipitation method. DEX-NPs were characterized by size (average diameter, AD), size distribution (polydispersity index, PDI), and surface charge (zeta-potential, ZP) using the dynamic light scattering technique. DEX encapsulation characteristics were determined using the UV-spectrophotometric method, and kinetics of DEX release from DEX-NPs was studied according to the dialysis method in PBS at 37°C. The obtained results showed that size of DEX-NPs varies within 143.6–164.1 nm depending on DEX content during the preparation. DEX incorporation characteristics were determined—encapsulation efficiency (EE) and actual drug loading (DL) were high enough and reached 55.1 and 10.2%, respectively. The kinetics of DEX release from DEX-NPs showed a typical biphasic release pattern—an initial rapid (burst) release and further much more continuous slow release. Based on the obtained data, we can conclude that the elaborated DEX-NPs have potential for the application in ophthalmology as ocular drug delivery nanocarriers.","PeriodicalId":16378,"journal":{"name":"Journal of Nanotechnology","volume":"132 1","pages":""},"PeriodicalIF":4.2,"publicationDate":"2023-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89728091","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Superhydrophobic cotton fabric with photoinduced reversibly switchable wettability was prepared by a coating of the hydrophobic copolymer and α-Fe2O3 nanoparticles. The surface morphology of the fabric was observed by scanning electron microscope (SEM). The wettability of the surface was tested under UV illumination and after storage in the dark. The chemical composition of the cotton fabric surfaces before and after UV illumination was analyzed using an X-ray photoelectron spectroscope (XPS) and FTIR. The experimental results showed that the prepared cotton fabric exhibited the excellent superhydrophobic property with a contact angle (CA) of 157.3 ± 2.9°, and became superhydrophilic after UV illumination for 64 h. The surface wettability reverted back to its initial superhydrophobic state after being stored in the dark for 30 d. Based on the XPS and FTIR analyses, the possible mechanism was discussed, and the switchable wettability was caused by the content change of the hydroxyl groups on the α-Fe2O3 surface. Moreover, the superhydrophobic cotton fabric also became superhydrophilic after sunlight illumination for 120 h.
{"title":"Study on the Cotton Fabrics with Photoinduced Reversibly Switchable Wettability","authors":"Caining Zhang, Xuman Wang","doi":"10.1155/2023/8422293","DOIUrl":"https://doi.org/10.1155/2023/8422293","url":null,"abstract":"Superhydrophobic cotton fabric with photoinduced reversibly switchable wettability was prepared by a coating of the hydrophobic copolymer and α-Fe2O3 nanoparticles. The surface morphology of the fabric was observed by scanning electron microscope (SEM). The wettability of the surface was tested under UV illumination and after storage in the dark. The chemical composition of the cotton fabric surfaces before and after UV illumination was analyzed using an X-ray photoelectron spectroscope (XPS) and FTIR. The experimental results showed that the prepared cotton fabric exhibited the excellent superhydrophobic property with a contact angle (CA) of 157.3 ± 2.9°, and became superhydrophilic after UV illumination for 64 h. The surface wettability reverted back to its initial superhydrophobic state after being stored in the dark for 30 d. Based on the XPS and FTIR analyses, the possible mechanism was discussed, and the switchable wettability was caused by the content change of the hydroxyl groups on the α-Fe2O3 surface. Moreover, the superhydrophobic cotton fabric also became superhydrophilic after sunlight illumination for 120 h.","PeriodicalId":16378,"journal":{"name":"Journal of Nanotechnology","volume":"30 1","pages":""},"PeriodicalIF":4.2,"publicationDate":"2023-04-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87827656","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Aminur Rahman, H. Rasid, Md. Isahak Ali, Nymul Yeachin, M. Alam, K. S. Hossain, M. A. Kafi
This study synthesized silver nanoparticles (Ag-NPs) using silver nitrate (AgNO3) as the ion source and sodium tripolyphosphate (STPP) as reducing as well as capping agents. The synthesized Ag-NPs were confirmed initially using Ag-NPs specific λmax at 410 nm with UV-Vis spectrophotometry and homogenously distributed, 100–300 nm size, and round-shaped particles were realized through atomic force microscopy (AFM) and transmission electron microscopy (TEM) image analysis. The various reaction condition-based studies revealed 0.01 M AgNO3 yields maximum particle after 4 h reduction with 1% STPP. Bacillus spp. (n = 23/90) and Pseudomonas spp. (n = 26/90) were isolated from three different poultry farms for evaluating the antibacterial activity of Ag-NPs. Among the PCR confirmed isolates, 52% (12/23) Bacillus spp. were resistant to ten antibiotics and 65% (17/26) Pseudomonas spp. were resistant to eleven antibiotics. The representative resistant isolates were subjected to antibacterial evaluation of synthesized Ag-NPs following the well diffusion method, revealing the maximum sensitive zone of inhibition 19 ± 0.2 mm against Bacillus spp. and 17 ± 0.38 mm against Pseudomonas spp. The minimum inhibitory concentration (MIC) and minimum bacterial concentration (MBC) of Ag-NPs were 2.1 μg/ml and 8.4 μg/ml, respectively, for broad-spectrum application. Finally, the biocompatibility was determined by observing the viability of Ag-NP-treated BHK-21 cell through trypan blue-based exclusion assay revealing nonsignificant decreased of cell viability ≤2MIC doses. Thus, the synthesized Ag-NPs were proven as biocompatible and sensitive to both Gram-positive and Gram-negative bacteria of the poultry farm environmental samples.
