Non-Abelian Parton Fractional Quantum Hall Effect in Multilayer Graphene.

The current proposals for producing non-Abelian anyons and Majorana particles, which are neither fermions nor bosons, are primarily based on the realization of topological superconductivity in two dimensions. We show theoretically that the unique Landau level structure of bilayer graphene provides a new possible avenue for achieving such exotic particles. Specifically, we demonstrate the feasibility of a "parton" fractional quantum Hall (FQH) state, which supports non-Abelian particles without the usual topological superconductivity. Furthermore, we advance this state as the fundamental explanation of the puzzling 1/2 FQH effect observed in bilayer graphene [ Kim et al. Nano Lett. 2015 , 15 , 7445 ] and predict that it will also occur in trilayer graphene. We indicate experimental signatures that differentiate the parton state from other candidate non-Abelian FQH states and predict that a transverse electric field can induce a topological quantum phase transition between two distinct non-Abelian FQH states.

Congenital Perisylvian Syndrome presenting as Post-partum Seizures with Preeclampsia.

Whether preceded by preeclampsia, or occuring without antecedent warning symptoms, eclamptic seizures usually occur in the antepartum period between 20 and 40 weeks of gestation or within a few hours to 2 days postpartum. We report the case of a patient with pre-eclampsia who developed seizures after more than 2 days of delivery. In view of late onset postpartum seizures and non-responsiveness to magnesium sulphate, she was further evaluated and diagnosed to have congenital perisylvian syndrome(CPS). In CPS, polymicrogyric cortex is distributed in variable extensions around the sylvian fissure i.e. a structural malformation of the brain with underlying anomaly of polymicrogyria.

Single-fluxon controlled resistance switching in centimeter-long superconducting gallium-indium eutectic nanowires.

The ability to manipulate a single quantum object, such as a single electron or a single spin, to induce a change in a macroscopic observable lies at the heart of nanodevices of the future. We report an experiment wherein a single superconducting flux quantum, or a fluxon, can be exploited to switch the resistance of a nanowire between two discrete values. The experimental geometry consists of centimeter-long nanowires of superconducting Ga-In eutectic, with spontaneously formed Ga nanodroplets along the length of the nanowire. The nonzero resistance occurs when a Ga nanodroplet traps one or more superconducting fluxons, thereby driving a Josephson weak-link created by a second nearby Ga nanodroplet normal. The fluxons can be inserted or flipped by careful manipulation of the magnetic field or temperature to produce one of many metastable states of the system.

Enigmatic 4/11 state: a prototype for unconventional fractional quantum Hall effect.

The origin of the fractional quantum Hall effect (FQHE) at 4/11 and 5/13 has remained controversial. We make a compelling case that the FQHE is possible here for fully spin polarized composite fermions, but with an unconventional underlying physics. Thanks to a rather unusual interaction between composite fermions, the FQHE here results from the suppression of pairs with a relative angular momentum of three rather than one, confirming the exotic mechanism proposed by Wójs, Yi, and Quinn [Phys. Rev. B 69, 205322 (2004)]. We predict that the 4/11 state reported a decade ago by Pan et al. [Phys. Rev. Lett. 90, 016801 (2003)] is a conventional partially spin polarized FQHE of composite fermions, and we estimate the Zeeman energy where a phase transition into the unconventional fully spin polarized state will occur.

Phase diagram of the two-component fractional quantum Hall effect.

We calculate the phase diagram of the two component fractional quantum Hall effect as a function of the spin or valley Zeeman energy and the filling factor, which reveals new phase transitions and phase boundaries spanning many fractional plateaus. This phase diagram is relevant to the fractional quantum Hall effect in graphene and in GaAs and AlAs quantum wells, when either the spin or valley degree of freedom is active.

Competing crystal phases in the lowest Landau level.

We show that the solid phase between the 1/5 and 2/9 fractional quantum Hall states arises from an extremely delicate interplay between type-1 and type-2 composite fermion crystals, clearly demonstrating its nontrivial, strongly correlated character. We also compute the phase diagram of various crystals occurring over a wide range of filling factors and demonstrate that the elastic constants exhibit nonmonotonic behavior as a function of the filling factor, possibly leading to distinctive experimental signatures that can help mark the phase boundaries separating different kinds of crystals.

Role of exciton screening in the 7/3 fractional quantum Hall effect.

The excitations of the 7/3 fractional Hall state, one of the most prominent states in the second Landau level, are not understood. We study the effect of screening by composite fermion excitons and find that it causes a strong renormalization at 7/3, thanks to a relatively small exciton gap and a relatively large residual interaction between composite fermions. The excitations of the 7/3 state are to be viewed as composite fermions dressed by a large exciton cloud. Their wide extent has implications for experiments as well as for analysis of finite system exact diagonalization studies.

