A Stress Stability Behavior and Development of an LC Assay Method for Anastrozole

This present work narrates the stress stability behavior and development of a liquid chromatographic method for the quantitative determination of anastrozole. Anastrozole is appropriately used when using substantial amounts of aromatizing steroids, or when one is prone to gynecomastia and using moderate amounts of such steroids. A chromatographic separation was achieved on a Hichrom RPB18 (250 × 4.6 mm, 5 μ) column using water and mixture of acetonitrile and methanol (1:1 ratio) as mobile phase. Forced degradation studies were performed on bulk samples of anastrozole using acid, base, hydrogen peroxide, heat and UV light. Degradation of the drug substance was observed in base hydrolysis. Degradation product formed under base hydrolysis was found to be Imp-C. The sample solution and mobile phase were found to be stable up to 48 h. The developed method was validated with respect to linearity, accuracy, precision, robustness and forced degradation studies prove the stability indicating power of the method.     

Inserts providing complete sample evaporation above the column entrance in vaporizing GC injectors

Completeness of sample evaporation in conventional vaporizing injection is a problem for many samples and calls for measures to arrest the sample liquid in the space between the needle exit and the column entrance. A visual testing procedure reveals that a small plug of loose glass or quartz wool ensures complete evaporation in all instances. Obstacles built into the liner also stop liquid, provided they force the sample to pass through narrow channels. Other important design characteristics concern access to the narrow channel. Evaporation in a packed insert usually occurs from a surface, whereas the sample hardly touches surfaces in the instance of an insert with obstacles. Evaporation from a packing is, in fact, more reliable, but creates more problems concerning inertness.     

Solventless injecction for packed column supercritical fluid chromatography

The adverse effects of injection solvent strength on microbore packed column SFC band broadening are demonstrated and a solventless injection system that eliminates these effects is introduced. The injection system removes solvent in a GC-like manner using a retention gap and an on-column capillary GC syringe. The analyte is delivered to the analytical column in a solvent-free plug of supercritical fluid mobile phase.     

A Stability-Indicating LC Assay Method for Pemetrexed Disodium

This present work describes the development of a stability-indicating high performance liquid chromatographic method for the quantitative determination of pemetrexed disodium. Pemetrexed disodium is an antifolate antineoplastic agent that exerts its action by disrupting folate-dependent metabolic processes essential for cell replication. The chromatographic separation was achieved on an ACE 3 C18 HPLC column using a mobile phase consisting of a mixture of buffer (solvent A) and organic modifier acetonitrile (solvent B). Forced degradation studies were performed on bulk sample of pemetrexed disodium using acid (0.5 N hydrochloric acid), base (0.5 N sodium hydroxide), oxidation (10% v/v hydrogen peroxide), heat (60 °C) and UV light (254 nm). Degradation of the drug substance was observed in base hydrolysis. Degradation product formed under acid and base hydrolysis was found to be starting material. The stressed samples were assayed using the developed LC method and the mass balance found was close to 99.5%, thus proving its stability-indicating power. The developed method was validated with respect to linearity, accuracy, precision and robustness.     

超声波光催化协同降解对甲基苯磺酸

以对甲基苯磺酸水溶液为研究对象,进行了超声波、光催化单独处理以及超声波与光催化联合处理的研究.探讨了超声功率、频率、溶液初始pH等因素对对甲基苯磺酸的降解效率的影响.结果表明,超声波和光催化之间存在着协同效应;当溶液初始质量浓度30mg/L、光催化剂Tio2投加量为1OOmg/L、超声功率和频率分别为80W和45kHz...     

Stress Degradation Studies on Dutasteride and Development of a Stability-Indicating HPLC Assay Method for Bulk Drug and Pharmaceutical Dosage Form

A simple stability-indicating LC method has been developed for the quantitative determination of dutasteride in bulk drug samples and in pharmaceutical dosage forms in the presence of degradation products. The retention time of dutasteride is about 7 min. The drug was subjected to stress conditions of hydrolysis, oxidation, photolysis and thermal degradation. Degradation was found to occur under hydrolysis and to a lesser extent under oxidation conditions but the compound was stable to photolytic and thermal stress. The assay of stress samples was calculated against a reference standard and the mass balance was found close to 99.3%. The developed method was validated with respect to linearity, accuracy, precision and ruggedness.     

Glass wool in the injector insert for quantitative analysis in splitless injection

Summary The use is suggested of a light packing of (silylated) glass wool in the injector insert between the end of the inserted syringe needle and the column inlet to improve quantitation in splitless injection for samples containing some involatile material. Glass wool reduces the standard deviation of the results but its major advantage is the improvment of the solute transfer onto the column. It reduces or eliminates matrix effects in splitless injection where solute transfer, and hence absolute and relative peak areas, depends on the sample composition (a source of serious systematic errors). High injector temperatures are required to overcome the retention of the solutes in the sample byproducts.     

