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微粒中负载双膦酸盐的纳米颗粒:一种潜在的巨噬细胞靶向和再极化药物递送系统。

Bisphosphonates loaded nanoparticles in microparticles: a potential macrophage targeting and repolarizing drug delivery system.

作者信息

Sagoe Paul N K, Zink Benjamin, Jain Era

机构信息

Department of Biomedical and Chemical Engineering, Syracuse University, Syracuse, NY, 13244, USA.

Bioinspired Syracuse: Institute for Material and Living System, Syracuse University, Syracuse, NY, 13244, USA.

出版信息

Drug Deliv Transl Res. 2025 Jun 6. doi: 10.1007/s13346-025-01889-7.

Abstract

Bisphosphonates (BPs) are widely used in treating bone-related conditions, with emerging evidence supporting their potential in treating both skeletal and extra-skeletal diseases. However, their clinical utility is limited by high cytotoxicity, particularly toward macrophages, leading to immune system disruption upon frequent use. This limitation highlights the need for an effective drug delivery system. While nanoparticle formulations improve pharmacokinetics and biodistribution, they often suffer from limited drug loading capacity, poor sustained-release ability, and increased cytotoxicity due to their rapid and excessive intracellular uptake.Here, we present a multifunctional formulation, composed of calcium-zoledronic acid nanoparticles (CaZol NP) encapsulated within polymeric microparticles (CaZol NiM), designed to address many challenges associated with therapeutic use of zoledronic acid (Zol). CaZol NiM improves cellular uptake of Zol, facilitates pH sensitive sustained release of Zol and allows ligand mediated uptake by macrophages. The controlled release of Zol from CaZol NiM effectively reduces Zol's cytotoxic effects on macrophages, enabling their immune modulation by suppressing NF-κB and reactive oxygen species (ROS) activity, while promoting macrophage repolarization from their pro-inflammatory M1 state.Altogether, these findings highlight the potential of CaZol NiM in minimizing off-target effect and expand the clinical applications of Zol in managing both skeletal and extra-skeletal inflammatory disorders.

摘要

双膦酸盐(BPs)被广泛用于治疗与骨骼相关的病症,越来越多的证据支持其在治疗骨骼和骨骼外疾病方面的潜力。然而,它们的临床应用受到高细胞毒性的限制,尤其是对巨噬细胞的毒性,频繁使用会导致免疫系统紊乱。这一局限性凸显了对有效药物递送系统的需求。虽然纳米颗粒制剂改善了药代动力学和生物分布,但它们往往存在载药量有限、缓释能力差以及由于细胞内快速过量摄取而导致细胞毒性增加等问题。在此,我们提出了一种多功能制剂,由包裹在聚合物微粒(CaZol NiM)中的唑来膦酸钙纳米颗粒(CaZol NP)组成,旨在解决与唑来膦酸(Zol)治疗应用相关的许多挑战。CaZol NiM改善了Zol的细胞摄取,促进了Zol的pH敏感型缓释,并允许巨噬细胞通过配体介导进行摄取。Zol从CaZol NiM中的控释有效降低了Zol对巨噬细胞的细胞毒性作用,通过抑制NF-κB和活性氧(ROS)活性实现对巨噬细胞的免疫调节,同时促进巨噬细胞从促炎M1状态重新极化。总之,这些发现凸显了CaZol NiM在最小化脱靶效应方面的潜力,并扩大了Zol在治疗骨骼和骨骼外炎症性疾病方面的临床应用。

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