Department of Geriatrics, Xinhua Hospital of Shanghai Jiaotong University, School of Medicine, Shanghai 200092, China.
Department of Chemistry, Fudan University, 220 Handan Road, Shanghai 200433, P.R. China.
Theranostics. 2020 Feb 10;10(7):3281-3292. doi: 10.7150/thno.37599. eCollection 2020.
Hormone therapy (HT) is one of the most effective treatments for osteoporosis. However, the nonselective accumulation of hormone in organs such as breast, heart and uterus other than bones causes serious side effects, which impedes the application of HT. Hence, it is critically important to develop a HT strategy with reduced non-specific enrichment of hormone drugs in non-target tissues and enhanced bone-targeting ability. : Herein, a 17β-estradiol (E)-laden mesoporous silica-coated upconversion nanoparticle with a surface modification of ethylenediaminetetraacetic acid (EDTA) (NaLuF:Yb,Tm@NaLuF@mSiO-EDTA-E, E-csUCNP@MSN-EDTA) is developed for bone-targeted osteoporosis hormone therapy. EDTA was attached onto the surface of E upconversion nanocomposite to enhance its affinity and efficiency targeting bone tissue and cells to optimize hormone replacement therapy for osteoporosis. We characterized the size, cytotoxicity, loading and release efficiency, and imaging. Further, and osteogenic ability was tested using preosteoblast and ovariectomy mouse model of osteoporosis. : The upconversion core of E-csUCNP@MSN-EDTA nanoparticle serves as an excellent imaging agent for tracking the loaded hormone drug . The mesoporous silica layer has a high loading efficiency for E and provides a relatively long-lasting drug release within 50 h. EDTA anchored on the silica layer endows the nanocomposite with a bone targeting property. The nanocomposite effectively reverses estrogen deficiency-induced osteoporosis and reduces the damage of hormone to the uterus. The bone mineral density in the nanocomposite treatment group is nearly twice that of the ovariectomized (OVX) group. Compared with the E group, the uterine weight and luminal epithelial height were significantly lower in the nanocomposite treatment group. : This work demonstrated that E-csUCNP@MSN-EDTA alleviates the side effect of hormone therapy while maintaining its therapeutic efficacy, which has great potential for developing the next generation of methods for osteoporosis treatment.
激素治疗(HT)是治疗骨质疏松症最有效的方法之一。然而,激素在骨骼以外的器官(如乳房、心脏和子宫)中的非选择性积累会导致严重的副作用,这阻碍了 HT 的应用。因此,开发一种 HT 策略,减少激素药物在非靶组织中的非特异性富集,增强骨靶向能力,是至关重要的。
在这里,开发了一种 17β-雌二醇(E)负载的介孔硅包覆上转换纳米粒子,其表面修饰为乙二胺四乙酸(EDTA)(NaLuF:Yb,Tm@NaLuF@mSiO-EDTA-E,E-csUCNP@MSN-EDTA),用于骨靶向骨质疏松症激素治疗。EDTA 被连接到 E 上转换纳米复合材料的表面上,以增强其与骨组织和细胞的亲和力和靶向效率,从而优化骨质疏松症的激素替代治疗。我们对其大小、细胞毒性、负载和释放效率进行了表征,并进行了成像和体内实验。进一步,通过成骨前体细胞和去卵巢骨质疏松症小鼠模型测试了其成骨能力。
E-csUCNP@MSN-EDTA 纳米颗粒的上转换核作为负载激素药物的优异成像剂。介孔硅层对 E 具有高负载效率,并在 50 h 内提供相对持久的药物释放。锚定在硅层上的 EDTA 赋予纳米复合材料骨靶向特性。该纳米复合材料有效逆转了雌激素缺乏引起的骨质疏松症,并降低了激素对子宫的损伤。与去卵巢(OVX)组相比,纳米复合材料治疗组的骨矿物质密度几乎是 OVX 组的两倍。与 E 组相比,纳米复合材料治疗组的子宫重量和腔上皮高度显著降低。
这项工作表明,E-csUCNP@MSN-EDTA 减轻了激素治疗的副作用,同时保持了其治疗效果,为开发下一代骨质疏松症治疗方法提供了巨大潜力。