Wound healing efficacy of curcumin-loaded sandalwood bark-derived carbon nanosphere/PVA nanofiber matrix.

The present investigation deals with the evaluation of the wound healing efficacy of sandalwood bark-derived carbon nanospheres loaded with curcumin-embedded polyvinyl alcohol (PVA) nanofiber membranes (NF). Carbon nanospheres (CNS) were prepared by pyrolyzing sandal wood bark powder at 750 °C. The morphology was confirmed by field emission scanning electron micrographs and a rich amount of carbon was confirmed by the energy dispersive X-ray technique. Curcumin, an active wound healing drug was loaded onto synthesized CNS and confirmed by ATR-IR studies. Drug-loaded CNS were anchored in a PVA matrix via electrospun nanofiber fabrication. The fabricated nanofiber membranes were characterized and evaluated for wound healing efficiency. The cytotoxicity assay proved the non-toxic nature of the prepared PVA/CNS-curcumin-loaded NF. Membranes with active CNS/drug showed better antimicrobial activity against S. aureus and E. coli, which was estimated using the zone of inhibition (ZOI) test. The in vitro scratch wound healing assay of prepared PVA/CNS-curcumin nanofibers was efficient enough and showed 92 to 98% wound closure, which was greater than the control (without drug) nanofiber membranes. The PVA nanofiber matrix with interconnected structure and carbon nanostructures together enhanced the wound healing efficacy of the considered wound healing membrane, which is a promising novel approach for future wound healing patches.

Spectroscopic, crystal structure and DFT-assisted studies of some nickel(II) chelates of a heterocyclic-based NNO donor aroylhydrazone: in vitro DNA binding and docking studies.

Five new nickel(II) complexes have been synthesised with an NNO donor tridentate aroylhydrazone (HFPB) employing the chloride, nitrate, acetate and perchlorate salts, and all the complexes are physiochemically characterized. Elemental analyses suggested stoichiometries as Ni(FPB)(NO3)]·2H2O (1), [Ni(HFPB)(FPB)]Cl (2), [Ni(FPB)(OAc)(DMF)] (3), [Ni(FPB)(ClO4)]·DMF (4), [Ni(FPB)2] (5). Aroylhydrazone is found coordinating in deprotonated iminolate form in four of the complexes (1, 3, 4, 5) however in one case (complex 2), two aroylhydrazone moieties are binding to the metal centre in the neutral and anionic forms. The structure of the bisligated complex 5, found using single crystal X ray diffraction studies confirmed that the metal has a distorted octahedral N4O2 coordination environment, with each of the two deprotonated ligands coordinating through the pyridine nitrogen, imino-hydrazone nitrogen and the enolate oxygen of the hydrazone moiety. To compare and study, the electronic interactions and stabilities of the metal complexes, various quantum chemical parameters were calculated. Moreover, Hirshfeld surface analysis was carried out for complex 5 to determine the intermolecular interactions. The biophysical attributes of the ligand and complex 5 have been investigated with CT-DNA and experimental outcomes show that the Ni(II) complex exhibited higher binding propensity towards DNA as compared to ligand. Furthermore, to specifically understand the type of interactions of the metal complexes with DNA, molecular docking studies were effectuated. In addition, the electronic and related reactivity behaviors of the ligand and five Ni(II) complexes were studied using B3LYP/6-31 + + G**/LANL2DZ level. As expected, the obtained results from Natural Bond Orbital (NBO) computations displayed that the resonance interactions (n → π* and π → π*) play a determinant role in evaluating the chemical attributes of the reported compounds.

Stretchable Substrates for the Assembly of Polymeric Microstructures.

