Superfield Approach to Nilpotency and Absolute Anticommutativity of Conserved Charges: 2D non-Abelian 1-Form Gauge Theory

We exploit the theoretical strength of augmented version of superfield approach (AVSA) to Becchi-Rouet-Stora-Tyutin (BRST) formalism to express the nilpotency and absolute anticommutativity properties of the (anti-)BRST and (anti-)co-BRST conserved charges for the two $(1+1)$-dimensional (2D) non-Abelian 1-form gauge theory (without any interaction with matter fields) in the language of superspace variables, their derivatives and suitable superfields. In the proof of absolute anticommutativity property, we invoke the strength of Curci-Ferrari (CF) condition for the (anti-)BRST charges. No such outside condition/restriction is required in the proof of absolute anticommutativity of the (anti-)co-BRST conserved charges. The latter observation (as well as other observations) connected with (anti-)co-BRST symmetries and corresponding conserved charges are novel results of our present investigation. We also discuss the (anti-)BRST and (anti-)co-BRST symmetry invariance of the appropriate Lagrangian densities within the framework of AVSA. In addition, we dwell a bit on the derivation of the above fermionic (nilpotent) symmetries by applying the AVSA to BRST formaism where only the (anti-)chiral superfields are used.Comment: LaTeX file, 33 pages, journal referenc

Modified 2D Proca Theory: Revisited Under BRST and (Anti-)Chiral Superfield Formalisms

Within the framework of Becchi-Rouet-Stora-Tyutin (BRST) approach, we discuss mainly the fermionic (i.e. off-shell nilpotent) (anti-)BRST, (anti-)co-BRST and some discrete dual-symmetries of the appropriate Lagrangian densities for a two (1+1)-dimensional (2D) modified Proca (i.e. a massive Abelian 1-form) theory without any interaction with matter fields. One of the novel observations of our present investigation is the existence of some kinds of restrictions in the case of our present St\"{u}ckelberg-modified version of the 2D Proca theory which is not like the standard Curci-Ferrari (CF)-condition of a non-Abelian 1-form gauge theory. Some kinds of similarities and a few differences between them have been pointed out in our present investigation. To establish the sanctity of the above off-shell nilpotent (anti-)BRST and (anti-)co-BRST symmetries, we derive them by using our newly proposed (anti-)chiral superfield formalism where a few specific and appropriate sets of invariant quantities play a decisive role. We express the (anti-)BRST and (anti-)co-BRST conserved charges in terms of the superfields that are obtained after the applications of (anti-)BRST and (anti-)co-BRST invariant restrictions and prove their off-shell nilpotency and absolute anticommutativity properties, too. Finally, we make some comments on (i) the novelty of our restrictions/obstructions, and (ii) the physics behind the negative kinetic term associated with the pseudo-scalar field of our present theory.Comment: LaTeX file, 58 pages, Journal reference give

Antipseudomonal property of honey and aminoglycosides

Pseudomonas aeruginosa has an ability to rapidly develop resistance to most antimicrobial compounds, and to check this ability. The isolates were collected from different pathological human sources and tested for their sensitivity to aminoglycoside antibiotic and to honey, a natural product that is generating renewed interest for its therapeutic application using Kirby Bauer disc diffusion technique. Aminoglycoside antibiotic which is normally active against gram-negative bacteria was used alongside honey. The 29 isolates of P. aeruginosa showed 100%sensitivity to honey tested in their undiluted form. This was not the case with gentamicin (10?g) and amikacin (30 ?g), both of which varied in their antipseudomonal activity, like even 1:2 aqueous dilution of honey appreciably inhibited pseudomonal isolates than either of the two aminoglycoside antibiotic. Honey is therefore suggested as an effective natural product in overcoming the widespread antibiotic resistance of P. aeruginosa

Two Gallium data sets, spin flavour precession and KamLAND

We reexamine the possibility of a time modulation of the low energy solar neutrino flux which is suggested by the average decrease of the Ga data in line with our previous arguments. We perform two separate fits to the solar neutrino data, one corresponding to 'high' and the other to 'low' Ga data, associated with low and high solar activity respectively. We therefore consider an alternative to the conventional solar+KamLAND fitting, which allows one to explore the much wider range of the $\theta_{12}$ angle permitted by the KamLAND fitting alone. We find a solution with parameters $\Delta m^2_{21}=8.2\times 10^{-5} eV^2, tan^{2}\theta=0.31$ in which the 'high' and the 'low' Ga rates lie far apart and are close to their central values and is of comparable quality to the global best fit, where these rates lie much closer to each other. This is an indication that the best fit in which all solar and KamLAND data are used is not a good measure of the separation of the two Ga data sets, as the information from the low energy neutrino modulation is dissimulated in the wealth of data. Furthermore for the parameter set proposed one obtains an equally good fit to the KamLAND energy spectrum and an even better fit than the 'conventional' LMA one for the reactor antineutrino survival probability as measured by KamLAND.Comment: V2: 15 pages, 3 eps figures, fit improved, final version to appear in Journal of Physics

