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[PDF] Top 20 High-performance Liquid Chromatographic Method for the Quantification of Gallic Acid in Simhanada Guggulu

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High-performance Liquid Chromatographic Method for the Quantification of Gallic Acid in Simhanada Guggulu

High-performance Liquid Chromatographic Method for the Quantification of Gallic Acid in Simhanada Guggulu

... RP-HPLC method was developed and validated for estimation of gallic acid in Simhanda ...The gallic acid content in Simhanda guggulu was ...HPLC method will help in ... See full document

6

UV HPLC METHOD DEVELOPMENT AND VALIDATION FOR QUANTIFICATION OF BESIFLOXACIN HYDROCHLORIDE

UV HPLC METHOD DEVELOPMENT AND VALIDATION FOR QUANTIFICATION OF BESIFLOXACIN HYDROCHLORIDE

... carboxylic acid hydrochloride) ...official method was available for the estimation of this drug in the pharmaceutical ...the method using ultraviolet-high performance liquid ... See full document

5

SIMULTANEOUS ESTIMATION OF CURCUMINOIDS, PIPERINE, AND GALLIC ACID IN AN AYURVEDIC FORMULATION BY VALIDATED HIGH PERFORMANCE THIN LAYER  CHROMATOGRAPHIC METHOD

SIMULTANEOUS ESTIMATION OF CURCUMINOIDS, PIPERINE, AND GALLIC ACID IN AN AYURVEDIC FORMULATION BY VALIDATED HIGH PERFORMANCE THIN LAYER CHROMATOGRAPHIC METHOD

... that high-performance thin layer chromatographic (HPTLC) [2-8], high-performance liquid chromatography [9-11], ultraviolet-visible spectroscopic [12], and spectrofluorimetric ... See full document

6

Journal of Applied Pharmaceutical Science

Journal of Applied Pharmaceutical Science

... phase high performance liquid chromatographic method was developed for the simultaneous determination of dutasteride in pharmaceutical formulations and bulk drugs using C-18 column (150 ... See full document

9

SIMULTANEOUS HIGH PERFORMANCE LIQUID CHROMATOGRAPHIC ANALYSIS OF OXICAMS IN PHARMACEUTICAL FORMULATIONS

SIMULTANEOUS HIGH PERFORMANCE LIQUID CHROMATOGRAPHIC ANALYSIS OF OXICAMS IN PHARMACEUTICAL FORMULATIONS

... analytical method for the determination of Tenoxicam (TEN), Piroxicam (PIR) and Meloxicam (MEL) in a finished dosage form was developed and ...citric acid) (60:40),at pH of ...of quantification for ... See full document

9

SIMULTANEOUS QUANTIFICATION OF PENTAZOCINE AND NALOXONE BY STABILITY INDICATING REVERSE PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHIC METHOD:

SIMULTANEOUS QUANTIFICATION OF PENTAZOCINE AND NALOXONE BY STABILITY INDICATING REVERSE PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHIC METHOD:

... The degradation was performed by adding 10 ml of reagent to 10 ml of tablet solution (2000 μg/ml pentazocine and 20 μg/ml naloxone). Hydrochloric acid (0.1 N), sodium hydroxide (0.1 N), deionized water, and ... See full document

6

Stability indicating high performance liquid chromatographic method for the quantification of aliskiren hemifumarate and its related substances

Stability indicating high performance liquid chromatographic method for the quantification of aliskiren hemifumarate and its related substances

... Significant degradation was observed in Aliskiren Hemifumarate stressed sample that were subjected to very sensitive in Acid hydrolysis, Base hydrolysis. Sensitive in Peroxide hydrolysis, Sunlight degradation and ... See full document

9

Liquid Chromatographic Technique for Stability Indicating Analytical Method Development and Validation of Salicylic Acid and Tolnaftate in Pharmaceutical Ointment by High Performance

Liquid Chromatographic Technique for Stability Indicating Analytical Method Development and Validation of Salicylic Acid and Tolnaftate in Pharmaceutical Ointment by High Performance

... indicating high performance liquid chromatography (HPLC) method is developed for the quantification of salicylic acid (SA) and Tolnaftate (TF) in combined pharmaceutical ointment ... See full document

6

Journal of Applied Pharmaceutical Science

Journal of Applied Pharmaceutical Science

... robust highperformance thin‐layer chromatographic (HPTLC) method has been developed for simultaneous estimation of β-sitosterol-D-glucoside, gallic acid, withaferin A and ... See full document

