Rapid micellar HPLC analysis of loratadine and its major metabolite desloratadine in nano-concentration range using monolithic column and fluorometric detection: application to pharmaceuticals and biological fluids

Background

Loratadine is a commonly used selective non-sedating antihistaminic drug. Desloratadine is the active metabolite of loratadine and, in addition, a potential impurity in loratadine bulk powder stated by the United States Pharmacopeia as a related substance of loratadine. Published methods for the determination of both analytes suffer from limited throughput due to the time-consuming steps and tedious extraction procedures needed for the analysis of biological samples. Therefore, there is a strong demand to develop a simple rapid and sensitive analytical method that can detect and quantitate both analytes in pharmaceutical preparations and biological fluids without prior sample extraction steps.

Results

A highly-sensitive and time-saving micellar liquid chromatographic method is developed for the simultaneous determination of loratadine and desloratadine. The proposed method is the first analytical method for the determination of this mixture using a monolithic column with a mobile phase composed of 0.15 M sodium dodecyl sulfate, 10% n-Butanol and 0.3% triethylamine in 0.02 M phosphoric acid, adjusted to pH 3.5 and pumped at a flow rate of 1.2 mL/min. The eluted analytes are monitored with fluorescence detection at 440 nm after excitation at 280 nm. The developed method is linear over the concentration range of 20.0–200.0 ng/mL for both analytes. The method detection limits are 15.0 and 13.0 ng/mL and the limits of quantification are 20.0 and 18.0 ng/mL for loratadine and desloratadine, respectively. Validation of the developed method reveals an accuracy of higher than 97% and intra- and inter-day precisions with relative standard deviations not exceeding 2%.

Conclusions

The method can be successfully applied to the determination of both analytes in various matrices including pharmaceutical preparations, human urine, plasma and breast milk samples with a run-time of less than 5 min and without prior extraction procedures. The method is ideally suited for use in quality control laboratories. Moreover, it could be a simple time-saving alternative to the official pharmacopeial method for testing desloratadine as a potential impurity in loratadine bulk powder.

Open image in new window

Graphical abstract Typical chromatogram of loratadine and its major metabolite desloratadine using the proposed micellar HPLC method

     

Square Integrable Representation of Groupoids

A notion of an irreducible representation, as well as of a square integrable representation on an arbitrary locally compact groupoid, is introduced. A generalization of a version of Schur＇s lemma on a locally compact groupoid is given. This is used in order to extend some well-known results from locally compact groups to the case of locally compact groupoids. Indeed, we have proved that if L is a continuous irreducible representation of a compact groupoid G defined by a continuous Hilbert bundle H = （Hu）u∈G^0, then each Hu is finite dimensional. It is also shown that if L is an irreducible representation of a principal locally compact groupoid defined by a Hilbert bundle （G^0, （Hu）,μ）, then dimHu = 1 （u ∈ G^0）. Furthermore it is proved that every square integrable representation of a locally compact groupoid is unitary equivalent to a subrepresentation of the left regular representation. Furthermore, for r-discrete groupoids, it is shown that every irreducible subrepresentation of the left regular representation is square integrable.     

Phytochemistry,Food Application,and Therapeutic Potential of the Medicinal Plant (Withania coagulans): A Review

Herbal plants have been utilized to treat and cure various health-related problems since ancient times. The use of Ayurvedic medicine is very significant because of its least reported side effects and host of advantages. Withania coagulans (Family; Solanaceae), a valuable medicinal plant, has been used to cure abnormal cell growth, wasting disorders, neural as well as physical problems, diabetes mellitus, insomnia, acute and chronic hepatic ailments. This review provides critical insight regarding the phytochemistry, biological activities, and pharmacognostic properties of W. coagulans. It has been known to possess diuretic, anti-inflammatory, anti-bacterial, anti-fungal, cardio-protective, hepato-protective, hypoglycemic, anti-oxidative, and anti-mutagenic properties owing to the existence of withanolides, an active compound present in it. Apart from withanolides, W. coagulans also contains many phytochemicals such as flavonoids, tannins, and β-sterols. Several studies indicate that various parts of W. coagulans and their active constituents have numerous pharmacological and therapeutic properties and thus can be considered as a new drug therapy against multiple diseases.     

