Adsorption reactions between surfaces of nanodiamond and nanosilica with diameter of 100 nm prepared as suspension solutions of 0.25μg/μL and lysozyme molecule with different concentrations of 7 mmol/L PPBS at pH=7,...Adsorption reactions between surfaces of nanodiamond and nanosilica with diameter of 100 nm prepared as suspension solutions of 0.25μg/μL and lysozyme molecule with different concentrations of 7 mmol/L PPBS at pH=7, 9, 11, and 13 have been investigated by fluores- cence spectroscopy. Adsorption reaction constants and coverages of lysozyme with different concentrations of 0-1000 nmol/L under the influences of different pH values have been ob- tained. Helicities and conformations of the adsorbed lysozyme molecules, free spaces of every adsorbed lysozyme molecule on the surfaces of nanopartieles at different concentrations and pH values have been deduced and discussed. The highest adsorption capabilities for both sys- tems and conformational efficiency of the adsorbed lysozyme molecule at pH=13 have been obtained. Lysozyme molecules can be prepared, adsorbed and carried with optimal activity and helicity, with 2 and 10 mg/m2 on unit nanosurface, 130 and 150 mg/g with respect to the weight of nanoparticle, within the linear regions of the coverages at around 150-250 nmol/L and four pH values for nanodiamond and nanosilica, respectively. They can be prepared in the tightest packed form, with 20 and 55 mg/m2, 810-1680 and 580-1100 mg/g at threshold concentrations and four pH values for nanodiamond and nanosilica, respectively.展开更多
<b>Introduction:</b> Local anesthetics (LAs) must be adsorbed to and permeate through membranes to reach their sites of action. The rates of these processes critically affect drug actions at the cellular l...<b>Introduction:</b> Local anesthetics (LAs) must be adsorbed to and permeate through membranes to reach their sites of action. The rates of these processes critically affect drug actions at the cellular level and also the <i>in vivo</i> pharmacokinetics of perineurally injected drugs. Therefore, we measured the adsorption equilibria and permeation kinetics of two LAs local anesthetics with markedly different hydrophobicities: tetracaine (TTC, P<sub>octanol:buffer</sub> = 3.6 × 10<sup>3</sup>) and procaine (PRO, P<sub>octanol:buffer</sub> = 8.1 × 10<sup>1</sup>), in unilamellar membranes of different composition and fluidity. <b>Methods:</b> Interactions with unilamellar vesicles made of dipalmitoylphosphatidylcholine (DPPC), at 23°C (solid gel state) or 45°C (liquid crystal state), without or with cholesterol (Chol), were investigated by a combination of fluorescence and stopped-flow techniques. Membrane adsorption was monitored by the LA’s fluorescence. Membrane permeation was monitored by the decrease of fluorescence intensity of intra-vesicular pyranine, when quenched by neighboring TTC or PRO. <b>Results:</b> Ionized TTC (TTCH<sup>+</sup>) and procaine (PROH<sup>+</sup>) adsorb to membranes more slowly and weakly than their neutral counterparts (time constant <i>τ</i> ~ 0.1 sec). Fluidizing of membranes, at the higher temperature (45°C) or by Chol inclusion, accelerated LA adsorption (faster than the mixing time of the stopped-flow device, 0.008 s). Permeation of protonated TTCH<sup>+</sup> through the solid gel DPPC membranes (23°C) occurred far more slowly than adsorption, (<i>τ</i> = 36.7 ± 0.7 s, n = 9), and 3 times slower than neutral TTC (<i>τ</i> = 10.9 ± 0.7 s, n = 9);neutral PRO permeated these membranes at the same rate as TTC. Inclusion of Chol with DPPC, disordering the fatty acyl tails of membrane phospholipids while crowding their polar headgroups, slowed permeation of TTC and of PRO to an even greater degree. <b>Conclusions:</b> Local anesthetic permeation through membranes is limited by the transport across the membrane core and not by the initial binding. Drug ionization greatly slows permeation, but greater hydrophobicity does not facilitate it. Lipid crowding caused by Chol, a normal membrane component, slows permeation by disorienting the LA bound at the surface.展开更多
Adsorption kinetics for a stilbene derivative type fluorescent whitening agent (FWA) on fiber surfaces was studied based on a real-time spectroscopic measurement system. Results showed that the time-dependent behavior...Adsorption kinetics for a stilbene derivative type fluorescent whitening agent (FWA) on fiber surfaces was studied based on a real-time spectroscopic measurement system. Results showed that the time-dependent behavior of FWA agrees to that of a mono-molecular adsorption layer on fiber surfaces,as characterized in Langmuir-type expression. The adsorption has two distinguishable stages includ-ing initial fast phase with the primary constant of 1.51×1014 and the later near-equilibrium phase with the secondary constant of 4.96×10-4. The maximum amount of FWA adsorbed on fiber surfaces is 1.67×10-4g (per dry weight based fiber) in the initial phase. A mathematical model of adsorption kinetics was therefore established and evaluated. This model is important for the optimization of FWA applica-tion in papermaking.展开更多
