A bis-bithiophene from Tridax procumbens L. (Asteraceae)

The ethyl acetate soluble part of hexane extract of Tridax procumbens yielded a new bis-bithiophene named tridbisbithiophene along with four known terpenoids: taraxasteryl acetate, beta-amyrenone, lupeol and oleanolic acid, which have never been reported so far from Tridax procumbens. The structures of all the isolated constituents were elucidated with the aid of 1D-NMR spectroscopy whereas, the structure of new constituent tridbisbithiophene was confirmed via COSY and HMBC interactions.     

Simultaneous determination of ofloxacin,tetrahydrozoline hydrochloride,and prednisolone acetate by high-performance liquid chromatography

A simple, specific, and precise high-performance liquid chromatographic method has been developed for the simultaneous determination of ofloxacin (OFX), tetrahydrozoline hydrochloride (THC), and prednisolone acetate (PAC) in ophthalmic suspension using propylparaben (POP) as the internal standard. The mobile phase consists of 0.05 M phosphate buffer-acetonitrile (65:35, v/v), and the pH is adjusted to 2.7 with orthophosphoric acid. A column containing octadecyl silane chemically bonded to porous silica particles (Waters Spherisorb, 5 microm ODS 1, 4.6 x 150 mm) is used as the stationary phase. The detection is carried out using a variable wavelength UV-vis detector set at 210 nm for OFX and THC and 254 nm for POP (internal standard) and PAC. The solutions are chromatographed at a constant flow rate of 1.2 mL/min. Retention times for OFX, THC, POP, and PAC are approximately 2.5, 4.5, 7.8, and 9.5 min, respectively. The relative retention times are approximately 0.14 min for OFX, 0.35 min for THC, 1.00 min for POP, and 1.22 min for PAC. The linearity range and percent recoveries for OFX, THC, and PAC are 24-120, 4-16, and 16-80 microg/mL and 100.48%, 100.34%, and 100.21%, respectively.     

Adsorption characteristics and the kinetics of the cation exchange of rhodamine-6G with Na+-montmorillonite

The adsorption and the kinetics of the cation exchange of rhodamine-6G (Rh-6G) with Na(+)-montmorillonite (Na(+)-MMT) have been studied. The binding parameters of Rh-6G have been determined by applying Freundlich and D-R isotherms. The enthalpy and the entropy of adsorption have been determined. The isosteric heat of adsorption has also been determined and decreases with increasing the concentration of Rh-6G. Increasing the concentration of Rh-6G led to a decrease in the adsorption capacity, which attributed to the formation of Rh-6G aggregates. Kinetic measurements of the cation exchange were followed up using a stopped-flow electrical conductivity detection unit. The cation-exchange process exhibited first-order kinetics with respect to the dye concentration and inversely proportional to the clay concentration. The measurements were accomplished at different temperatures and the activation parameters were determined. Increasing the Na(+)-MMT concentration led to a decrease in the rate constant. The latter is also affected by changing the exchangeable cation.     

Cobalt determination with FI-FAAS after on-line sorbent preconcentration using 1-nitroso-2-naphthol

The suitability of 1-nitroso-2-naphthol (NN) as a complexing agent for on-line preconcentration of cobalt using C(18) microcolumn with FI-FAAS system has been tested. Various parameters affecting the complex formation and its elution were optimized. Reagent solution (2.5x10(-3) mol l(-1)) and aqueous sample solution acidified with 0.1% (v/v) nitric acid were on-line mixed in a reaction coil set at 65+/-1 degrees C and flowed through the microcolumn for 30 s. The pH of the mixed solution was adjusted to 3 approximately 4 by adding HNO(3) (1 mol l(-1)) or NaOH (1 mol l(-1)) in the reagent solution. The adsorbed complexes in the microcolumn were eluted with ethanol (acidified to 1% nitric acid) in 10 s into the nebulizer of FAAS. A good precision (1.6% for 100 mug l(-1) Co(II), n=10), high enrichment factor 17.2, with detection limit (3sigma) 3.2 mug l(-1), and sample throughput (90 h(-1)) were obtained. The method was applied on the certified reference materials (CRMs) i.e. NBS-362 and NBS-364 (special low alloy steel), for the determination of cobalt and the results were in good agreement with the certified values.     

One-step SFE-plus-C(18) selective extraction of low-polarity compounds,with lipid removal,from smoked fish and bovine milk

Co-extraction of lipid materials is the major source of interference in determinations of low-polarity compounds in many biological matrixes. "SFE-plus-C(18)", a recently developed supercritical fluid extraction method employing C(18) adsorbent in the extraction chamber, can enable selective extraction of low-polarity compounds in lipid-rich biological matrixes without a cleanup step. This study reports the application of the SFE-plus-C(18) method to the quantification of: 1. polycyclic aromatic hydrocarbons (PAH) in commercially purchased smoked fish; and 2. anti-cancer agents cyclophosphamide (CP) and suberoylanilide hydroxamic acid (SAHA) spiked into homogenized whole bovine milk.Over the course of SFE-plus-C(18)extraction, indigenous lipids are preferentially retained on the C(18) adsorbent. Compared with the conventional method, only 8-15% of the lipids in the smoked fish sample, and only 6-18% of the lipids in the milk sample, were co-extracted by SFE-plus-C(18). This reduction in the quantity of background lipids significantly improved chromatographic separations, retarded deterioration of the column, and dramatically improved the ability to quantify PAH present at trace levels in smoked fish by GC-MS. Using the SFE-plus-C(18) method, ten targeted PAH were detected in the range 9.5-13.5 ng g(-1) in the smoked fish sample. Compared with these levels, PAH extractions by use of conventional SFE gave values that were lower by 38-86%. Recoveries of CP and SAHA spiked into milk were close to 100% in both SFE-plus-C(18)and conventional SFE, where the lipid background during the chromatographic elution of CP and SAHA was not so severe.     

