Photodynamic therapy(PDT)has been established as one of the most promising novel cancer therapies with fewer side-effects and enhanced efficacy compared to the currently available conventional treatments.However,its a...Photodynamic therapy(PDT)has been established as one of the most promising novel cancer therapies with fewer side-effects and enhanced efficacy compared to the currently available conventional treatments.However,its application has been hindered by the limitations that photosensitizers(PS)have.The combination of PS with metallic nanoparticles like platinum nanoparticles(PtNPs),can help to overcome these intrinsic drawbacks.In this work,the combination of PtNPs and the natural photosensitizer riboflavin(RF)is proposed.PtNPs are synthesized using RF(Pt@RF)as reducing and stabilizing agent in a one-step method,obtaining nanoparticles with mesoporous structure for UV triggered PDT.In view of possible future UV irradiation treatments,the degradation products of RF,ribitol(RB)and lumichrome(LC),this last being a photosensitizing byproduct,are also employed for the synthesis of porous PtNPs,obtaining Pt@LC and Pt@RB.When administered in vitro to lung cancer cells,all the samples elicit a strong decrease of cell viability and a decrease of intracellular ATP levels.The antitumoral effect of both Pt@RF and Pt@LC is triggered by UV-A irradiation.This antitumoral activity is caused by the induction of oxidative stress,shown in our study by the decrease in intracellular glutathione and increased expression of antioxidant enzymes.展开更多
Developing biomass platform compounds into high value-added chemicals is a key step in renewable resource utilization.Herein,we report porous carbon-supported Ni-ZnO nanoparticles catalyst(Ni-ZnO/AC)synthesized via lo...Developing biomass platform compounds into high value-added chemicals is a key step in renewable resource utilization.Herein,we report porous carbon-supported Ni-ZnO nanoparticles catalyst(Ni-ZnO/AC)synthesized via low-temperature coprecipitation,exhibiting excellent performance for the selective hydrogenation of 5-hydroxymethylfurfural(HMF).A linear correlation is first observed between solvent polarity(E_(T)(30))and product selectivity within both polar aprotic and protic solvent classes,suggesting that solvent properties play a vital role in directing reaction pathways.Among these,1,4-dioxane(aprotic)favors the formation of 2,5-bis(hydroxymethyl)furan(BHMF)with 97.5%selectivity,while isopropanol(iPrOH,protic)promotes 2,5-dimethylfuran production with up to 99.5%selectivity.Mechanistic investigations further reveal that beyond polarity,proton-donating ability is critical in facilitating hydrodeoxygenation.iPrOH enables a hydrogen shuttle mechanism where protons assist in hydroxyl group removal,lowering the activation barrier.In contrast,1,4-dioxane,lacking hydrogen bond donors,stabilizes BHMF and hinders further conversion.Density functional theory calculations confirm a lower activation energy in iPrOH(0.60 eV)compared to 1,4-dioxane(1.07 eV).This work offers mechanistic insights and a practical strategy for solvent-mediated control of product selectivity in biomass hydrogenation,highlighting the decisive role of solvent-catalyst-substrate interactions.展开更多
Porous functionalized silica nanoparticles have attracted the interest of researchers as they are excellent carriers for antibacterial drug delivery applications.In this work,porous aminated-silica nanoparticles(SiO2-...Porous functionalized silica nanoparticles have attracted the interest of researchers as they are excellent carriers for antibacterial drug delivery applications.In this work,porous aminated-silica nanoparticles(SiO2-NH2 NPs) were prepared via one-step approach through the ammonia-catalyzed hydrolysis of tetraethylorthosilicate(TEOS) and(3-aminopropyl) triethoxysilane(APTES) in a mixed water-ethanol system.The obtained SiO2-NH2 NPs displayed a spherical morphology and relatively uniform size distribution,while the morphology and structure of SiO2-NH2 NPs were mainly determined by the order of the reagents added and the pH value of the solution.After characterization,the results showed that there were a large number of-NH2 groups on the surface of porous SiO2-NH2 NPs and that the porous SiO2-NH2 NPs had a large surface area of 476 m2 g-1 with an average pore width of 4.3 nm.Through an absorbing-releasing experiment and bacterial test,those SiO2-NH2 NPs were found to exhibit efficient absorption and release of drugs as well as a pH-de pendent release pattern of epirubicin-loaded SiO2-NH2 NPs.Meanwhile,SiO2-NH2@capsaicin NPs exhibited antibacterial properties.Those porous SiO2-NH2 NPs could be a candidate for drug delivery for antibacterial applications owing to their tailored porous structure and high surface area.展开更多