6

Development and validation of stability indicating RP-HPLC method for estimation of Brexpiprazole from bulk and tablet form

Development and validation of stability indicating RP-HPLC method for estimation of Brexpiprazole from bulk and tablet form

... Phase High Performance Liquid Chromatographic (RP-HPLC) method were developed for the quantification of Brexpiprazole in bulk and pharmaceutical dosage form was performed on ... See full document

5

DEVELOPMENT AND VALIDATION OF RP HPLC METHOD TO DETERMINE URSODEOXYCHOLIC ACID IN PHARMACEUTICAL DOSAGE FORMS

DEVELOPMENT AND VALIDATION OF RP HPLC METHOD TO DETERMINE URSODEOXYCHOLIC ACID IN PHARMACEUTICAL DOSAGE FORMS

... phase high performance liquid chromatographic (RP- HPLC) method for the estimation of ursodeoxycholic acid used to solubilize cholesterol gallstones, in conventional tablet ... See full document

6

Reverse Phase High Performance Liquid Chromatographic Method for the Estimation of Curcumin

Reverse Phase High Performance Liquid Chromatographic Method for the Estimation of Curcumin

... phase high performance liquid chromatographic method has been developed for the determination of curcumin, Demethoxy curcumin and Bismethoxy curcumin with short run ...time. ... See full document

6

DEVELOPMENT AND VALIDATION OF REVERSE PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHIC METHOD FOR DETERMINATION OF TIROFIBAN IN SERUM

DEVELOPMENT AND VALIDATION OF REVERSE PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHIC METHOD FOR DETERMINATION OF TIROFIBAN IN SERUM

... the Method: The precision and reproducibility were checked for the period ofseveral days; both within day (n = 5) and between days (n = 5) for two different ...the method. The precision and reproducibility ... See full document

6

Journal of Applied Pharmaceutical Science

Journal of Applied Pharmaceutical Science

... Nigella sativa oil (NSO) has been exploited for medical purposes for many generations. The fabrication of microparticles containing NSO intended for sustained release was done to be used in treating osteomyelitis. ... See full document

7

Development and validation of stability-indicating high performance liquid chromatographic method for the estimation of everolimus in tablets

Development and validation of stability-indicating high performance liquid chromatographic method for the estimation of everolimus in tablets

... of chromatographic conditions were performed to obtain the good peak shape, resolution and peak parameter (tailing factor, theoretical ...orthophosphoric acid (50:50 v/v) at a flow rate of 1 ml/min was ... See full document

6

A 100% Water Mobile Phase HPLC PDA Analysis of Meamine and Related Analogues

A 100% Water Mobile Phase HPLC PDA Analysis of Meamine and Related Analogues

... nized method for residue monitoring in foods is urgently- ...harmonized method must be easy- to-use, economical in time and cost, and must cause no harm to the environment and ... See full document

5

DETERMINATION OF AMOXYCYLLIN AND CLAVULANIC ACID IN PHARMACEUTICAL DOSAGE FORMS BY HPLC WITH AMPEROMETRIC DETECTION

DETERMINATION OF AMOXYCYLLIN AND CLAVULANIC ACID IN PHARMACEUTICAL DOSAGE FORMS BY HPLC WITH AMPEROMETRIC DETECTION

... sensitive high performance liquid chromatographic method with electrochemical detection is described for the quantitative determination of the amoxycillin and clavulanic acid in ... See full document

5

Analytical quality by design approach in RP-HPLC method development for the assay of etofenamate in dosage forms

Analytical quality by design approach in RP-HPLC method development for the assay of etofenamate in dosage forms

... in chromatographic condition is very ...between method results (Y; such as t R ) and input variables, a central composite design was designed and ... See full document

7

Development and Validation of Spectrophotometric and Chromatographic Method for the Estimation of Apremilast in Bulk and Formulations

Development and Validation of Spectrophotometric and Chromatographic Method for the Estimation of Apremilast in Bulk and Formulations

... Phase High Performance Liquid Chromatography Method for Determination of Assay and Forced Degradation Study of Apremilast from Active Pharmaceutical Dosage Form, Journal of Chemical and ... See full document

7

Development and validation of reversed-phase high performance liquid chromatographic method for hydroxychloroquine sulphate

Development and validation of reversed-phase high performance liquid chromatographic method for hydroxychloroquine sulphate

... The drug HCQ and internal standard CQ stock solutions of 100 µg/ml were prepared by dissolving 10 mg of each in 100 ml of volumetric flasks separately with distilled water. This was further diluted by pH 1.5 of HCl ... See full document

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