The directed assembly of micro-/nanoscale objects relies on physical or chemical processes to generate structures that are not possible via self-assembly alone. A relatively unexplored strategy in directed assembly is the "active" manipulation of building blocks through deformations of elastomeric substrates. This manuscript reports a method which uses macroscopic mechanical deformations of chemically modified silicone films to realize the rational assembly of microscopic polymer structures. Specifically, polystyrene microparticles are deposited onto polydimethylsiloxane substrates using microcontact-printing where, through a process that involved stretching/relaxing the substrates and bonding of the particles, they are elaborated into microstructures of various sizes, shapes, symmetries, periodicities, and functionalities. The resulting polymeric microstructures can be released and redeposited onto planar/nonplanar surfaces. When building blocks with different properties (e.g., those with fluorescent and catalytic properties) are used, it is possible to fabricate structures with heterogeneous functionality. This method can be extended to the assembly of numerous micro-/nanoscale building blocks (e.g., colloidal organic/inorganic materials) with rational control over the size, shape, and functionality of the product. As a strategy, the use of substrate deformations to enable the micromanipulation and fabrication of a potentially diverse set of assemblies represents a powerful tool useful to, for example, nanotechnology and micromanufacturing.

Correction: Stacking interactions by two Phe side chains stabilize and orient assemblies of even the minimal amphiphilic ß-sheet motif.

Correction for 'Stacking interactions by two Phe side chains stabilize and orient assemblies of even the minimal amphiphilic ß-sheet motif' by Shlomo Zarzhitsky et al., Chem. Commun., 2015, 51, 3154-3157.

Photocatalytic hybrid Au/ZnO nanoparticles assembled through a one-pot method.

Growth of metal domains on semiconductor nanoparticles is known to enhance their photocatalytic properties. We prepared ZnO nanoparticles decorated with metallic Au domains through a new one-pot microwave-based strategy. The synthetic route utilized microwave-heating of a mixture of only three components: Zn(2+) salt, Au(SCN)4(-) which served as a precursor for metallic gold, and Tris base. The Tris molecules had a dual role in the process, both shaping the morphology of the ZnO particles, as well as constituting docking and nucleation sites for the Au(SCN)4(-) ions. The Au complex subsequently underwent spontaneous crystallization/reduction without co-addition of reducing or stabilizing agents, yielding Au nanoparticles attached to the ZnO surface. We show that the hybrid Au/ZnO nanoparticles exhibited enhanced photocatalytic properties compared to the plain ZnO nanoparticles.

Unilamellar vesicles from amphiphilic graphene quantum dots.

Graphene quantum dots (GQDs) have attracted considerable interest due to their unique physicochemical properties and various applications. For the first time it is shown that GQDs surface-functionalized with hydrocarbon chains (i.e., amphiphilic GQDs) self-assemble into unilamellar spherical vesicles in aqueous solution. The amphiphilic GQD vesicles exhibit multicolor luminescence that can be readily exploited for membrane studies by fluorescence spectroscopy and microscopy. The GQD vesicles were used for microscopic analysis of membrane interactions and disruption by the peptide beta-amyloid.

Stacking interactions by two Phe side chains stabilize and orient assemblies of even the minimal amphiphilic ß-sheet motif.

Here we demonstrate that the smallest possible motif of the amphiphilic and pleated ß-strand structure can be generated using tri-peptides stabilized by π-π stacking interactions. Monitoring the early stages of Phe-Glu-Phe fibril formation revealed unique angular orientations. Phe-Glu-Phe fibrils were further exploited as adsorbing templates for metal ions.

Nanostructure synthesis at the solid-water interface: spontaneous assembly and chemical transformations of tellurium nanorods.

Bottom-up synthesis offers novel routes to obtain nanostructures for nanotechnology applications. Most self-assembly processes are carried out in three dimensions (i.e. solutions); however, the large majority of nanostructure-based devices function in two dimensions (i.e. on surfaces). Accordingly, an essential and often cumbersome step in bottom-up applications involves harvesting and transferring the synthesized nanostructures from the solution onto target surfaces. We demonstrate a simple strategy for the synthesis and chemical transformation of tellurium nanorods, which is carried out directly at the solid-solution interface. The technique involves binding the nanorod precursors onto amine-functionalized surfaces, followed by in situ crystallization/oxidation. We show that the surface-anchored tellurium nanorods can be further transformed in situ into Ag2Te, Cu2Te, and SERS-active Au-Te nanorods. This new approach offers a way to construct functional nanostructures directly on surfaces.

