Toxicity in vitro and in Zebrafish Embryonic Development of Gold Nanoparticles Biosynthesized Using Cystoseira Macroalgae Extracts

References

• Amini SM. Gold nanostructures absorption capacities of various energy forms for thermal therapy applications. J Therm Biol. 2019;79:81–84.
   PubMedGoogle Scholar
• Bouché M, Hsu JC, Dong YC, Kim J, Taing K, Cormode DP. Recent advances in molecular imaging with gold nanoparticles. Bioconjug Chem. 2020;31:303–314.
   PubMed Web of Science ®Google Scholar
• Goddard ZR, Marín MJ, Russell DA, Searcey M. Active targeting of gold nanoparticles as cancer therapeutics. Chem Soc Rev. 2020;49:8774–8789.
   PubMed Web of Science ®Google Scholar
• Kang MS, Lee SY, Kim KS, Han DW. State of the art biocompatible gold nanoparticles for cancer theragnosis. Pharmaceutics. 2020;12(701):1–22.
   Google Scholar
• Prado-López S, González-Ballesteros N, Rodríguez-Argüelles MC. Nanometals in cancer diagnosis and therapy. In: Zivic F, Affatato S, Trajanovic M, Schnabelrauch M, Grujovic N, Choy KL, editors. Biomaterial in Clinical Practice. Advances in Clinical Research and Medical Devices. Switzerland: Springer; 2018:407–428.
   Google Scholar
• Yan L, Zhao F, Wang J, Zu Y, Gu Z, Zhao Y. A safe-by-design strategy towards safer nanomaterials in nanomedicines. Adv Mater. 2019;1805391:1–33.
   Google Scholar
• Miller MR, Poland CA. Nanotoxicology: the need for a human touch? Small. 2020;16(2001516):1–12.
   Google Scholar
• Zielinska A, Costa B, Ferreira MV, et al. Nanotoxicology and nanosafety: safety-by-design and testing at a glance. Int J Environ Res Public Health. 2020;17(4657):1–23.
   Google Scholar
• Dlugosz O, Szostak K, Staron A, Pulit-Prociak J, Banach M. Methods for reducing the toxicity of metal and metal oxide NPs as biomedicine. Materials. 2020;13(2):279–298.
   PubMed Web of Science ®Google Scholar
• Lee KX, Shameli K, Yew YP, et al. Recent developments in the facile bio-synthesis of gold nanoparticles (AuNPs) and their biomedical applications. Int J Nanomedicine. 2020;15:275–300.
   PubMed Web of Science ®Google Scholar
• Kalimuthu K, Cha BS, Kim S, Park KS. Eco-friendly synthesis and biomedical applications of gold nanoparticles: a review. Microchem J. 2020;152:104296–104315.
   Google Scholar
• González-Ballesteros N, Rodríguez-Argüelles MC. Seaweeds: a promising bionanofactory for ecofriendly synthesis of gold and silver nanoparticles. In: Torres MD, Kraan S, Dominguez H, editors. Advances in Green and Sustainable Chemistry. Sustainable Seaweed Technologies Cultivation, Biorefinery, and Applications. 1st ed. Elsevier; 2020:507–541.
   Google Scholar
• Bruno de Sousa C, Gangadhar KN, Macridachis J, et al. Cystoseira algae (fucaceae): update on their chemical entities and biological activities. Tetrahedron Asymmetry. 2017;28(11):1486–1505.
   Google Scholar
• Ammar HH, Lajili S, Said RB, Cerf DL, Bouraoui A, Majdoub H. Physico-chemical characterization and pharmacological evaluation of sulfated polysaccharides from three species of Mediterranean brown algae of the genus. DARU J Pharmaceutical Sci. 2015;23(1):1–8.
   Google Scholar
• Vizetto-Duarte C, Custódio L, Acosta G, et al. Can macroalgae provide promising anti-tumoral compounds? A closer look at Cystoseira tamariscifolia as a source for antioxidant and anti-hepatocarcinoma compounds. PeerJ. 2016;4:e1704–e1704.
   PubMed Web of Science ®Google Scholar
• Vizetto-Duarte C, Custódio L, Gangadhar KN, et al. Isololiolide, a carotenoid metabolite isolated from the brown alga Cystoseira tamariscifolia, is cytotoxic and able to induce apoptosis in hepatocarcinoma cells through caspase-3 activation, decreased bcl-2 levels, increased p53 expression and PARP cleava. Phytomedicine. 2016;23(5):550–557.
   PubMed Web of Science ®Google Scholar
• Alarif WM, Basaif SA, Badria FA, Ayyadd SN. Two new cytotoxic C-29 steroids from the red sea brown alga Cystoseira Trinodis. Chem Nat Comp. 2015;51(4):697–702.
