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骨靶向纳米载体辅助递送腺苷以防治骨质疏松性骨丢失。

Bone targeting nanocarrier-assisted delivery of adenosine to combat osteoporotic bone loss.

机构信息

Department of Orthopaedic Surgery, Duke University School of Medicine, Durham, NC, 27710, USA.

Department of Orthopaedic Surgery, Duke University School of Medicine, Durham, NC, 27710, USA; Department of Mechanical Engineering and Materials Science, Duke University, Durham, NC, 27710, USA.

出版信息

Biomaterials. 2021 Jun;273:120819. doi: 10.1016/j.biomaterials.2021.120819. Epub 2021 Apr 14.

Abstract

Extracellular adenosine has been shown to play a key role in maintaining bone health and could potentially be used to treat bone loss. However, systemic administration of exogenous adenosine to treat bone disorders remains a challenge due to the ubiquitous presence of adenosine receptors in different organs and the short half-life of adenosine in circulation. Towards this, we have developed a bone-targeting nanocarrier and determined its potential for systemic administration of adenosine. The nanocarrier, synthesized via emulsion suspension photopolymerization, is comprised of hyaluronic acid (HA) copolymerized with phenylboronic acid (PBA), a moiety that can form reversible bonds with adenosine. The bone binding affinity of the nanocarrier was achieved by alendronate (Aln) conjugation. Nanocarriers functionalized with the alendronate (Aln-NC) showed a 45% higher accumulation in the mice vertebrae in vivo compared to those lacking alendronate molecules (NCs). Systemic administration of adenosine via bone-targeting nanocarriers (Aln-NC) attenuated bone loss in ovariectomized (OVX) mice. Furthermore, bone tissue of mice treated with adenosine-loaded Aln-NC displayed trabecular bone characteristics comparable to healthy controls as shown by microcomputed tomography, histochemical staining, bone labeling, and mechanical strength. Overall, our results demonstrate the use of a bone-targeting nanocarrier towards systemic administration of adenosine and its application in treating bone degenerative diseases such as osteoporosis.

摘要

细胞外腺苷已被证明在维持骨骼健康方面发挥着关键作用,并且可能被用于治疗骨质疏松症。然而,由于腺苷受体在不同器官中的普遍存在以及腺苷在循环中的半衰期较短,将外源性腺苷全身给药用于治疗骨疾病仍然是一个挑战。针对这一问题,我们开发了一种靶向骨骼的纳米载体,并确定了其用于全身给予腺苷的潜力。该纳米载体通过乳液悬浮光聚合合成,由透明质酸(HA)与苯硼酸(PBA)共聚而成,PBA 是一种可以与腺苷形成可逆键的部分。通过阿仑膦酸钠(Aln)缀合实现了纳米载体的骨结合亲和力。在体内,与缺乏阿仑膦酸钠分子的纳米载体(NCs)相比,用阿仑膦酸钠(Aln-NC)功能化的纳米载体在小鼠椎骨中的积累增加了 45%。通过靶向骨骼的纳米载体(Aln-NC)全身给予腺苷可减轻去卵巢(OVX)小鼠的骨质流失。此外,用载有腺苷的 Aln-NC 治疗的小鼠的骨组织显示出与健康对照组相当的小梁骨特征,这通过微计算机断层扫描、组织化学染色、骨标记和机械强度来显示。总的来说,我们的研究结果表明,使用靶向骨骼的纳米载体进行全身给予腺苷,并将其应用于治疗骨质疏松症等骨骼退行性疾病。

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