Poly(methyl methacrylate)-supported polydiacetylene films: unique chromatic transitions and molecular sensing.

Polydiacetylenes (PDAs) constitute a family of conjugated polymers exhibiting unique colorimetric and fluorescence transitions, and have attracted significant interest as chemo- and biosensing materials. We spin-coated PDA films upon poly(methyl methacrylate) (PMMA), and investigated the photophysical properties and sensing applications of the new PDA configuration. Specifically, the as-polymerized blue PDA layer underwent distinct transformations to purple, red, and yellow phases, which could be quantified through conventional color scanning combined with application of image analysis algorithms. Furthermore, we recorded a reversible red-purple PDA transition that was induced by ultraviolet irradiation, a phenomenon that had not been reported previously in PDA film systems. We show that distinct color and fluorescence transitions were induced in the PMMA-supported PDA films by amphiphilic substances-surfactants and ionic liquids-and that the chromatic transformations were correlated to the analyte structures and properties. Overall, this study presents a new chromatic PDA film system in which noncovalent interactions between the PMMA substrate and spin-coated PDA give rise to distinct chromatic properties and molecular sensing capabilities.

Nonplanar conductive surfaces via "bottom-up" nanostructured gold coating.

Development of technologies for the construction of bent, curved, and flexible conductive surfaces is among the most important albeit challenging goals in the promising field of "flexible electronics". We present a generic solution-based "bottom-up" approach for assembling conductive gold nanostructured layers on nonplanar polymer surfaces. The simple two-step experimental scheme is based upon incubation of an amine-displaying polymer [the abundantly used poly(dimethylsiloxane) (PDMS), selected here as a proof of concept] with Au(SCN)4(-), followed by a brief treatment with a conductive polymer [poly(3,4-thylenedioxythiophene)/poly(styrenesulfonate)] solution. Importantly, no reducing agent is co-added to the gold complex solution. The resultant surfaces are conductive and exhibit a unique "nanoribbon" gold morphology. The scheme yields conductive layers upon PDMS in varied configurations: planar, "wrinkled", and mechanically bent surfaces. The technology is simple, inexpensive, and easy to implement for varied polymer surfaces (and other substances), opening the way for practical applications in flexible electronics and related fields.

Transparent, conductive, and SERS-active Au nanofiber films assembled on an amphiphilic peptide template.

The use of biological materials as templates for functional molecular assemblies is an active research field at the interface between chemistry, biology, and materials science. We demonstrate the formation of gold nanofiber films on ß-sheet peptide domains assembled at the air/water interface. The gold deposition scheme employed a recently discovered chemical process involving spontaneous crystallization and reduction of water-soluble Au(SCN)4(1-) upon anchoring to surface-displayed amine moieties. Here we show that an interlinked network of crystalline Au nanofibers is readily formed upon incubation of the Au(iii) thiocyanate complex with the peptide monolayers. Intriguingly, the resultant films were optically transparent, enabled electrical conductivity, and displayed pronounced surface enhanced Raman spectroscopy (SERS) activity, making the approach a promising avenue for construction of nano-structured films exhibiting practical applications.

A novel aqueous phase synthetic route for CuInSe2 nanocrystals.

A novel aqueous phase synthetic route for CuInSe2 nanoparticles is presented. In our synthesis, the Se precursor used was Na2SeSO3 and CuI, while InCl3 were used as precursors for copper and indium, respectively. The reaction was performed in water under basic condition in the presence of thioglycolic acid (TGA). TGA has a crucial effect on the formation of CIS nanocrystals in aqueous media. With less amount of TGA compared to the optimum amount, only amorphous CIS was formed while larger amount caused the formation of Cu2-xSe crystals because TGA had a lower reactivity of In3+ to Se2- ion. The ratio of reagents used optimized the structure, while the composition and properties of the nanomaterials obtained were studied applying various techniques such as XRD, SEM, TEM, TG/DSC, and XPS.

