Effective immunity to dental caries: enhancement of salivary anti-Streptococcus mutans antibody responses with oral adjuvants

In the present study, we compared the ability of the soluble adjuvants concanavalin A (ConA), muramyl dipeptide (MDP), and peptidoglycan (PG) to enhance immune responses to orally administered particulate antigens of Streptococcus mutans 6715 in gnotobiotic rats. The isotype and levels of antibody in saliva and in serum from experimental rats were determined by an enzyme-linked immunosorbent assay using S. mutans whole cells (WC) as the coating antigen. The specificities of salivary and serum immunoglobulin A (IgA) antibodies to particulate S. mutans antigens, lipoteichoic acid, S. mutans serotype g carbohydrate, and dextran were also determined. When 50 micrograms of ConA was used as the oral adjuvant with S. mutans 6715 WC immunogen, a slight enhancement of immune responses was obtained. A higher dose of ConA suppressed humoral responses to the immunogen. Enhanced immune responses, especially of the IgA isotype, in both serum and saliva were induced in gnotobiotic rats given MDP and either S. mutans 6715 WC or purified cell walls (CW) by gastric intubation. Elevated IgA antibody levels to CW, lipoteichoic acid, and carbohydrate were observed in rats given S. mutans WC and MDP by gastric intubation, whereas oral immunization with S. mutans CW and MDP resulted in higher antibody levels to CW and carbohydrate and lower levels to lipoteichoic acid when compared with the antibody levels in rats given antigen alone. Rats orally immunized with either S. mutans WC or CW and MDP and challenged with virulent S. mutans 6715 exhibited significantly (P less than or equal to 0.05) lower plaque scores, numbers of viable S. mutans in plaque, and caries scores than did rats immunized with antigen alone or in infected-only controls. In another series of experiments, a PG fraction derived from S. mutans 6715 CW was assessed for adjuvant properties. The oral administration of PG and either S. mutans WC or CW induced good salivary and serum IgA antibody responses. The specificity of the antibodies was similar to that obtained in rats given antigen and MDP. Rats receiving either S. mutans WC or CW and PG and challenged with virulent S. mutans 6715 had lower plaque scores, fewer numbers of viable S. mutans in plaque, and lower caries activity than did infected rats receiving S. mutans WC or CW immunogen alone. These results provide evidence that soluble adjuvants derived from the gram-positive bacterial CW, e.g., MDP and PG, are effective oral adjuvants and augment IgA immune responses to particulate S. mutans antigens which are protective against the mucosally associated disease, dental caries.     

Responses of dairy cows supplemented with somatotropin during weeks 5 through 43 of lactation

Beginning at wk 5 of lactation, 136 cows (34 per treatment) were supplemented daily for 38 wk with 0, 10.3, 20.6, or 41.2 mg of recombinantly derived bST monomer. Cows were obtained from University of Kentucky, University of Minnesota, University of Pennsylvania, and The Ohio State University. Nine cows (4 at 0 mg/d, 1 at 10.3 mg/d, 1 at 20.6 mg/d, and 3 at 41.2 mg/d) did not complete the experiment because of health problems. Data from these cows were included in the reproduction and health databases but not in the production database. Cows supplemented with bST produced more milk, consumed more feed, had lower rates of BW gain, and had improved efficiencies of milk production (conversion of feed and NEL to milk). Additional increases in productivity were modest at 20.6 and 41.2 mg/d versus productivity at 10.3 mg/d of bST. Concentrations of fat, protein, and TS in milk were unaffected. At 10.3 mg/d, bST did not adversely affect reproduction or health.     