   Web of Science ®Google Scholar
• Klebowski B, Depciuch J, Parlinska-Wojtan M, Baran J. Applications of noble metal-based nanoparticles in medicine. J Mol Sci. 2018;19(4031):1–17.
   Google Scholar
• Daraee H, Eatemadi A, Abbasi E, Aval SF, Kouhi M, Akbarzadeh A. Application of gold nanoparticles in biomedical and drug delivery. Artif Cells Nanomed Biotechnol. 2016;44(1):410–422.
   PubMed Web of Science ®Google Scholar
• Bai C, Tang M. Toxicological study of metal and metal oxide nanoparticles in zebrafish. J Applied Toxicol. 2020;40(1):37–63.
   PubMed Web of Science ®Google Scholar
• Botha TL, Brand SJ, Ikenaka Y, Nakayama SMM, Ishizuka M, Wepener V. How toxic is a non-toxic nanomaterial: behaviour as an indicator of effect in Danio rerio exposed to nanogold. Aquatic Toxicology. 2019;215:105287–105297.
   PubMedGoogle Scholar
• Dumitrescu E, Wallace K, Andreescu S. Nanotoxicity assessment using embryonic zebrafish. Methods Mol Biol. 2019;1894:331–343.
   PubMedGoogle Scholar
• Haque E, Ward AC. Zebrafish as a model to evaluate nanoparticle toxicity. Nanomaterials. 2018;8:561.
   Web of Science ®Google Scholar
• Pereira AC, Gomes T, Machado MRF, Rocha TL. The zebrafish embryotoxicity test (ZET) for nanotoxicity assessment: from morphological to molecular approach. Environ Pollut. 2019;252:1841–1853.
   PubMedGoogle Scholar
• Liu H, Wang X, Wu Y, et al. Toxicity responses of different organs of zebrafish (Danio rerio) to silver nanoparticles with different particle sizes and surface coatings. Environ Pollut. 2019;246:414–422.
   PubMed Web of Science ®Google Scholar
• Khoshnamvand M, Hao Z, Fadare OO, Hanachi P, Chen Y, Liu J. Toxicity of biosynthesized silver nanoparticles to aquatic organisms of different trophic levels. Chemosphere. 2020;258:127346.
   PubMedGoogle Scholar
• Aksakal FI, Sisman T. Developmental toxicity induced by Cu(OH)2 nanopesticide in zebrafish embryos. Environ Toxicol. 2020;35:1289–1298.
   PubMedGoogle Scholar
• Pereira AC, Gonçalves BB, Brito RS, Vieira LG, Lima ECO, Rocha TL. Comparative developmental toxicity of iron oxide nanoparticles and ferric chloride to zebrafish (Danio rerio) after static and semi-static exposure. Chemosphere. 2020;254:126792.
   PubMedGoogle Scholar
• Tang T, Zhang Z, Zhu X. Toxic effects of TiO2 NPs on zebrafish. Int J Environ Res Public Health. 2019;16:523.
   PubMed Web of Science ®Google Scholar
• González-Ballesteros N, Prado-López S, Rodríguez-González JB, Lastra-Valdor M, Rodríguez-Argüelles MC. Green synthesis of gold nanoparticles using brown seaweed Cystoseira baccata: its activity in colon cancer cells. Colloids Surf B Biointerfaces. 2017;153:190–198.
   PubMed Web of Science ®Google Scholar
• González-Ballesteros N, Rodríguez-González JB, Lastra-Valdor M, Rodríguez-Argüelles MC. New application of two Antarctic macroalgae Palmaria decipiens and Desmarestia menziesii in the synthesis of gold and silver nanoparticles. Polar Sci. 2018;15:49–54.
   Google Scholar
• Wang H, Cheng H, Wang F, Wei D, Wang X. An improved 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) reduction assay for evaluating the viability of Escherichia coli cells. J Microbiol Methods. 2010;82(3):330–333.
   PubMed Web of Science ®Google Scholar
• Gellert G, Heinrichsdorff J. Effect of age on the susceptibility of zebrafish eggs to industrial wastewater. Water Res. 2001;35(15):3754–3757.
   PubMedGoogle Scholar
• Mohapatra DP, Brar SK, Daghrir R, et al. Photocatalytic degradation of carbamazepine in wastewater by using a new class of whey-stabilized nanocrystalline TiO2 and ZnO. Sci Total Environ. 2014;485:263–269.
   PubMed Web of Science ®Google Scholar
• Bhattacharjee S. DLS and zeta potential – what they are and what they are not? J Control Release. 2016;235:337–351.