Porous nanocarbons with average particle size 20–40 nm were developed using biowaste oil palm leaves as a precursor.Simple pyrolysis was carried out at 700 °C under nitrogen atmosphere.Obtained porous nanocarbon...Porous nanocarbons with average particle size 20–40 nm were developed using biowaste oil palm leaves as a precursor.Simple pyrolysis was carried out at 700 °C under nitrogen atmosphere.Obtained porous nanocarbons showed excellent porous nature along with spherical shape.Symmetric supercapacitor fabricated from porous nanocarbons showed superior supercapacitance performance where high specific capacitance of 368 F/g at 0.06 A/g in 5 M KOH were reported.It also exhibited high stability(96% over 1700cycles) and energy density of 13 Wh/kg.Low resistance values were obtained by fitting the impedance spectra,thus indicating the availability of these materials as supercapacitors electrode.The presented method is cost effective and also in line with waste to wealth approach.展开更多
New viral infections,due to their rapid spread,lack of effective antiviral drugs and vaccines,kill millions of people every year.The global pandemic SARS-CoV-2 in 2019-2021 has shown that new strains of viruses can wi...New viral infections,due to their rapid spread,lack of effective antiviral drugs and vaccines,kill millions of people every year.The global pandemic SARS-CoV-2 in 2019-2021 has shown that new strains of viruses can widespread very quickly,causing disease and death,with significant socio-economic consequences.Therefore,the search for new methods of combating different pathogenic viruses is an urgent task,and strategies based on nanoparticles are of significant interest.This work demonstrates the antiviral adsorption(virucidal)efficacy of nanoparticles of porous silicon(PSi NPs)against various enveloped and non-enveloped pathogenic human viruses,such as Influenza A virus,Poliovirus,Human immunodeficiency virus,West Nile virus,and Hepatitis virus.PSi NPs sized 60 nm with the average pore diameter of 2 nm and specific surface area of 200 m^(2)/g were obtained by ball-milling of electrochemically-etched microporous silicon films.After interaction with PSi NPs,a strong suppression of the infectious activity of the virus-contaminated fluid was observed,which was manifested in a decrease in the infectious titer of all studied types of viruses by approximately 104 times,and corresponded to an inactivation of 99.99%viruses in vitro.This sorption capacity of PSi NPs is possible due to their microporous structure and huge specific surface area,which ensures efficient capture of virions,as confirmed by ELISA analysis,dynamic light scattering measurements and transmission electron microscopy images.The results obtained indicate the great potential of using PSi NPs as universal viral sorbents and disinfectants for the detection and treatment of viral diseases.展开更多
There has been a lot of basic and clinical research on Alzheimer’s disease(AD)over the last 100 years,but its mechanisms and treatments have not been fully clarified.Despite some controversies,the amyloid-beta hypoth...There has been a lot of basic and clinical research on Alzheimer’s disease(AD)over the last 100 years,but its mechanisms and treatments have not been fully clarified.Despite some controversies,the amyloid-beta hypothesis is one of the most widely accepted causes of AD.In this study,we disclose a new amyloid-beta plaque disaggregating agent and an AD brain-targeted delivery system using porous silicon nanoparticles(pSiNPs)as a therapeutic nano-platform to overcome AD.We hypothesized that the negatively charged sulfonic acid functional group could disaggregate plaques and construct a chemical library.As a result of the in vitro assay of amyloid plaques and library screening,we confirmed that 6-amino-2-naphthalenesulfonic acid(ANA)showed the highest efficacy for plaque disaggregation as a hit compound.To confirm the targeted delivery of ANA to the AD brain,a nano-platform was created using porous silicon nanoparticles(pSiNPs)with ANA loaded into the pore of pSiNPs and biotin-polyethylene glycol(PEG)surface functionalization.The resulting nano-formulation,named Biotin-CaCl2-ANA-pSiNPs(BCAP),delivered a large amount of ANA to the AD brain and ameliorated memory impairment of the AD mouse model through the disaggregation of amyloid plaques in the brain.This study presents a new bioactive small molecule for amyloid plaque disaggregation and its promising therapeutic nano-platform for AD brain-targeted delivery.展开更多