A Stability-Indicating LC Assay and Degradation Behavior of Temozolomide Drug Substances

This study deals with a stability indicating HPLC reverse phase method for quantitative determination of temozolomide. A chromatographic separation was achieved on an Inertsil ODS 3V, 250 × 4.6 mm ID, 5 μm column using mobile phase A (buffer 5 mL glacial acetic acid in 1,000 mL of Milli Q water ) and mobile phase B (methanol). Forced degradation studies were performed on bulk sample of temozolomide using acid (0.5 N hydrochloric acid), base (0.5 N sodium hydroxide), oxidation (10% v/v hydrogen peroxide), heat (60 °C) and UV light (254 nm). Degradation of the drug substance was observed in base hydrolysis and oxidation. Degradation product formed under these conditions was found to be Imp-A. When the stress samples were assayed, the mass balance was close to 99.5%. The sample solution was stable up to 48 h at 5 °C and mobile phase was found to be stable up to 48 h at 25 °C. The developed method was validated with respect to linearity, accuracy, precision, robustness and forced degradation studies prove the stability indicating power of the method.     

Pyridinium aldoxime analysis by HPLC: the method for studies on pharmacokinetics and stability

Reversed-phase separation of various pyridinium aldoximes requires a certain concentration of ion-pairing agent, as their chemical structures contain two quaternary amines in the pyridinium ring. Adequate mobile phase is scouted on the basis of retention of pyridinium aldoxime (using the graph of k′ versus concentration of an ion-pairing agent) compared to the chromatogram of the background peaks originated from the homogenate. Change in the ion-pairing agent concentration was more expressed for the elution of K-203 than that of the background peaks from the serum, brain and cerebrospinal fluid. Stability of K-203 was investigated using HPLC. Determination of K-203 in tissue samples requires homogenization using either trichloroacetic acid or perchloric acid. Fast degradation takes place at acidic pH. Adjusting pH to neutral in the possible shortest time frame helps to avoid degradation. Degradation of K-203 was easily followed by HPLC separation and monitoring the elution with an ultraviolet absorbance detector at 276 nm. Amperometric detection indicates only the decrease of K-203 content.     

A spark modulator for correlation chromatography

Summary A spark modulator has been tested as an injection system for correlation gas chromatography. An air/hydrocarbon vapour mixture was used as the carrier gas. Single negative sample injections were performed using a single spark period. The experiments resulted in negative sample peaks and a positive product peak. The intensity of all peaks showed a characteristic dependence on the spark frequency and power used. Ghostpeaks were absent when a correlation experiment was performed with a high concentration of a test compound in pure air. The signal to noise ratio enhancement however, was lower than the theoretical value. More experiments are necessary to expalain this phenomenon.     

Continuous wave laser induced degradation of polystyrene monitored by time-of-flight mass spectrometry

The laser induced degradation of polystyrene within the ion-source housing of a time-of-flight mass spectrometer is described. A low power, CO₂ laser was used to produce a steady state flux of degradation products. This method permits the use of normal recording techniques. The degradation of polystyrene is reported using this technique. Evidence is presented that the monomer is ejected from the irradiated surface. Degradation in the presence of oxygen and nitrogen is also described. Oxygen promotes the fragmentation of styrene while nitrogen shows the opposite effect.     

Direct injection of large sample volumes into capillary columns with packed column injector

A direct injection method for large volume samples which avoids severe tailing of the solvent peak has been developed using a packed column injector (up to 100 μl) leading into an ordinary capillary column (0.3 mm i.d.). Modifications are made to the cooler zones of the inlet port and on the carrier gas flow control system. This injection technique is based on the effective use of phase soaking and cold trapping using a retention gap. The large volume of solvent vapor is rapidly purged out of the injector with a higher flow of carrier gas while the solutes trapped at the head of the column are subsequently analyzed with another optimum flow rate. The proposed carrier gas flow regulation system is also compared with conventional split/splitless injection methods.     

Comparison of different injection modes in edible oil minor components analysis

Waxes and fatty acid alkyl esters are minor components used as official parameters to control the authenticity and quality of a high‐value olive oil product. A poor measurement can lead to a misleading classification of the oil. The official method requires their analysis together by capillary gas chromatography equipped with a flame ionization detector and an on‐column injector to avoid discrimination and thermal degradation. The degradation can occur to a different extent if different (and not properly optimized) injectors are used. However, other injection techniques, such as programmed‐temperature vaporizer, are much more versatile and more widespread. The aim of the present work was to compare the performance of a programmed‐temperature vaporizer injector, in on‐column and splitless mode, with the on‐column injector to analyze alkyl esters and waxes. Discrimination among high‐boiling compounds was evaluated, as well as the occurrence of thermal degradation, especially of sterols and diterpene alcohol (phytyl and geranylgeraniol) esters. A proper optimization of a programmed‐temperature vaporizer injection, with particular attention to the liner selection, was proven to provide comparable results to the traditional on‐column injection. A performance comparison was carried out both on standard mixtures and on real oil samples.     