Cu/low-k dielectric TDDB reliability issues for advanced CMOS technologies

With the wide application of low-k and ultra-low-k dielectric materials at the 90 nm technology node and beyond, the long-term reliability of such materials is rapidly becoming a critical challenge for technology qualification. Low-k time-dependent dielectric breakdown (TDDB) is usually considered as one of the most important reliability issues during Cu/low-k technology development because low-k materials generally have weaker intrinsic breakdown strength than traditional SiO₂ dielectrics. This problem is further exacerbated by the aggressive shrinking of the interconnect pitch size due to continuous technology scaling. In this paper, three critical issues of low-k TDDB characteristics during low-k development and qualification will be reviewed. In the first part, a low-k TDDB field acceleration model and its determination will be discussed. In the second part, low-k dielectric time-to-breakdown (t_BD) statistical distribution and TDDB area scaling law for reliability projection will be examined. In the last part, as low-k TDDB has been found to be sensitive to all aspects of integration, the effects of process variations on low-k TDDB degradation will be demonstrated. Some key aspects which need to be carefully addressed to control overall low-k TDDB performance from process and integration side will be discussed.     

Environmentally Friendly Radiation Hard d-Limonene and Laccol Copolymers Synthesized via Cationic Copolymerization

In the modern world, petroleum-based synthetic polymers have a great number of applications in fields ranging from food packaging to space travel. However, the processing of petroleum products and the resulting depletion of fossil fuels are major environmental concerns in today's society. As a result, the development of sustainable polymers which are made up of renewable resources and waste products is an immerging area of research. Considering the world food production, citrus fruit is most abundant and its contribution to waste generation is immense. Therefore, this study focuses on offering an alternative to the use of petroleum-based polymers and also providing a regulatory pathway to manage citrus waste by developing novel copolymers of laccol and limonene. Two environmentally friendly compounds, laccol, derived from the sap of Toxicodendron succedaneum tree and limonene, extracted from orange peels, were copolymerized via cationic polymerization to generate d-limonene:laccol copolymers with radiation hardening capabilities which is relevant in fields such as nuclear energy generation, medicinal sterilization, commercial irradiation, and space exploration. Formation of these copolymers was verified with infrared and nuclear magnetic resonance analysis. The synthesized copolymers were characterized using different methods and exposed to Co-60 gamma radiation to identify alterations to their properties. POLYM. ENG. SCI., 60:607–618, 2020. © 2019 Society of Plastics Engineers     

Thermal analysis of novel underfill materials with optimum processing characteristics

This work encompasses the development of low‐viscosity cyclic oligomer underfill formulations that cure without heat evolution. Boron nitride, silica‐coated aluminum nitride, and alumina ceramic powders were used as fillers in cyclic butylene terephthalate oligomer melts. The melts were heated with a suitable catalyst to induce polymerization. The effects of the filler type and composition on the thermal and mechanical properties of the poly(butylene terephthalate)/filler composites were examined with differential scanning calorimetry, temperature‐modulated differential scanning calorimetry, thermogravimetric analysis, thermomechanical analysis, and dynamic mechanical analysis. Scanning electron microscopy was employed to elucidate the morphology of these composites. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 1300–1307, 2005     

Dielectric properties of PMMA/Soot nanocomposites

Dielectric analysis (DEA) of relaxation behavior in poly(methyl methacrylate) (PMMA) soot nanocomposites is described herein. The soot, an inexpensive material, consists of carbon nanotubes, amorphous and graphitic carbon and metal particles. Results are compared to earlier studies on PMMA/multi-walled nanotube (MWNT) composites and PMMA/single-walled nanotube (SWNT) composites. The beta relaxation process appeared to be unaffected by the presence of the soot, as was noted earlier in nanotube composites. The gamma relaxation region in PMMA, normally dielectrically inactive, was "awakened" in the PMMA/soot composite. This occurrence is consistent with previously published data on nanotube composites. The dielectric permittivity, s', increased with soot content. The sample with 1% soot exhibited a permittivity (at 100 Hz and 25 degrees C) of 7.3 as compared to 5.1 for neat PMMA. Soot increased the dielectric strength, deltaE, of the composites. The 1% soot sample exhibited a dielectric strength of 6.38, while the neat PMMA had a value of 2.95 at 40 degrees C. The symmetric broadening term (alpha) was slightly higher for the 1% composite at temperatures near the secondary relaxation and near the primary relaxation, but all samples deviated from symmetrical semi-circular behavior (alpha = 1). The impact of the soot filler is seen more clearly in dielectric properties than in mechanical properties studies conducted earlier.     

