Effect of IFN-λ2 on combined allergic rhinitis with nasal polyps.

OBJECTIVE: This study sought to investigate the expression of interferon-λ2 (IFN-λ2) in patients with combined allergic rhinitis and nasal polyps (AR+NP), analyze the correlation between IFN-λ2 and tryptase, interleukin 10 (IL-10), and interleukin 12 (IL-12), and identify its peripheral blood cell origins. PATIENTS AND METHODS: ELISA kits were used to investigate plasma levels of IFN-λ2, tryptase, IL-10, and IL-12 in AR+NP patients and healthy controls (HC). Flow cytometry analysis was carried out to detect IFN-λ2 expression in peripheral blood leukocytes. Immunocytochemical staining was performed to detect nasal polyp IFN-λ2 expression in AR+NP patients. RESULTS: Elevated plasma IFN-λ2 levels and positive correlations between plasma IFN-λ2 and tryptase levels in AR+NP patients indicated that IFN-λ2 likely contributes to AR+NP pathogenesis. IFN-λ2 expression was upregulated in cytotoxic T cells and eosinophils in AR+NP patients. Nasal polyp mast cells and macrophages in AR+NP patients expressed IFN-λ2. CONCLUSIONS: The close correlation between IFN-λ2 expression and AR+NP may provide experimental evidence for a possible effect of IFN-λ2 against the allergic inflammatory reaction. Therefore, IFN-λ2 actions may have a potential utility for the treatment and prevention of AR+AP.

The effect of three-dimensional conformal radiotherapy on locally recurrent nasopharyngeal carcinoma and on the expression of succinate dehydrogenase B.

OBJECTIVE: Investigate the effect of three-dimensional conformal radiotherapy (3DCRT) on locally recurrent nasopharyngeal carcinoma (NPC) on the expression of succinate dehydrogenase B (SDHB). PATIENTS AND METHODS: Eighty-six patients diagnosed with locally recurrent NPC in our hospital were selected and divided into the control group (43 cases) and observation group (43 cases). Conventional two-dimensional radiotherapy was applied in the control group, and 3DCRT was adopted in the observation group. The curative effect of both groups was compared. RESULTS: The effective rate and the degree of alleviation of the observation group were higher than those of the control group, and the differences were statistically significant (p<0.05). There were no differences in the occurrence rate of complications from radiotherapy between the two groups (p>0.05). The survival rate and median survival time of the observation group were significantly higher than those of the control group (p<0.05). The positive expression rate of SDHB in the observation group after radiotherapy was significantly higher than that of the control group (p<0.05), and the median survival time of patients with positive expression of SDHB was significantly higher than patients with negative expression (p<0.05). CONCLUSIONS: 3DCRT applied for treatment of locally recurrent NPC was safe and effective. It also improved the positive expression rate of SDHB, which was associated with increased survival time.

Single-molecule and single-nanoparticle SERS: from fundamental mechanisms to biomedical applications.

This tutorial review discusses a new class of colloidal metal nanoparticles that is able to enhance the efficiencies of surface-enhanced Raman scattering (SERS) by as much as 10(14)-10(15) fold. This enormous enhancement allows spectroscopic detection and identification of single molecules located on the nanoparticle surface or at the junction of two particles under ambient conditions. Considerable progress has been made in understanding the enhancement mechanisms, including definitive evidence for the single-molecule origin of fluctuating SERS signals. For applications, SERS nanoparticle tags have been developed based on the use of embedded reporter molecules and a silica or polymer encapsulation layer. The SERS nanoparticle tags are capable of providing detailed spectroscopic information and are much brighter than semiconductor quantum dots in the near-infrared spectral window. These properties have raised new opportunities for multiplexed molecular diagnosis and in vivo Raman spectroscopy and imaging.

Combined vacuum ultraviolet laser and synchrotron pulsed field ionization study of CH2BrCl.

