The effect of sunset yellow food coloring (E110) on the zebrafish (Danio rerio) embryos development

Penulis

  • Galuh Mahardika Agustin Universitas Sebelas Maret
  • Dewi Puspita Sari Universitas Sebelas Maret

DOI:

https://doi.org/10.33751/injast.v7i1.51

Kata Kunci:

Embryotoxicity, LC50, Somite development, Sunset Yellow, Zebrafish

Abstrak

Synthetic food coloring sunset yellow (E110) is widely used due to its color stability and low production cost; however, it may pose toxic effects during the early developmental stages of aquatic organisms. This study aimed to evaluate the embryotoxicity of sunset yellow in zebrafish (Danio rerio) embryos, determine the median lethal concentration (LC₅₀) as an indicator of acute toxicity, and analyze its effects on embryonic development, with a particular focus on somite formation. The study employed a completely randomized design (CRD) using the fish embryo toxicity test, with one control group and three treatment groups exposed to sunset yellow at 200 ppm, 400 ppm, and 800 ppm. Observed parameters included survival rate, hatching rate, heart rate, somite development, and morphological alterations in the embryo. Data were analyzed using One-Way ANOVA and Two-Way ANOVA with IBM SPSS software at a significance level of α = 0.05. The results showed that the LC50 value of Sunset yellow for zebrafish embryos was 416.67 ppm. Exposure to sunset yellow significantly decreased survival rate and hatching rate (p = 0.004 and p = 0.033, respectively) and significantly affected embryonic heart rate based on concentration and exposure duration (p < 0.001). Disruption of somite development was primarily observed during early embryogenesis, characterized by indistinct somite boundaries at higher concentrations. Additionally, concentration-dependent morphological abnormalities were observed, including shortened body length, delayed hatching, and increased body curvature. These findings suggest that Sunset yellow exhibits embryotoxic effects in zebrafish and may pose an ecological risk to aquatic organisms.

Referensi

Al-Zghoul, M. B., & El-Bahr, S. M. (2019). Basal And Dynamics Mrna Expression Of Muscular Hsp108, Hsp90, Hsf-1 And Hsf-2 In Thermally Manipulated Broilers During Embryogenesis. Bmc Veterinary Research, 15(1), 1–11.

Barciela, P., Perez-Vazquez, A., & Prieto, M. A. (2023). Azo dyes in the food industry: Features, classification, toxicity, alternatives, and regulation. Food and Chemical Toxicology, 178, 113935.

Gao, C., Ran, C., Zhang, Z., Ding, Q., Xie, M., Zhang, H., Yang, Y., Duan, M., & Zhou, Z. (2017). Chemical-induced oxidative stress affects melanocyte distribution during zebrafish embryogenesis. Aquatic Toxicology.

Hahn, M. E., McArthur, A. G., Karchner, S. I., Franks, D. G., Jenny, M. J., & Di Giulio, R. T. (2014). The Transcriptional Response to Oxidative Stress during Vertebrate Development Effects of tert-Butylhydroquinone and 2,3,7,8-Tetrachlorodibenzo-p-Dioxin. PLOS ONE, 9(11), e113158. https://doi.org/https://doi.org/10.1371/journal.pone.0113158

He, J., Zhang, Y., Yang, Y., Wang, X., & Li, H. (2020). Effects of environmental toxicants on cardiac development and function in zebrafish embryos. Environmental Toxicology and Pharmacology.

Huang, D., Li, H., He, Q., Yuan, W., Chen, Z., & Yang, H. (2018). Developmental Toxicity of Diethylnitrosamine in Zebrafish Embryos/Juveniles Related to Excessive Oxidative Stress. Water, Air, and Soil Pollution, 229(3). https://doi.org/10.1007/s11270-018 3739-8

Jiang, L. L., Li, K., Yan, D. L., Yang, M. F., Ma, L., & Xie, L. Z. (2020). Toxicity assessment of four azo dyes in zebrafish embryos. International Journal of Toxicology, 39(2), 115–123.