Porous and single crystalline platinum （Pt） nanoparticles （NPs） have been successfully synthesized by reduction of H2PtC16.6H20 and then investigated by optical spectroscopy and transmission electron microscopy. H...Porous and single crystalline platinum （Pt） nanoparticles （NPs） have been successfully synthesized by reduction of H2PtC16.6H20 and then investigated by optical spectroscopy and transmission electron microscopy. H2PtCI6-6H20 was reduced using ethylene glycol in the presence of polyvinylpyrrolidone under highly acidic conditions （pH 〈 1） to form single crystalline Pt particles about 5 nm in size. These particles were then stacked via {100} facets, forming 50-nm length porous nanocubes with a mosaic structure. The porous Pt NPs exhibited excellent catalytic properties for methanol oxidation. In particular, the electrochemical surface area was -63 m2/g, five times higher than that for non-porous Pt NPs prepared using a conventional method. We suggest that the high catalytic activity of porous Pt NPs is due to a combination of the crystalline structure having exposed {100} facets and a porous morphology.展开更多
A silicon（Si） surface with a nanosized porous structure was formed via simple wet chemical etching catalyzed by gold（Au） nanoparticles on p-type Cz-Si（100）.The average reflectivity from 300 to 1200 nm was less t...A silicon（Si） surface with a nanosized porous structure was formed via simple wet chemical etching catalyzed by gold（Au） nanoparticles on p-type Cz-Si（100）.The average reflectivity from 300 to 1200 nm was less than 1.5%.Black Si solar cells were then fabricated using a conventional production process.The results reflected the output characteristics of the cells fabricated using different etching depths and emitter dopant profiles.Heavier dopants and shallower etching depths should be adopted to optimize the black Si solar cell output characteristics. The efficiency at the optimized etching time and dopant profile was 12.17%.However,surface passivation and electrode contact due to the nanosized porous surface structure are still obstacles to obtaining high conversion efficiency for the black Si solar cells.展开更多
Pd-based egg-shell nano-catalysts were prepared using porous hollow silica nanoparticles （PHSNs） as support, and the as-prepared catalysts were modified with TiO2 to promote their selectivity for hydro-genation of a...Pd-based egg-shell nano-catalysts were prepared using porous hollow silica nanoparticles （PHSNs） as support, and the as-prepared catalysts were modified with TiO2 to promote their selectivity for hydro-genation of acetylene. Pd nanoparticles were loaded evenly on PHSNs and TiO2 was loaded on the active Pd particles. The effects of reduction time and temperature and the amount of TiO2 added on catalytic per-formances were investigated by using a fixed-bed micro-reactor. It was found that the catalysts showed better performance when reduced at 300 ℃ than at 500℃, and if reduced for 1 h than 3 h. When the amount of Ti added was 6 times that of Pd, the catalyst showed the highest ethylene selectivity.展开更多
基金funded by the Horizon Europe Project"PERSEUS"(No.101099423)financed by the Ministry of Universities under application 33.50.460A.752by the European Union NextGenerationEU/PRTR through a contract Margarita Salas from Universidade de Vigo.
文摘Photodynamic therapy(PDT)has been established as one of the most promising novel cancer therapies with fewer side-effects and enhanced efficacy compared to the currently available conventional treatments.However,its application has been hindered by the limitations that photosensitizers(PS)have.The combination of PS with metallic nanoparticles like platinum nanoparticles(PtNPs),can help to overcome these intrinsic drawbacks.In this work,the combination of PtNPs and the natural photosensitizer riboflavin(RF)is proposed.PtNPs are synthesized using RF(Pt@RF)as reducing and stabilizing agent in a one-step method,obtaining nanoparticles with mesoporous structure for UV triggered PDT.In view of possible future UV irradiation treatments,the degradation products of RF,ribitol(RB)and lumichrome(LC),this last being a photosensitizing byproduct,are also employed for the synthesis of porous PtNPs,obtaining Pt@LC and Pt@RB.When administered in vitro to lung cancer cells,all the samples elicit a strong decrease of cell viability and a decrease of intracellular ATP levels.The antitumoral effect of both Pt@RF and Pt@LC is triggered by UV-A irradiation.This antitumoral activity is caused by the induction of oxidative stress,shown in our study by the decrease in intracellular glutathione and increased expression of antioxidant enzymes.
基金the National Nature Science Foundation of China for Excellent Young Scientists Fund(32222058)Fundamental Research Foundation of CAF(CAFYBB2022QB001).