Possible anti-Pfaffian pairing of composite fermions at ν = 3/8.

We predict that an incompressible fractional quantum Hall state is likely to form at ν = 3/8 as a result of a chiral p-wave pairing of fully spin polarized composite fermions carrying four quantized vortices, and that the pairing is of the anti-Pfaffian kind. Experimental ramifications include quasiparticles with non-Abelian braid statistics and upstream neutral edge modes.

Synthesis, characterization and evaluation of mannich bases as potent antifungal and hydrogen peroxide scavenging agents.

In the present study, (E)-2-{ [-2-(2,4-Dinitrophenyl)hydrazono]methyl} phenol (3) was synthesized and used as key intermediate for the synthesis of new Mannich bases. All the synthesized compounds were evaluated for their antifungal activity against three fungal strains Candida albicans, Candida tropicalis and Aspergillus niger and antioxidant activity. The structure of these compounds was confirmed by IR, 1H NMR and 13C NMR studies. Most of the compounds exhibited moderate to significant activities.

Capacity Building for Vaccine Manufacturing Across Developing Countries: The Way Forward.

Approved vaccines prevent 2 to 3 million deaths per year. There is a lack of equitable access to vaccines in the low- and middle-income developing nations. Challenges in the life cycle of vaccine production include process development, lead time, intellectual property, and local vaccine production. A robust and stable manufacturing process and constant raw material supplies over decades is critical. In a continuously evolving vaccine landscape, the need of the hour for developing nations is to manufacture their own vaccines besides having supply security, control over production scheduling and sustainability, control of costs, socio-economic development, and rapid response to local epidemics. There is a need for capacity building of workforce development, technology transfer, and financial support. Technology transfer has improved vaccine access and reduced prices of vaccines. Capacity building for the manufacturing of vaccines in developing countries has always been an area of paramount importance and more so in a pandemic situation.

Higher-energy composite fermion levels in the fractional quantum Hall effect.

Even though composite fermions in the fractional quantum Hall liquid are well established, it is not yet known up to what energies they remain intact. We probe the high-energy spectrum of the 1/3 liquid directly by resonant inelastic light scattering, and report the observation of a large number of new collective modes. Supported by our theoretical calculations, we associate these with transitions across two or more composite fermions levels. The formation of quasiparticle levels up to high energies is direct evidence for the robustness of topological order in the fractional quantum Hall effect.

Landau-level mixing and the emergence of Pfaffian excitations for the 5/2 fractional quantum Hall effect.

We report on exact diagonalization studies for fully spin polarized 5/2 fractional quantum Hall effect, incorporating Landau-level mixing through the Bishara-Nayak effective interaction. We find that there is an experimentally accessible region in the phase diagram where the Pfaffian model accurately describes not only the ground state but also the neutral and charged excitations. These results are consistent with the observed persistence of the 5/2 Hall effect down to very low magnetic fields; they are also relevant to the experimental attempts to detect non-Abelian braid statistics.

Global phase diagram of the fractional quantum Hall effect arising from repulsive three-body interactions.

The model of fermions in a magnetic field interacting via a purely three-body repulsive interaction has attracted interest because it produces, in the limit of short range interaction, the Pfaffian state with non-Abelian excitations. We show that this is part of a rich phase diagram containing a host of fractional quantum Hall states, a composite fermion Fermi sea, and a pairing transition. This is entirely unexpected, because the appearance of composite fermions and fractional quantum Hall effect is ordinarily thought to be a result of strong two-body repulsion. Recent breakthroughs in ultracold atoms have facilitated the realization of such a system, where this physics can be tested.

Design, Synthesis and Anticancer Activity of Site Specific Short Chain Cationic Peptide.