Khosim, N., Latuconsina, H., & Suhada, R. A. (2023). Perkembangan Embrio dan Rasio Penetasan Telur Ikan Zebra Danio rerio (Hamilton, 1822) di Instalasi Perikanan Budidaya Punten Batu. JUSTE (Journal of Science and Technology), 3(2), 152–165. https://doi.org/10.51135/justevol3issue2page152-165

Kimmel, C. B., Ballard, W. W., Kimmel, S. R., Ullmann, B., & Schilling, T. F. (1995). Stages of embryonic development of the zebrafish. Developmental Dynamics, 203(3), 253 310.

https://doi.org/10.1002/aja.1002030302

Koca, Y. B., Ozmen, M., & Yildirim, M. Z. (2015). Developmental toxicity of food additives on fish embryos.

Environmental Science and Pollution Research.

Lockwood, B. L., Julick, C. R., & Montooth, K. L. (2017). Maternal Loading Of A Small Heat Shock Protein Increases Embryo Thermal Tolerance In Drosophila Melanogaster. Journal Of Experimental Biology, 220(23), 4492–4501.

Oetelaar, D. Van Den, Tobor-kapłon, M. A., Reijnaers, M., & Beekhuijzen, M. (2025). Zebrafish Embryo Developmental Toxicity Assay ( ZEDTA ) for Regulatory Testing — Protocol Optimization and Historical Control Data. Toxics, 13, 1–19.

Rarassari, M. A., Riani, Ira, G., Ritonga, Nia, B., & Cahya, G. (2023). Sosialisasi Penyalahgunaan Zat Pewarna Dan Pengawet Makanan Berbahaya Sebagai Upaya Penjaminan Keamanan Pangan. Jurdimas (Jurnal Pengabdian Kepada Masyarakat) Royal, 6(3), 398–403. https://doi.org/https://doi.org/10.33330/jurdimas.v6i3.2503

Rousseaux, C. (2005). Trouble shooting in toxicopathology. Toxicology and Applied Pharmacology, 207(2), 214–224. https://doi.org/10.1016/j.taap.2005.01.036

Roy, N. M., Carneiro, B., & Ochs, J. (2016). Glyphosate induces neurotoxicity in zebrafish. Environmental Toxicology and Pharmacology, 42, 45–54. https://doi.org/10.1016/j.etap.2016.01.003

Sano, K., Inohaya, K., Kawaguchi, M., Yoshizaki, N., Iuchi, I., & Yasumasu, S. (2008). Purification and characterization of zebrafish hatching enzyme - an evolutionary aspect of the mechanism of egg envelope digestion. FEBS Journal, 275(23), 5934–5946. https://doi.org/https://doi.org/10.1111/j.1742- 4658.2008.06722.x

Scholz, S., Fischer, S., Gündel, U., Küster, E., Luckenbach, T., & Voelker, D. (2008). The zebrafish embryo model in environmental risk assessment - Applications beyond acute toxicity testing. Environmental Science and Pollution Research, 15(5), 394–404. https://doi.org/10.1007/s11356-008-0018-z

Small, C. D., Liss, S. E., & Burggren, W. W. (2020). Matrix Metalloproteinase 13 Activity is Required for Normal and Hypoxia-Induced Precocious Hatching in Zebrafish Embryos. Journal of Developmental Biology, 8(1), 3. https://doi.org/https://doi.org/10.3390/jdb8010003

Sunu, B. (2018). Penggunaan Zat Pewarna Sintetis pada Sirup Yang Dijual di Pasar Modern Kota Makassar. Jurnal Kesmas Untika Luwuk : Public Health Journal, 9(2), 11–17. https://doi.org/10.51888/phj.v9i2.9

OECD. (2013). Test No. 236: Fish Embryo Acute Toxicity (FET) Test. OECD Guidelines for the Testing of Chemicals, Section 2, OECD Publishing, July, 1–22. http://www.oecd ilibrary.org

Yesudhason, B. V., Selvan Christyraj, J. R. S., Ganesan, M., Subbiahanadar Chelladurai, K., Venkatachalam, S., Ramalingam, A., Benedict, J., Paulraj, V. D., & Selvan Christyraj, J. D. (2020). Developmental stages of zebrafish (Danio rerio) embryos and toxicological studies using foldscope microscope. Cell Biology International, 44(10), 1968–1980. https://doi.org/10.1002/cbin.11412

Diterbitkan

2026-04-30

Cara Mengutip

Agustin, G. M., & Sari, D. P. (2026). The effect of sunset yellow food coloring (E110) on the zebrafish (Danio rerio) embryos development. Indonesian Journal of Applied Environmental Studies, 7(1), 52–59. https://doi.org/10.33751/injast.v7i1.51