Spectrophotometric determination of diphenhydramine hydrochloride in pharmaceutical preparations and biological fluids via ion-pair formation

A simple, sensitive and accurate spectrophotometric method has been described for the assay of diphenhydramine hydrochloride (DPH) in raw material and in biological samples. The method is based on extraction of DPH into dichloromethane as ion-pair complexes with patent blue (PB), eriochrome black T (EBT), methyl orange (MO) and bromocresol purple (BCP) in acidic medium. The coloured species exhibited absorption maxima at 632, 514, 428 and 414 nm for PB, EBT, MO and BCP, with molar absorptivity values of 1.32 × 10⁵, 2.36 × 10⁴, 3.68 × 10⁴ and 3.07 × 10⁴ l mol^?1 cm^?1, respectively. The reaction conditions were optimized to obtain the maximum colour intensity. Beer’s law was obeyed with a good correlation coefficient (0.9982–0.9993) in the concentration ranges 0.5–3, 2.0–16, 2.0–10 and 1.0–10 μg ml^?1 for PB, EBT, MO and BCP methods, respectively. The composition ratio of the ion-association complexes was found to be 1:1 in all cases as established by Job’s method. The conditional stability constant (K_f) and the free energy changes (ΔG°) were determined for all complexes formed. The proposed method was successfully applied for the determination of DPH in tablets and human urine with good accuracy and precision. Statistical comparison of the results with those obtained by the official method showed good agreement and indicated no significant difference in accuracy and precision.     

Spectroscopy and photoredox properties of soluble platinum(II) alkynyl complexes

Six complexes of platinum(II) with a terdentate π-acceptor ligand, 2,6-(N-(n-hexyl)benzimidazol-2′-yl)pyridine), and different ethynylbenzene ligands were synthesized and investigated by means of optical absorption, luminescence, and time-resolved emission spectroscopy. These complexes display similar photophysical and electrochemical properties as previously investigated analogs with the 2,2′:6′,2″-terpyridine ligand. The energy of the luminescence band maximum is a function of the nature of the chemical substituents attached to the ethynylbenzene ligand, luminescence intensities and lifetimes correlate with the luminescence wavelength according to the energy-gap law. The emissive excited states of some of these complexes are quenched reductively with efficiencies near the diffusion-controlled limit, even for moderate electron donors such as phenothiazine or triphenylamine. A complex with a dimethylamine substituent attached to the ethynylbenzene ligand exhibits photophysical properties that are strongly dependent on the protonation state of the amine. A dimer complex with a diethynyl-substituted xanthene bridging ligand displays absorption and emission behavior that is essentially identical to that of some of the monomeric platinum complexes investigated in this work. Short Pt(II)–Pt(II) contacts are only observed in the crystal structure of a precursor complex. A key feature of the new complexes is their good solubility in common organic solvents, thanks to the presence of two hexyl chains that are attached to the terdentate ligands.     

Micellar properties of a phenothiazine drug in presence of additives

In this study micellar properties of a phenothiazine drug, promazine hydrochloride, at different concentrations of NaCl and cationic surfactants (conventional as well as gemini surfactants) are presented. The parameters studied are cmc (critical micelle concentration), X ₁ (mole fraction of surfactant in micelles), f ₁, f ₂ (activity coefficients) and ΔG _ex (excess free energy). Cl⁻ ions (from NaCl) get adsorbed on the micellar head groups and, by decreasing the repulsion among them, lower the cmc. Surfactants form mixed micelles with the drug and the values of X ₁, X ₁^id (mole fraction of the surfactant in micelles in ideal state), interaction parameter β, f ₁ and f ₂ all suggest non-ideal but synergistic nature. The ΔG _ex values are negative indicating that the mixed state is more stable than the pure micelle state. The article is published in the original.     

Spectrofluorimetric Determination of the Hypertensive Drug Captopril Based on Its Oxidation with Cerium(IV)

A highly sensitive and specific spectrofluorimetric method for the analysis of captopril (CAP) in the pure form and in the tablet dosage forms has been described. The method was based on the oxidation of captopril by cerium(IV) in the presence of sulphuric acid and subsequent monitoring the fluorescence of the induced Ce(III) ion produced at λ_ex = 256 nm and λ_em = 354 nm. All variables affecting the reaction conditions such as cerium(IV) concentration, type and concentration of acid medium, reaction time, diluting solvents, temperature and heating time were carefully studied and optimized. Under the experimental conditions used, an excellent linear relationship was obtained between fluorescence intensity and the concentration of CAP. A linear range of determination was verified for captopril concentrations between 0.1–1.3 μg mL^?1 and the correlation coefficient of determination was 0.9997. Quantitation and detection limits were calculated. The precision of the method was satisfactory; the values of relative standard deviations did not exceed 1.14%. No interference could be observed from the excipients and additives are commonly presented in dosage forms. The proposed method was applied successfully for the assay of the studied drug in pure form and in pharmaceutical dosage forms. Recovery experiments revealed recovery of 99.82–100.21%. The results of the analysis show a good agreement with those obtained by official method stated in the United State Pharmacopoeia.     

