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Photocrosslinkable chitosan hydrogels functionalized with the RGD peptide and phosphoserine to enhance osteogenesis.用RGD肽和磷酸丝氨酸功能化的可光交联壳聚糖水凝胶以增强成骨作用。
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Biocompatibility Assessment of Detonation Nanodiamond in Non-Human Primates and Rats Using Histological, Hematologic, and Urine Analysis.用组织学、血液学和尿液分析评估在非人类灵长类动物和大鼠中的爆轰纳米金刚石的生物相容性。
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Evidence for Mechanisms Underlying the Functional Benefits of a Myocardial Matrix Hydrogel for Post-MI Treatment.心肌基质水凝胶用于心肌梗死后治疗功能益处的潜在机制证据。
J Am Coll Cardiol. 2016 Mar 8;67(9):1074-1086. doi: 10.1016/j.jacc.2015.12.035.
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Nanodiamonds: The intersection of nanotechnology, drug development, and personalized medicine.纳米金刚石:纳米技术、药物研发与个性化医疗的交叉领域。
Sci Adv. 2015 Aug 21;1(7):e1500439. doi: 10.1126/sciadv.1500439. eCollection 2015 Aug.
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Biodegradable, phosphate-containing, dual-gelling macromers for cellular delivery in bone tissue engineering.用于骨组织工程中细胞递送的可生物降解、含磷酸盐的双凝胶大分子单体。
Biomaterials. 2015 Oct;67:286-96. doi: 10.1016/j.biomaterials.2015.07.016. Epub 2015 Jul 21.
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Evaluating the effect of laser irradiation on bone regeneration in midpalatal suture concurrent to rapid palatal expansion in rats.评估激光照射对大鼠快速腭扩展同期腭中缝骨再生的影响。
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The endocrine role of estrogens on human male skeleton.雌激素对人类男性骨骼的内分泌作用。
Int J Endocrinol. 2015;2015:165215. doi: 10.1155/2015/165215. Epub 2015 Mar 19.
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Bioactive nanoengineered hydrogels for bone tissue engineering: a growth-factor-free approach.用于骨组织工程的生物活性纳米工程水凝胶:一种无生长因子的方法。
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Visible-light-initiated hydrogels preserving cartilage extracellular signaling for inducing chondrogenesis of mesenchymal stem cells.可见光引发水凝胶保留软骨细胞外信号诱导间充质干细胞软骨分化
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采用可注射雌激素-纳米金刚石水凝胶降低腭裂扩张术后复发。

Reducing posttreatment relapse in cleft lip palatal expansion using an injectable estrogen-nanodiamond hydrogel.

机构信息

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.

出版信息

Proc Natl Acad Sci U S A. 2017 Aug 29;114(35):E7218-E7225. doi: 10.1073/pnas.1704027114. Epub 2017 Aug 14.

DOI:10.1073/pnas.1704027114
PMID:28808036
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5584423/
Abstract

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.

摘要

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。