BACKGROUND: In spite of current progress in treatment methods, cancer is a major source of morbidity and death rate all over the world. Traditional chemotherapeutic agents aim to divide cancerous cells, are often associated with deleterious side effects to healthy cells and tissues. Host defense peptides Cecropin A and B obtained from insects are capable to lyses various types of human cancer cells at peptide concentrations which are not fatal to normal eukaryotic cells. METHODS: In the present work we have designed short chain α-helical linear and cyclic peptide from cecropin A having same cationic charge, hydrophobicity and helicity. Synthesis of designed novel short chain linear (10) and cyclic compound (12) was accomplished by using solution phase method. All the coupling reactions were carried out by using dicyclohexylcarbodiimide (DCC) as the coupling reagent at room temperature in the presence of N-methylmorpholine (NMM) as the base. The Structure of newly synthesized peptidse were elucidated by 1H-NMR, 13C-NMR, FT-IR, FABMS and elemental analysis data.Cytotoxicity of synthesized compound was tested against Dalton's Lymphoma Ascites (DLA), Ehrlich's Ascites Carcinoma (EAC) and MCF-7 cell lines by using MTT assay and 5-FU as reference compound. RESULT: From biological assessment,it was found that short chain cyclicpeptide12 showed high level of cytotoxic activity against DLA and EAC cell lines. CONCLUSION: By utilizing a structure-based rational approach to anticancer peptide design from cecropin A, we were able to develop short chain linear and cyclic peptides having same charge, hydrophobicity and with improved activity. Systematically removing amino acids, we were able to retaining peptide charge and hydrophobicity/hydrophilicity in linear and cyclic peptide which results to optimize the anticancer activity against DLA and EAC cell lines.

Screening of Some Novel 4, 5 Disubstituted 1, 2, 4-Triazole-3-thiones for Anticonvulsant Activity.

OBJECTIVE: In the present study, we synthesized fifteen 4, 5-disubstituted 1, 2, 4-triazol- 3-thione derivatives and evaluated for anticonvulsant activity with neurotoxicity determination. METHODS: The synthesized compounds were characterized using FTIR, 1H-NMR and MS. The molecular docking study was also performed to study the interactions of compounds with LYS329 residue of gamma amino butyric acid aminotransferase (GABA-AT) using Autodock 4.2 software. The anticonvulsant activity was assessed by maximal electroshock (MES) test and subcutaneous pentylenetetrazol (scPTZ) tests. The neurotoxicity was assessed by rotarod ataxia test. RESULTS: In MES test, compounds 5a, 8a and 9a were found active at 100 mg/kg and five compounds were found active at 300 mg/kg dose after 1 hr of administration. After 4 hr of drug administration, only two compounds 8a and 9a exhibited protection at 100 mg/kg. In scPTZ test, three compounds 2a, 6a and 8a were found active at 100 mg/kg and 7a was active at 300 mg/kg after 1 hr of test drug administration. Most of the compounds were found active in MES test with 8a and 9a being the most active among all. In docking study, 2a was found to be best compound based on the binding energy of -6.5 kcal/mol and estimated inhibition constant of 17.2 µM. CONCLUSION: Majority of synthesized compounds were found active in MES test, whereas only few were found to possess anti scPTZ activity. Among all compounds, only 14a caused motor coordination impairment in rotarod ataxia test at 300 mg/kg 1 hr duration.

Design, Synthesis and Biological Activity of Some 4, 5-Disubstituted-2, 4- Dihydro-3H-1, 2, 4- Triazole-3-Thione Derivatives.

BACKGROUND: In the present study, 4, 5-disubstituted triazol-3-thione derivatives were synthesized and evaluated for anticonvulsant activity along with neurotoxicity determination. MATERIALS AND METHODS: The synthesized compounds were characterized using FTIR, 1H-NMR and MS. The anticonvulsant activity was assessed by Maximal Electroshock (MES) test and subcutaneous Pentylenetetrazole (scPTZ) tests and neurotoxicity was assessed by rotarod test. Docking was also performed to study the interactions of compounds with LYS329 residue of gamma amino butyric acid aminotransferase (GABA-AT) using Autodock 4.2 software. RESULTS: The compounds 7a and 9a with significant pharmacological activity were also found to interact with LYS329 residue of GABA-AT by H-bond with a docking score of -5.92 kcal/mol (Ki = 41.99 µM) and -5.87 kcal/mol (Ki = 49.83 µM) respectively. CONCLUSION: Most of the compounds were found to be active in MES test but only seven showed protection in scPTZ test.

Simultaneous determination of multi drug components Theophylline, Etofylline, Guaiphenesine and Ambroxol Hydrochloride by validated RP-HPLC method in liquid dosage form.

The RP-HPLC (reverse phase high performance liquid chromatography) method was developed and validated for simultaneous determination of Multi drug components i.e., Theophylline, Etofylline, Guaiphenesine and Ambroxol Hydrochloride in a liquid dosage form. Chromatographic separation of the four drugs was performed on a Hypersil Phenyl BDS (25cmX4.6mm, 5mm). The mobile phase constituted of triethylamine pH 3.0 buffer: methanol (85:15) v/v was delivered at the flow rate 1.5 mL/min. Detection was performed at 235 nm. The peak purity of Theophylline, Etofylline, Guaiphenesine and Ambroxol Hydrochloride were 0.99970, 0.99979, 0.99986 and 0.99949 respectively. Calibration curves were linear with correlation coefficient between 0.99995 to 0.99997 over a concentration range of 5 to 37 microg/mL for Theophylline, 19 to 140 microg/mL for Etofylline, 20 to 149 microg/mL for Guaiphenesine and 6 to 45 microg/mL for Ambroxol hydrochloride. The relative standard deviation (RSD) was found < 2.0%. The percentage recovery was found between the range of 98.6% and 100.5% at three different levels. Robustness and ruggedness were performed and result found within the RSD of 2%. All the parameters of validation were found in the acceptance range of ICH guideline.