Synthesis of some cyclopentenones and crystal structure of 4-hydroxy-3,4-bis(4-methoxyphenyl)-5,5-dimethyl-2-cyclopenten-1-one

Abstract  

Sodium-hydroxide-catalyzed condensation of di-p-methyl- and di-p-methoxybenzil with acetone derivatives was investigated in methanol. Di- and trisubstituted products were obtained as cyclopentenones, while tetraaryl-substituted systems were isolated as cyclopentadienones. The structures of the products were identified by elemental analysis, infrared (IR), nuclear magnetic resonance (¹H NMR), and mass spectroscopy. The solid-state structure of 4-hydroxy-3,4-bis(4-methoxyphenyl)-5,5-dimethyl-2-cyclopenten-1-one was further studied by single-crystal X-ray diffraction analysis. The title compound crystallizes in an orthorhombic space group and intermolecular O–H···O and C–H···O hydrogen bonds stabilize the crystal lattice.     

Application of Calcium Alginate–Starch Entrapped Bitter Gourd (<Emphasis Type="Italic">Momordica charantia</Emphasis>) Peroxidase for the Removal of Colored Compounds from a Textile Effluent in Batch as well as in Continuous Reactor

Calcium alginate–starch entrapped bitter gourd peroxidase has been employed for the treatment of a textile industrial effluent in batch as well as in continuous reactor. The textile effluent was recalcitrant to decolorization by bitter gourd peroxidase; thus, its decolorization was examined in the presence of a redox mediator, 1.0 mM 1-hydroxybenzotriazole. Immobilized enzyme exhibited same pH and temperature optima for effluent decolorization as attained by soluble enzyme. Immobilized enzyme could effectively remove more than 70% of effluent color in a stirred batch process after 3 h of incubation. Entrapped bitter gourd peroxidase retained 59% effluent decolorization reusability even after its tenth repeated use. The two-reactor system containing calcium alginate–starch entrapped enzyme retained more than 50% textile effluent decolorization efficiency even after 2 months of its operation. The absorption spectra of the treated effluent exhibited a marked difference in the absorption at various wavelengths as compared to untreated effluent. The use of a two-reactor system containing immobilized enzyme and an adsorbent will be significantly successful for treating industrial effluents at large scale, and it will help in getting water free from aromatic pollutants.     

On the construction of normal wildly ramified extensions over Q 2

It is well known that a finite totally ramified extension of a local field can be generated by a uniformising element the minimal polynomial of which is also Eisenstein. The quadratic and the quartic normal totally ramified extensions of Q ₂ are well known and well characterized. In this note we characterize the Eisenstein polynomials of degree 4 with coefficients in Z ₂ that define normal totally ramified extensions of Q ₂. Furthermore we give some necessary conditions for the cyclic case of degree 2 ⁿ . Also examples are given.     

Identification of low amount of irradiated spices (red pepper,garlic, ginger powder) with luminescence analysis

For the identification of irradiated food, current analysis methods have limitations regarding presence and stability of radiation-induced markers. In this study, different spice blends with small quantity of different irradiated (0, 1 and 10 kGy) spice powders, such as red pepper, garlic or ginger, were investigated using PSL and TL techniques. In PSL-based screening analysis, the spice blends containing 10% of irradiated materials (1 or 10 kGy) were determined as intermediate or positive. In TL results, the blends containing 1% of 1 or 10 kGy-irradiated spices showed the typical TL glow curves that could be interpreted as positive. The blends with irradiated garlic powder provided more good results where identification was possible at 0.5% mixing of irradiated sample. However, the TL ratios of all spice blends were <0.1 and only TL glow curve shape and intensity may be used to discriminate the samples having irradiated component.     

Enhancement in sensitivity of nitro blue tetrazolium polyvinyl alcohol film dosimeters by sodium formate and Triton X-100

Nitro blue tetrazolium polyvinyl alcohol film dosimeters, NBT-PVA were prepared and evaluated based on radiation-induced reduction of NBT²⁺. NBT-PVA film dosimeters containing different concentrations of NBT dye from 1 to 5 mM were prepared in a solution of ethanol. The dosimeters were irradiated with ?-ray from ⁶⁰Co source at doses up to 50 kGy. UV/vis spectrophotometer was used to investigate the optical density of un-irradiated and irradiated films in terms of absorbance at 529 nm. The absorbance increases with absorbed dose up to 50 kGy for NBT-PVA film dosimeters. The dose sensitivity of NBT-PVA film increases strongly with increase of concentrations of NBT dye. The effects of irradiation temperature, humidity, dose rate and the stability of the response of the films after irradiation were investigated. A considerable increase was observed in the dose response of NBT-PVA film by adding appropriate concentration of sodium formate and Triton X-100.     

Thermoluminescence analyses of irradiated dried sea foods using different methods of mineral separation

This research was conducted to find the most suitable parameters to separate minerals from irradiated dried shrimps and mussels (0 and 5 kGy) for thermoluminescence analysis using density separation and modified acid hydrolysis (at 50 °C with continuous agitation) methods. Nonirradiated samples gave TL glow curve of low intensity with peak after 300 °C except dried mussel sample, which gave false positive result. This problem was absent in minerals separated by acid hydrolysis. TL ratios of all nonirradiated samples were <0.1 irrespective of method used for mineral separation. Minerals separated from irradiated samples by density separation showed very high intensity of TL glow peak before 200 °C, where results from irradiated dried shrimp samples were better because of good availability of minerals. The minerals separated from irradiated samples by acid hydrolysis showed slightly low TL intensity and glow curve peak was found at about 200 °C. However, acid hydrolysis method was less laborious and required less sample weight as compared to density separation method. TL ratios of all irradiated samples were >0.1 confirming the quality of minerals on TL discs.