The nanoplatforms based on upconversion nanoparticles(UCNPs)have shown great promise in amplified photodynamic therapy(PDT)triggered by near-infrared(NIR)light.However,their practical in vivo applications are hindered...The nanoplatforms based on upconversion nanoparticles(UCNPs)have shown great promise in amplified photodynamic therapy(PDT)triggered by near-infrared(NIR)light.However,their practical in vivo applications are hindered by the overheating effect of 980 nm excitation and low utilization of upconversion luminescence(UCL)by photosensitizers.To solve these defects,core-satellite metal-organic framework@UCNP superstructures,composed of a single metal-organic framework(MOF)NP as the core and Nd3+-sensitized UCNPs as the satellites,are designed and synthesized via a facile electrostatic self-assembly strategy.The superstructures realize a high co-loading capacity of chlorin e6(Ce6)and rose bengal(RB)benefitted from the highly porous nature of MOF NPs,showing a strong spectral overlap between maximum absorption of photosensitizers and emission of UCNPs.The in vitro and in vivo experiments demonstrate that the dual-photosensitizer superstructures have trimodal(magnetic resonance(MR)/UCL/fluorescence(FL))imaging functions and excellent antitumor effectiveness of PDT at 808 nm NIR light excitation,avoiding the laser irradiation-induced overheating issue.This study provides new insights for the development of highly efficient PDT nanodrugs toward precision theranostics.展开更多
The bioaccumulation of mercury(Hg)in aquatic ecosystem poses a potential health risk to human being and aquatic organism.Bioaccumulations by plankton represent a crucial process of Hg transfer from water to aquatic fo...The bioaccumulation of mercury(Hg)in aquatic ecosystem poses a potential health risk to human being and aquatic organism.Bioaccumulations by plankton represent a crucial process of Hg transfer from water to aquatic food chain.However,the current understanding of major factors affecting Hg accumulation by plankton is inadequate.In this study,a data set of 89 aquatic ecosystems worldwide,including inland water,nearshore water and open sea,was established.Key factors influencing plankton Hg bioaccumulation(i.e.,plankton species,cell sizes and biomasses)were discussed.The results indicated that total Hg(THg)and methylmercury(MeHg)concentrations in plankton in inland waters were significantly higher than those in nearshore waters and open seas.Bioaccumulation factors for the logarithm of THg and MeHg of phytoplankton were 2.4–6.0 and 2.6–6.7 L/kg,respectively,in all aquatic ecosystems.They could be further biomagnified by a factor of 2.1–15.1 and 5.3–28.2 from phytoplankton to zooplankton.Higher MeHg concentrations were observed with the increases of cell size for both phyto-and zooplankton.A contrasting trend was observed between the plankton biomasses and BAF_(MeHg),with a positive relationship for zooplankton and a negative relationship for phytoplankton.Plankton physiologic traits impose constraints on the rates of nutrients and contaminants obtaining process from water.Nowadays,many aquatic ecosystems are facing rapid shifts in nutrient compositions.We suggested that these potential influences on the growth and composition of plankton should be incorporated in future aquatic Hg modeling and ecological risk assessments.展开更多
In this study,K+-doped γ-Ce2 S3 was successfully prepared via a gas-solid reaction method using CeO2,K2 CO3,and CS2 as raw materials.The effects of the suitable sulfide system and different molar ratios of K to Ce(nK...In this study,K+-doped γ-Ce2 S3 was successfully prepared via a gas-solid reaction method using CeO2,K2 CO3,and CS2 as raw materials.The effects of the suitable sulfide system and different molar ratios of K to Ce(nK/Ce=0-0.30) on the phase composition,crystal structure,chromaticity and thermal stability ofγ-Ce2 S3 were systematically investigated.Pure γ-Ce2 S3 was obtained by calcining the doped samples at840℃ for 150 min.After calcination at the same temperature the undoped K+samples exhibit a pure α-phase.Samples with a K/Ce molar ratio(nK/Ce) of 0.10-0.25 comprise only the γ-phase;and when nK/Ce exceeds 0.25,a new heterogeneous phase,KCeS2,emerges.For values of nK/Ce in the range of0-0.25,the γ-Ce2 S3 lattice parameters gradually increases with increasing K+ content.When nK/Ceexceedes 0.25,the lattice parameters remains unchanged.As nK/Ce increased,the synthesized color gradually changes from red to orange—red and finally,to yellow.The redness value a* reaches the maximum(L*=33.86,a*=36.68,b*=38.15) when nK/Ce=0.10,The nK/Ce=0.10 composition continues to exhibit the y-phase after heat treatment at 420℃ for 10 min in air.The K+doping fills the internal vacancies of γ-Ce2 S3 and formed a solid solution,which is beneficial for the stability of its lattice,thus improving the thermal stability of γ-Ce2 S3(from 350 to 420℃).展开更多
基金This work was financially supported by National Natural Science Foundation of China(NSFC,Nos.21601140 and 21871214)the Fundamental Research Funds for the Central Universities,and Open Research Fund of State Key Laboratory of Bioelectronics.
