Chen Yun-Fang, Hsu Chun-Chieh, Chung Ching-Hu
Department of Medicine, Mackay Medical College, New Taipei City 252, Taiwan.
Nanomaterials (Basel). 2022 Nov 2;12(21):3868. doi: 10.3390/nano12213868.
Fluorescent gold nanoclusters conjugated with α-lipoic acid (FANC) is a promising biocompatible fluorescent nanomaterial with a high potential for drug development. However, there is still no FANC-related research on toxicology, which is very important for future research and the development of healthy food supplements or drugs. This study uses oral administration of FANC to determine the most appropriate dose range in ICR mice for further evaluation. The acute and subacute toxicity study was conducted by oral administration of FANC to male and female ICR mice. Animal survival, body weight, daily food consumption, hematological profile, organ coefficient, serum biochemistry profile, and histopathological changes were analyzed. FANC did not show any form of morbidity or mortality at acute and subacute toxicity in both male and female ICR mice. Animal behavior, daily food consumption, hematological profile, organ coefficient, and histopathology showed no treatment-related malignant changes at single and repeated doses. Furthermore, serum glutamic-oxaloacetic transaminase (GOT), glutamic-pyruvic transaminase (GPT), lactate dehydrogenase (LDH), blood urea nitrogen (BUN), and creatinine (CRE) levels showed no significant malignant changes, which indicated that FANC does not cause liver and renal damage. The only change observed in this study was the change in body weight. The body weight of the FANC-treated group was slightly decreased in female mice but increased in male mice; however, the body weight decreases were below the threshold of concern, and there was no dose-response effect. In conclusion, no observed adverse effect level (NOAEL) in repeated doses was considered in 20 μM/100 μL/25 g male and female ICR mice.
与α-硫辛酸共轭的荧光金纳米簇(FANC)是一种很有前景的生物相容性荧光纳米材料,在药物开发方面具有很高的潜力。然而,目前仍没有关于FANC毒理学的相关研究,而这对于未来的研究以及健康食品补充剂或药物的开发非常重要。本研究通过对ICR小鼠口服FANC来确定最适宜的剂量范围,以便进行进一步评估。通过对雄性和雌性ICR小鼠口服FANC来进行急性和亚急性毒性研究。分析动物的存活率、体重、每日食物消耗量、血液学指标、器官系数、血清生化指标以及组织病理学变化。在雄性和雌性ICR小鼠的急性和亚急性毒性实验中,FANC均未表现出任何形式的发病或死亡。动物行为、每日食物消耗量、血液学指标、器官系数和组织病理学在单次和重复给药时均未显示出与治疗相关的恶性变化。此外,血清谷草转氨酶(GOT)、谷丙转氨酶(GPT)、乳酸脱氢酶(LDH)、血尿素氮(BUN)和肌酐(CRE)水平均未显示出明显的恶性变化,这表明FANC不会导致肝和肾损伤。本研究中观察到的唯一变化是体重的改变。FANC处理组的雌性小鼠体重略有下降,而雄性小鼠体重增加;然而,体重下降低于关注阈值,且不存在剂量反应效应。总之,在20 μM/100 μL/25 g的雄性和雌性ICR小鼠中,重复给药未观察到有害作用水平(NOAEL)。