文摘Developing biomass platform compounds into high value-added chemicals is a key step in renewable resource utilization.Herein,we report porous carbon-supported Ni-ZnO nanoparticles catalyst(Ni-ZnO/AC)synthesized via low-temperature coprecipitation,exhibiting excellent performance for the selective hydrogenation of 5-hydroxymethylfurfural(HMF).A linear correlation is first observed between solvent polarity(E_(T)(30))and product selectivity within both polar aprotic and protic solvent classes,suggesting that solvent properties play a vital role in directing reaction pathways.Among these,1,4-dioxane(aprotic)favors the formation of 2,5-bis(hydroxymethyl)furan(BHMF)with 97.5%selectivity,while isopropanol(iPrOH,protic)promotes 2,5-dimethylfuran production with up to 99.5%selectivity.Mechanistic investigations further reveal that beyond polarity,proton-donating ability is critical in facilitating hydrodeoxygenation.iPrOH enables a hydrogen shuttle mechanism where protons assist in hydroxyl group removal,lowering the activation barrier.In contrast,1,4-dioxane,lacking hydrogen bond donors,stabilizes BHMF and hinders further conversion.Density functional theory calculations confirm a lower activation energy in iPrOH(0.60 eV)compared to 1,4-dioxane(1.07 eV).This work offers mechanistic insights and a practical strategy for solvent-mediated control of product selectivity in biomass hydrogenation,highlighting the decisive role of solvent-catalyst-substrate interactions.
基金supported financially by National Natural Science Foundation of China (No. 51706166 and No. 51773163)Innovation Group of Natural Science Foundation of Hubei Province (No. 2016CFA008)Joint Funds of China (No. 20171f0107)。
文摘Porous functionalized silica nanoparticles have attracted the interest of researchers as they are excellent carriers for antibacterial drug delivery applications.In this work,porous aminated-silica nanoparticles(SiO2-NH2 NPs) were prepared via one-step approach through the ammonia-catalyzed hydrolysis of tetraethylorthosilicate(TEOS) and(3-aminopropyl) triethoxysilane(APTES) in a mixed water-ethanol system.The obtained SiO2-NH2 NPs displayed a spherical morphology and relatively uniform size distribution,while the morphology and structure of SiO2-NH2 NPs were mainly determined by the order of the reagents added and the pH value of the solution.After characterization,the results showed that there were a large number of-NH2 groups on the surface of porous SiO2-NH2 NPs and that the porous SiO2-NH2 NPs had a large surface area of 476 m2 g-1 with an average pore width of 4.3 nm.Through an absorbing-releasing experiment and bacterial test,those SiO2-NH2 NPs were found to exhibit efficient absorption and release of drugs as well as a pH-de pendent release pattern of epirubicin-loaded SiO2-NH2 NPs.Meanwhile,SiO2-NH2@capsaicin NPs exhibited antibacterial properties.Those porous SiO2-NH2 NPs could be a candidate for drug delivery for antibacterial applications owing to their tailored porous structure and high surface area.
文摘Porous nanocarbons with average particle size 20–40 nm were developed using biowaste oil palm leaves as a precursor.Simple pyrolysis was carried out at 700 °C under nitrogen atmosphere.Obtained porous nanocarbons showed excellent porous nature along with spherical shape.Symmetric supercapacitor fabricated from porous nanocarbons showed superior supercapacitance performance where high specific capacitance of 368 F/g at 0.06 A/g in 5 M KOH were reported.It also exhibited high stability(96% over 1700cycles) and energy density of 13 Wh/kg.Low resistance values were obtained by fitting the impedance spectra,thus indicating the availability of these materials as supercapacitors electrode.The presented method is cost effective and also in line with waste to wealth approach.
基金The research was funded by the Russian Science Foundation(Grant number 20-12-00297).
文摘New viral infections,due to their rapid spread,lack of effective antiviral drugs and vaccines,kill millions of people every year.The global pandemic SARS-CoV-2 in 2019-2021 has shown that new strains of viruses can widespread very quickly,causing disease and death,with significant socio-economic consequences.Therefore,the search for new methods of combating different pathogenic viruses is an urgent task,and strategies based on nanoparticles are of significant interest.This work demonstrates the antiviral adsorption(virucidal)efficacy of nanoparticles of porous silicon(PSi NPs)against various enveloped and non-enveloped pathogenic human viruses,such as Influenza A virus,Poliovirus,Human immunodeficiency virus,West Nile virus,and Hepatitis virus.PSi NPs sized 60 nm with the average pore diameter of 2 nm and specific surface area of 200 m^(2)/g were obtained by ball-milling of electrochemically-etched microporous silicon films.After interaction with PSi NPs,a strong suppression of the infectious activity of the virus-contaminated fluid was observed,which was manifested in a decrease in the infectious titer of all studied types of viruses by approximately 104 times,and corresponded to an inactivation of 99.99%viruses in vitro.This sorption capacity of PSi NPs is possible due to their microporous structure and huge specific surface area,which ensures efficient capture of virions,as confirmed by ELISA analysis,dynamic light scattering measurements and transmission electron microscopy images.The results obtained indicate the great potential of using PSi NPs as universal viral sorbents and disinfectants for the detection and treatment of viral diseases.