This work investigated the effect of granular activated carbon adsorption （GACA） on fluorescence characteristics of dissolved organic matter （DOM） in secondary effluent, by means of excitation-emission matrix （EE...This work investigated the effect of granular activated carbon adsorption （GACA） on fluorescence characteristics of dissolved organic matter （DOM） in secondary effluent, by means of excitation-emission matrix （EEM） spectra, the fluorescence regional integra- tion （FRI） method, synchronous spectra, the fluorescence index defined as the ratio of fluorescence emission intensity at wavelength 450nm to that at 500nm at excitation （λex）= 370 am, and the wavelength that corre- sponds to the position of the normalized emission band at its half intensity （λ0.5）. DOM in the secondary effluent from the North Wastewater Treatment Plant （Shenyang, China） was fractionated using XAD resins into 5 fractions： hydrophobic acid （HPO-A）, hydrophobic neutral （HPO- N）, transphilic acid （TPI-A）, transphi｜ic neutral （TPI-N） and hydrophilic fraction （HPI）. Results showed that fluorescent materials in HPO-N and TPI-N were less readily removed than those in the other fractions by GACA. The relative content of fluorescent materials in HPO-A, TPI-A and HPI decreased whereas that in HPO- N and TPI-N increased as a consequence of GACA. Polycyclic aromatics in all DOM fractions were preferen- tially absorbed by GACA, in comparison with bulk DOM expressed as DOC. On the other hand, the adsorption of aromatic amino acids and humic acid-like fluorophores exhibiting fluorescence peaks in synchronous spectra by GACA seemed to be dependent on the acid/neutralproperties of DOM fractions. All five fractions had decreased fluorescence indices as a result of GACA. GACA led to a decreased λ0.5 value for HPO-A, increased ,λ0.5 values for HPO-N, TPI-A and HPI, and a consistent λ0.5 value for TPI-N.展开更多
Solid surface fluorescence (SSF) spectra of fibrinogen (FG) adsorbed on a glass surface were measured. For comparison, solution fluorescence (SF) spectra of native, thermally denatured, urea denatured FG solution wit...Solid surface fluorescence (SSF) spectra of fibrinogen (FG) adsorbed on a glass surface were measured. For comparison, solution fluorescence (SF) spectra of native, thermally denatured, urea denatured FG solution with FG desorbed from a glass surface and the SSF spectra of native FG powder were recorded. To analyze the structural changes induced by the surface adsorption, all the aqueous samples mentioned above were analyzed by circular dichroism (CD) spectroscopy. The results demonstrated that the structural changes of FG induced by glass adsorption caused changes in the spectroscopic features of the SSF spectra, especially in the excitation (EX) spectra. It is suggested that SSF spectroscopy may be a useful tool for studying the structures of surface/interface biomolecules and for evaluating the biocompatibility of biomaterials.展开更多
文摘Adsorption reactions between surfaces of nanodiamond and nanosilica with diameter of 100 nm prepared as suspension solutions of 0.25μg/μL and lysozyme molecule with different concentrations of 7 mmol/L PPBS at pH=7, 9, 11, and 13 have been investigated by fluores- cence spectroscopy. Adsorption reaction constants and coverages of lysozyme with different concentrations of 0-1000 nmol/L under the influences of different pH values have been ob- tained. Helicities and conformations of the adsorbed lysozyme molecules, free spaces of every adsorbed lysozyme molecule on the surfaces of nanopartieles at different concentrations and pH values have been deduced and discussed. The highest adsorption capabilities for both sys- tems and conformational efficiency of the adsorbed lysozyme molecule at pH=13 have been obtained. Lysozyme molecules can be prepared, adsorbed and carried with optimal activity and helicity, with 2 and 10 mg/m2 on unit nanosurface, 130 and 150 mg/g with respect to the weight of nanoparticle, within the linear regions of the coverages at around 150-250 nmol/L and four pH values for nanodiamond and nanosilica, respectively. They can be prepared in the tightest packed form, with 20 and 55 mg/m2, 810-1680 and 580-1100 mg/g at threshold concentrations and four pH values for nanodiamond and nanosilica, respectively.