Evaluation of the MMCLIFE 3.0 code in predicting crack growth in titanium aluminide composites

Crack growth and fatigue life predictions made with the MMCLIFE 3.0 code are compared to test data for unidirectional, continuously reinforced SCS-6/Ti-14Al-21Nb (wt pct) composite laminates. The MMCLIFE 3.0 analysis package is a design tool capable of predicting strength and fatigue performance in metal matrix composite (MMC) laminates. The code uses a combination of micromechanic lamina and macromechanic laminate analyses to predict stresses and uses linear elastic fracture mechanics to predict crack growth. The crack growth analysis includes a fiber bridging model to predict the growth of matrix flaws in 0-deg laminates and is capable of predicting the effects of interfacial shear stress and thermal residual stresses. The code has also been modified to include edge-notch flaws in addition to center-notch flaws. The model was correlated with constant amplitude, isothermal data from crack growth tests conducted on 0- and 90-deg SCS-6/Ti-14-21 laminates. Spectrum fatigue tests were conducted, which included dwell times and frequency effects. Strengths and areas for improvement for the analysis are discussed. This article is based on a presentation made in the symposium “Fatigue and Creep of Composite Materials” presented at the TMS Fall Meeting in Indianapolis, Indiana, September 14–18, 1997, under the auspices of the TMS/ASM Composite Materials Committee.     

A linkage moment approach to modeling condensation polymerization with multiple monomers. I. Linear polymers

In recent years, industrial interest in condensation copolymers with controlled microstructures has been increasing as these systems add an additional dimension to the design and manipulation of product properties without requiring completely new routes for monomer or polymer synthesis. The techniques used to control the compositional microstructure in condensation systems differ greatly from those in vinyl polymerization, as condensation polymers are continuously broken apart and reformed during the course of the polymerization. Blocky copolymers may be produced in a melt blending process only by limiting the contact time at reaction temperatures because the ultimate result of the polymerization and interchange reactions is complete randomization of the copolymer with a structure similar to that obtained in vinyl polymerization with all reactivity ratios equal to one. The design of processes yielding the desired product microstructure therefore requires a quantitative understanding of the effect of each reaction on the copolymer composition. As typical copolymer recipes include multiple monomers with different functionalities, in this paper a general copolycondensation model is presented that can accommodate an arbitrary number of monomers of differing reactivities. In this paper, only monofunctional and bifunctional monomers are considered; the extension to the case of gelating systems is left for a future paper. The use of this framework and the validity of the approach is demonstrated for an example situation in which a polyarylate is melt blended with PBT to produce a copolymer whose average sequence length may be controlled by limiting the extent of reaction. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 79: 246–265, 2001     

Modeling of solid-state polycondensation. II. Reactor design issues

The relative merits of the moving packed bed, fluidized bed, and stirred bed reactors for solid-state polycondensation are discussed along with methods for improving these designs. A general model to describe continuous solid-state polymerization reactors is then developed and illustrated by a case study of a moving packed bed reactor showing the relative importance of operating variables. The model also predicts the dynamic behavior in response to several process inputs. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 69: 1775–1788, 1998     

An empirical correlation between glass transition temperatures and structural parameters for polymers with linear and branched alkyl substituents

A new quantitative model is proposed to correlate glass transition temperatures with bond radii-based structural parameters for poly(p-alkyl styrenes), poly-olefins, poly(alkyl methacrylates), and poly(alkyl acrylates). The model provides a consistent prediction of the glass transition temperatures for both the linear and highly branched polymers up to the entanglement offset points for long side groups. Polymers with highly branched side chains, such as t-butyl and t-pentyl groups that contain quaternary C groups, are predicted to have much higher glass transition temperatures, followed by the methylated, the unsubstituted, and the linearly alkylated polymers. The predictions are confirmed by the experimental results from the authors' research and literature. The current model also allows the extraction of the contribution of hydrogen bonding to glass transition temperatures in polymethacrylates and polyacrylates by comparing differences between the modeled hydrogen-bonding free values with the experimental data. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 64: 507–517, 1997