2,701 research outputs found

    Correlation effects during liquid infiltration into hydrophobic nanoporous mediums

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    Correlation effects arising during liquid infiltration into hydrophobic porous medium are considered. On the basis of these effects a mechanism of energy absorption at filling porous medium by nonwetting liquid is suggested. In accordance with this mechanism, the absorption of mechanical energy is a result expenditure of energy for the formation of menisci in the pores on the shell of the infinite cluster and expenditure of energy for the formation of liquid-porous medium interface in the pores belonging to the infinite cluster of filled pores. It was found that in dependences on the porosity and, consequently, in dependences on the number of filled pores neighbors, the thermal effect of filling can be either positive or negative and the cycle of infiltration-defiltration can be closed with full outflow of liquid. It can occur under certain relation between percolation properties of porous medium and the energy characteristics of the liquid-porous medium interface and the liquid-gas interface. It is shown that a consecutive account of these correlation effects and percolation properties of the pores space during infiltration allow to describe all experimental data under discussion

    Impact of Intracranial Artery Disease and Prior Cerebral Infarction on Central Nervous System Complications After Off-Pump Coronary Artery Bypass Grafting

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    We tried to determine whether postoperative CNS complications after off-pump coronary artery bypass grafting (OPCABG) are related to prior cerebral infarction or intracranial artery disease. Fifty-five patients (40 men, mean age 64.59 ± 8.86 years) subjected