Integrated Routing Algorithms for Provisioning “Sub-Wavelength” Connections in IP-Over-WDM Networks

This work focuses on developing and implementing comprehensive unified constraint-based routing algorithms within the generalized multi-protocol label switching framework (GMPLS) to provision sub-wavelength circuits (low-rate traffic streams). Constraint-based routing is further augmented in this work by dynamically routing both an active and another alternate link/node-disjoint backup path at the same time in order to provision a given connection request. This new integrated approach combines both IP routing and optical resource allocation to setup end-to-end connections.     

Implications of $B \to \rho \gamma$ measurements in the standard model and supersymmetric theories

We study the implications of the recently improved upper limits on the branching ratios for the decays , expressed as . We work out the constraints that the current bound on implies on the parameters of the quark mixing matrix in the standard model (SM). Using the present profile of the unitarity triangle, we predict this ratio to lie in the range (at 95% C.L.), with the central value . We also work out the correlations involving , the isospin-violating ratio , and the direct CP-violating asymmetry in decays in the SM, in the minimal supersymmetric extension of the SM (MSSM), and in an extension of the MSSM involving an additional flavor-changing structure in transitions. Received: 19 August 2002 / Published online: 18 October 2002 RID="a" ID="a" e-mail: ali@mail.desy.de RID="b" ID="b" e-mail: lunghi@mail.desy.de     

An enhancement to the IEEE 802.11e EDCA providing QoS guarantees

One of the challenges that must be overcome to realize the practical benefits of ad hoc networks is quality of service (QoS). However, the IEEE 802.11 standard, which undeniably is the most widespread wireless technology of choice for WLANs and ad hoc networks, does not address this issue. In order to support applications with QoS requirements, the upcoming IEEE 802.11e standard enhances the original IEEE 802.11 MAC protocol by introducing a new coordination function which has both contention-based and contention-free medium access methods. In this paper, we consider the contention-based medium access method, the EDCA, and propose an extension to it such that it can be used to provide QoS guarantees in WLANs operating in ad hoc mode. Our solution is fully distributed, uses admission control to regulate the usage of resources and gives stations with high-priority traffic streams an opportunity to reserve time for collision-free access to the medium.     

Spatially variant morphological restoration and skeleton representation.

The theory of spatially variant (SV) mathematical morphology is used to extend and analyze two important image processing applications: morphological image restoration and skeleton representation of binary images. For morphological image restoration, we propose the SV alternating sequential filters and SV median filters. We establish the relation of SV median filters to the basic SV morphological operators (i.e., SV erosions and SV dilations). For skeleton representation, we present a general framework for the SV morphological skeleton representation of binary images. We study the properties of the SV morphological skeleton representation and derive conditions for its invertibility. We also develop an algorithm for the implementation of the SV morphological skeleton representation of binary images. The latter algorithm is based on the optimal construction of the SV structuring element mapping designed to minimize the cardinality of the SV morphological skeleton representation. Experimental results show the dramatic improvement in the performance of the SV morphological restoration and SV morphological skeleton representation algorithms in comparison to their translation-invariant counterparts.     

Acquisition of high-precision images for non-contact atomic force microscopy

The atomic force microscope (AFM) system has evolved into a useful tool for direct measurements of intermolecular forces with atomic-resolution characterization that can be employed in a broad spectrum of applications. The distance between cantilever tip and sample surface in non-contact AFM is a time-varying parameter even for a fixed sample height, and typically difficult to identify. A remedy to this problem is to directly identify the sample height in order to generate high-precision atomic-resolution images. For this, the microcantilever (which forms the basis for the operation of AFM) is modeled as a single mode approximation and the interaction between the sample and cantilever is derived from a van der Waals potential. Since in most practical applications only the microcantilever deflection is accessible, we will use merely this measurement to identify the sample height. In most non-contact AFMs, cantilevers with high-quality factors are employed essentially for acquiring high-resolution images. However, due to high-quality factor, the settling time is relatively large and the required time to achieve a periodic motion is long. As a result, identification methods based on amplitude and phase measurements cannot be efficiently utilized. The proposed method overcomes this shortfall by using a small fraction of the transient motion for parameter identification, so the scanning speed can be increased significantly. Furthermore, for acquiring atomic-scale images of atomically flat samples, the need for feedback loop to achieve setpoint amplitude is basically eliminated. On the other hand, for acquiring atomic-scale images of highly uneven samples, a simple PI controller is designed to track the desired constant sample height. Simulation results are provided to demonstrate the feasibility of the approach for both sample height identification and tracking the desired sample height.