   PubMed Web of Science ®Google Scholar
• Ainane T, Abourriche A, Kabbaj M. Physico-chemical analysis by SEM-EDX and FTIR two brown algae Cystoseira tamariscifolia and Bifurcaria bifurcata. Anal Chem. 2007;6(2):4–8.
   Google Scholar
• Vizetto-Duarte C, Custódio L, Barreira L, et al. Proximate biochemical composition and mineral content of edible species from the genus Cystoseira in Portugal. Bot Mar. 2016;59(4):251–257.
   Web of Science ®Google Scholar
• Rodrigues D, Freitas AC, Pereira L, et al. Chemical composition of red, brown and green macroalgae from buarcos bay in central west coast of Portugal. Food Chem. 2015;183:197–207.
   PubMed Web of Science ®Google Scholar
• Balboa EM, Gallego-Fabrega C, Moure A, Dominguez H. Study of the seasonal variation on proximate composition of oven-dried Sargassum muticum biomass collected in Vigo ria, Spain. J Appl Phycol. 2016;28(3):1943–1953.
   Google Scholar
• Belattmani Z, El Atouani S, Kaidi S, et al. Protonated biomass of the brown seaweed Cystoseira tamariscifolia: a potential biosorbent for toxic chromium ions removal. Res J Environ Sci. 2018;12(3):106–113.
   Google Scholar
• Zhu B, Ni F, Xiong Q, Yao Z. Marine oligosaccharides originated from seaweeds: source, preparation, structure, physiological activity and applications. Crit Rev Food Sci Nutr. 2020. doi:10.1080/10408398.2020.1716207
   Google Scholar
• Fernández PV, Ciancia M, Estévez JM. Cell wall variability in the green seaweed Codium vermilara (bryopsidales chlorophyta) from the Argentine coast. J Phycol. 2011;47:802–810.
   PubMed Web of Science ®Google Scholar
• Estévez JM, Fernández PV, Kasulin L, Dupree P, Ciancia M. Chemical and in situ characterization of macromolecular components of the cell walls from the green seaweed Codium fragile. Glycobiology. 2009;19(3):212–228.
   PubMed Web of Science ®Google Scholar
• Tabarsa M, You S, Dabaghian EH, Surayot U. Water-soluble polysaccharides from Ulva intestinalis: molecular properties, structural elucidation and immunomodulatory activities. J Food Drug Anal. 2018;26(2):599–608.
   PubMed Web of Science ®Google Scholar
• El-Rafie H, El-Rafie M, Zahran MK. Green synthesis of silver nanoparticles using polysaccharides extracted from marine macro algae. Carbohydr Polym. 2013;96(2):403–410.
   PubMed Web of Science ®Google Scholar
• Alipour HJ, Rezaei M, Shabanpour B, Tabarsa M. Effects of sulfated polysaccharides from green alga Ulva intestinalis on physicochemical properties and microstructure of silver carp surimi. Food Hydrocoll. 2018;74:87–96.
   Google Scholar
• Abdala-Diaz RT, Cabellor-Pasisni A, Márquez-Garrido E, López-Figueroa F. Intra-thallus variation of phenolic compounds, antioxidant activity, and phenolsulphatase activity in Cystoseira tamariscifolia (phaeophyceae) from southern Spain. Cienc Mar. 2014;40(1):1–10.
   Google Scholar
• Celis-Plá PSM, Bouzon ZL, Hall-Spencer JM, Schmidt EC, Korbee N, Figueroa FL. Seasonal biochemical and photophysiological responses in the intertidal macroalga Cystoseira tamariscifolia (ochrophyta). Mar Environ Res. 2016;115:89–97.
   PubMed Web of Science ®Google Scholar
• Custódio L, Silvestre L, Rocha MI, et al. Methanol extracts from cystoseira tamariscifolia and Cystoseira nodicaulis are able to inhibit cholinesterases and protect a human dopaminergic cell line from hydrogen peroxide-induced cytotoxicity. Pharm Biol. 2016;54(9):1687–1696.
   PubMed Web of Science ®Google Scholar
• Pinteus S, Silva J, Alves C, et al. Cytoprotective effect of seaweeds with high antioxidant activity from the Peniche coast (Portugal). Food Chem. 2017;218:591–599.
   PubMed Web of Science ®Google Scholar
• Samri N, Hsaine L, El Kafhi S, Khlifi S, Etahiri S. Radical scavenging activity and phenolic contents of brown seaweeds harvested from the coast of Sidi Bouzid (El Jadida, Morocco). Int J Pharm Sci Rev Res. 2019;54(21):116–122.
   Google Scholar
• Andrade PB, Barbosa M, Matos RP, et al. Valuable compounds in macroalgae extracts. Food Chem. 2013;138:1819–1828.