{"title":"Facile Synthesis and Application of Ag-NPs for Controlling Antibiotic-ResistantPseudomonas spp. and Bacillus spp. in a Poultry Farm Environment","authors":"Aminur Rahman, H. Rasid, Md. Isahak Ali, Nymul Yeachin, M. Alam, K. S. Hossain, M. A. Kafi","doi":"10.1155/2023/6260066","DOIUrl":"https://doi.org/10.1155/2023/6260066","url":null,"abstract":"This study synthesized silver nanoparticles (Ag-NPs) using silver nitrate (AgNO3) as the ion source and sodium tripolyphosphate (STPP) as reducing as well as capping agents. The synthesized Ag-NPs were confirmed initially using Ag-NPs specific λmax at 410 nm with UV-Vis spectrophotometry and homogenously distributed, 100–300 nm size, and round-shaped particles were realized through atomic force microscopy (AFM) and transmission electron microscopy (TEM) image analysis. The various reaction condition-based studies revealed 0.01 M AgNO3 yields maximum particle after 4 h reduction with 1% STPP. Bacillus spp. (n = 23/90) and Pseudomonas spp. (n = 26/90) were isolated from three different poultry farms for evaluating the antibacterial activity of Ag-NPs. Among the PCR confirmed isolates, 52% (12/23) Bacillus spp. were resistant to ten antibiotics and 65% (17/26) Pseudomonas spp. were resistant to eleven antibiotics. The representative resistant isolates were subjected to antibacterial evaluation of synthesized Ag-NPs following the well diffusion method, revealing the maximum sensitive zone of inhibition 19 ± 0.2 mm against Bacillus spp. and 17 ± 0.38 mm against Pseudomonas spp. The minimum inhibitory concentration (MIC) and minimum bacterial concentration (MBC) of Ag-NPs were 2.1 μg/ml and 8.4 μg/ml, respectively, for broad-spectrum application. Finally, the biocompatibility was determined by observing the viability of Ag-NP-treated BHK-21 cell through trypan blue-based exclusion assay revealing nonsignificant decreased of cell viability ≤2MIC doses. Thus, the synthesized Ag-NPs were proven as biocompatible and sensitive to both Gram-positive and Gram-negative bacteria of the poultry farm environmental samples.","PeriodicalId":16378,"journal":{"name":"Journal of Nanotechnology","volume":"16 1","pages":""},"PeriodicalIF":4.2,"publicationDate":"2023-04-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83395901","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Moeko Fukada, T. Chhetri, Agasthya Suresh, Anandhi Upendran, Z. Afrasiabi
Hydroxyapatite nanoparticles (nHAPs) have been recognized for potent antitumor effects in certain cancer cells, making them good candidates as drug delivery agents and tumor therapeutics with fewer than normal side effects. This study is aimed to correlate cell proliferation inhibition with the size and morphology of nHAPs in a human breast cancer cell line as well as in normal tissue cells. We present our in vitro experimental evidence that nHAPs with sizes smaller than 50 nm have high inhibitory activity against human MCF-7 breast cancer cell lines. Based on our experimental data, normal fibroblast cells (NIH 3T3) were relatively more viable upon treatment with the nanoconstructs. The present study indicates that nHAPs can be engineered as nontoxic specific inhibitors as efficient breast cancer therapeutics in humans.