An Intricate Review on Nutritional and Analytical Profiling of Coconut,Flaxseed, Olive,and Sunflower Oil Blends

Vegetable oils (VOs), being our major dietary fat source, play a vital role in nourishment. Different VOs have highly contrasting fatty acid (FA) profiles and hence possess varying levels of health protectiveness. Consumption of a single VO cannot meet the recommended allowances of various FA either from saturated FA (SFA), monounsaturated FA (MUFA), polyunsaturated FA (PUFA), Ω-3 PUFAs, and medium-chain triglycerides (MCTs). Coconut oil (CO), flaxseed oil (FO), olive oil (OO), and sunflower oil (SFO) are among the top listed contrast VOs that are highly appreciated based on their rich contents of SFAs, Ω-3 PUFAs, MUFAs, and Ω-6 PUFA, respectively. Besides being protective against various disease biomarkers, these contrasting VOs are still inappropriate when consumed alone in 100% of daily fat recommendations. This review compiles the available data on blending of such contrasting VOs into single tailored blended oil (BO) with suitable FA composition to meet the recommended levels of SFA, MUFA, PUFA, MCTs, and Ω-3 to Ω-6 PUFA ratios which could ultimately serve as a cost-effective dietary intervention towards the health protectiveness and improvement of the whole population in general. The blending of any two or more VOs from CO, FO, OO, and SFO in the form of binary, ternary, or another type of blending was found to be very conclusive towards balancing FA composition; enhancing physiochemical and stability properties; and promising the therapeutic protectiveness of the resultant BOs.     

Improved visible light photocatalytic activity of TiO<Subscript>2</Subscript> nano powders with metal ions doping for glazed ceramic tiles

Self-cleaning and anti-bacterial activities of the photo-catalyst titanium dioxide make it a superior compound for use in the ceramics and glass industry. In order to achieve high self-cleaning efficiency for building products, it is important that Titania is present as anatase phase. Moreover, it is desirable that the particle sizes are in Nano-range, so that a large enough surface area is available for enhanced catalytic performance. In the present paper, Cobalt and Nickel co-doped (4%mol Ni and 4%mol Co doped TiO₂) and un-doped TiO₂ Nano powders have been prepared by sol–gel technique. They were calcined at the temperatures in the range of 475–1075 °C. Ni/Co co-doped TiO₂ postponed the anatase to rutile transformation of TiO₂ by about 200–300°C, such that before calcination at 775°C, no rutile was detected for 4 mol% Ni/Co co-doped TiO₂. A systematic decreasing on crystallite size and increasing on specific surface area of Ni/Co co-doped TiO₂ were observed. Photo-catalytic activity of anatase polymorph was measured by the decomposition rate of methylene blue under visible light. The results showed enhanced catalysis under visible light for Ni/Co co-doped TiO₂ as compared to pure TiO₂. The enhanced performance was attributed to surface chemistry change associated with a slight shift in the band gap. Depending on the temperatures ranging from 475 to 1075 °C, band gap energy of Ni and Co doped TiO₂ crystals decreased. For all samples there is a general reduction of the band gap energy from 3.00 to 2.96 eV.     

A simple humidity sensor utilizing air-gap as sensing part of the Mach–Zehnder interferometer

A simple high-resolution refractive index (RI) and phase sensor has been demonstrated and the results numerically verified. A free space gap is employed in one arm of a Mach–Zehnder interferometer (MZI) to serve as the sensing mechanism with a physical spacing of 1.4 mm. The propagation constant of transmitted light in the MZI’s gap changes due to the small variation in the ambient RI that will further shift the optical phase of the signal. A free space optical delay line is embedded within the MZI’s other arm to set the phase reference point and compensate for variations in the optical phase difference. The ambient RI is computed by measuring the phase shift in the transmission spectrum A high-resolution sensing of 0.8 pm/%RH corresponds to phase change of 0.012°/%RH has been achieved in 1520 nm.     

