PVC建筑膜材的表面处理及其亲水性能研究

为制备具有亲水和防污自清洁性能的PVC建筑薄膜,在经低温等离子体改性的PVC薄膜表面涂覆SiO2作为隔离层,然后采用旋涂法将TiO2涂覆于薄膜表面,制备得到PVC/SiO2/TiO2复合膜。利用XRD、FTIR、SEM、EDS等测试手段对复合膜的形貌和结构进行表征,并用接触角测试仪测定了其亲水性能,经紫外光照后,复合膜的接触角由42.2°降为10.9°,结果表明TiO2层的涂覆大大地提高了PVC薄膜的亲水性能。     

Adaptive evolution of human immunodeficiency virus-type 1 during the natural course of infection

The rate of progression to disease varies considerably among individuals infected with human immunodeficiency virus-type 1 (HIV-1). Analyses of semiannual blood samples obtained from six infected men showed that a rapid rate of CD4 T cell loss was associated with relative evolutionary stasis of the HIV-1 quasispecies virus population. More moderate rates of CD4 T cell loss correlated with genetic evolution within three of four subjects. Consistent with selection by the immune constraints of these subjects, amino acid changes were apparent within the appropriate epitopes of human leukocyte antigen class I-restricted cytotoxic T lymphocytes. Thus, the evolutionary dynamics exhibited by the HIV-1 quasispecies virus populations under natural selection are compatible with adaptive evolution.     

Cranial cystic epidermoid: report of two cases and review of the literature

Among non-Hodgkin's lymphomas occurring in childhood two major histologic subgroups can be identified: (1) Burkitt's lymphoma and (2) T-cell lymphoblastic lymphoma, an uncommon high-grade malignant non-Hodgkin's lymphoma. Although Burkitt's lymphoma with maxillofacial involvement is a well-documented disease, T-cell lymphoblastic lymphoma in the perioral region is rare. An unusual case of T-cell lymphoblastic lymphoma with initial oral manifestation in an 18-month-old child is presented.     

Influence of delayed viral production on viral dynamics in HIV-1 infected patients

We present and analyze a model for the interaction of human immunodeficiency virus type 1 (HIV-1) with target cells that includes a time delay between initial infection and the formation of productively infected cells. Assuming that the variation among cells with respect to this 'intracellular' delay can be approximated by a gamma distribution, a high flexible distribution that can mimic a variety of biologically plausible delays, we provide analytical solutions for the expected decline in plasma virus concentration after the initiation of antiretroviral therapy with one or more protease inhibitors. We then use the model to investigate whether the parameters that characterize viral dynamics can be identified from biological data. Using non-linear least-squares regression to fit the model to simulated data in which the delays conform to a gamma distribution, we show that good estimates for free viral clearance rates, infected cell death rates, and parameters characterizing the gamma distribution can be obtained. For simulated data sets in which the delays were generated using other biologically plausible distributions, reasonably good estimates for viral clearance rates, infected cell death rates, and mean delay times can be obtained using the gamma-delay model. For simulated data sets that include added simulated noise, viral clearance rate estimates are not as reliable. If the mean intracellular delay is known, however, we show that reasonable estimates for the viral clearance rate can be obtained by taking the harmonic mean of viral clearance rate estimates from a group of patients. These results demonstrate that it is possible to incorporate distributed intracellular delays into existing models for HIV dynamics and to use these refined models to estimate the half-life of free virus from data on the decline in HIV-1 RNA following treatment.     

Injectable bioactive glass/biodegradable polymer composite for bone and cartilage reconstruction: Concept and experimental outcome with thermoplastic composites of poly(ε-caprolactone-co-D,L-lactide) and bioactive glass S53P4

Injectable composites (Glepron) of particulate bioactive glass S53P4 (BAG) and Poly(epsilon-caprolactone-co-D,L-lactide) as thermoplastic carrier matrix were investigated as bone fillers in cancellous and cartilagineous subchondral bone defects in rabbits. Composites were injected as viscous liquid or mouldable paste. The glass granules of the composites resulted in good osteoconductivity and bone bonding that occurred initially at the interface between the glass and the host bone. The bone bioactivity index (BBI) indicating bone contacts between BAG and bone, as well as the bone coverage index (BCI) indicating bone ongrowth, correlated with the amount of glass in the composites. The indices were highest with 70 wt % of BAG, granule size 90-315 microm and did not improve by the addition of sucrose as in situ porosity creating agent in the composite or by using smaller (<45 microm) glass granules. The percentage of new bone ingrowth into the composite with 70 wt % of BAG was 6-8% at 23 weeks. At the articular surface cartilage regeneration with chondroblasts and mature chondrocytes was often evident. The composites were osteoconductive and easy to handle with short setting time. They were biocompatible with low foreign body cellular reaction. Results indicate a suitable working concept as a filler bone substitute for subchondral cancellous bone defects.     