   PubMed Web of Science ®Google Scholar
• Ramachandran R, Krishnaraj C, Kumar VKA, Harper SL, Kalaichelvan TP, Yun SI. In vivo toxicity evaluation of biologically synthesized silver nanoparticles and gold nanoparticles on adult zebrafish: a comparative study. Biotech. 2018;8(441).
   Google Scholar
• Kimmel CB, Ballard WW, Kimmel SR, Ullmann B, Schilling TF. Stages of embryonic development of the zebrafish. Dev Dyn. 1995;203(3):253–310.
   PubMed Web of Science ®Google Scholar
• Bonsignorio D, Perego L, Del Giacco L, Cotelli F. Structure and macromolecular composition of the zebrafish egg chorion. Zygote. 1996;4(2):101–108.
   PubMed Web of Science ®Google Scholar
• Rawson DM, Zhang T, Kalicharan D, Jongebloed WL. Field emission scanning electron microscopy and transmission electron microscopy studies of the chorion, plasma membrane and syncytial layers of the gastrula‐stage embryo of the zebrafish Brachydanio rerio: a consideration of the structural and functional relationships with respect to cryoprotectant penetration. Aquaculture Res. 2000;31:325–336.
   Google Scholar
• Fraher D, Sanigorski A, Mellett NA, Meikle PJ, Sinclair AJ, Gibert Y. Zebrafish embryonic lipidomic analysis reveals that the yolk cell is metabolically active in processing lipid. Cell Rep. 2016;14(6):1317–1329.
   PubMed Web of Science ®Google Scholar
• Saint-Amant L, Drapeau P. Time course of the development of motor behaviors in the zebrafish embryo. J Neurobiol. 1998;37(4):622–632.
   PubMedGoogle Scholar
• Kinkhabwala A, Riley M, Koyama M, et al. A structural and functional ground plan for neurons in the hindbrain of zebrafish. Proc Natl Acad Sci USA. 2011;108(3):1164–1169.
   PubMedGoogle Scholar
• Fuiman LA. Special considerations of fish eggs and larval. In: Fuiman LA, Werner RG, editors. Fishery Science: The Unique Contributions of Early Life Stage. Oxford: Blacwell Science; 2002:1–32.
   Google Scholar
• Teixidó E, Barenys M, Piqué E, Llobet JM, Gómez-Catalán J. Cardiovascular effects of PCB 126 (3,3ʹ,4,4ʹ,5-pentachlorobiphenyl) in zebrafish embryos and impact of co-exposure to redox modulating chemicals. Int J Mol Sci. 2019;20(5):1065.
   PubMedGoogle Scholar
• Asharani PV, Lianwu Y, Gong Z, Valiyaveettil S. Comparison of the toxicity of silver, gold and platinum nanoparticles in developing zebrafish embryos. Nanotoxicology. 2011;5:43–54.
   PubMed Web of Science ®Google Scholar
• Bar-Ilan O, Albrecht RM, Fako VE, Furgeson DY. Toxicity assessments of multisized gold and silver nanoparticles in zebrafish embryos. Small. 2009;5(16):1897–1910.
   PubMed Web of Science ®Google Scholar
• Schmid G, Kreyling WG, Simon U. Toxic effects and biodistribution of ultrasmall gold nanoparticles. Arch Toxicol. 2017;91(9):3011–3037.
   PubMed Web of Science ®Google Scholar
• Patibandla S, Zhang Y, Tohari AM, et al. Comparative analysis of the toxicity of gold nanoparticles in zebrafish. J Appl Toxicol. 2018;38(8):1153–1161.
   PubMedGoogle Scholar
• Premarathna AD, Ranahewa TH, Wijesekera SK, et al. Wound healing properties of aqueous extracts of Sargassum ilicifolium: an in vitro assay. Wound Medicine. 2019;24(1):1–7.
   Google Scholar
• Sellimi S, Maalej H, Rekik DM, et al. Antioxidant, antibacterial and in vivo wound healing properties of laminaran purified from Cystoseira barbata seaweed. Int J Biol Macromol. 2018;119:633–644.
   PubMedGoogle Scholar
• Nethi SK, Das S, Patra CR, Mukherjee S. Recent advances in inorganic nanomaterials for wound-healing applications. Biomater Sci. 2019;7(7):2652–2674.
   PubMed Web of Science ®Google Scholar
• Mihai MM, Dima MB, Dima B, Holban AM. Nanomaterials for wound healing and infection control. Materials. 2019;12(13):2176.
   PubMed Web of Science ®Google Scholar
• Vijayakumar V, Samal SK, Mohanty S, Nayak SK. Recent advancements in biopolymer and metal nanoparticle-based materials in diabetic wound healing management. Int J Biol Macromol. 2019;122:137–148.
   PubMed Web of Science ®Google Scholar