Hu Yiping, Xiao Kui, Chen Ziang, Ou Shali, Sima Chao, Wang Haiyang, Zhang Jinli, Zhang Zhi, Li Xiaojian
Department of Burns and Plastic Surgery, Guangzhou Red Cross Hospital, Jinan University, Guangzhou, Guangdong, 510000, People's Republic of China.
Department of Oral and Maxillofacial Surgery, Women and Children's Medical Center Affiliated to Guangzhou Medical University, Guangzhou, Guangdong, 510000, People's Republic of China.
Int J Nanomedicine. 2025 Aug 2;20:9559-9572. doi: 10.2147/IJN.S520656. eCollection 2025.
Non-invasive fat reduction and body contouring technologies have rapidly advanced in plastic surgery. Although various devices have been developed globally for body sculpting, the mechanisms and long-term efficacy of non-surgical fat reduction are still debated. While gold nanorods (AuNRs) have been extensively studied in cancer treatment, their potential in fat reduction has not been explored. This study aims to design a novel nanoplatform combining AuNRs with a PPARγ monoclonal antibody (PPARγmAb) for effective photothermal fat reduction therapy.
AuNRs were chemically activated by adding 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC) activator, followed by the addition of PPARγmAb for reaction. Simultaneously, adipose-derived stem cells were induced to differentiate into adipocytes, and an obese mouse model was established. Differentiated adipocytes and obese mice were treated with AuNRs-PPARγmAb and exposed to 808nm near-infrared (NIR) laser irradiation to evaluate fat reduction effects and biocompatibility.
The PPARγmAb modification did not significantly affect the optical properties of AuNRs but greatly increased their retention in adipocytes. Compared to AuNRs alone, AuNRs-PPARγmAb showed a stronger photothermal effect on adipocytes under 808 nm near-infrared laser irradiation, inducing cell apoptosis. In obese mice, AuNRs-PPARγmAb treatment significantly reduced adipose tissue weight, size, and thickness, with no major histopathological damage observed in organs. Hematological parameters, as well as liver and kidney function, remained unchanged, confirming the biocompatibility and fat-reducing efficacy of the treatment.
AuNRs-PPARγmAb, when exposed to 808nm NIR laser irradiation, effectively targets and induces apoptosis in adipocytes, leading to significant fat reduction. This targeted approach offers a promising method for non-surgical, localized fat reduction. Compared to other fat reduction treatments, it provides the advantages of high specificity, minimal invasiveness, and fewer side effects, highlighting its potential for clinical application.
非侵入性减脂和身体塑形技术在整形手术中发展迅速。尽管全球已开发出各种用于身体塑形的设备,但非手术减脂的机制和长期疗效仍存在争议。虽然金纳米棒(AuNRs)在癌症治疗方面已得到广泛研究,但其在减脂方面的潜力尚未得到探索。本研究旨在设计一种将AuNRs与过氧化物酶体增殖物激活受体γ单克隆抗体(PPARγmAb)相结合的新型纳米平台,用于有效的光热减脂治疗。
通过添加1-乙基-3-(3-二甲基氨基丙基)碳二亚胺(EDC)活化剂对AuNRs进行化学活化,随后添加PPARγmAb进行反应。同时,诱导脂肪来源的干细胞分化为脂肪细胞,并建立肥胖小鼠模型。用AuNRs-PPARγmAb处理分化的脂肪细胞和肥胖小鼠,并暴露于808nm近红外(NIR)激光照射下,以评估减脂效果和生物相容性。
PPARγmAb修饰对AuNRs的光学性质没有显著影响,但大大增加了它们在脂肪细胞中的保留率。与单独的AuNRs相比,AuNRs-PPARγmAb在808nm近红外激光照射下对脂肪细胞表现出更强的光热效应,诱导细胞凋亡。在肥胖小鼠中,AuNRs-PPARγmAb治疗显著降低了脂肪组织的重量、大小和厚度,器官未观察到主要的组织病理学损伤。血液学参数以及肝肾功能保持不变,证实了该治疗的生物相容性和减脂效果。
AuNRs-PPARγmAb在暴露于808nm NIR激光照射时,能有效靶向并诱导脂肪细胞凋亡,从而显著减少脂肪。这种靶向方法为非手术局部减脂提供了一种有前景的方法。与其他减脂治疗相比,它具有高特异性、微创性和较少副作用的优点,突出了其临床应用潜力。