Development and Validation of a Normal-Phase HPTLC-Densitometric Method for the Quantitative Analysis of Fluconazole in Tablets

JPC – Journal of Planar Chromatography – Modern TLC - This paper presents the development and validation of an improved method for the analysis of fluconazole using high-performance...     

Thin-Layer Chromatographic Method for the Quality Control of Dexamethasone and Betamethasone Tablets

Abstract

A rapia, sensitive and specific metnoa for the assay and identincation of corticosteriods (dexamethasone and betamethasone) in tablet forms is described. The method involves a rapia single step extraction of the sterolas with extremely low volume of solvents (0.1 ml water + 0.4 ml ethanol) followed by identifiction and estimation by thin layer chromatography using the solvenc system choroform : methanol : water : 180 : 15 : 1, v/v). The sterolas extracted from the chromatogram by ethanol were assayed directly by measuring the extinotion of the extract at the respective adsorption maxima (around 240 nm). The resuts agree with those obtained by the BP, 1980 and IP, 1966 methods.     

Development and Validation of a High-Performance Thin-Layer Chromatographic Fingerprint Method for the Evaluation of QiYi Capsules with the Reference of Myotonin

JPC – Journal of Planar Chromatography – Modern TLC - The newly developed high-performance thin-layer chromatography (HPTLC) method allowed for the differentiation of QiYi capsules from...     

Development and Validation of a Stability-Indicating High-Performance Thin-Layer Chromatographic Method for the Simultaneous Quantification of Sparfloxacin and Flurbiprofen in Nanoparticulate Formulation

JPC – Journal of Planar Chromatography – Modern TLC - A simple, sensitive, precise, rapid, and reliable high-performance thin-layer chromatographic (HPTLC) method for the simultaneous...     

Comparative Analysis of Rhein Content in Cassia fistula Pod Extract by Thin-Layer Chromatographic-Densitometric and TLC Image Methods

JPC – Journal of Planar Chromatography – Modern TLC - A simple, rapid, and cost-effective thin-layer chromatography (TLC) image analysis was developed and validated to quantify rhein...     

Method Development and Validation of a Rapid Determination of Ropinirole in Tablets by LC-UV

A reversed-phase high-performance liquid chromatographic (HPLC) method with UV detection was developed and validated for the determination of ropinirole (ROP) in tablets. The assay utilized UV detection at 250 nm and a Luna CN column (250 × 4.6 mm I.D, 5 μm). The mobile phases were comprised of acetonitrile: 10 mM nitric acid (pH 3.0) (75:25, v/v). Validation experiments were performed to demonstrate linearity, accuracy, precision, limit of quantitation (LOQ), limit of detection (LOD), and robustness. The method was linear over the concentration range of 0.5–10.0 μg mL⁻¹. The method showed good recoveries (99.75–100.20%) and the relative standard deviations of intra and inter-day assays were 0.38–1.69 and 0.45–1.95%, respectively. The method can be used for quality control assay of ropinirole.     

Separation and Determination of Lamivudine,Tenofovir Disoproxil Fumarate and Efavirenz in Tablet Dosage Form by Thin-Layer Chromatographic-Densitometric Method

JPC – Journal of Planar Chromatography – Modern TLC - This paper describes the development and validation of high-performance thin-layer chromatography (HPTLC) method for the...     

Development and Validation of a High Performance Liquid Chromatographic Method for the Determination of Voriconazole Content in Tablets

This paper describes the validation of an isocratic HPLC method for the assay of voriconazole in tablets. The method employs a Merck LiChrospher^? 100 RP-8 (125 × 4.6 mm I.D., 5 μm particle size) column, with a mobile phase of methanol : triethylamine solutions 0.6 %, pH 6.0 (50:50, v/v) and UV detection at 255 nm. A linear response (r > 0.9999) was observed in the range of 20.0–100.0 μg mL⁻¹. The method showed good recoveries (average 100.4%) and the relative standard deviation intra and inter-day were ≤ 1.0 %. Validation parameters as specificity and robustness were also determined. The method can be used for both quality control assay of voriconazole in tablets and for stability studies as the method separates voriconazole from its degradation products and tablet excipients.     

Development and Validation of a High-Performance Thin-Layer Chromatographic Method for the Simultaneous Estimation of Torsemide and Eplerenone by Quality by Design Approach

JPC – Journal of Planar Chromatography – Modern TLC - This paper includes the development of a novel, systematic, quality by design (QbD)-based high-performance thin-layer...     

Multivariate Optimization and Validation of a CZE Method for the Analysis of Pridinol Mesylate and Meloxicam in Tablets

A capillary zone electrophoresis method for the simultaneous determination of pridinol mesylate (PRI) and meloxicam (MEL) employing epinastine hydrochloride and piroxicam as internal standards, was developed and optimized employing experimental design and response surface methodologies. The separation was optimally achieved in less than 2 min at 30 kV in an uncoated fused-silica capillary (41.4 cm × 75 ??m I.D.), employing an 18 mmol L^?1 sodium phosphate buffer solution (pH 5.90) at 25 °C. Samples were injected in hydrodynamic mode (50 mbar, 5 s) and the analytes were spectrophotometrically detected at 200 nm. Method robustness was demonstrated by ANOVA of determinations performed under conditions slightly different from the optimum. The method was validated regarding separation selectivity (peak purity factors > 0.99), linearity and range (PRI = 17.6?C31.4 mg L^?1; MEL = 66.5?C122.5 mg L^?1), accuracy (PRI = 100.2?C101.9%; MEL = 98.9?C100.7%) and precision. The RSD values obtained were ??1.3% for injection repeatability and ??1.9% for intra-day precision. The limits of detection (1.0 and 0.9 mg L^?1) and quantification (3.3 and 16.5 mg L^?1) of PRI and MEL, respectively, were also determined. The method was successfully applied to the determination of both drugs in three brands of tablet formulations. No statistically significant differences were observed when these results were compared with those of a RP-HPLC method.     