Coagulation factor VII R353Q polymorphism and the risk of puerperal cerebral venous thrombosis.

Puerperal cerebral venous thrombosis (CVT) is a relatively common form of stroke in young women in India. The blood coagulation factor VII (FVII) R353Q polymorphism increases the risk for venous thrombosis. Our aim was to investigate the association of FVII R353Q polymorphism with the risk of puerperal CVT. A total of 100 women with puerperal CVT and 102 age-matched women without postpartum complications were investigated. FVII R353Q genotypes were identified using restriction fragment length polymorphism analysis. Our results showed that the homozygous FVII 353QQ genotype was present in 9% and 8% of patients and controls, respectively; and 42% of patients and 31.4% of controls had the heterozygous 353RQ genotype (odds ratio = 1.55, 95% confidence interval = 0.89-2.70; p = 0.243). Our findings suggest that the FVII R353Q polymorphism is not associated with increased risk for CVT occurring during the puerperal period in Indian women.

Postnatal variations in blood free and acylcarnitines.

BACKGROUND: Alteration in concentrations of blood carnitine and its esters are diagnostic of a number of inherited metabolic disorders. Acylcarnitine (AC) profiles of newborns obtained from dried blood spots by tandem mass spectrometric analysis are being used for the diagnosis of these disorders. There are no data of the postnatal variations of free carnitine (FC) and AC in Indian neonates. OBJECTIVES: Evaluation of postnatal variations in free and AC levels in newborns. METHODS: Blood FC and AC levels were evaluated in 2,727 healthy neonates of postnatal day 2-30 by electrospray ionization tandem mass spectrometry. RESULTS: Blood C2, C5DC, C16, C16:1, C18, C18:1, C18:2, and C18:OH carnitines were increased in groups A (aged 8-14 days) and B (aged 15-30 days), compared with the control group (aged 2-7 days), whereas C3, C4, C4OH, C6, C6DC, and C12 carnitines were increased only in group B. No sex-related differences were found except for C3DC, C4, and C5 carnitine concentrations, which were higher in female neonates. CONCLUSIONS: Our data can be used as a reference for the assessment of carnitine status in Indian newborns, hence reducing the risk of misdiagnosis of fatty acid oxidation disorders and organic acidemias during interpretation of the results of tandem mass spectrometry-based newborn screening.

Multisegmented Se-Te-Se hybrid nanowires: a building unit with inbuilt block and glue functionality.

A novel hybrid nanomaterial incorporating Te and Se components within a multisegmented nanowire morphology is synthesized through a facile aqueous phase reaction at room temperature. Te nanowires were used as templates to grow Se segments at their terminal locations. The Se-Te-Se structures obtained exhibit a self-organization property thereby enabling the formation of "nanotweezers" at elevated temperatures. The physical and chemical properties of its individual components are expected to provide interesting functionality and promising utility to these nanostructures. The inbuilt block and glue features associated with its components make it a potential building unit toward nanoarchitectures of higher sophistication.

Self-guided one-sided metal reduction in te nanowires leading to Au-Te matchsticks.

Highly anisotropic nanoscale structures are fundamentally important for understanding the properties of hybrid nanoscale systems and self-organization phenomena, but they are typically difficult to prepare experimentally. Hybrid Au and Te matchstick-like nanostructures, which display high structural anisotropy, were synthesized using small Au clusters as seeds. The matchsticks were found to be an exclusive product of this reaction. We hypothesize that the mechanism of the synthesis is based on self-directed site-specific reduction of Au ions due to the gradually increasing dipole moment facilitating this process on one side of Te nanorods, which is supported by quantum mechanical calculations.

The prothrombin gene G20210A variant and puerperal cerebral venous and sinus thrombosis in South Indian women.