Effect of the particle size and solids volume fraction on the thermal degradation behaviour of Invar 36 feedstocks

Degradation kinetics and the thermal stability of Invar 36 powder injection moulding feedstocks (PIM) based on cellulose acetate butyrate (CAB) and polyethylene glycol (PEG) binders were investigated using simultaneous thermogravimetric analysis (STA) and differential scanning calorimetry (DSC). The initial decomposition temperature (IDT) and the integral procedure decomposition temperature (IPDT) were used to analyse the thermal stability of the binder system as a function of the solid loading content and powder particle size. The degradation kinetics was studied, and the process apparent activation energies were assessed using isoconversional methods. All the methodologies revealed changes in the thermal degradation behaviours of the feedstocks for solid loadings that were previously determined to correspond to optimal solid loadings using other experimental procedures. The studies also contrast previous similar findings with a ceramic powder. Therefore these results strengthen the proposal of thermodynamic degradation studies of feedstocks as an alternative or complementary technique to determine optimal solid loading contents in metal injection moulding (MIM).     

A Stability-Indicating LC Assay Method for Bicalutamide

A stability-indicating HPLC method for the quantitative determination of Bicalutamide is described. Bicalutamide is a nonsteroidal antiandrogen and is an oral medication that is used for treating prostate cancer. Separation was achieved on a Waters Symmetry shield RP18 HPLC column using a mobile phase consists of a mixture of phosphate buffer (Solvent A) and organic modifier acetonitrile (Solvent B). Degradation studies were performed on bulk samples of bicalutamide using acid (0.5 N methanolic hydrochloric acid), base (0.5 N methanolic sodium hydroxide), oxidation (10% v/v methanolic hydrogen peroxide), heat (60 °C) and UV light (254 nm). Degradation was observed under base hydrolysis to give the starting material used during the synthesis of bicalutamide. The degraded samples were assayed and gave a mass balance greater than 99.5%, thus proving the stability-indicating power of the developed method. The method was validated with respect to linearity, accuracy, precision and robustness.     

Thermal analysis applied to the characterization of degradation in soil of polylactide: I. Calorimetric and viscoelastic analyses

An accelerated soil burial test has been performed on a commercial polylactide (PLA) for simulating non-controlled disposal. Degradation in soil promotes physical and chemical changes in polylactide properties, which can be characterized by Thermal Analysis techniques. Physical changes occurred in polylactide due to the degradation in soil were evaluated by correlating their calorimetric and viscoelastic properties. It is highly remarkable that each calorimetric scan offers specific and enlightening information. Degradation in soil affects the polylactide chains reorganization. A multimodal melting behavior is observed for buried PLA, degradation in soil also promotes the enlarging the lamellar thickness distribution of the population with bigger average size. Morphological changes due to degradation in soil lead to an increase in the free volume of the polylactide chains in the amorphous phase that highly affected the bulk properties. Thermal Analysis techniques provide reliable indicators of the degradation stage of polylactide induced by degradation in soil, as corroborated by molecular weight analysis.     

Evaluation of gamma radiation for degradation of a polychlorinated biphenyl in solution and on activated carbon

A polychlorinated biphenyl isomer was irradiated in aqueous solution and in deoxygenated alkaline 2-propanol /0.3M KOH/. Recovery of original PCB was diminished in aqueous solution but no degradation products were seen. Degradation in alkaline 2-propanol was readily achieved by a chain reaction. Polychlorinated biphenyl adsorbed on activated carbon was also irradiated, but no degradation was evident.     

Gas chromatography in qualitative analysis Part 16. An investigation of the oxidation of reference stationary phases used in column characterization by the Rohrschneider and McReynolds methods

Summary The on-column oxidation of hydrocarbons commonly used as stationary phases in column characterization is investigated. In each case significant shifts of retention are observed, which may be negative or positive depending upon the polarity of the test solutes and the adsorptivity of the support material. In order to reduce the consequent uncertainties in the Rohrschneider [1] and McReynolds [2] polarity values, a new method of column characterization is proposed. The applicability of the new method is illustrated by a consideration of a range of silicone liquid phases.     

多路气体自动进样器的研制

研制了一种新型的多路气体自动进样器,可与气相色谱联机,用于钢瓶中气体组分的定性、定量分析,最多可同时分析16个钢瓶气体样品。通过对色谱工作站参数的设定,可自动调整钢瓶气体的进样顺序、进样次数和进样时间。实验表明,与手动进样方式相比,气体自动进样器的应用可显著提高色谱分析的重复性、稳定性,以及气体分析的工作效率和分析精确度。     

Total degradation of fenitrothion and other organophosphorus pesticides by catalytic oxidation employing Fe-TAML peroxide activators

A Fe-TAML/H2O2 catalytic oxidation process achieves facile in-solution total degradation of fenitrothion and two other organophosphorus (OP) pesticides. Degradation products have been identified and quantified providing evidence for oxidative hydrolysis, oxidative desulfuration, perhydrolysis, and deep oxidation. Degradation pathways can be selected by pH control to completely obviate all toxic residuals. Aquatic toxicity assays support the environmental compatibility of the degradation process.