Section of Orthodontics, Division of Growth and Development, School of Dentistry, University of California, Los Angeles, CA 90095;
Section of Orthodontics, Division of Growth and Development, School of Dentistry, University of California, Los Angeles, CA 90095.
Proc Natl Acad Sci U S A. 2017 Aug 29;114(35):E7218-E7225. doi: 10.1073/pnas.1704027114. Epub 2017 Aug 14.
Patients with cleft lip and/or palate (CLP), who undergo numerous medical interventions from infancy, can suffer from lifelong debilitation caused by underdeveloped maxillae. Conventional treatment approaches use maxillary expansion techniques to develop normal speech, achieve functional occlusion for nutrition intake, and improve esthetics. However, as patients with CLP congenitally lack bone in the cleft site with diminished capacity for bone formation in the expanded palate, more than 80% of the patient population experiences significant postexpansion relapse. While such relapse has been a long-standing battle in craniofacial care of patients, currently there are no available strategies to address this pervasive problem. Estrogen, 17β-estradiol (E2), is a powerful therapeutic agent that plays a critical role in bone homeostasis. However, E2's clinical application is less appreciated due to several limitations, including its pleiotropic effects and short half-life. Here, we developed a treatment strategy using an injectable system with photo-cross-linkable hydrogel (G) and nanodiamond (ND) technology to facilitate the targeted and sustained delivery of E2 to promote bone formation. In a preclinical expansion/relapse model, this functionalized E2/ND/G complex substantially reduced postexpansion relapse by nearly threefold through enhancements in sutural remodeling compared with unmodified E2 administration. The E2/ND/G group demonstrated greater bone volume by twofold and higher osteoblast number by threefold, compared with the control group. The E2/ND/G platform maximized the beneficial effects of E2 through its extended release with superior efficacy and safety at the local level. This broadly applicable E2 delivery platform shows promise as an adjuvant therapy in craniofacial care of patients.
唇腭裂(CLP)患者在婴儿期接受了多次医学干预,可能会因上颌骨发育不良而终生虚弱。传统的治疗方法使用上颌扩张技术来发展正常的语音,实现营养摄入的功能性咬合,并改善美观。然而,由于 CLP 患者先天在裂隙部位缺乏骨骼,并且在扩张的腭部形成骨骼的能力减弱,超过 80%的患者群体经历了显著的扩张后复发。虽然这种复发一直是颅面患者护理中的一个长期问题,但目前尚无解决这一普遍问题的策略。雌激素,17β-雌二醇(E2),是一种强大的治疗剂,在骨骼动态平衡中发挥着关键作用。然而,由于其多种作用和半衰期短等限制,E2 的临床应用尚未得到充分认识。在这里,我们开发了一种使用可注射系统结合光交联水凝胶(G)和纳米金刚石(ND)技术的治疗策略,以促进 E2 的靶向和持续递送,从而促进骨形成。在临床前扩张/复发模型中,与未修饰的 E2 给药相比,这种功能化的 E2/ND/G 复合物通过缝合重塑的增强,使扩张后复发的比例降低了近三倍。与对照组相比,E2/ND/G 组的骨体积增加了两倍,成骨细胞数量增加了三倍。E2/ND/G 平台通过其延长释放最大限度地提高了 E2 的有益效果,在局部水平具有更好的疗效和安全性。这种广泛适用的 E2 递送平台有望成为颅面患者护理的辅助治疗方法。