Predictions from non trivial Quark-Lepton complementarity

The complementarity between the quark and lepton mixing matrices is shown to provide robust predictions. We obtain these predictions by first showing that the matrix V_M, product of the quark (CKM) and lepton (PMNS) mixing matrices, may have a zero (1,3) entry which is favored by experimental data. We obtain that any theoretical model with a vanishing (1,3) entry of V_M that is in agreement with quark data, solar, and atmospheric mixing angle leads to $\theta_{13}^{PMNS}=(9{^{+1}_{-2}})^\circ$. This value is consistent with the present 90% CL experimental upper limit. We also investigate the prediction on the lepton phases. We show that the actual evidence, under the only assumption that the correlation matrix V_M product of CKM and PMNS has a zero in the entry (1,3), gives us a prediction for the three CP-violating invariants J, S_1, and S_2. A better determination of the lepton mixing angles will give stronger prediction for the CP-violating invariants in the lepton sector. These will be tested in the next generation experiments. Finally we compute the effect of non diagonal neutrino mass in "l_i -> l_j gamma" in SUSY theories with non trivial Quark-Lepton complementarity and a flavor symmetry. The Quark-Lepton complementarity and the flavor symmetry strongly constrain the theory and we obtain a clear prediction for the contribution to "mu -> e gamma" and the "tau" decays "tau -> e gamma" and "tau -> mu gamma". If the Dirac neutrino Yukawa couplings are degenerate but the low energy neutrino masses are not degenerate, then the lepton decays are related among them by the V_M entries. On the other hand, if the Dirac neutrino Yukawa couplings are hierarchical or the low energy neutrino masses are degenerate, then the prediction for the lepton decays comes from the CKM hierarchy.Comment: 15 pages, 5 figures, ws-ijmpa class included, Proceedings of the CTP Symposium on Sypersymmetry at LH

QQˉQ\bar Q (Q∈{b,c}Q\in \{b, c\}) spectroscopy using Cornell potential

The mass spectra and decay properties of heavy quarkonia are computed in nonrelativistic quark-antiquark Cornell potential model. We have employed the numerical solution of Schr\"odinger equation to obtain their mass spectra using only four parameters namely quark mass ($m_c$, $m_b$) and confinement strength ($A_{c\bar c}$, $A_{b\bar b}$). The spin hyperfine, spin-orbit and tensor components of the one gluon exchange interaction are computed perturbatively to determine the mass spectra of excited $S$, $P$, $D$ and $F$ states. Digamma, digluon and dilepton decays of these mesons are computed using the model parameters and numerical wave functions. The predicted spectroscopy and decay properties for quarkonia are found to be consistent with available experimental observations and results from other theoretical models. We also compute mass spectra and life time of the $B_c$ meson without additional parameters. The computed electromagnetic transition widths of heavy quarkonia and $B_c$ mesons are in tune with available experimental data and other theoretical approaches

Niosomes as vesicular carriers for delivery of proteins and biologicals

Over the past several years, treatment of infectious diseases and immunization has undergone a paradigm shift. Stemming from the nanobiotechnology research, not only a large number of disease-specific biologicals have been developed, but also enormous efforts have been made to effectively deliver these biologicals. Niosomes are vesicular systems prepared from self-assembly of hydrated non-ionic surfactants. Opinions of the usefulness of niosomes in delivery of proteins and biologicals range from unsubstantiated optimism to undeserved pessimism. This article reviews the current deepening and widening of interest of niosomes in many scientific disciplines, and their application in medicine particularly for the delivery of proteins (insulin, cyclosporine, bacitracin, trypsin), vaccines and antigens (bovine serum albumin, antigen tetanus toxoid, haemagglutinin). This article also presents an overview of techniques of noisome preparation, characterization of niosomes and their applications.Keywords: Niosomes, Proteins, Biologicals, Vaccines, Oral deliver

Niosomes as vesicular carriers for delivery of proteins and biologicals

Over the past several years, treatment of infectious diseases and immunization has undergone a paradigm shift. Stemming from the nanobiotechnology research, not only a large number of disease-specific biologicals have been developed, but also enormous efforts have been made to effectively deliver these biologicals. Niosomes are vesicular systems prepared from self-assembly of hydrated non-ionic surfactants. Opinions of the usefulness of niosomes in delivery of proteins and biologicals range from unsubstantiated optimism to undeserved pessimism. This article reviews the current deepening and widening of interest of niosomes in many scientific disciplines, and their application in medicine particularly for the delivery of proteins (insulin, cyclosporine, bacitracin, trypsin), vaccines and antigens (bovine serum albumin, antigen tetanus toxoid, haemagglutinin). This article also presents an overview of techniques of noisome preparation, characterization of niosomes and their applications.Keywords: Niosomes, Proteins, Biologicals, Vaccines, Oral deliver