A comparative study on the Ge6C14 heterofullerene nanocages: a density functional survey

Ten C₁₄Ge₆ heterofullerene isomers of C₂₀ have been investigated by density functional theory (DFT) methods with Becke 3‐Parameter (Exchange), Lee, Yang and Parr (B3LYP) functional at the 6‐311 + G*, 6‐311++G** and AUG‐cc‐pVTZ levels. In contrast to identical bonds in the latter, contractions of C═C double bonds are encountered at the expense of longer C―Ge bonds in the former. Vibrational frequency analysis confirms that all of the nanocages are true minima. In contrast to the common belief, for obtaining highly silicon‐doped stable heterofullerenes, that the silicon dopants must be completely isolated from each other by means of strong C═C double bonds. Here, linking the germanium substitutions together is an applicable strategy for obtaining highly doped stable isolated heterofullerenes since it avoids weak heteroatom─heteroatom bonds. Therefore, none of the computed heterofullerenes collapses to open, to deform, or to segregate fullerenic cages. As to band gaps (ΔE_HOMO‐LUMO), and nucleus‐independent chemical shifts at cage centers (NICS (0)), C₁₄Ge₆‐2 immerges with the highest value. Hence, it is predicted to be the most stable against electronic excitation. It contains 2 Ge─Ge single bonds at the cap‐equatorial positions. On the other hand, as to zero‐point vibrational energy and heat of atomization (ΔH_at), C₁₄Ge₆‐8 appears with the lowest and highest value, respectively. It contains 6 alternating germanium atoms in the equatorial and cap positions. Thus, it is predicted to be the most thermodynamically stable. So, germanium substitution leads to a high charge distribution on the surfaces of all the isomers specially C₁₄Ge₆‐9 with +1.496 charged germanum atoms. C₁₄Ge₆ isomers seem to be a good candidate for the hydrogen storage material.     

Synthesis and characterization of nickel(II) complexes with three potentially hexadentate Schiff-base ligands and polyamines: X-ray crystal structure determination of one nickel(II) complex

Three new potentially hexadentate N₄O₂ Schiff-base ligands (H₂L¹, H₂L² and H₂L³) were prepared from the reaction of the polyamines N,N′-bis(2-aminophenyl)-1,2-ethanediamine (L¹), N,N′-bis(2-aminophenyl)-1,3-propanediamine (L²) and N,N′-bis(2-aminophenyl)-1,4-butanediamine (L³), respectively with salicylaldehyde. Reaction of the Schiff bases with Ni(II) salts in the presence of N(Et)₃ gave the neutral complexes [NiL⁴], [NiL⁵] and [NiL⁶]. Ni(II) complexes of the polyamines were also prepared. One of complexes [Ni(L¹)(MeCN)₂](ClO₄)₂·MeCN has been characterized through X-ray diffraction methods.     

PTSA catalyzed simple and green synthesis of benzothiazole derivatives in water

Abstract  

p-Toluenesulfonic acid (10 mol%) was found to be an effective and efficient catalyst for the synthesis of 2-substituted benzothiazoles from aromatic aldehydes and 2-aminothiophenol in moderate to excellent yields in water. This method provides a simple and efficient protocol in terms of mild reaction conditions, clean reaction profiles, small quantity of catalyst, and simple workup procedure.     

Effects of external electromagnetic field on binodal curve of (water + propionic acid + dichloromethane) ternary system

The effects of an external electromagnetic field on the binodal curve of the (water + propionic acid + dichloromethane) ternary system was investigated at 91.3 kPa and T = (294.15 and 284.15) K. The experimental binodal curve values for the ternary system were obtained by the cloud point method using a new setup with a flat capacitor. The effects of variation of frequencies and amplitude of voltages of the applied external electromagnetic field on the binodal curve results have been evaluated. The results obtained indicate that the heterogeneous two-phase area increases with increasing frequency of the applied external electromagnetic field. At constant frequency, a similar effect has been found by increasing the amplitude of the voltage of the applied external electromagnetic field. The comparison between the results obtained for this work with those reported in previous work indicates that the treatment efficiency in liquid–liquid extraction process of (water + propionic acid + dichloromethane) ternary system can be governed by the applied external electromagnetic field.