The self-assembled monolayers （SAMs） of imidazoline （IM） on the iron surface were characterized by scanning electron microscope （SEM） and scanning electrochemical microscopy （SECM）. The results showed that SAM...The self-assembled monolayers （SAMs） of imidazoline （IM） on the iron surface were characterized by scanning electron microscope （SEM） and scanning electrochemical microscopy （SECM）. The results showed that SAMs were an effective inhibition film for iron.展开更多
Oligo（ethylene glycol） （-OEG） and amino （-NH2） mixed self-assembled monolayers （SAMs） were employed as model substrates to investigate the effect of charge density on the fate of mesenchymal stem cells （MSCs...Oligo（ethylene glycol） （-OEG） and amino （-NH2） mixed self-assembled monolayers （SAMs） were employed as model substrates to investigate the effect of charge density on the fate of mesenchymal stem cells （MSCs） and osteopontin （OPN） adsorption. We found that all surfaces presenting -NH2 groups favored cell responses regardless of the surface charge. Meanwhile, OPN adsorption could remain stable on the mixed SAMs over a certain range of charge densities. Our work provides some insights into cell responses and protein adsorption to surface charge.展开更多
Gravimetric resonant-inspired biosensors have attracted increasing attention in industrial and point-ofcare applications,enabling label-free detection of biomarkers such as DNA and antibodies.Capacitive micromachined ...Gravimetric resonant-inspired biosensors have attracted increasing attention in industrial and point-ofcare applications,enabling label-free detection of biomarkers such as DNA and antibodies.Capacitive micromachined ultrasonic transducers(CMUTs)are promising tools for developing miniaturized highperformance biosensing complementary metal–oxide–silicon(CMOS)platforms.However,their operability is limited by inefficient functionalization,aggregation,crosstalk in the buffer,and the requirement for an external high-voltage(HV)power supply.In this study,we aimed to propose a CMUTs-based resonant biosensor integrated with a CMOS front–end interface coupled with ethylene–glycol alkanethiols to detect single-stranded DNA oligonucleotides with large specificity.The topography of the functionalized surface was characterized by energy-dispersive X-ray microanalysis.Improved selectivity for onchip hybridization was demonstrated by comparing complementary and non-complementary singlestranded DNA oligonucleotides using fluorescence imaging technology.The sensor array was further characterized using a five-element lumped equivalent model.The 4 mm^(2) application-specific integrated circuit chip was designed and developed through 0.18 lm HV bipolar-CMOS-double diffused metal–oxide–silicon(DMOS)technology(BCD)to generate on-chip 20 V HV boosting and to track feedback frequency under a standard 1.8 V supply,with a total power consumption of 3.8 mW in a continuous mode.The measured results indicated a detection sensitivity of 7.943×10^(-3) lmol·L^(-1)·Hz^(-1) over a concentration range of 1 to 100 lmol·L^(-1).In conclusion,the label-free biosensing of DNA under dry conditions was successfully demonstrated using a microfabricated CMUT array with a 2 MHz frequency on CMOS electronics with an internal HV supplier.Moreover,ethylene–glycol alkanethiols successfully deposited self-assembled monolayers on aluminum electrodes,which has never been attempted thus far on CMUTs,to enhance the selectivity of bio-functionalization.The findings of this study indicate the possibility of full-on-chip DNA biosensing with CMUTs.展开更多
All-cis-hexafluoro-and all-cis-pentafluoro-cyclohexane(PFCH)derivatives are new kinds of materials,the structures and properties of which are dominated by the highly dipolar Janus-face motif.Here,we report on the effe...All-cis-hexafluoro-and all-cis-pentafluoro-cyclohexane(PFCH)derivatives are new kinds of materials,the structures and properties of which are dominated by the highly dipolar Janus-face motif.Here,we report on the effects of integrating the PFCH groups into self-assembled monolayers(SAMs)of alkanethiolates on Au(111).Monolayers with an odd(eleven)and even(twelve)number of methylene groups were characterized in detail by several complementary experimental tools,supported by theoretical calculations.Surprisingly,all the data show a high similarity of both kinds of monolayers,nearly lacking the typically observed odd-even effects.These new monolayers have a packing density about 1/3 lower than that of non-substituted alkanethiolate monolayers,caused by the bulkiness of the PFCH moieties.The orientations of the PFCH groups and the alkyl chains could be determined independently,suggesting a conformation similar to the one found in the solid state structure of an analogous compound.Although in the SAMs the PFCH groups are slightly tilted away from the surface normal with the axial fluorine atoms pointing downwards,most of the dipole moments of the group remain oriented parallel to the surface,which is a unique feature for a SAM system.The consequences are much lower water contact angles compared to other partly fluorinated SAMs as well as rather moderate work function values.The interaction between the terminal PFCH moieties results in an enhanced stability of the PFCH-decorated SAMs toward exchange reaction with potential molecular substituents in spite of the lower packing density of these films.展开更多