The pulsed field ionization-photoelectron (PFI-PE) spectrum of bromochloromethane (CH2BrCl) in the region of 85,320-88,200 cm-1 has been measured using vacuum ultraviolet laser. The vibrational structure resolved in the PFI-PE spectrum was assigned based on ab initio quantum chemical calculations and Franck-Condon factor predictions. At energies 0-1400 cm-1 above the adiabatic ionization energy (IE) of CH2BrCl, the Br-C-Cl bending vibration progression (nu1+=0-8) of CH2BrCl+ is well resolved and constitutes the major structure in the PFI-PE spectrum, whereas the spectrum at energies 1400-2600 cm-1 above the IE(CH2BrCl) is found to exhibit complex vibrational features, suggesting perturbation by the low lying excited CH2BrCl+(A 2A") state. The assignment of the PFI-PE vibrational bands gives the IE(CH2BrCl)=85,612.4+/-2.0 cm-1 (10.6146+/-0.0003 eV) and the bending frequencies nu1+(a1')=209.7+/-2.0 cm-1 for CH2BrCl+(X2A'). We have also examined the dissociative photoionization process, CH2BrCl+hnu-->CH2Cl++Br+e-, in the energy range of 11.36-11.57 eV using the synchrotron based PFI-PE-photoion coincidence method, yielding the 0 K threshold or appearance energy AE(CH2Cl+)=11.509+/-0.002 eV. Combining the 0 K AE(CH2Cl+) and IE(CH2BrCl) values obtained in this study, together with the known IE(CH2Cl), we have determined the 0 K bond dissociation energies (D0) for CH2Cl+-Br (0.894+/-0.002 eV) and CH2Cl-Br (2.76+/-0.01 eV). We have also performed CCSD(T, full)/complete basis set (CBS) calculations with high-level corrections for the predictions of the IE(CH2BrCl), AE(CH2Cl+), IE(CH2Cl), D0(CH2Cl+-Br), and D0(CH2Cl-Br). The comparison between the theoretical predictions and experimental determinations indicates that the CCSD(T, full)/CBS calculations with high-level corrections are highly reliable with estimated error limits of <17 meV.

A vacuum ultraviolet pulsed field ionization-photoelectron study of cyanogen cation in the energy range of 13.2-15.9 eV.

The vacuum ultraviolet pulsed field ionization-photoelectron and photoionization efficiency spectra of NCCN have been measured in the energy region of 13.25-17.75 eV. The analyses of these spectra have provided accurate ionization energy (IE) values of 13.371+/-0.001, 14.529+/-0.001, 14.770+/-0.001, and 15.516+/-0.001 eV for the formation of NCCN(+) in the X(2)Pi(g), A(2)Sigma(g) (+), B(2)Sigma(u) (+), and C(2)Pi(u) states, respectively. The ionization energy [NCCN(+)(B(2)Sigma(u) (+))] value determined here indicates that the origin of the NCCN(+)(B(2)Sigma(u) (+)) state lies lower in energy by 25 meV than previously reported. A set of spectroscopic parameters for NCCN(+)(X(2)Pi(g)) has been calculated using high level ab initio calculations. The experimental spectra are found to consist of ionizing transitions populating the vibronic levels of NCCN(+), which consist of pure vibronic progressions, combination modes involving the symmetric CN stretch, the CC stretch, and even quanta of the antisymmetric CN stretch, and bending vibrations. These bands are identified with the guidance of the present ab initio calculations.

A combined vacuum ultraviolet laser and synchrotron pulsed field ionization study of BCl3.

The pulsed field ionization-photoelectron (PFI-PE) spectrum of boron trichloride (BCl3) in the region of 93 590-95 640 cm(-1) has been measured using vacuum ultraviolet (VUV) laser. At energies 0-1100 cm(-1) above the adiabatic ionization energy (IE) of BCl3, the bending vibration progression of BCl3+ is clearly resolved in the PFI-PE spectrum, whereas the spectrum at energies 1200-1900 cm(-1) above the IE (BCl3) is found to exhibit dense vibrational structure. This observation unambiguously shows that BCl3+ in its ground state has C2v symmetry. Ab initio calculations performed at the CCSD(T)/CBS level with high-level corrections are consistent with this observation, indicating that the BCl3+(X 2B2) ground state has two long and one short B-Cl bonds. Furthermore, the CCSD(T)/CBS calculations predict the existence of two BCl3+ transitional structures with D3h and C2v symmetries lying 800 and 1300 cm(-1), respectively, above the BCl3+ (X 2B2) ground state. This prediction is also consistent with the dense features observed in the PFI-PE spectrum in the region of 1200-1900 cm(-1) above the IE (BCl3). The assignment of the PFI-PE vibrational bands gives the IE (BCl3) = 93 891 +/- 2 cm (11.6410 +/- 0.0003 eV) and the bending frequencies for BCl3+ (X 2B2), v1+ (b2) = 194 cm(-1) and v1+ (a1) = 209 cm We have also examined the dissociative photoionization process BCl3 + hu --> BCl2 (+) + Cl + e- using the synchrotron based PFI-PE-photoion coincidence method, yielding the 0 K threshold or appearance energy (AE) for this process to be 12.495 +/- 0.002 eV. Combining this 0 K AE value and the IE (BCl3), we have determined the 0 K bond dissociation energy (D0) for Cl2B(+) -Cl as 0.854 +/- 0.002 eV. This experimental and theoretical study indicates that the CCSD (T, Full)/CBS calculations with high-level corrections are highly reliable for the predictions of IE (BCl3), AE (BCI2+) and D0 (Cl2B(+) -Cl) with error limits of less than 35 meV. However, the CCSD (T, Full)/CBS predictions for deltaH(f0) degrees (BCl3), deltaH(f0) degrees (BCl2+), and deltaH(f0)degrees (BCl3+) are less reliable with discrepancies up to 0.1 eV as compared to the experimental determinations.

