N′-(2-Methoxy­benzyl­idene)nicotinohydrazide

The title compound, C14H13N3O2, was prepared by the reaction of 2-methoxy­benzyaldehyde with nicotinic acid hydrazide in methanol. The dihedral angle between the benzene and pyridine rings is 5.9 (3)°. In the crystal structure, mol­ecules are linked by inter­molecular N—H⋯O hydrogen bonds, leading to the formation of chains along the c axis; adjacent chains are linked via C—H⋯O and C—H⋯N hydrogen bonds

Improved D-S evidence theory for pipeline damage identification

Identification of the location of damages in pipeline is important and still needs to be improved due to the problems such as limited number of sensors that can be placed in the pipeline, uncertainty of the working environment. In this paper, a new approach is presented, which shows an improved diagnosis performance. The new approach is based on combining an improved D-S evidence theory and an improved index which is based on three specific identification techniques known to the pipeline community. The improved D-S evidence theory is based on the idea of preserving similar evidences and using weighted average evidence to represent the conflict evidence. The paper also presents an experiment to verify the new approach by comparing the result of the new approach with the traditional D-S approach. The experimental result has shown that the new approach is promising. The new approach also renders the possibility to visualize the location of the damages in the pipeline, which facilitates the access to the damage for repair and any compensation measure

N′-(2-Meth­oxy-1-naphthyl­idene)nicotino­hydrazide

The title compound, C18H15N3O2, was prepared by the reaction of 2-methoxy­naphthaldehyde with nicotinic acid hydrazide in methanol. The dihedral angle between the naphthalene ring system and the pyridine ring is 9.2 (3)°. An intra­molecular C—H⋯N hydrogen bond is observed. In the crystal structure, mol­ecules are linked into chains running along the c axis by inter­molecular N—H⋯O hydrogen bonds

(E)-N′-(3,5-Dibromo-2-hydroxy­benzyl­idene)nicotinohydrazide

In the title Schiff base compound, C13H9Br2N3O2, there is an intra­molecular O-H⋯N hydrogen bond involving the hydroxyl substituent and the adjacent hydrazine N atom. The mol­ecule is almost planar, the dihedral angle between the benzene ring and the pyridine ring being 5.7 (2)°. In the crystal structure, symmetry-related mol­ecules are linked via N—H⋯O hydrogen bonds, forming chains propagating in [001]

3β,11α-Dihy­droxy-12-ursen-3-yl palmitate

In the title compound, C46H80O3, a natural ursane-type triperpenoid, four of the five six-membered rings adopt chair conformations; the fifth, which has a C=C double bond, adopts an approximate half-boat conformation. In the crystal, mol­ecules are linked by O—H⋯O hydrogen bonds, forming chains along [010]

Surpassing the repeaterless bound with a photon-number encoded measurement-device-independent quantum key distribution protocol

Decoherence is detrimental to quantum key distribution (QKD) over large distances. One of the proposed solutions is to use quantum repeaters, which divide the total distance between the users into smaller segments to minimise the effects of the losses in the channel. However, the secret key rates that repeater protocols can achieve are fundamentally bounded by the separation between each neighbouring node. Here we introduce a measurement-device-independent protocol which uses high-dimensional states prepared by two distant trusted parties and a coherent total photon number detection for the entanglement swapping measurement at the repeater station. We present an experimentally feasible protocol that can be implemented with current technology as the required states reduce down to the single-photon level over large distances. This protocol outperforms the existing measurement-device-independent and twin-field QKD protocols by surpassing the fundamental limit of the repeaterless bound for the pure-loss channel at a shorter distance and achieves a higher transmission distance in total when experimental imperfections are considered