Bioactive glass induced in vitro apatite formation on composite GBR membranes

The aim of this study was to investigate in vitro bioactivity of different thermoplastic biodegradable barrier membranes. Three experimental GBR membranes were fabricated using Poly(epsilon-caprolactone-co-D: ,L-lactide) P(CL/DL-LA) and particulate bioactive glass S53P4 (BAG; granule size 90-315 microm): (A) composite membrane with 60-wt.% of BAG, (B) membrane coated with BAG; and (C) copolymer membrane without BAG. Membranes were immersed in simulated body fluid (SBF), and their surfaces were characterized with SEM, XRD and EDS after 6 and 12 h and after 1, 3, 5, 7, and 14 days. Calcium phosphate (Ca-P) surface formation was observed on both composite membranes (A and B) but not on the copolymer membrane without bioactive glass (C). The Ca-P precipitation appeared to be initiated on the bioactive glass followed by growth of the layer along the polymer surface. In 6-12 h ion dissolution of the bioactive glass led to formation of the silica rich layer on the surface of the exposed glass granules on composite membrane B whereas only small amounts of silica was observed on the polymer surface of the composite membrane A. At 24 h nucleation of Ca-P precipitation was observed, and by 3-5 days membrane surface was covered with a uniform Ca-P layer transforming from amorphous to low crystalline structure. At 7 days composition and structure of the apatite surface resembled the apatite in bone. Once nucleated, the surface topography seemed to have significant effect on the growth of the apatite layer.     

UPPC梁的开裂截面惯性矩及挠度计算研究

为满足无粘结部分预应力混凝土(UPPC)梁正常使用极限状态的设计要求, 必须合理估算使用荷载下构件的挠度。由于预应力筋与其周围混凝土没有粘结, 加之部分预应力混凝土梁的中性轴随外荷载而动, 开裂截面形心轴及开裂截面惯性矩也跟着变, 这给UPPC梁的挠度计算带来了困难。该文建立了一个UPPC梁的开裂截面惯性矩计算方法, 在此基础上, 可以按Branson方法很容易地计算出截面有效惯性矩。该有效惯性矩与按《混凝土设计规范》(GB50010-2010)方法所得的有效惯性矩较接近, 前者与后者之比在0.89~1.10。计算挠度与3个不同研究者的试验对比表明所建立方法是正确的并具有较广泛的适用性, 可用于无粘结预应力筋为纤维复合材料的混凝土梁, 而目前的混凝土结构设计规范方法则无法应用于此类构件。     

Improvement of Mechanical Properties of Oligomer-modified Acrylic Bone Cement with Glass-fibers

Some mechanical properties of oligomer-modified acrylic bone cement with glass-fibers were studied. Under wet environments, oligomer-filler forms a porous structure in the acrylic bone cement. Test specimens were manufactured using commercial bone cement (Palacos^® R) with different quantities of an experimental oligomer-filler (0–20 wt%), and included continuous unidirectional E-glass fibers (l=65 mm) or chopped E-glass fibers (l=2 mm). The specimens were either tested dry, or after being immersed under wet environments for one week. The three-point bending test was used to measure the flexural strength and modulus of the acrylic bone cement composites (analysis with ANOVA). A scanning electron microscope (SEM) was used to examine the surface structure of the acrylic bone cement composites. Using continuous glass-fiber reinforcement, the dry flexural strength was 145 MPa and modulus was 4.6 GPa for the plain bone cement. For the test specimens with 20 wt% of oligomer-filler and continuous unidirectional glass-fibers, the dry flexural strength was 118 MPa and modulus was 4.2 GPa, whereas the wet flexural strength was 66 MPa and modulus was 3.0 GPa. The results suggest that the reduced flexural properties caused by the porosity of oligomer-modified bone cement can be compensated with glass-fiber reinforcement.