Vacuum ultraviolet pulsed field ionization study of ND3: accurate thermochemistry for the ND2-ND2+ and ND3-ND3+ system.

The dissociation of energy-selected ND(3) (+) to form ND(2) (+)+D near its threshold has been investigated using the pulsed field ionization-photoelectron (PFI-PE)-photoion coincidence method. The breakdown curves for ND(3) (+) and ND(2) (+) give a value of 15.891+/-0.001 eV for the 0 K dissociation threshold or appearance energy (AE) for ND(2) (+) from ND(3). We have also measured the PFI-PE vibrational bands for ND(3) (+)(X;v(2) (+)=0, 1, 2, and 3), revealing partially resolved rotational structures. The simulation of these bands yields precise ionization energies (IEs) for ND(3) (+) X(0,v(2) (+)=0-3,0,0)<--ND(3) X(0,0,0,0). Using the 0 K AE (ND(2) (+)) and IE(ND(3))=10.200+/-0.001 eV determined in the present study, together with the known 0 K bond dissociation energy for ND(3) [D(0)(D-ND(2))=4.7126+/-0.0025 eV], we have determined the D(0)(ND(2) (+)-D), IE(ND(2)), and 0 K heat of formation for ND(2) (+) to be 5.691+/-0.001 eV, 11.1784+/-0.0025 eV, and 1261.82+/-0.4 kJ/mol, respectively. The PFI-PE spectrum is found to exhibit a steplike feature near the AE(ND(2) (+)), indicating that the dissociation of excited ND(3) (+) at energies slightly above the dissociation threshold is prompt, occurring in the time scale

A high-resolution pulsed field ionization-photoelectron-photoion coincidence study of vinyl bromide.

By employing the high-resolution pulsed field ionization-photoelectron (PFI-PE)-photoion coincidence method, we have examined the unimolecular dissociation reaction of energy-selected C(2)H(3)Br(+) to form C(2)H(3) (+)+Br near its threshold. The analysis of the breakdown curves for C(2)H(3)Br(+) and C(2)H(3) (+) yields a value of 11.9010+/-0.0015 eV for the 0 K dissociative photoionization threshold or appearance energy (AE) for C(2)H(3) (+) from C(2)H(3)Br. This AE(C(2)H(3) (+)) value, together with the ionization energy (IE) for C(2)H(3)Br (9.8200+/-0.0015 eV) obtained by PFI-PE and threshold photoelectron (TPE) measurements, has allowed the determination of the 0 K dissociation energy (D(0)) for the C(2)H(3) (+)-Br bond to be 2.081+/-0.002 eV. The 0 K AE(C(2)H(3) (+)) from C(2)H(3)Br obtained in this study corresponds to DeltaH(f0) ( composite function )(C(2)H(3) (+))=1123.7+/-1.9 kJ/mol. Combining the latter value and the known DeltaH(f0) ( composite function )(C(2)H(3))=306.7+/-2.1 kJ/mol, we calculated a value of 8.468+/-0.029 eV for the IE(C(2)H(3)), which is in accord with the result obtained in the previous photoionization efficiency study. We have also carried out high-level ab initio calculations for the IE(C(2)H(3)) at the Gaussian-3 and the CCSD(T,full)/CBS level of theory. The CCSD(T,full)/CBS prediction of 8.487 eV for the IE(C(2)H(3)-->bridged-C(2)H(3) (+)) is in good agreement with the IE(C(2)H(3)) value derived in the present experiment. Combining the 0 K AE(C(2)H(3) (+))=11.9010+/-0.0015 eV and the IE(C(2)H(3))=8.468+/-0.029 eV yields the value of 3.433+/-0.029 eV for D(0)(C(2)H(3)-Br). We have also recorded the TPE spectrum of C(2)H(3)Br in the energy range of 9.80-12.20 eV. Members (n=5-14) of four autoionizing Rydberg series converging to the C(2)H(3)Br(+)(A (2)A(')) state are observed in the TPE spectrum. The analysis of the converging limit of these Rydberg series and the vibrational TPE bands for C(2)H(3)Br(+)(A (2)A(')) has provided more precise values for the nu(6) (+) (1217+/-10 cm(-1)) and nu(8) (+) (478+/-8 cm(-1)) modes and the IE (10.9156+/-0.0010 eV) for the formation of C(2)H(3)Br(+)(A (2)A(')) from C(2)H(3)Br.