Development and Validation of a Novel Stability-Indicating LC Method for the Determination of Riluzole in Bulk Drug and Tablets

A novel stability indicating LC method was developed and validated for the quantitative determination of riluzole in bulk drugs and in pharmaceutical dosage forms in the presence of its isomers, related substances and degradation products. The drug was subjected to stress conditions of hydrolysis (acid, base and neutral), oxidation, photolysis and thermal degradation. Considerable degradation was observed under base hydrolysis and oxidation. The stress samples were assayed against a qualified reference standard and the mass balance was found close to 99.5%. The developed method was validated with respect to linearity, accuracy, precision, specificity, ruggedness and robustness.     

Development and Validation of a High-Performance Thin-Layer Chromatographic Method for the Assay of Ternary Mixtures Containing Cetirizine Dihydrochloride in Pharmaceutical Dosage Forms

JPC – Journal of Planar Chromatography – Modern TLC - A highly validated and selective high-performance thin-layer chromatography (HPTLC) method was developed for the determination of...     

Development and Validation of a High-Performance Thin-Layer Chromatography Based Method for the Quantification of Trigonelline in Fenugreek (Trigonella foenum-graecum) Seeds

JPC – Journal of Planar Chromatography – Modern TLC - The present research work was undertaken to develop and validate a sensitive, fast, and reproducible high-performance thin-layer...     

Development and Validation of a Stability-Indicating LC Method for Simultaneous Analysis of Aceclofenac and Paracetamol in Conventional Tablets and in Microsphere Formulations

A stability-indicating reversed-phase LC method for analysis of aceclofenac and paracetamol in tablets and in microsphere formulations has been developed and validated. The mobile phase was 80:20 (v/v) methanol–phosphate buffer (10 mM at pH 2.5 ± 0.02). UV detection was at 276 nm. The method was linear over the concentration ranges 16–24 and 80–120 μg mL^?1 for aceclofenac and paracetamol, respectively, with recovery in the range 100.9–102.22%. The limits of detection and quantitation for ACF were 0.0369 and 0.1120 μg mL^?1, respectively; those for PCM were 0.0631 and 0.1911 μg mL^?1, respectively.     

Development and Validation of a Stability-Indicating High-Performance Thin-Layer Chromatographic Method for Determination of Pyridostigmine Bromide in the Presence of Its Alkaline-Induced Degradation Product

JPC – Journal of Planar Chromatography – Modern TLC - A validated, sensitive, and highly selective stability-indicating high-performance thin-layer chromatographic (HPTLC) method has...     

Development and Validation of a High-Performance Thin-Layer Chromatographic Method,with Densitometry,for Quantitative Analysis of Tizoxanide (a Metabolite of Nitazoxanide) in Human Plasma

JPC – Journal of Planar Chromatography – Modern TLC - A new simple, rapid, and selective high-performance thin-layer chromatographic (HPTLC) method with metronidazole as the internal...     

Development and Validation of a Novel High-Performance Thin-Layer Chromatography Method for the Simultaneous Determination of Apigenin and Luteolin in Hygrophila spinosa T. Anders

JPC – Journal of Planar Chromatography – Modern TLC - The present study was undertaken to develop and validate a novel high-performance thin-layer chromatography (HPTLC) method for the...     

Development and Validation of an RP-HPLC Method for Determination of Valganciclovir in Human Serum and Tablets

This paper describes the validation of an isocratic high-performance liquid chromatographic method for the assay of valganciclovir in raw materials, tablets and human serum samples. Valganciclovir and fluvastatin (internal standard) were well separated using a reversed phase column and a mobile phase consisting of a mixture of acetonitrile:methanol:KH₂PO₄ (0.02 M) (40:20:40; v/v/v) (at pH 5.0). The mobile phase was pumped at 1.0 mL min⁻¹ flow rate and valganciclovir was detected by diode-array detection at 255 nm. The retention times for valganciclovir and fluvastatin were 3.41 and 5.60 min, respectively. A linear response (r > 0.999) was observed in the range of 10–30,000 ng mL⁻¹ in mobile phase and serum. The limit of detection and limit of quantification were found as 2.95 and 9.82 ng mL⁻¹ in mobile phase and 1.73 and 5.77 ng mL⁻¹ in human serum samples, respectively. Validation parameters as precision, accuracy, selectivity, reproducibility and system suitability tests were also determined. The method can be used for valganciclovir assay of tablets and human serum samples as the method separates valganciclovir from tablet excipients and endogenous substances.

     

Development and Validation of a High-Performance Thin-Layer Chromatographic—Densitometric Method for the Quantification of Guggulsterones E and Z in a Polyherbal Formulation Containing Commiphora Mukul

JPC – Journal of Planar Chromatography – Modern TLC - The present article focuses on the quantitative analysis of a polyherbal formulation containing arjuna, guggul, and pushkarmoola in...     

Development and Validation of a High-Performance Thin-Layer Chromatography Method for the Quantification of Rutin in the Fruit Pulp of Benincasa hispida (Thunb.) Cogniaux

JPC – Journal of Planar Chromatography – Modern TLC - The fruits of Benincasa hispida (Thunb.) Cogniaux, a ‘rasayana’ in ‘Ayurveda’, are enriched with several...