Multiple genus-specific markers in PCR assays improve the specificity and sensitivity of diagnosis of brucellosis in field animals.

Brucella-specific nucleotide sequences encoding the BCSP 31 kDa protein, Omp2 and the 16S rRNA were employed in three independent diagnostic PCR assays. Results of the three PCR assays on six reference strains of Brucella were in complete agreement. The results of PCR assays based on bcsp and omp2 on 19 Indian field isolates (human, bovine and murine tissues) also agreed completely. However, when the 16S rRNA gene was employed as the diagnostic target in the PCR, only 14 out of these 19 isolates and 2 out of 7 bovine milk isolates were identified as the genus Brucella. The bovine blood samples were insensitive to 16S rRNA PCR. The antibody-detecting ELISA results of field samples (n=87) from a serologically positive herd in India were compared separately with omp2 and bcsp PCRs of blood (n=62). While the bcsp PCR was the most sensitive, the degree of association of ELISA with omp2 blood PCR (kappa=0.37 at P <0.05) was similar to that with the bcsp blood PCR (kappa =0.34 at P <0.05). An improvement in the correlation between ELISA and blood PCR was noticed (kappa =0.5 at P <0.05) when a consensus result of omp2 and bcsp blood PCR was considered for comparison with ELISA. The use of more than one marker-based PCR gave increased sensitivity and higher specificity and appears to be a more reliable molecular diagnostic approach for screening of field animals.

In silico validation and structure activity relationship study of a series of pyridine-3-carbohydrazide derivatives as potential anticonvulsants in generalized and partial seizures.

A series of twelve compounds (Compounds RNH1-RNH12) of acid hydrazones of pyridine-3-carbohydrazide or nicotinic acid hydrazide was synthesized and evaluated for anticonvulsant activity by MES, scPTZ, minimal clonic seizure and corneal kindling seizure test. Neurotoxicity was also determined for these compounds by rotarod test. Results showed that halogen substitution at meta and para position of phenyl ring exhibited better protection than ortho substitution. Compounds RNH4 and RNH12, were found to be the active analogs displaying 6Hz ED50 of 75.4 and 14.77 mg/kg while the corresponding MES ED50 values were 113.4 and 29.3 mg/kg respectively. In addition, compound RNH12 also showed scPTZ ED50 of 54.2 mg/kg. In the series, compound RNH12 with trifluoromethoxy substituted phenyl ring was the most potent analog exhibiting protection in all four animal models of epilepsy. Molecular docking study has also shown significant binding interactions of these two compounds with 1OHV, 2A1H and 1PBQ receptors. Thus, N-[(meta or para halogen substituted) benzylidene] pyridine-3-carbohydrazides could be used as lead compounds in anticonvulsant drug design and discovery.

Synthesis, characterization of (Z)-N-(1-(2-(2-amino-3-(dimethylamino) methyl)phenyl)-5-phenyl-1,3,4, oxadiazol-3(2H)-yl)ethanone analogs as potent antimicrobial and hydrogen peroxide scavenging agents.

A series of (Z)-N-(1-(2-(2-amino-3-((dimethylamino) methyl) phenyl)-5-phenyl-1,3,4,oxadiazol-3(2H)- yl)ethanone derivatives was prepared and studied for its antimicrobial and antioxidant activities. Among the synthesized derivatives, compounds (7c) (Z)-N-(1-(2-(2-amino-3-((dimethylamino)methyl)phenyl)-5-phenyl-1,3,4-oxadiazol-3(2H)- yl)ethylidene)-4-chloroaniline, (7g) (Z)-N-(1-(2-(2-amino-3-((dimethylamino)methyl)phenyl)-5-phenyl-1,3,4-oxadiazol- 3(2H)-yl)ethylidene)-4-nitroaniline and (7i) (Z)-N-(1-(2-(2-amino-3-((dimethylamino)methyl)phenyl)-5-phenyl-1,3,4- oxadiazol-3(2H)-yl)ethylidene)-4-methoxyaniline were found to be the most effective antimicrobial compounds. While the compounds 7c and 7g were the most potent antioxidant compounds with significant hydrogen peroxide scavenging activity.