to OPCABG underwent neurological and neuropsychological examinations 24 h before surgery. MRI was used to identify old and/or new ischemic lesions before surgery, and MRA was used to determine the presence and severity of intracranial artery disease. The patients were examined eight days after surgery; possible development of stroke or cognitive dysfunction was evaluated. Associations between postoperative stroke and potential predictors, including prior cerebral infarction and intracranial artery disease, were analyzed using univariate methods. Two of 55 (3.64%) patients had postoperative stroke, and no patient showed cognitive decline. Univariate analysis found no significant association between postoperative stroke and prior cerebral infarction detected by MRI (P = 0.378) or intracranial artery disease detected by MRA (P = 0.103). Our results suggest that intracranial artery disease and prior cerebral infarction are not independent risk factors for stroke after OPCABG. Nonetheless, further investigation of these associations is necessary.Мо ĐœĐ°ĐŒĐ°ĐłĐ°Đ»ĐžŃŃ ĐČŃŃ‚Đ°ĐœĐŸĐČото, чо Đ·Đ°Đ»Đ”Đ¶Đ°Ń‚ŃŒ ĐżŃ–ŃĐ»ŃĐŸĐżĐ”Ń€Đ°Ń†Ń–ĐčĐœŃ– усĐșĐ»Đ°ĐŽĐœĐ”ĐœĐœŃ ĐČ ĐŠĐĐĄ ĐżŃ–ŃĐ»Ń ŃˆŃƒĐœŃ‚ŃƒĐČĐ°ĐœĐœŃ ĐșĐŸŃ€ĐŸĐœĐ°Ń€ĐœĐŸŃ— артДрії бДз Đ·Đ°ŃŃ‚ĐŸŃŃƒĐČĐ°ĐœĐœŃ ŃˆŃ‚ŃƒŃ‡ĐœĐŸĐłĐŸ ĐșŃ€ĐŸĐČĐŸĐŸĐ±Ń–ĐłŃƒ ĐČіЮ ĐœĐ°ŃĐČĐœĐŸŃŃ‚Ń– ĐČ ĐżĐŸĐżĐ”Ń€Đ”ĐŽĐœŃ–Đč ĐżĐ”Ń€Ń–ĐŸĐŽ Ń†Đ”Ń€Đ”Đ±Ń€Đ°Đ»ŃŒĐœĐŸĐłĐŸ ĐłĐ”ĐŒĐŸŃ€Đ°ĐłŃ–Ń‡ĐœĐŸĐłĐŸ Ń–ĐœŃŃƒĐ»ŃŒŃ‚Ńƒ Đ°Đ±ĐŸ ŃŃ‚Đ”ĐœĐŸĐ·Ńƒ ĐșŃ€Đ°ĐœŃ–Đ°Đ»ŃŒĐœĐžŃ… артДріĐč. 55 ĐżĐ°Ń†Ń–Ń”ĐœŃ‚Ń–ĐČ (40 Ń‡ĐŸĐ»ĐŸĐČіĐșіĐČ Ń– 15 Đ¶Ń–ĐœĐŸĐș, ŃĐ”Ń€Đ”ĐŽĐœŃ–Đč ĐČіĐș 64.59 ± 8.86 Ń€ĐŸĐșу), ĐșĐŸŃ‚Ń€ĐžĐŒ була ĐżŃ€ĐžĐ·ĐœĐ°Ń‡Đ”ĐœĐ° ĐČĐșĐ°Đ·Đ°ĐœĐ° ĐŸĐżĐ”Ń€Đ°Ń†Ń–Ń, булО Đ·Đ° ĐŽĐŸĐ±Ńƒ пДрДЎ ĐœĐ”ŃŽ ĐżŃ–ĐŽĐŽĐ°ĐœŃ– ĐœĐ”ĐČŃ€ĐŸĐ»ĐŸĐłŃ–Ń‡ĐœĐŸĐŒŃƒ та ĐœĐ”ĐčŃ€ĐŸĐżŃĐžŃ…ĐŸĐ»ĐŸĐłŃ–Ń‡ĐœĐŸĐŒŃƒ ĐŸĐ±ŃŃ‚Đ”Đ¶Đ”ĐœĐœŃŽ. ĐœĐ°ĐłĐœŃ–Ń‚ĐŸŃ€Đ”Đ·ĐŸĐœĐ°ĐœŃĐœĐ” сĐșĐ°ĐœŃƒĐČĐ°ĐœĐœŃ (MRI) Đ±ŃƒĐ»ĐŸ ĐČĐžĐșĐŸŃ€ĐžŃŃ‚Đ°ĐœĐ” ĐŽĐ»Ń Ń–ĐŽĐ”ĐœŃ‚ĐžŃ„Ń–Đșації старох та/Đ°Đ±ĐŸ ĐœĐŸĐČох Ń–ŃˆĐ”ĐŒŃ–Ń‡ĐœĐžŃ… ŃƒŃ€Đ°Đ¶Đ”ĐœŃŒ, Đ° ĐŒĐ°ĐłĐœŃ–Ń‚ĐŸŃ€Đ”Đ·ĐŸĐœĐ°ĐœŃĐœĐ° Đ°ĐœĐłŃ–ĐŸĐłŃ€Đ°Ń„Ń–Ń (MRA) Đ·Đ°ŃŃ‚ĐŸŃĐŸĐČуĐČĐ°Đ»Đ°ŃŃ ĐŽĐ»Ń ĐČŃŃ‚Đ°ĐœĐŸĐČĐ»Đ”ĐœĐœŃ ĐœĐ°ŃĐČĐœĐŸŃŃ‚Ń– та ŃŃ‚ŃƒĐżĐ”ĐœŃŽ ŃŃ‚Đ”ĐœĐŸĐ·Ńƒ ĐșŃ€Đ°ĐœŃ–Đ°Đ»ŃŒĐœĐžŃ… артДріĐč. ĐŸĐ°Ń†Ń–Ń”ĐœŃ‚Đž булО ĐżĐŸĐČŃ‚ĐŸŃ€ĐœĐŸ ĐŸĐ±ŃŃ‚Đ”Đ¶Đ”ĐœŃ– чДрДз ĐČŃ–ŃŃ–ĐŒ Ўіб ĐżŃ–ŃĐ»Ń ĐŸĐżĐ”Ń€Đ°Ń†Ń–Ń— ĐŽĐ»Ń ĐČояĐČĐ»Đ”ĐœĐœŃ ĐŒĐŸĐ¶Đ»ĐžĐČох усĐșĐ»Đ°ĐŽĐœĐ”ĐœŃŒ (Ń€ĐŸĐ·ĐČотĐșу Ń–ĐœŃŃƒĐ»ŃŒŃ‚Ńƒ Đ°Đ±ĐŸ ĐșĐŸĐłĐœŃ–Ń‚ĐžĐČĐœĐŸŃ— ĐŽĐžŃŃ„ŃƒĐœĐșції). ЗĐČâ€™ŃĐ·ĐșĐž ĐŒŃ–Đ¶ Ń€ĐŸĐ·ĐČотĐșĐŸĐŒ ĐżĐŸŃŃ‚ĐŸĐżĐ”Ń€Đ°Ń†Ń–ĐčĐœĐŸĐłĐŸ Ń–ĐœŃŃƒĐ»ŃŒŃ‚Ńƒ та ĐŒĐŸĐ¶Đ»ĐžĐČĐžĐŒĐž прДЎОĐșŃ‚ĐŸŃ€Đ°ĐŒĐž (ĐżĐŸĐżĐ”Ń€Đ”ĐŽĐœŃ–ĐŒ Ń–ĐœŃŃƒĐ»ŃŒŃ‚ĐŸĐŒ та ŃŃ‚Đ”ĐœĐŸĐ·ĐŸĐŒ ĐșŃ€Đ°ĐœŃ–Đ°Đ»ŃŒĐœĐžŃ… артДріĐč) булО ĐżŃ€ĐŸĐ°ĐœĐ°Đ»Ń–Đ·ĐŸĐČĐ°ĐœŃ– Ń–Đ· Đ·Đ°ŃŃ‚ĐŸŃŃƒĐČĐ°ĐœĐœŃĐŒ ĐŒĐ”Ń‚ĐŸĐŽŃ–ĐČ ĐČаріаціĐčĐœĐŸŃ— статостоĐșĐž. ĐŸŃ–ŃĐ»ŃĐŸĐżĐ”Ń€Đ°Ń†Ń–ĐčĐœĐžĐč Ń–ĐœŃŃƒĐ»ŃŒŃ‚ Ń€ĐŸĐ·ĐČĐžĐČся у ĐŽĐČĐŸŃ… Ń–Đ· 55 ĐżĐ°Ń†Ń–Ń”ĐœŃ‚Ń–ĐČ (3.64 %); Đ·ĐœĐžĐ¶Đ”ĐœĐœŃ ріĐČĐœŃ ĐșĐŸĐłĐœŃ–Ń‚ĐžĐČĐœĐŸŃ— Đ°ĐșтоĐČĐœĐŸŃŃ‚Ń– ĐœĐ” ŃĐżĐŸŃŃ‚Đ”Ń€Ń–ĐłĐ°Đ»ĐŸŃŃ ĐČ Đ¶ĐŸĐŽĐœĐŸĐŒŃƒ ĐČОпаЎĐșу. ĐĐœĐ°Đ»Ń–Đ· ĐœĐ” ĐżĐŸĐșĐ°Đ·Đ°ĐČ ĐČŃ–Ń€ĐŸĐłŃ–ĐŽĐœĐŸĐłĐŸ Đ·ĐČâ€™ŃĐ·Đșу ĐŒŃ–Đ¶ Ń€ĐŸĐ·ĐČотĐșĐŸĐŒ ĐżŃ–ŃĐ»ŃĐŸĐżĐ”Ń€Đ°Ń†Ń–ĐčĐœĐŸĐłĐŸ Ń–ĐœŃŃƒĐ»ŃŒŃ‚Ńƒ та ĐœĐ°ŃĐČĐœŃ–ŃŃ‚ŃŽ ĐżĐŸĐżĐ”Ń€Đ”ĐŽĐœŃŒĐŸĐłĐŸ ĐłĐ”ĐŒĐŸŃ€Đ°ĐłŃ–Ń‡ĐœĐŸĐłĐŸ Ń–ĐœŃŃƒĐ»ŃŒŃ‚Ńƒ (ĐŽĐ°ĐœŃ– MRI; P = 0.378) Đ°Đ±ĐŸ ŃŃ‚Đ”ĐœĐŸĐ·Ńƒ ĐșŃ€Đ°ĐœŃ–Đ°Đ»ŃŒĐœĐžŃ… артДріĐč (ĐŽĐ°ĐœŃ– MRA; P= 0.103). Наші Ń€Đ”Đ·ŃƒĐ»ŃŒŃ‚Đ°Ń‚Đž ĐŽĐŸĐ·ĐČĐŸĐ»ŃŃŽŃ‚ŃŒ ĐČĐČажатО, Ń‰ĐŸ ŃŃ‚Đ”ĐœĐŸĐ· ĐșŃ€Đ°ĐœŃ–Đ°Đ»ŃŒĐœĐžŃ… артДріĐč та ĐżĐŸĐżĐ”Ń€Đ”ĐŽĐœŃ–Đč Ń–ĐœŃŃƒĐ»ŃŒŃ‚ ĐœĐ” є ĐœĐ”Đ·Đ°Đ»Đ”Đ¶ĐœĐžĐŒĐž фаĐșŃ‚ĐŸŃ€Đ°ĐŒĐž рОзОĐșу Ń‰ĐŸĐŽĐŸ Ń–ĐœŃŃƒĐ»ŃŒŃ‚Ńƒ ĐżŃ–ŃĐ»Ń ŃˆŃƒĐœŃ‚ŃƒĐČĐ°ĐœĐœŃ ĐșĐŸŃ€ĐŸĐœĐ°Ń€ĐœĐŸŃ— артДрії, алД ĐżĐŸĐŽĐ°Đ»ŃŒŃˆŃ– ĐŽĐŸŃĐ»Ń–ĐŽĐ¶Đ”ĐœĐœŃ ĐŒĐŸĐ¶Đ»ĐžĐČĐŸŃŃ‚Ń– таĐșох Đ·ĐČâ€™ŃĐ·ĐșіĐČ Ń” ĐœĐ”ĐŸĐ±Ń…Ń–ĐŽĐœĐžĐŒĐž

