STABILITY OF VITAMIN C UNDER INFLUENCE OF RUTIN ADDITION AS ANTIOXIDANT
Background: Beverage supplements containing high dose of vitamin C (L-ascorbic acid) are widely available in the market. However vitamin C is unstable and can be easily oxidized to form L-dehydroascorbic. This reaction will be influenced by contact with air, moisture and water, under exposure to...
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Format: | Theses |
Language: | Indonesia |
Online Access: | https://digilib.itb.ac.id/gdl/view/45724 |
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Institution: | Institut Teknologi Bandung |
Language: | Indonesia |
Summary: | Background: Beverage supplements containing high dose of vitamin C (L-ascorbic
acid) are widely available in the market. However vitamin C is unstable and can be
easily oxidized to form L-dehydroascorbic. This reaction will be influenced by
contact with air, moisture and water, under exposure to light, and high temperature.
Addition of water-soluble antioxidant is a common method to prevent this reaction
in beverage products. Rutin is a water-soluble bioflavonoid compound containing
phenol groups and hence reported to show good antioxidant activities. The aims of
this research were to obtain analytical method for the determination of vitamin C in
the presence of rutin and to obtain data whether the addition of rutin is able to
prevent the degradation of vitamin C under standardized experimental conditions.
For this purposes a High Performance Liquid Chromatographic (HPLC) method for
the quantification of vitamin C will be applied. Method: Prior the stability test, due
to possible interference from rutin, an analytical method development for the
determination of vitamin C in the presence of rutin should be performed which
includes system suitability test and method validation. An HPLC method using
Phenomenex C18 column (3.90 x 150 mm, 10µm), UV detector at 254 nm and
methanol –formic acid 0.05% (20 : 80) mobile phase by gradient elution at 1.2 mL
min
-1
of flow rate was applied. The stabilities of vitamin C in solutions under
influence and no influence of rutin were tested at incubation temperatures of 50 and
70
o
C up to 2 days for test substance dissolved in phosphate buffer pH 5.4, while
for that dissolved in mineral-free water up to 16 days. Result: Under the optimal
condition, the method gave linear calibration curve over the range of 5.06 - 13.15
µg/mL for vitamin C with a regression equation of y = 36161.72x –96094 and
regression coefficient of r = 0.9992. The limit of detection and limit of
quantification for vitamin C were 0.75 dan 1.83 µg/mL respectively. The intra-day
relative standard deviation (RSD) of the method were 0.595, 0.211 and 0.349 %
respectively and inter-day RSD was 0.43 %. The recovery for vitamin C in sample
simulation was in a range of 98.29 - 103.92 %. Independent of incubation
temperatures, the results of stability test revealed that the addition of rutin was failed
to prevent the degradation of vitamin C dissolved in both mineral-free water and
phosphate buffer pH 5.4. Only slight inhibition of vitamin C degradation was
observed from the 0 to 240
th
hours in the case of vitamin C dissolved in mineralfree water and incubated at both 50 and 70
o
C. The rate of degradation reaction
occurred at second order for vitamin C and first order for vitamin C with addition
of rutin (10:1) Conclusion: The method is suitable for the simultaneous
determination of vitamin C and rutin in mixture solution without prior separation.
The overall results of stability test revealed that the addition of rutin was failed to
prevent the degradation of vitamin C under these experimental conditions.
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