Department of Biomedical Engineering, University of Utah, Salt Lake City, Utah, USA.
Scientific Computing and Imaging Institute, University of Utah, Salt Lake City, Utah, USA.
J Orthop Res. 2023 Nov;41(11):2424-2432. doi: 10.1002/jor.25577. Epub 2023 May 2.
The objective of this study was to investigate the potential of collagen hybridizing peptides (CHPs), which bind to denatured collagen, to extend the retention time of near-infrared fluorophores (NIRF) following intra-articular (IA) injection in rat knee joints. CHPs were synthesized with a NIRF conjugated to the N-terminus. Male Sprague-Dawley rats were assigned to one of four experimental groups: healthy, CHP; osteoarthritis (OA), CHP; healthy, scrambled-sequence CHP (sCHP), which has no collagen binding affinity; or OA, sCHP. Animals in the OA groups received an IA injection of monosodium iodoacetate to induce OA. All animals then received the corresponding CHP injection. Animals were imaged repeatedly over 2 weeks using an in vivo fluorescence imaging system. Joint components were isolated and imaged to determine CHP binding distribution. Safranin-O and Fast Green histological staining was performed to confirm the development of OA. CHPs were found to be retained within the joint following IA injection in both healthy and OA animals for the full study period. In contrast, sCHP signal was negligible by 24-48 h. CHP signal was significantly greater (p < 0.05) in OA joints when compared to healthy joints. At the 2-week end point, multiple joint components retained CHPs, including cartilage, meniscus, and synovium. CHPs dramatically extended the retention time of NIRFs following IA injection in healthy and OA knee joints by binding to multiple collagenous tissues in the joint. These results support the pursuit of further research to develop CHP based therapeutics for IA treatment of OA.
本研究旨在探讨胶原杂交肽(CHP)的潜力,CHP 可与变性胶原结合,从而延长近红外荧光团(NIRF)在大鼠膝关节腔内注射后的保留时间。CHP 是通过将 NIRF 连接到 N 端合成的。雄性 Sprague-Dawley 大鼠被分为四组:健康组、CHP 组;骨关节炎(OA)组、CHP 组;健康组、无胶原结合亲和力的乱序 CHP(sCHP)组;OA 组、sCHP 组。OA 组动物接受关节内注射单碘乙酸钠以诱导 OA。所有动物随后接受相应的 CHP 注射。使用体内荧光成像系统在 2 周内重复对动物进行成像。分离关节成分并进行成像以确定 CHP 结合分布。用番红 O 和 Fast Green 进行组织学染色以确认 OA 的发展。CHP 在健康和 OA 动物的关节内注射后,在整个研究期间均保留在关节内。相比之下,sCHP 信号在 24-48 小时内几乎检测不到。与健康关节相比,OA 关节中的 CHP 信号显著更高(p<0.05)。在 2 周终点时,多个关节成分保留了 CHP,包括软骨、半月板和滑膜。CHP 通过与关节中的多种胶原组织结合,极大地延长了 NIRF 在健康和 OA 膝关节腔内注射后的保留时间。这些结果支持进一步研究开发基于 CHP 的治疗方法,用于 IA 治疗 OA。