Europium doped Gd_2 O_3 nanotubes(Gd_2 O_3:Eu~(3+) NTs) were synthesized and characterized. Then,the neurotoxicity and brain localization of Gd_2 O_3:Eu~(3+) NTs were evaluated. All experimental rats were administered by intranasal instillation with 30 μL Gd_2 O_3:Eu~(3+) NTs suspension 3.0 and 15.0 mg/mL respectively every other day for 35 consecutive days, and the rats of control group were administered with an equal volume of physiological saline. The Morris water maze was used to assess the rats’ spatial learning and memory ability. The oxidative stress-related biomarkers and the activity of AChE in striatum and hippocampus were analyzed, and the histopathology of hippocampus and striatum was observed.The brain localization of gadolinium(Gd) was measured. The results showed that the escape latency of the rats in high-dose group prolonged significantly compared with that of control group after treatment of six weeks(p < 0.05), and the swimming time in D quadrant of high-dose group shortened significantly compared with the control group(p < 0.01). In addition, high-dose Gd_2 O_3:Eu~(3+) NTs could decrease the activity of GSH-Px and CAT in hippocampus and the activity of SOD in striatum(p < 0.05). MDA content in hippocampus and striatum of high-dose group increased(p < 0.05). High dose Gd_2 O_3:Eu~(3+) NTs could increase the activity of AChE in hippocampus(p < 0.05) and in striatum(p < 0.001). But there were no significant differences between the low-dose group and control group(p > 0.05). The results of Gd localization in brain showed that the ranking of Gd levels was olfactory bulb > striatum > hippocampus> cerebellum > brain stem > frontal cortex. The pathology results indicated that high dose Gd_2 O_3:Eu~(3+)NTs resulted in degeneration necrosis, nucleus pycnosis, and axons disappearance of the nerve cells at CA1, CA3 and DG area of hippocampus. Therefore, the results implied that Gd_2 O_3:Eu~(3+) NTs have the potential neurotoxicity and a possible danger in causing neurodegenerative disorders after intranasal instillation. Then, the neurotoxicity and brain localization of Gd_2 O_3: Eu ~ (3+) NTs were evaluated. All experimental rats were administered by intranasal Instillation with 30 μL Gd 2 O 3: Eu 3+ NTs suspension 3.0 and 15.0 mg / mL respectively every other day for 35 consecutive days, and the rats of control group were administered with an equal volume of physiological saline. The Morris water maze was used to assess the rats’ spatial learning and memory ability. The oxidative stress-related biomarkers and the activity of AChE in striatum and hippocampus were analyzed, and the histopathology of hippocampus and striatum was observed. The brain localization of gadolinium (Gd) was measured. The results showed that the escape latency of the rats in high-dose group prolonged significantly compared with that of control group after treatment of six weeks (p <0.05), and the swimming time in D quadrant of high-dose group In addition, high-dose Gd_2 O_3: Eu ~ (3+) NTs could decrease the activity of GSH-Px and CAT in hippocampus and the activity of SOD in striatum (p <0.05). MDA content in hippocampus and striatum of high-dose group increased (p <0.05). High dose Gd_2 O_3: Eu ~ (3+) NTs could increase the activity of AChE in hippocampus (p <0.001). There results no Gd localization in brain showed that the ranking of Gd levels was olfactory bulb> striatum> hippocampus> cerebellum The pathology results indicated that high dose Gd_2 O_3: Eu ~ (3+) NTs resulted in degeneration necrosis, nucleus pycnosis, and axons disappearance of the nerve cells at CA1, CA3 and DG area of ​​hippocampus. , the results implied that Gd_2 O_3: Eu ~ (3+) NTs have the potential neurotoxicity and a possible danger in c ausing neurodegenerative disorders after intranasal instillation.