Mol Pharm. 2019 Mar 4;16(3):1234-1244. doi: 10.1021/acs.molpharmaceut.8b01197. Epub 2019 Feb 14.
The addictive potential of clinically used opioids as a result of their direct action on the dopaminergic reward system in the brain has limited their application. In an attempt to reduce negative side effects as well as to improve the overall effectiveness of these analgesics, we have designed, synthesized, and evaluated an N-(2-hydroxypropyl)methacrylamide (HPMA)-based macromolecular prodrug of hydromorphone (HMP), a commonly used opioid. To this end, P-HMP was synthesized via RAFT polymerization and a subsequent polymer analogous reaction. Its interaction with inflammatory cells in arthritic joints was evaluated in vitro using a RAW 264.7 cell culture, and subsequent confocal microscopy analysis confirmed that P-HMP could be internalized by the cells via endocytosis. In vivo imaging studies indicated that the prodrug can passively target the arthritic joint after systemic administration in a rodent model of monoarticular adjuvant-induced arthritis (MAA). The inflammatory pain-alleviating properties of the prodrug were assessed in MAA rats using the incapacitance test and were observed to be similar to dose-equivalent HMP. Analgesia through mechanisms at the spinal cord level was further measured using the tail flick test, and it was determined that the prodrug significantly reduced spinal cord analgesia versus free HMP, further validating the peripheral restriction of the macromolecular prodrug. Immunohistochemical analysis of cellular uptake of the P-HMP within the MAA knee joint proved the internalization of the prodrug by phagocytic synoviocytes, colocalized with HMP's target receptor as well as with pain-modulating ion channels. Therefore, it can be concluded that the novel inflammation-targeting polymeric prodrug of HMP (P-HMP) has the potential to be developed as an effective and safe analgesic agent for musculoskeletal pain.
临床上使用的阿片类药物由于其直接作用于大脑中的多巴胺奖赏系统而具有成瘾潜力,这限制了它们的应用。为了降低这些阿片类药物的负面副作用,并提高其整体疗效,我们设计、合成并评估了一种羟丙基甲基丙烯酰胺(HPMA)基氢吗啡酮(HMP)的大分子前药。为此,通过 RAFT 聚合和随后的聚合物类似物反应合成了 P-HMP。使用 RAW 264.7 细胞培养物在体外评估了其与关节炎关节中炎症细胞的相互作用,随后的共焦显微镜分析证实 P-HMP 可以通过胞吞作用被细胞内化。体内成像研究表明,在单关节炎佐剂诱导关节炎(MAA)的啮齿动物模型中,前药可以在系统给药后被动靶向关节炎关节。在 MAA 大鼠中使用失能试验评估了前药的抗炎性疼痛缓解特性,结果与等效剂量的 HMP 相似。通过尾巴拍打试验进一步测量了脊髓水平的镇痛机制,结果表明前药与游离 HMP 相比显著减少了脊髓镇痛,进一步验证了大分子前药的外周限制。在 MAA 膝关节中对 P-HMP 细胞内摄取的免疫组织化学分析证明了前药被吞噬性滑膜细胞内化,与 HMP 的靶受体以及疼痛调节离子通道共定位。因此,可以得出结论,新型炎症靶向 HMP(P-HMP)聚合物前药有可能开发为治疗肌肉骨骼疼痛的有效和安全的镇痛药。