IN SILICO TOXICITY PREDICTION OF ANTIOXIDANT FOOD ADDITIVES
Antioxidant food additives are used to prevent or slowing down the oxidation process in foods. European Food Safety Authority (EFSA) by EC257/2010 regulation set up a programme for reevaluation of approved antioxidant food additives. Safety of the food additive was one of its concern. The aim of...
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Format: | Theses |
Language: | Indonesia |
Online Access: | https://digilib.itb.ac.id/gdl/view/45295 |
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Institution: | Institut Teknologi Bandung |
Language: | Indonesia |
Summary: | Antioxidant food additives are used to prevent or slowing down the oxidation
process in foods. European Food Safety Authority (EFSA) by EC257/2010
regulation set up a programme for reevaluation of approved antioxidant food
additives. Safety of the food additive was one of its concern. The aim of the
present research was to predict toxicity of antioxidant food additives using in
silico toxicity prediction as preliminary evaluation of safety antioxidant food
additives. The in silico prediction was conducted for acute toxicity (LD50),
mutagenicity, carcinogenicity, reproduction toxicity, chronic toxicity (NOEL),
Acceptable Daily Intake (ADI) value and metabolit toxicity. The applied software
for the study were Toxtree, TEST, Admet Predictor and OECD QSAR Toolbox.
Among 42 antioxidant food additives, the prediction methods predict that 7
compounds as carcinogen (carnosic acid, citric acid, ethylene diamine tetra
acetate, isopropyl citrate, octyl gallate, ascorbyl stearate and stearyl citrate); 2
compounds as mutagen (ascorbyl palmitate and 2,4,5-trihydroxybutyrophenone);
6 compounds as reproduction toxic (4 hexyl resorcinol, alpha tocopherol, delta
tocopherol, ethoxyquine, gamma tocopherol, tertiary butyl hydroquinone); 2
compounds as carcinogen and reproduction toxic (butylated hydroxy anisole,
isomer butylated hydroxy anisole); and 1 compound as mutagen and reproduction
toxic, that is norhydroguairetic acid. Acute toxicity prediction was conducted by
LD50 prediction. The lowest LD50 value was shown by ethoxyquine, 937.84
mg/kg, while the highest LD50 value was observed of dilauryl thiodipropionate,
13367.79 mg/kg. The comparison between LD50 prediction and LD50
experimental using paired t-test method. Showed that there is no significantly
difference between predict LD50 and experimental LD50. Chronic toxicity
prediction was conducted by NOEL value predcition, and ADI value was
calculated from NOEL value. The compound with lowest ADI value is carnosic
acid (0.38 mg/kg bw/day), while the highest ADI value was shown citric acid
(1.67 mg/kg bw/day). The camparison between ADI prediction and ADI
experimental using paired t-test method showed that there is no significant
difference between predicted ADI and experimental ADI. Metabolite prediction
was conducted using two software, that were Toxtree and Admet Predictor. The
metabolite prediction showed a change in prediction result compared to its parent
compound. In concluson, the in silico toxicity prediction method can be used as
one supportive method to performe food additive safety evaluation by prediction
of carcinogen, genotoxicity, reproduction toxicity, LD50 value and ADI value.
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