文摘The nanoplatforms based on upconversion nanoparticles(UCNPs)have shown great promise in amplified photodynamic therapy(PDT)triggered by near-infrared(NIR)light.However,their practical in vivo applications are hindered by the overheating effect of 980 nm excitation and low utilization of upconversion luminescence(UCL)by photosensitizers.To solve these defects,core-satellite metal-organic framework@UCNP superstructures,composed of a single metal-organic framework(MOF)NP as the core and Nd3+-sensitized UCNPs as the satellites,are designed and synthesized via a facile electrostatic self-assembly strategy.The superstructures realize a high co-loading capacity of chlorin e6(Ce6)and rose bengal(RB)benefitted from the highly porous nature of MOF NPs,showing a strong spectral overlap between maximum absorption of photosensitizers and emission of UCNPs.The in vitro and in vivo experiments demonstrate that the dual-photosensitizer superstructures have trimodal(magnetic resonance(MR)/UCL/fluorescence(FL))imaging functions and excellent antitumor effectiveness of PDT at 808 nm NIR light excitation,avoiding the laser irradiation-induced overheating issue.This study provides new insights for the development of highly efficient PDT nanodrugs toward precision theranostics.
基金funded by National Natural Science Foundation of China(Grant Nos.41977324 and 41630748)the Natural Science Foundation of Tianjin(No.20JCYBJC01080).
文摘The bioaccumulation of mercury(Hg)in aquatic ecosystem poses a potential health risk to human being and aquatic organism.Bioaccumulations by plankton represent a crucial process of Hg transfer from water to aquatic food chain.However,the current understanding of major factors affecting Hg accumulation by plankton is inadequate.In this study,a data set of 89 aquatic ecosystems worldwide,including inland water,nearshore water and open sea,was established.Key factors influencing plankton Hg bioaccumulation(i.e.,plankton species,cell sizes and biomasses)were discussed.The results indicated that total Hg(THg)and methylmercury(MeHg)concentrations in plankton in inland waters were significantly higher than those in nearshore waters and open seas.Bioaccumulation factors for the logarithm of THg and MeHg of phytoplankton were 2.4–6.0 and 2.6–6.7 L/kg,respectively,in all aquatic ecosystems.They could be further biomagnified by a factor of 2.1–15.1 and 5.3–28.2 from phytoplankton to zooplankton.Higher MeHg concentrations were observed with the increases of cell size for both phyto-and zooplankton.A contrasting trend was observed between the plankton biomasses and BAF_(MeHg),with a positive relationship for zooplankton and a negative relationship for phytoplankton.Plankton physiologic traits impose constraints on the rates of nutrients and contaminants obtaining process from water.Nowadays,many aquatic ecosystems are facing rapid shifts in nutrient compositions.We suggested that these potential influences on the growth and composition of plankton should be incorporated in future aquatic Hg modeling and ecological risk assessments.
基金Project supported by National Natural Science Foundation of China (51462010)Natural Science Foundation of Jiangxi Province(20161BAB206132,20171ACB20022)The Innovation fund of Jingdezhen Ceramic Institute (JYC-201803)。
文摘In this study,K+-doped γ-Ce2 S3 was successfully prepared via a gas-solid reaction method using CeO2,K2 CO3,and CS2 as raw materials.The effects of the suitable sulfide system and different molar ratios of K to Ce(nK/Ce=0-0.30) on the phase composition,crystal structure,chromaticity and thermal stability ofγ-Ce2 S3 were systematically investigated.Pure γ-Ce2 S3 was obtained by calcining the doped samples at840℃ for 150 min.After calcination at the same temperature the undoped K+samples exhibit a pure α-phase.Samples with a K/Ce molar ratio(nK/Ce) of 0.10-0.25 comprise only the γ-phase;and when nK/Ce exceeds 0.25,a new heterogeneous phase,KCeS2,emerges.For values of nK/Ce in the range of0-0.25,the γ-Ce2 S3 lattice parameters gradually increases with increasing K+ content.When nK/Ceexceedes 0.25,the lattice parameters remains unchanged.As nK/Ce increased,the synthesized color gradually changes from red to orange—red and finally,to yellow.The redness value a* reaches the maximum(L*=33.86,a*=36.68,b*=38.15) when nK/Ce=0.10,The nK/Ce=0.10 composition continues to exhibit the y-phase after heat treatment at 420℃ for 10 min in air.The K+doping fills the internal vacancies of γ-Ce2 S3 and formed a solid solution,which is beneficial for the stability of its lattice,thus improving the thermal stability of γ-Ce2 S3(from 350 to 420℃).