THE electrochemical and/or photochemical active organic molecules have attracted much atten-.tion due to their potential applications in the field of molecular electronics. The azobenzenederivatives have been widely s...THE electrochemical and/or photochemical active organic molecules have attracted much atten-.tion due to their potential applications in the field of molecular electronics. The azobenzenederivatives have been widely studied as typical systems, owing to their reversible trans-cis iso-merization and reduction/oxidation reactions (see fig. 1 (a) ). We have studied the char-acteristic photochromic and electrochemical behavior of azobenzene Langmuir-Blodgett mono-展开更多
The self-assembly monolayers （SAMs） of n-dodecyltriethoxysilane （DTES） and 1 H, 1 H, 2H, 2H-perflu- orodecyltriethoxysilane （PFDS） on the surface of the 430 stainless steel （430SS） were prepared and their corr...The self-assembly monolayers （SAMs） of n-dodecyltriethoxysilane （DTES） and 1 H, 1 H, 2H, 2H-perflu- orodecyltriethoxysilane （PFDS） on the surface of the 430 stainless steel （430SS） were prepared and their corrosion protection performance was investigated by potentiodynamic polarization, Fourier transform infrared spectroscopy （FTIR） -attenuated total reflection （ATR）, static contact angle and atomic force microscopy （AFM）. The results showed that the alkali pretreatment and the water added into the self-assembly solution could generate more hydrox- yls on the 430SS surface, and then enhanced the adsorption of the SAMs. A suitable temperature of the self-assem- bly solution is important for the formation of the SAMs. The silane SAMs were chemically adsorbed on the 430SS substrates by Fe-O-Si bonds. In all cases tested, PFDS has a better inhibition effect compared with DTES, and the difference in inhibition effect is most marked at the lowest concentration of 1 mmol/L.展开更多
Phage contamination is a very serious and unavoidable problem in modem fermentation industry. It is necessary to develop sensitive and rapid phage detection methods for the early detection of phage contamination. In t...Phage contamination is a very serious and unavoidable problem in modem fermentation industry. It is necessary to develop sensitive and rapid phage detection methods for the early detection of phage contamination. In the present work, a real-time, rapid, specific and quantitative phage T4 detection method based on surface plasmon resonance （SPR） technique has been in- troduced. Escherichia coli was immobilized onto the preformed MPA self-assembled monolayer （SAM） through the widely used EDC/NHS cross-linking reaction as the recognition element. The bacteria immobilization was verified efficiently through the electrochemical measurements and fluorescence microscopy observations. The specific adsorption was much stronger than the non-specific adsorption of phage T4 binding to the biosensor surface modified by E. coli, and the latter could be neglected. The detection sensitivity reached 1×10^7 PFU/mL within 10 min. Within the experimental phage concentrations, the linear cor- relation between the SPR response and the phage concentration was good. The results suggest that the SPR technique is a po- tentially powerful tool for the phage or other virus detections, as a label-free, real-time, and rapid method.展开更多
基金the National Natural Science Foundation of China(No.20573069)for financial support of this research.
文摘The self-assembled monolayers （SAMs） of imidazoline （IM） on the iron surface were characterized by scanning electron microscope （SEM） and scanning electrochemical microscopy （SECM）. The results showed that SAMs were an effective inhibition film for iron.
基金supported by the National Basic Research Program of China(No.2012CB619100)the National Natural Science Foundation of China(No.51232002)+1 种基金the 111 Project(No.B13039)the Science and Technology Program of Guangdong Province(No.2013B010403007)
文摘Oligo（ethylene glycol） （-OEG） and amino （-NH2） mixed self-assembled monolayers （SAMs） were employed as model substrates to investigate the effect of charge density on the fate of mesenchymal stem cells （MSCs） and osteopontin （OPN） adsorption. We found that all surfaces presenting -NH2 groups favored cell responses regardless of the surface charge. Meanwhile, OPN adsorption could remain stable on the mixed SAMs over a certain range of charge densities. Our work provides some insights into cell responses and protein adsorption to surface charge.
基金supported by the National Key Research and Development Program of China(2022YFB3205400)the National Natural Science Foundation of China(52275570)+1 种基金the Postdoctoral Innovation Talents Support Program(BX20230288)the Postdoctoral Science Foundation of Shaanxi Province(2018BSHEDZZ08).