Pregnancy and puerperium raise the risk of thrombotic events, and these risks are likely to be increased in women who are carriers of thrombophilic gene polymorphisms. Prothrombin G20210A variant is reported to be the second most frequent prothrombotic polymorphism in Caucasians. Our aim was to determine the prevalence of this variant in south Indian women and examine its association with cerebral venous and sinus thrombosis occurring during puerperium. We investigated 96 women with puerperal cerebral veno-sinus thrombosis (CVT) and 103 age-matched women with no post-partum complications. We used restriction fragment length polymorphism analysis to identify their genotypes. The prothrombin G20210A variant was not detected in either the CVT patients or the healthy control subjects. Our study on a large series of patients with puerperal CVT shows that the prothrombin G20210A variant is not present in south Indian women and is not associated with puerperal CVT. This study also highlights the fact that there are racial differences in the risk factors for thrombosis, which should be considered when investigating these patients.

Factor V gene A4070G mutation and the risk of cerebral veno-sinus thrombosis occurring during puerperium.

INTRODUCTION: Cerebral veno-sinus thrombosis (CVT) occurring during puerperium is a common form of stroke in young women in India, associated with high mortality and morbidity. Genetic polymorphisms involving coagulation factors are considered to be risk factors for thrombosis. A recently identified polymorphism in factor V gene, A4070G (R2 allele), has been reported as a risk factor for venous thrombosis in some studies. Moreover, the R2 allele has been reported to increase factor V Leiden-related thrombosis risk in doubly heterozygous individuals. The risk associated with the R2 allele has not yet been evaluated in CVT. Our aim was to determine the prevalence of factor V A4070G mutation in Indians and examine its role as a possible risk factor for CVT occurring during puerperium. MATERIALS AND METHODS: We investigated 50 patients with puerperal CVT and 100 healthy women with no post-partum complications for factor V A4070G and G1691A (factor V Leiden) polymorphisms using polymerase chain reaction and restriction fragment length polymorphism. RESULTS AND CONCLUSION: Among cases, 6 (12%) were heterozygous for the factor V A4070G mutation and none were homozygous. In the control group, 9 (9%) were heterozygous and 3 (3%) were homozygous. The odds ratio was 1.00 (95% CI: 0.31-3.13, p=1.000), suggesting that the risk for CVT was not increased in the presence of the R2 allele. There was no co-inheritance of factor V A4070G with factor V G1691A in any of the subjects. Our study shows that the A4070G mutation in factor V though highly prevalent in the Indian population is not associated with an increased risk of CVT occurring during puerperium in Indian women.

Thrombophilic gene polymorphisms in puerperal cerebral veno-sinus thrombosis.

Puerperal cerebral veno-sinus thrombosis (PCVT) is a common form of stroke in young women in India, which is associated with high morbidity and mortality. The frequency of PCVT in India is 10 to 12 times more compared to western population. As yet, the etiology of this condition is unclear. Our aim was to study the prevalence and the role of the common genetic polymorphisms associated with thrombophilia such as factor V Leiden, prothrombin G20210A and methylene tetrahydrofolate reductase (MTHFR) C677T, in aseptic PCVT. We investigated 86 women with PCVT and 86 age-matched women with no post-partum complications. Polymerase chain reaction (PCR)/restriction fragment length polymorphism analysis was used to identify their genotypes. The frequency of the three polymorphisms in cases and controls were: factor V Leiden, 2.3% versus 1.2% (OR 0.49, 95% CI=0.02-7.12, p=1.000) and MTHFR C677T, 16.3% versus 17.4% (OR 0.92, 95% CI=0.39-2.19, p=0.838). The prothrombin G20210A variant was not detected in either patients or controls. The clinical characteristics of the PCVT patients with the polymorphisms did not differ significantly from those without them. In our series of PCVT patients, the risk associated with the established thrombophilic risk factors is insignificant. Exploration of these gene polymorphisms seems to be of limited value in the investigation of PCVT in south Indian women.