    A muscle-targeting peptide displayed on AAV2 improves muscle tropism on systemic delivery

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    Adeno-associated virus (AAV) has become a leading gene transfer vector for striated muscles. However, the AAV vectors also exhibit broad tropisms after systemic delivery. In an attempt to improve muscle tropism, we inserted a 7-amino-acid (ASSLNIA) muscle-targeting peptide (MTP) in the capsids of AAV2 at residue 587 or 588, generating AAV587MTP and AAV588MTP. In vitro studies showed that both viruses diminished their infectivity on non-muscle cell lines as well as on un-differentiated myoblasts, however, preserved or enhanced their infectivity on differentiated myotubes. AAV587MTP, but not AAV588MTP, also abolished its heparin-binding capacity and infected myotubes in a heparin-independent manner. Furthermore, in vivo studies by intravenous vector administration in mice showed that AAV587MTP enhanced its tropism to various muscles and particularly to the heart (24.3 fold of unmodified AAV2), whereas reduced its tropism to the non-muscle tissues such as the liver, lungs and spleen, etc. This alteration of tissue tropism is not simply due to the loss of heparin-binding, since a mutant AAV2 (AAVHBSMut) containing heparin-binding site mutations lost infectivity on both non-muscle and muscle cells. Furthermore, free MTP peptide, but not the scrambled control peptide, competitively inhibited AAV587MTP infection on myotubes. These results suggest that AAV2 could be re-targeted to the striated muscles by a muscle-targeting peptide inserted after residue 587 of the capsids. This proof of principle study showed first evidence of peptide-directed muscle targeting upon systemic administration of AAV vectors

    First observation of the M1 transition ψ(3686)→γηc(2S)\psi(3686)\to \gamma\eta_c(2S)