基金supported by Basic Science Research Program through the National Research Foundation(NRF)of Korea funded by the Ministry of Education(2018-R1A6A1A03025124D.K.)+5 种基金supported by Bio&Medical Technology Development Program of the NRF of Korea funded by the Ministry of Science&ICT(2022-M3A9H1014157,2021-M3A9I5030523D.K.)a grant from Korea Health Technology R&D Project of the Korea Health Industry Development Institute(KHIDI)funded by the Ministry of Health&Welfare,Republic of Korea(HI21C0239D.K.)supported by the National Research Foundation of Korea(NRF)grant funded by the Korea government(MSIT)(2022-R1F1A1069954D.K.).
文摘There has been a lot of basic and clinical research on Alzheimer’s disease(AD)over the last 100 years,but its mechanisms and treatments have not been fully clarified.Despite some controversies,the amyloid-beta hypothesis is one of the most widely accepted causes of AD.In this study,we disclose a new amyloid-beta plaque disaggregating agent and an AD brain-targeted delivery system using porous silicon nanoparticles(pSiNPs)as a therapeutic nano-platform to overcome AD.We hypothesized that the negatively charged sulfonic acid functional group could disaggregate plaques and construct a chemical library.As a result of the in vitro assay of amyloid plaques and library screening,we confirmed that 6-amino-2-naphthalenesulfonic acid(ANA)showed the highest efficacy for plaque disaggregation as a hit compound.To confirm the targeted delivery of ANA to the AD brain,a nano-platform was created using porous silicon nanoparticles(pSiNPs)with ANA loaded into the pore of pSiNPs and biotin-polyethylene glycol(PEG)surface functionalization.The resulting nano-formulation,named Biotin-CaCl2-ANA-pSiNPs(BCAP),delivered a large amount of ANA to the AD brain and ameliorated memory impairment of the AD mouse model through the disaggregation of amyloid plaques in the brain.This study presents a new bioactive small molecule for amyloid plaque disaggregation and its promising therapeutic nano-platform for AD brain-targeted delivery.
文摘Porous and single crystalline platinum （Pt） nanoparticles （NPs） have been successfully synthesized by reduction of H2PtC16.6H20 and then investigated by optical spectroscopy and transmission electron microscopy. H2PtCI6-6H20 was reduced using ethylene glycol in the presence of polyvinylpyrrolidone under highly acidic conditions （pH 〈 1） to form single crystalline Pt particles about 5 nm in size. These particles were then stacked via {100} facets, forming 50-nm length porous nanocubes with a mosaic structure. The porous Pt NPs exhibited excellent catalytic properties for methanol oxidation. In particular, the electrochemical surface area was -63 m2/g, five times higher than that for non-porous Pt NPs prepared using a conventional method. We suggest that the high catalytic activity of porous Pt NPs is due to a combination of the crystalline structure having exposed {100} facets and a porous morphology.
基金supported by the Knowledge Innovation Program of the Chinese Academy of Sciences(No.KGCX2-YW-382)the National Program on Key Basic Research Project of China(No.2010CB933804)
文摘A silicon（Si） surface with a nanosized porous structure was formed via simple wet chemical etching catalyzed by gold（Au） nanoparticles on p-type Cz-Si（100）.The average reflectivity from 300 to 1200 nm was less than 1.5%.Black Si solar cells were then fabricated using a conventional production process.The results reflected the output characteristics of the cells fabricated using different etching depths and emitter dopant profiles.Heavier dopants and shallower etching depths should be adopted to optimize the black Si solar cell output characteristics. The efficiency at the optimized etching time and dopant profile was 12.17%.However,surface passivation and electrode contact due to the nanosized porous surface structure are still obstacles to obtaining high conversion efficiency for the black Si solar cells.
基金the financial support provided by National Natural Science Foundation of China (Nos.20821004 and 50642042)the Key Research Program of Ministry ofEducation of China (No. 108009)+1 种基金CNPC Innovation Foundation (No.06-04D-01-01-02)the Chinese Universities Scientific Fund
文摘Pd-based egg-shell nano-catalysts were prepared using porous hollow silica nanoparticles （PHSNs） as support, and the as-prepared catalysts were modified with TiO2 to promote their selectivity for hydro-genation of acetylene. Pd nanoparticles were loaded evenly on PHSNs and TiO2 was loaded on the active Pd particles. The effects of reduction time and temperature and the amount of TiO2 added on catalytic per-formances were investigated by using a fixed-bed micro-reactor. It was found that the catalysts showed better performance when reduced at 300 ℃ than at 500℃, and if reduced for 1 h than 3 h. When the amount of Ti added was 6 times that of Pd, the catalyst showed the highest ethylene selectivity.