文摘Gravimetric resonant-inspired biosensors have attracted increasing attention in industrial and point-ofcare applications,enabling label-free detection of biomarkers such as DNA and antibodies.Capacitive micromachined ultrasonic transducers(CMUTs)are promising tools for developing miniaturized highperformance biosensing complementary metal–oxide–silicon(CMOS)platforms.However,their operability is limited by inefficient functionalization,aggregation,crosstalk in the buffer,and the requirement for an external high-voltage(HV)power supply.In this study,we aimed to propose a CMUTs-based resonant biosensor integrated with a CMOS front–end interface coupled with ethylene–glycol alkanethiols to detect single-stranded DNA oligonucleotides with large specificity.The topography of the functionalized surface was characterized by energy-dispersive X-ray microanalysis.Improved selectivity for onchip hybridization was demonstrated by comparing complementary and non-complementary singlestranded DNA oligonucleotides using fluorescence imaging technology.The sensor array was further characterized using a five-element lumped equivalent model.The 4 mm^(2) application-specific integrated circuit chip was designed and developed through 0.18 lm HV bipolar-CMOS-double diffused metal–oxide–silicon(DMOS)technology(BCD)to generate on-chip 20 V HV boosting and to track feedback frequency under a standard 1.8 V supply,with a total power consumption of 3.8 mW in a continuous mode.The measured results indicated a detection sensitivity of 7.943×10^(-3) lmol·L^(-1)·Hz^(-1) over a concentration range of 1 to 100 lmol·L^(-1).In conclusion,the label-free biosensing of DNA under dry conditions was successfully demonstrated using a microfabricated CMUT array with a 2 MHz frequency on CMOS electronics with an internal HV supplier.Moreover,ethylene–glycol alkanethiols successfully deposited self-assembled monolayers on aluminum electrodes,which has never been attempted thus far on CMUTs,to enhance the selectivity of bio-functionalization.The findings of this study indicate the possibility of full-on-chip DNA biosensing with CMUTs.
文摘All-cis-hexafluoro-and all-cis-pentafluoro-cyclohexane(PFCH)derivatives are new kinds of materials,the structures and properties of which are dominated by the highly dipolar Janus-face motif.Here,we report on the effects of integrating the PFCH groups into self-assembled monolayers(SAMs)of alkanethiolates on Au(111).Monolayers with an odd(eleven)and even(twelve)number of methylene groups were characterized in detail by several complementary experimental tools,supported by theoretical calculations.Surprisingly,all the data show a high similarity of both kinds of monolayers,nearly lacking the typically observed odd-even effects.These new monolayers have a packing density about 1/3 lower than that of non-substituted alkanethiolate monolayers,caused by the bulkiness of the PFCH moieties.The orientations of the PFCH groups and the alkyl chains could be determined independently,suggesting a conformation similar to the one found in the solid state structure of an analogous compound.Although in the SAMs the PFCH groups are slightly tilted away from the surface normal with the axial fluorine atoms pointing downwards,most of the dipole moments of the group remain oriented parallel to the surface,which is a unique feature for a SAM system.The consequences are much lower water contact angles compared to other partly fluorinated SAMs as well as rather moderate work function values.The interaction between the terminal PFCH moieties results in an enhanced stability of the PFCH-decorated SAMs toward exchange reaction with potential molecular substituents in spite of the lower packing density of these films.
文摘THE electrochemical and/or photochemical active organic molecules have attracted much atten-.tion due to their potential applications in the field of molecular electronics. The azobenzenederivatives have been widely studied as typical systems, owing to their reversible trans-cis iso-merization and reduction/oxidation reactions (see fig. 1 (a) ). We have studied the char-acteristic photochromic and electrochemical behavior of azobenzene Langmuir-Blodgett mono-
文摘The self-assembly monolayers （SAMs） of n-dodecyltriethoxysilane （DTES） and 1 H, 1 H, 2H, 2H-perflu- orodecyltriethoxysilane （PFDS） on the surface of the 430 stainless steel （430SS） were prepared and their corrosion protection performance was investigated by potentiodynamic polarization, Fourier transform infrared spectroscopy （FTIR） -attenuated total reflection （ATR）, static contact angle and atomic force microscopy （AFM）. The results showed that the alkali pretreatment and the water added into the self-assembly solution could generate more hydrox- yls on the 430SS surface, and then enhanced the adsorption of the SAMs. A suitable temperature of the self-assem- bly solution is important for the formation of the SAMs. The silane SAMs were chemically adsorbed on the 430SS substrates by Fe-O-Si bonds. In all cases tested, PFDS has a better inhibition effect compared with DTES, and the difference in inhibition effect is most marked at the lowest concentration of 1 mmol/L.
基金support from the National Basic Research Program of China (2011CB933600)the National Natural Science Foundation of China (21077081,20921062)+1 种基金the Natural Science Foundation of Hubei Province (2010CDB01302)the Fundamental Research Funds for Central Universities (1103005 and 1101007)
文摘Phage contamination is a very serious and unavoidable problem in modem fermentation industry. It is necessary to develop sensitive and rapid phage detection methods for the early detection of phage contamination. In the present work, a real-time, rapid, specific and quantitative phage T4 detection method based on surface plasmon resonance （SPR） technique has been in- troduced. Escherichia coli was immobilized onto the preformed MPA self-assembled monolayer （SAM） through the widely used EDC/NHS cross-linking reaction as the recognition element. The bacteria immobilization was verified efficiently through the electrochemical measurements and fluorescence microscopy observations. The specific adsorption was much stronger than the non-specific adsorption of phage T4 binding to the biosensor surface modified by E. coli, and the latter could be neglected. The detection sensitivity reached 1×10^7 PFU/mL within 10 min. Within the experimental phage concentrations, the linear cor- relation between the SPR response and the phage concentration was good. The results suggest that the SPR technique is a po- tentially powerful tool for the phage or other virus detections, as a label-free, real-time, and rapid method.