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    Using a sample of 106 million \psi(3686) events collected with the BESIII detector at the BEPCII storage ring, we have made the first measurement of the M1 transition between the radially excited charmonium S-wave spin-triplet and the radially excited S-wave spin-singlet states: \psi(3686)\to\gamma\eta_c(2S). Analyses of the processes \psi(2S)\to \gamma\eta_c(2S) with \eta_c(2S)\to \K_S^0 K\pi and K^+K^-\pi^0 gave an \eta_c(2S) signal with a statistical significance of greater than 10 standard deviations under a wide range of assumptions about the signal and background properties. The data are used to obtain measurements of the \eta_c(2S) mass (M(\eta_c(2S))=3637.6\pm 2.9_\mathrm{stat}\pm 1.6_\mathrm{sys} MeV/c^2), width (\Gamma(\eta_c(2S))=16.9\pm 6.4_\mathrm{stat}\pm 4.8_\mathrm{sys} MeV), and the product branching fraction (\BR(\psi(3686)\to \gamma\eta_c(2S))\times \BR(\eta_c(2S)\to K\bar K\pi) = (1.30\pm 0.20_\mathrm{stat}\pm 0.30_\mathrm{sys})\times 10^{-5}). Combining our result with a BaBar measurement of \BR(\eta_c(2S)\to K\bar K \pi), we find the branching fraction of the M1 transition to be \BR(\psi(3686)\to\gamma\eta_c(2S)) = (6.8\pm 1.1_\mathrm{stat}\pm 4.5_\mathrm{sys})\times 10^{-4}.Comment: 7 pages, 1 figure, 1 tabl

    Precision measurement of the branching fractions of J/psi -> pi+pi-pi0 and psi' -> pi+pi-pi0

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    We study the decays of the J/psi and psi' mesons to pi+pi-pi0 using data samples at both resonances collected with the BES III detector in 2009. We measure the corresponding branching fractions with unprecedented precision and provide mass spectra and Dalitz plots. The branching fraction for J/psi -> pi+pi-pi0 is determined to be (2.137 +- 0.004 (stat.) +0.058-0.056 (syst.) +0.027-0.026 (norm.))*10-2, and the branching fraction for psi' -> pi+pi-pi0 is measured as (2.14 +- 0.03 (stat.) +0.08-0.07 (syst.) +0.09-0.08 (norm.))*10-4. The J/psi decay is found to be dominated by an intermediate rho(770) state, whereas the psi' decay is dominated by di-pion masses around 2.2 GeV/c2, leading to strikingly different Dalitz distributions.Comment: 15 pages, 2 figure

    Observation and study of the decay J/ψ→ϕηηâ€ČJ/\psi\rightarrow\phi\eta\eta'

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    We report the observation and study of the decay J/ψ→ϕηηâ€ČJ/\psi\rightarrow\phi\eta\eta' using 1.3×1091.3\times{10^9} J/ψJ/\psi events collected with the BESIII detector. Its branching fraction, including all possible intermediate states, is measured to be (2.32±0.06±0.16)×10−4(2.32\pm0.06\pm0.16)\times{10^{-4}}. We also report evidence for a structure, denoted as XX, in the ϕηâ€Č\phi\eta' mass spectrum in the 2.0−2.12.0-2.1 GeV/c2c^2 region. Using two decay modes of the ηâ€Č\eta' meson (ÎłÏ€+π−\gamma\pi^+\pi^- and ηπ+π−\eta\pi^+\pi^-), a simultaneous fit to the ϕηâ€Č\phi\eta' mass spectra is performed. Assuming the quantum numbers of the XX to be JP=1−J^P = 1^-, its significance is found to be 4.4σ\sigma, with a mass and width of (2002.1±27.5±21.4)(2002.1 \pm 27.5 \pm 21.4) MeV/c2c^2 and (129±17±9)(129 \pm 17 \pm 9) MeV, respectively, and a product branching fraction B(J/ψ→ηX)×B(X→ϕηâ€Č)=(9.8±1.2±1.7)×10−5\mathcal{B}(J/\psi\rightarrow\eta{}X)\times{}\mathcal{B}(X\rightarrow\phi\eta')=(9.8 \pm 1.2 \pm 1.7)\times10^{-5}. Alternatively, assuming JP=1+J^P = 1^+, the significance is 3.8σ\sigma, with a mass and width of (2062.8±13.1±7.2)(2062.8 \pm 13.1 \pm 7.2) MeV/c2c^2 and (177±36±35)(177 \pm 36 \pm 35) MeV, respectively, and a product branching fraction B(J/ψ→ηX)×B(X→ϕηâ€Č)=(9.6±1.4±2.0)×10−5\mathcal{B}(J/\psi\rightarrow\eta{}X)\times{}\mathcal{B}(X\rightarrow\phi\eta')=(9.6 \pm 1.4 \pm 2.0)\times10^{-5}. The angular distribution of J/ψ→ηXJ/\psi\rightarrow\eta{}X is studied and the two JPJ^P assumptions of the XX cannot be clearly distinguished due to the limited statistics. In all measurements the first uncertainties are statistical and the second systematic.Comment: 10 pages, 6 figures and 4 table

