The widespread use of zinc oxide nanoparticles (ZnO NPs) in multiple applications has increased the importance of safety considerations. ZnO NPs were synthesized, characterized, and evaluated for toxicity in Artemia salina and zebrafish (Danio rerio). NPs were characterized by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), and ultraviolet-visible (UV-Vis) spectroscopy. The hydrodynamic size and stability of the ZnO NP surface were examined using a Zetasizer. Characterization techniques confirmed the ZnO wurtzite structure with a particle size of 32.2 ± 5.2 nm. Synthesized ZnO NPs were evaluated for acute toxicity in Artemia salina using the Probit and Reed and Muench methods to assess for lethal concentration at 50% (LC50). The LC50 was 86.95 ± 0.21 μg/mL in Artemia salina. Physical malformations were observed after 96 h at 50 μg/mL of exposure. The total protein and cytochrome P450 contents were determined. Further analysis was performed to assess the bioaccumulation capacity of zebrafish (Danio rerio) using ICP-OES. ZnO NP content in adult zebrafish was greater in the gastrointestinal tract than in the other tissues under study. The present analysis of ZnO NPs supports the use of Artemia salina and adult zebrafish as relevant models for assessing toxicity and bioaccumulation while considering absorption quantities.

The benzophenone (BP) family, including oxybenzone (BP-3), a prevalent sunscreen ingredient and environmental contaminant, has raised concerns since the year 2005. This study investigated oxybenzone toxicity in zebrafish (Danio rerio) eleutheroembryos and brine shrimp (Artemia salina) nauplii, focusing on the LC₅₀ and developmental impacts. Zebrafish embryos (0.100–1.50 mg/L BP-3, 96 h) and A. salina (0.100–5.00 mg/L BP-3, 48 h) were tested with ultrasound-assisted emulsified liquid-phase microextraction (UA-ELPME) used for zebrafish tissue analysis. HPLC-DAD determined BP-3 concentrations (highest: 0.74 ± 0.13 mg/L). Although no significant zebrafish embryo mortality or hatching changes occurred, developmental effects were evident. Lethal concentrations were determined (A. salina LC₅₀ at 24 h = 3.19 ± 2.02 mg/L; D. rerio embryos LC₅₀ at 24 h = 4.19 ± 3.60 mg/L), with malformations indicating potential teratogenic effects. A. salina displayed intestinal tract alterations and D. rerio embryos exhibited pericardial edema and spinal deformities. These findings highlight oxybenzone’s environmental risks, posing threats to species and ecosystem health.

Among nanoparticles (NPs), titanium dioxide is one of the most highly manufactured worldwide and widely used in multiple products for both industrial use and personal care products. This increases the probability of release into aquatic environments, potentially affecting these ecosystems. The present study aimed to evaluate TiO₂ P25 NP toxicity in zebrafish embryos and eleutheroembryos by evaluating LC₅₀, hatching rate, embryo development, and chemical analysis of the TiO₂ concentration accumulated in eleutheroembryo tissues. Zebrafish embryos ~2 h post-fertilization (hpf) were exposed to 75, 100, 150, 200, and 250 mg/L TiO₂ P25 NPs for 48 and 96 h. A total of 40–60 embryos were placed in each Petri dish for the respective treatments. Three replicates were used for each treatment group. Ti⁴⁺ concentrations were determined by inductively coupled plasma optical emission spectrometry (ICP-OES), and a conversion factor was used to calculate the TiO₂ concentrations in the tissues. The highest calculated concentrations of TiO₂ in zebrafish larvae were 1.0199 mg/L after 48 h and 1.2679 mg/L after 96 h of exposure. The toxicological results indicated that these NPs did not have a significant effect on the mortality and hatching of zebrafish embryos but did have an effect on their development. LC₂₀ and LC₃₀ were determined experimentally, and LC₅₀ and LC₈₀ were estimated using four different methods. Up to 11% of embryos also presented physical malformations. These effects can be detrimental to a species and affect ecosystems. Physical malformations were observed in all treatments, indicating teratogenic effects.

Plastic pollution is a growing environmental crisis, with millions of tons of plastic entering the ocean each year and breaking down into microplastics and nanoplastics. These tiny particles pose a serious threat to marine life, particularly to zooplankton, which are essential to aquatic ecosystems. This study investigated the distribution and toxicity of polystyrene nanoplastics in Artemia salina (brine shrimp), a key model organism in ecotoxicology. Using specialized imaging and spectroscopy techniques, we tracked the presence of nanoplastics in A. salina and examined their effects on survival, behavior, and body structure. The results showed that nanoplastics accumulated in the gut and, at higher concentrations, caused gut deformities. The toxicity assay revealed that after 48 h of exposure, lethal concentrations decreased by nearly half compared with 24 h, demonstrating a time-dependent toxic effect. The estimated concentration that caused 50% mortality was 30.21 ± 6.44 mg/L. Additionally, these findings suggest that nanoplastics may impair the salt gland, affecting osmoregulation and energy allocation, leading to reduced feeding and pigmentation. These results highlight the potential risks of nanoplastics to marine organisms and emphasize the need for further research to understand their broader ecological and health impacts.

Oxybenzone (BP-3) and polystyrene microplastics (PS MPs) are pervasive aquatic contaminants whose combined biological effects remain insufficiently characterized. This study investigated co-exposure to BP-3 and PS MPs in zebrafish embryos (Danio rerio), focusing on developmental endpoints, tissue bioaccumulation, and time-dependent sorption behavior. Embryos were exposed to 0.10–1.50 mg/L BP-3 for 96 h in the presence of PS MPs. Mortality, developmental abnormalities, and tissue BP-3 concentrations were measured, and chemical analysis was performed by HPLC-DAD. Although mortality was not significantly affected, embryos exhibited developmental abnormalities, particularly in swim bladder formation. Tissue BP-3 accumulation increased with exposure concentration. The influence of PS MPs on BP-3 uptake was concentration-dependent: at lower BP-3 exposures, PS MPs reduced tissue accumulation, whereas at higher exposures this reduction became negligible or was no longer observed. This suggests a dual role for PS MPs: mitigating direct aqueous exposure by sequestering BP-3 yet simultaneously acting as potential vectors for its environmental persistence and trophic transfer through alternative pathways. Independent time-resolved experiments showed rapid BP-3 removal from the aqueous phase in the presence of PS MPs, with early stabilization consistent with rapid partitioning behavior. These findings highlight the complex interactions between emerging contaminants and MPs, underscoring the need for further research into their ecological implications.