{"title":"Size and Morphology-Mediated Antiproliferative Activity of Hydroxyapatite Nanoparticles in Human Breast Cancer Cells","authors":"Moeko Fukada, T. Chhetri, Agasthya Suresh, Anandhi Upendran, Z. Afrasiabi","doi":"10.1155/2023/5381158","DOIUrl":"https://doi.org/10.1155/2023/5381158","url":null,"abstract":"Hydroxyapatite nanoparticles (nHAPs) have been recognized for potent antitumor effects in certain cancer cells, making them good candidates as drug delivery agents and tumor therapeutics with fewer than normal side effects. This study is aimed to correlate cell proliferation inhibition with the size and morphology of nHAPs in a human breast cancer cell line as well as in normal tissue cells. We present our in vitro experimental evidence that nHAPs with sizes smaller than 50 nm have high inhibitory activity against human MCF-7 breast cancer cell lines. Based on our experimental data, normal fibroblast cells (NIH 3T3) were relatively more viable upon treatment with the nanoconstructs. The present study indicates that nHAPs can be engineered as nontoxic specific inhibitors as efficient breast cancer therapeutics in humans.","PeriodicalId":16378,"journal":{"name":"Journal of Nanotechnology","volume":"18 1","pages":""},"PeriodicalIF":4.2,"publicationDate":"2023-04-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85538855","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Astuti, S. Arief, Muldarisnur, Zulhadjri, R. A. Usna
A Fe3O4@ZnO/C nanocomposite with a core-shell structure was synthesized using the co-precipitation method. To prevent the aggregation of the Fe3O4 magnetic particles, polyethylene glycol (PEG) was added. The X-ray diffractometer (XRD) results confirmed the formation of Fe3O4 and ZnO phases, with Fe3O4 having a cubic crystal system and ZnO having a hexagonal crystal system. Carbon in Fe3O4@ZnO/C had no effect on the crystal structure of Fe3O4@ZnO. Images from transmission electron microscopy (TEM) and scanning electron microscopy (SEM) revealed that the nanocomposite formed a core-shell structure. The Fourier transform infrared (FTIR) spectra verified the presence of bonds among ZnO, Fe3O4, and carbon. The appearance of the stretching vibration of the C≡C bond on the Fe3O4@ZnO/C sample revealed the nanocomposites’ carbon coupling. Photoluminescence (PL) spectroscopy was used to characterize the optical properties of the nanocomposites. Based on the results of the PL, the sample absorption of visible light was in the wavelength range of 400–700 nm. The photoluminescence of Fe3O4@ZnO differed from that of the Fe3O4@ZnO/C, especially in the deep-level emission (DLE) band. There was a phenomenon of broadening and shift of the band at a shorter wavelength, namely, in the blue wavelength region. Magnetic properties were characterized by vibrating-sample magnetometry (VSM). Based on the VSM results, the sample coupled with carbon exhibited a decrease in magnetic saturation. The presence of carbon changed photon energy into thermal energy. So, this material, apart from being a bioimaging material, can also be developed as a photothermal therapy material.
{"title":"Synthesis and Properties of Magnetic-Luminescent Fe3O4@ZnO/C Nanocomposites","authors":"Astuti, S. Arief, Muldarisnur, Zulhadjri, R. A. Usna","doi":"10.1155/2023/2381623","DOIUrl":"https://doi.org/10.1155/2023/2381623","url":null,"abstract":"A Fe3O4@ZnO/C nanocomposite with a core-shell structure was synthesized using the co-precipitation method. To prevent the aggregation of the Fe3O4 magnetic particles, polyethylene glycol (PEG) was added. The X-ray diffractometer (XRD) results confirmed the formation of Fe3O4 and ZnO phases, with Fe3O4 having a cubic crystal system and ZnO having a hexagonal crystal system. Carbon in Fe3O4@ZnO/C had no effect on the crystal structure of Fe3O4@ZnO. Images from transmission electron microscopy (TEM) and scanning electron microscopy (SEM) revealed that the nanocomposite formed a core-shell structure. The Fourier transform infrared (FTIR) spectra verified the presence of bonds among ZnO, Fe3O4, and carbon. The appearance of the stretching vibration of the C≡C bond on the Fe3O4@ZnO/C sample revealed the nanocomposites’ carbon coupling. Photoluminescence (PL) spectroscopy was used to characterize the optical properties of the nanocomposites. Based on the results of the PL, the sample absorption of visible light was in the wavelength range of 400–700 nm. The photoluminescence of Fe3O4@ZnO differed from that of the Fe3O4@ZnO/C, especially in the deep-level emission (DLE) band. There was a phenomenon of broadening and shift of the band at a shorter wavelength, namely, in the blue wavelength region. Magnetic properties were characterized by vibrating-sample magnetometry (VSM). Based on the VSM results, the sample coupled with carbon exhibited a decrease in magnetic saturation. The presence of carbon changed photon energy into thermal energy. So, this material, apart from being a bioimaging material, can also be developed as a photothermal therapy material.","PeriodicalId":16378,"journal":{"name":"Journal of Nanotechnology","volume":"1 1","pages":""},"PeriodicalIF":4.2,"publicationDate":"2023-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88852837","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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