Rovibrational-state-selected photoionization of acetylene by the two-color IR+VUV scheme: observation of rotationally resolved Rydberg transitions.

We have demonstrated a rovibrational-state-selected photoionization experiment using an IR laser and high-resolution VUV-synchrotron radiation. The VUV photoionization of acetylene [C2H2(Xtilde; (1)Sigma(+)(g);nu(3)=1,J(')=8 or 10)] prepared by IR excitation reveals three strong autoionizing Rydberg series converging to C2H+2(Xtilde; (2)Pi(u);nu(+)(3)=1) with little ion background interference. Rotational transitions resolved for the Rydberg states provide an estimate of approximately 1.8 ps for their lifetimes. This experiment opens the way for state-selective photoionization studies of polyatomic molecules using VUV-synchrotron radiation.

Xerocomus badius - Picea abies, an ectomycorrhiza of high activity and element storage capacity in acidic soil.

Mycorrhizas were collected from three Norway spruce (Picea abies) stands in southwest Germany, sorted on the morphotype level and analysed by fluorescein diacetate vital fluorescence staining and the accumulation of elements using inductively coupled plasma-atomic emission spectrometry (ICP-AES) and electron energy-loss spectroscopy (EELS). Xerocomus badius - Picea abies mycorrhizas showed a higher frequency of active hyphal sheaths and a higher potential to store nitrogen, phosphorus, potassium, magnesium, iron and zinc than other mycorrhizal types. Phosphorus and nitrogen were localized by EELS in vacuolar bodies which occurred consistently in the sheath of X. badius mycorrhizas. The results indicate that X. badius is well adapted to acidic stands and that its mycorrhizas are very efficient in uptake and storage of macronutrients.

[Clinical study of sudden deafness treated with method of integrated traditional Chinese and Western medicine].

OBJECTIVE: To explore the mechanisms of sudden deafness treated with integrated traditional Chinese and Western medicine (TCM-WM). METHODS: One hundred and forty-six patients suffering from sudden deafness were divided into two groups, 64 cases of treated group treated with the method of integrated TCM-WM and the other 82 cases treated with Western medicine alone for control. RESULTS: The total effective rate of the treated group was 92.19%, that of the control group was 75.61%. The difference between two groups was significant, P < 0.01. CONCLUSION: The integrated method is very effective in treating sudden deafness. Its mechanism might be: (1) Decrease the blood viscosity and increase the red blood cell's tenacity, so that the blood stream is passing through unimpeded. (2) Decrease the plasma TXA2 level and increase the PGI2 level, keep the blood supply for inner ear. (3) Increase the activity of SOD and clear away the free radicals so as to reduce the damage of inner ear.

Modelling for waste water treatment by Rhodopseudomonas palustris Y6 immobilized on fibre in a columnar bioreactor.

A kinetic model of continuous treatment of waste water by Rhodopseudomonas palustris Y6 immobilized on soft fibre in a columnar bioreaction system was established. Good agreement was found between the model prediction and the experimental data from continuous operation [initial chemical oxygen demand (COD) concentration = 29.700 g/l] of the system. The optimum operational conditions for the maximum COD reduction capacity were investigated from the model prediction and the experimental data. The waste water treatment process may significantly increase the waste reduction capacity because a large amount of active biomass for COD reduction is immobilized in the system, resulting in operation stability. The results presented here provide a useful basis for further scaling up and efficient operation of waste water treatment processes.

Factors affecting gibberellic acid production by Fusarium moniliforme in solid-state cultivation on starch.

The production of gibberellic acid (GA3) by Fusarium moniliforme M-7121 in solid-state culture was evaluated in flask cultures as well as in 3-I horizontal rotary reactors. The highest production rate of GA3 was with 80% (w/v) maize flour mixed with wheat bran. The optimum initial moisture content was inversely dependent on the ambient relative humidity. The initial water activity range for optimal growth and GA3 accumulation was about 0.98 to 0.99, which is unusually high for a filamentous fungus. A low O2 concentration resulted in a much decreased GA3 yield and the appearance of a yellow to reddish pigmentation in the mycelium. The lag phase was short and rapid growth continued for up to 2 days in the rotary reactor, with a maximum specific growth rate of 0.12 h(-1). The maximum rate of GA3 production occurred during the subsequent 3 to 10 days of incubation and the final GA3 concentration reached was 18.7 mg to 19.3 mg/g dry culture. The point of maximum GA3 accumulation after 10 to 12 days of incubation was usually marked by a sharp increase in pH.