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Drug-Free ROS Sponge Polymeric Microspheres Reduce Tissue Damage from Ischemic and Mechanical Injury

机译:不含药物的ROS海绵聚合物微球减少了缺血和机械损伤引起的组织损伤

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摘要

The inherent antioxidant function of poly(propylene sulfide) (PPS) microspheres (MS) was dissected for different reactive oxygen species (ROS), and therapeutic benefits of PPS-MS were explored in models of diabetic peripheral arterial disease (PAD) and mechanically induced post-traumatic osteoarthritis (PTOA). PPS-MS (∼1 μm diameter) significantly scavenged hydrogen peroxide (H2O2), hypochlorite, and peroxynitrite but not superoxide in vitro in cell-free and cell-based assays. Elevated ROS levels (specifically H2O2) were confirmed in both a mouse model of diabetic PAD and in a mouse model of PTOA, with greater than 5- and 2-fold increases in H2O2, respectively. PPS-MS treatment functionally improved recovery from hind limb ischemia based on ∼15–25% increases in hemoglobin saturation and perfusion in the footpads as well as earlier remodeling of vessels in the proximal limb. In the PTOA model, PPS-MS reduced matrix metalloproteinase (MMP) activity by 30% and mitigated the resultant articular cartilage damage. These results suggest that local delivery of PPS-MS at sites of injury-induced inflammation improves the vascular response to ischemic injury in the setting of chronic hyperglycemia and reduces articular cartilage destruction following joint trauma. These results motivate further exploration of PPS as a stand-alone, locally sustained antioxidant therapy and as a material for microsphere-based, sustained local drug delivery to inflamed tissues at risk of ROS damage.
机译:剖析了聚(丙烯硫醚)(PPS)微球(MS)固有的抗氧化功能,以用于不同的活性氧(ROS),并在糖尿病性外周动脉疾病(PAD)和机械诱导的模型中探索了PPS-MS的治疗益处创伤后骨关节炎(PTOA)。在无细胞和基于细胞的测定中,PPS-MS(直径约1μm)可在体外清除过氧化氢(H2O2),次氯酸盐和过氧亚硝酸盐,但不能清除超氧化物。在糖尿病性PAD的小鼠模型和PTOA的小鼠模型中,均证实了ROS水平升高(特别是H2O2),H2O2升高分别超过5倍和2倍。 PPS-MS治疗在功能上改善了后肢缺血的恢复,这是由于脚垫中血红蛋白饱和度和灌注增加了约15–25%,以及较早的肢体近端血管重构。在PTOA模型中,PPS-MS将基质金属蛋白酶(MMP)活性降低了30%,并减轻了由此引起的关节软骨损伤。这些结果表明,在慢性高血糖情况下,在损伤诱导的炎症部位局部递送PPS-MS可改善对缺血性损伤的血管反应,并减少关节损伤后关节软骨的破坏。这些结果激发了对PPS的进一步探索,它是一种独立的,局部持续的抗氧化剂治疗,并且是一种基于微球的,持续的局部药物输送到有ROS风险的发炎组织的材料。

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