    Measurement of azimuthal asymmetries in inclusive charged dipion production in e+e−e^+e^- annihilations at s\sqrt{s} = 3.65 GeV

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    We present a measurement of the azimuthal asymmetries of two charged pions in the inclusive process e+e−→ππXe^+e^-\rightarrow \pi\pi X based on a data set of 62 pb−1\rm{pb}^{-1} at the center-of-mass energy s=3.65\sqrt{s}=3.65 GeV collected with the BESIII detector. These asymmetries can be attributed to the Collins fragmentation function. We observe a nonzero asymmetry, which increases with increasing pion momentum. As our energy scale is close to that of the existing semi-inclusive deep inelastic scattering experimental data, the measured asymmetries are important inputs for the global analysis of extracting the quark transversity distribution inside the nucleon and are valuable to explore the energy evolution of the spin-dependent fragmentation function.Comment: 7 pages, 5 figure

    Study of J/ψ→ppˉJ/\psi\to p\bar{p} and J/ψ→nnˉJ/\psi\to n\bar{n}

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    The decays J/ψ→ppˉJ/\psi\to p\bar{p} and J/ψ→nnˉJ/\psi\to n\bar{n} have been investigated with a sample of 225.2 million J/ψJ/\psi events collected with the BESIII detector at the BEPCII e+e−e^+e^- collider. The branching fractions are determined to be B(J/ψ→ppˉ)=(2.112±0.004±0.031)×10−3\mathcal{B}(J/\psi\to p\bar{p})=(2.112\pm0.004\pm0.031)\times10^{-3} and B(J/ψ→nnˉ)=(2.07±0.01±0.17)×10−3\mathcal{B}(J/\psi\to n\bar{n})=(2.07\pm0.01\pm0.17)\times10^{-3}. Distributions of the angle Ξ\theta between the proton or anti-neutron and the beam direction are well described by the form 1+αcos⁥2Ξ1+\alpha\cos^2\theta, and we find α=0.595±0.012±0.015\alpha=0.595\pm0.012\pm0.015 for J/ψ→ppˉJ/\psi\to p\bar{p} and α=0.50±0.04±0.21\alpha=0.50\pm0.04\pm0.21 for J/ψ→nnˉJ/\psi\to n\bar{n}. Our branching-fraction results suggest a large phase angle between the strong and electromagnetic amplitudes describing the J/ψ→NNˉJ/\psi\to N\bar{N} decay.Comment: 16 pages, 13 figures, the 2nd version, submitted to PR

    Measurement of the e+e−→π+π−\mathrm e^+\mathrm e^-\rightarrow\mathrm\pi^+\mathrm\pi^- Cross Section between 600 and 900 MeV Using Initial State Radiation

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    We extract the e+e−→π+π−e^+e^-\rightarrow \pi^+\pi^- cross section in the energy range between 600 and 900 MeV, exploiting the method of initial state radiation. A data set with an integrated luminosity of 2.93 fb−1^{-1} taken at a center-of-mass energy of 3.773 GeV with the BESIII detector at the BEPCII collider is used. The cross section is measured with a systematic uncertainty of 0.9%. We extract the pion form factor ∣FÏ€âˆŁ2|F_\pi|^2 as well as the contribution of the measured cross section to the leading order hadronic vacuum polarization contribution to (g−2)ÎŒ(g-2)_\mu. We find this value to be aΌππ,LO(600−900  MeV)=(368.2±2.5stat±3.3sys)⋅10−10a_\mu^{\pi\pi,\rm LO}(600-900\;\rm MeV) = (368.2 \pm 2.5_{\rm stat} \pm 3.3_{\rm sys})\cdot 10^{-10}.Comment: 14 pages, 7 figures, accepted by PL
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