Spectrophotometric Methods For The Determination Of Lipoic Acid By Using MBTH And Ferric Chloride

DOI : 10.17577/IJERTV1IS7173

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Spectrophotometric Methods For The Determination Of Lipoic Acid By Using MBTH And Ferric Chloride

The oxidative coupling of the proposed method is simple, rapid and sensitive with reasonable precision and accuracy. The precision of the method was found by analyzing a set of eight solutions, each containing a final concentration value approximately in the middle of the Beers law range. The percent relative standard deviation in this method is presented in table-2. The accuracy of the method was determined by taking different known amounts (with in Beers law limits) of the drug and analyzing them by proposed method. The results are given in table 3. In the determination of Lipoic acid the excipients usually present in formulations (glucose, starch, sodium hexa phosphate and some vitamins) and the other antioxidants and antidiabetics did not interfere.

A very few physico-chemical methods have appeared in the literature for the determination of Alpha-Lipoic Acid (-LA) in bulk and pharmaceutical formulations. The literature suggested and reported only a few chromatographic techniques like Gas chromatographic methods with flame ionization detection and flame photometric detection, High-performance liquid chromatographic methods with ultraviolet, fluorescence and electrochemical detection, spectrophotometric using palladium(II) chloride, Reversed phase liquid chromatography, LC-MS/MS with atmospheric pressure chemical ionization and electro spray ionization interfaces, Tandem mass spectrometry, Electrophoresis, Extractive spectrophotometry and potentiometric techniques. The analytically important functional groups of -LA are not fully exploited for designing suitable spectrophotometric methods for the determination of -LA. Hence the need arises to develop certain sensitive, precise, accurate and flexible visible spectrophotometric methods, which prompted the authors to

choose -LA for the investigation based on various chemical reactions, by exploiting various functional groups from the structure.

These methods are based on the reaction of -LA with MBTH and compounds like ferric chloride and to produce colored species of reasonable stability, paving the possibility for spectrophotometric determination of -LA in its bulk from and pharmaceutical formulations.

I) Lipoic acid (0.25mg/ml): The stock solution (0.25mg/ml) of Lipoic Acid was prepared by dissolving 100mg of the drug in 400ml of distilled water to get a clear solution. A portion of this stock solution was diluted to get the working standard solutions of concentration 100 g/ml.

All the other chemical reagents were of analytical grade.

  1. MBTH(0.2%):this solution was prepared by dissolving 200mg of analytical grade,MBTH in 100ml of double distilled water.

  2. ferric chloride solution(0.7%):700mg of analytical grade ferric chloride in 100ml of 0.5N HCL.

    Procedure : An aliquotes of standard lipoicacid solution (100 g/ml) ranging from 0.4 to 2.0ml are taken into a series of 10ml graduated test tubes and aqueous solutions of MBTH(1.5ml), Fecl3 (2ml) were added. The solution was kept aside for 10minuites and solutions were stir occasionally. The solutions were finally made up to the mark with distilled water and absorbance of the green colored solution was measured at 450nm against the corresponding reagent blank.

    Comparison of the results incorporated in Tables 1 4 reveal that the proposed method is simple, rapid and sensitive with reasonable precision and accuracy.

    Fig 5.1: absorption spectra of

    Lipoic acid with MBTH and Ferric chloride

    Concentration range(µg/ml) (or) Beers law limit

    4.0 to 20.0

    * Regression equation

    A=0.1369-0.0023C

    Correlation coefficient

    0.9989

    Molar absorptivity (1-mole -1 cm-1)

    2.55*104

    Sandells sensitivity

    (µg / cm2 / 0.001 absorbance unit)

    0.0083

    Optimum photometric range (µg/ml)

    5.2 to 16.8

    *Found in this work; it must be determined independently by users of the method.

    Compound

    % RSD**

    % Range of errors confidence limit

    0.05 level

    0.01level

    Lipoic acid

    1.002

    ±0.8456

    ±1.246

    Amount of Lipoic acid ( µg)

    % Error

    Taken

    Found

    450

    442.2

    1.73

    Sample

    Labeled amount

    **Amount found(µg) in method

    *Recovery proposed method

    Proposed

    Reported

    Tablet

    150

    148.1

    146.8

    98.7

    Capsule

    150

    147.3

    146.1

    99.3

    Capsule

    300

    298.1

    297.2

    99.3

    Capsule

    450

    447.9

    446.3

    99.6

    * Each result is an average of three determinations ** After adding 5 mg of drug.

    The proposed method is simple, rapid and sensitive with reasonable precision and accuracy and it is useful for the determination of Lipoic acid in bulk samples, pharmaceutical preparations and biological fluids.

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