文摘<b>Introduction:</b> Local anesthetics (LAs) must be adsorbed to and permeate through membranes to reach their sites of action. The rates of these processes critically affect drug actions at the cellular level and also the <i>in vivo</i> pharmacokinetics of perineurally injected drugs. Therefore, we measured the adsorption equilibria and permeation kinetics of two LAs local anesthetics with markedly different hydrophobicities: tetracaine (TTC, P<sub>octanol:buffer</sub> = 3.6 × 10<sup>3</sup>) and procaine (PRO, P<sub>octanol:buffer</sub> = 8.1 × 10<sup>1</sup>), in unilamellar membranes of different composition and fluidity. <b>Methods:</b> Interactions with unilamellar vesicles made of dipalmitoylphosphatidylcholine (DPPC), at 23°C (solid gel state) or 45°C (liquid crystal state), without or with cholesterol (Chol), were investigated by a combination of fluorescence and stopped-flow techniques. Membrane adsorption was monitored by the LA’s fluorescence. Membrane permeation was monitored by the decrease of fluorescence intensity of intra-vesicular pyranine, when quenched by neighboring TTC or PRO. <b>Results:</b> Ionized TTC (TTCH<sup>+</sup>) and procaine (PROH<sup>+</sup>) adsorb to membranes more slowly and weakly than their neutral counterparts (time constant <i>τ</i> ~ 0.1 sec). Fluidizing of membranes, at the higher temperature (45°C) or by Chol inclusion, accelerated LA adsorption (faster than the mixing time of the stopped-flow device, 0.008 s). Permeation of protonated TTCH<sup>+</sup> through the solid gel DPPC membranes (23°C) occurred far more slowly than adsorption, (<i>τ</i> = 36.7 ± 0.7 s, n = 9), and 3 times slower than neutral TTC (<i>τ</i> = 10.9 ± 0.7 s, n = 9);neutral PRO permeated these membranes at the same rate as TTC. Inclusion of Chol with DPPC, disordering the fatty acyl tails of membrane phospholipids while crowding their polar headgroups, slowed permeation of TTC and of PRO to an even greater degree. <b>Conclusions:</b> Local anesthetic permeation through membranes is limited by the transport across the membrane core and not by the initial binding. Drug ionization greatly slows permeation, but greater hydrophobicity does not facilitate it. Lipid crowding caused by Chol, a normal membrane component, slows permeation by disorienting the LA bound at the surface.
文摘Adsorption kinetics for a stilbene derivative type fluorescent whitening agent (FWA) on fiber surfaces was studied based on a real-time spectroscopic measurement system. Results showed that the time-dependent behavior of FWA agrees to that of a mono-molecular adsorption layer on fiber surfaces,as characterized in Langmuir-type expression. The adsorption has two distinguishable stages includ-ing initial fast phase with the primary constant of 1.51×1014 and the later near-equilibrium phase with the secondary constant of 4.96×10-4. The maximum amount of FWA adsorbed on fiber surfaces is 1.67×10-4g (per dry weight based fiber) in the initial phase. A mathematical model of adsorption kinetics was therefore established and evaluated. This model is important for the optimization of FWA applica-tion in papermaking.
基金国家自然科学基金项目(21922814,22138012,21961160745,21921005,22178349,22078333,22108281,31961133019)中国科学院青年创新促进会优秀会员(Y202014)山东能源研究所(Grant Number SEI I202133)资助
文摘This work investigated the effect of granular activated carbon adsorption （GACA） on fluorescence characteristics of dissolved organic matter （DOM） in secondary effluent, by means of excitation-emission matrix （EEM） spectra, the fluorescence regional integra- tion （FRI） method, synchronous spectra, the fluorescence index defined as the ratio of fluorescence emission intensity at wavelength 450nm to that at 500nm at excitation （λex）= 370 am, and the wavelength that corre- sponds to the position of the normalized emission band at its half intensity （λ0.5）. DOM in the secondary effluent from the North Wastewater Treatment Plant （Shenyang, China） was fractionated using XAD resins into 5 fractions： hydrophobic acid （HPO-A）, hydrophobic neutral （HPO- N）, transphilic acid （TPI-A）, transphi｜ic neutral （TPI-N） and hydrophilic fraction （HPI）. Results showed that fluorescent materials in HPO-N and TPI-N were less readily removed than those in the other fractions by GACA. The relative content of fluorescent materials in HPO-A, TPI-A and HPI decreased whereas that in HPO- N and TPI-N increased as a consequence of GACA. Polycyclic aromatics in all DOM fractions were preferen- tially absorbed by GACA, in comparison with bulk DOM expressed as DOC. On the other hand, the adsorption of aromatic amino acids and humic acid-like fluorophores exhibiting fluorescence peaks in synchronous spectra by GACA seemed to be dependent on the acid/neutralproperties of DOM fractions. All five fractions had decreased fluorescence indices as a result of GACA. GACA led to a decreased λ0.5 value for HPO-A, increased ,λ0.5 values for HPO-N, TPI-A and HPI, and a consistent λ0.5 value for TPI-N.
文摘Solid surface fluorescence (SSF) spectra of fibrinogen (FG) adsorbed on a glass surface were measured. For comparison, solution fluorescence (SF) spectra of native, thermally denatured, urea denatured FG solution with FG desorbed from a glass surface and the SSF spectra of native FG powder were recorded. To analyze the structural changes induced by the surface adsorption, all the aqueous samples mentioned above were analyzed by circular dichroism (CD) spectroscopy. The results demonstrated that the structural changes of FG induced by glass adsorption caused changes in the spectroscopic features of the SSF spectra, especially in the excitation (EX) spectra. It is suggested that SSF spectroscopy may be a useful tool for studying the structures of surface/interface biomolecules and for evaluating the biocompatibility of biomaterials.