In vitro cellular uptake of evodiamine and rutaecarpine using a microemulsion

Yong-Tai Zhang, Zhe-Bin Huang, Su-Juan Zhang, Ji-Hui Zhao, Zhi Wang, Ying Liu, Nian-Ping FengDepartment of Pharmaceutics, Shanghai University of Traditional Chinese Medicine, Shanghai, The People's Republic of ChinaObjective: To investigate the cellular uptake of evodiamine and rutaecarpine in a microemulsion in comparison with aqueous suspensions and tinctures.Materials and methods: A microemulsion was prepared using the dropwise addition method. Mouse skin fibroblasts were cultured in vitro to investigate the optimal conditions for evodiamine and rutaecarpine uptake with different drug concentrations and administration times. Under optimal conditions, the cellular uptake of microemulsified drugs was assayed and compared to tinctures and aqueous suspensions. Rhodamine B labeling and laser scanning confocal microscopy (LSCM) were used to explore the distribution of fluorochrome transferred with the microemulsion in fibroblasts. Cellular morphology was also investigated, using optical microscopy to evaluate microemulsion-induced cellular toxicity.Results: The maximum cellular drug uptake amounts were obtained with a 20% concentration (v/v) of microemulsion and an 8 hour administration time. Drug uptake by mouse skin fibroblasts was lowest when the drugs were loaded in microemulsion. After incubation with rhodamine B-labeled microemulsion for 8 hours, the highest fluorescence intensity was achieved, and the fluorochrome was primarily distributed in the cytochylema. No obvious cellular morphologic changes were observed with the administration of either the microemulsion or the aqueous suspension; for the tincture group, however, massive cellular necrocytosis was observed.Conclusion: The lower cellular uptake with microemulsion may be due to the fact that most of the drug loaded in the microemulsion vehicle was transported via the intercellular space, while a small quantity of free drug (released from the vehicle) was ingested through transmembrane transport. Mouse skin fibroblasts rarely endocytosed evodiamine and rutaecarpine with a microemulsion as the vehicle. The microemulsion had no obvious effect on cellular morphology, suggesting there is little or no cellular toxicity associated with the administration of microemulsion on mouse skin fibroblasts.Keywords: mouse skin fibroblasts, evodiamine, rutaecarpine, microemulsion, cellular uptake, in vitr

Enhanced transdermal delivery of evodiamine and rutaecarpine using microemulsion

Yong-Tai Zhang, Ji-Hui Zhao, Su-Juan Zhang, Yang-Zi Zhong, Zhi Wang, Ying Liu, Feng Shi, Nian-Ping FengSchool of Pharmacy, Shanghai University of Traditional Chinese Medicine, Shanghai, People’s Republic of ChinaObjective: The purpose of this study was to improve skin permeation of evodiamine and rutaecarpine for transdermal delivery with microemulsion as vehicle and investigate real-time cutaneous absorption of the drugs via in vivo microdialysis.Methods: Pseudoternary phase diagrams were constructed to evaluate microemulsion regions with various surfactants and cosurfactants. Nine formulations of oil in water microemulsions were selected as vehicles for assessing skin permeation of evodiamine and rutaecarpine in ex vivo transdermal experiments. With a microdialysis hollow fiber membrane implanted in the skin beneath the site of topical drug administration, dialysis sampling was maintained for 10 hours and the samples were detected directly by high performance liquid chromatography. Real-time concentrations of the drugs in rat skin were investigated and compared with those of conventional formulations, such as ointment and tincture. Furthermore, the drugs were applied to various regions of the skin using microemulsion as vehicle.Results: In ex vivo transdermal experiments, cutaneous fluxes of evodiamine and rutaecarpine microemulsions were 2.55-fold to 11.36-fold and 1.17-fold to 6.33-fold higher, respectively, than those of aqueous suspensions. Different drug loadings, microemulsion water content, and transdermal enhancers markedly influenced the permeation of evodiamine and rutaecarpine. In microemulsion application with in vivo microdialysis, the maximum concentration of the drugs (evodiamine: 18.23 ± 1.54 ng/mL; rutaecarpine: 16.04 ± 0.69 ng/mL) were the highest, and the area under the curve0–t of evodiamine and rutaecarpine was 1.52-fold and 2.27-fold higher than ointment and 3.06-fold and 4.23-fold higher than tincture, respectively. A greater amount of drugs penetrated through and was absorbed by rat abdominal skin than shoulder and chest, and a reservoir in the skin was found to supply drugs even after the microemulsion was withdrawn.Conclusion: Compared to conventional formulations, higher cutaneous fluxes of evodiamine and rutaecarpine were achieved with microemulsion. Based on this novel transdermal delivery, the transdermal route was effective for the administration of the two active alkaloids.Keywords: microemulsion, evodiamine, rutaecarpine, transdermal delivery, microdialysi