Laboratory of Nanostructures and Nanomedicine, Institute of High Pressure Physics, Polish Academy of Sciences, Warsaw, Poland.
Medicinal and Aromatic Plants Research Department, Pharmaceutical and Drug Industries Research Division, National Research Centre (NRC), P.C.12622, Dokki, Giza, Egypt.
Int J Nanomedicine. 2020 Jul 22;15:5181-5202. doi: 10.2147/IJN.S247692. eCollection 2020.
Combating infectious diseases caused by influenza virus is a major challenge due to its resistance to available drugs and vaccines, side effects, and cost of treatment. Nanomedicines are being developed to allow targeted delivery of drugs to attack specific cells or viruses.
In this study, mesoporous silica nanoparticles (MSNs) functionalized with amino groups and loaded with natural prodrugs of shikimic acid (SH), quercetin (QR) or both were explored as a novel antiviral nanoformulations targeting the highly pathogenic avian influenza H5N1 virus. Also, the immunomodulatory effects were investigated in vitro tests and anti-inflammatory activity was determined in vivo using the acute carrageenan-induced paw edema rat model.
Prodrugs alone or the MSNs displayed weaker antiviral effects as evidenced by virus titers and plaque formation compared to nanoformulations. The MSNs-NH-SH and MSNs-NH-SH-QR2 nanoformulations displayed a strong virucidal by inactivating the H5N1 virus. They induced also strong immunomodulatory effects: they inhibited cytokines (TNF-α, IL-1β) and nitric oxide production by approximately 50% for MSNs-NH-SH-QR2 (containing both SH and QR). Remarkable anti-inflammatory effects were observed during in vivo tests in an acute carrageenan-induced rat model.
Our preliminary findings show the potential of nanotechnology for the application of natural prodrug substances to produce a novel safe, effective, and affordable antiviral drug.
由于流感病毒对现有药物和疫苗的耐药性、副作用以及治疗成本,防治其引发的传染病是一项重大挑战。正在开发的纳米药物可实现药物的靶向递送来攻击特定的细胞或病毒。
在这项研究中,用氨基官能化的介孔硅纳米颗粒(MSNs)负载天然前药莽草酸(SH)、槲皮素(QR)或两者的混合物,探索其作为针对高致病性禽流感 H5N1 病毒的新型抗病毒纳米制剂。还在体外试验中研究了其免疫调节作用,并在急性角叉菜胶诱导的大鼠足肿胀模型中测定了抗炎活性。
单独的前药或 MSNs 的抗病毒效果较弱,病毒滴度和蚀斑形成试验均表明如此。MSNs-NH-SH 和 MSNs-NH-SH-QR2 纳米制剂具有很强的病毒灭活作用,可灭活 H5N1 病毒。它们还具有很强的免疫调节作用:MSNs-NH-SH-QR2(同时含有 SH 和 QR)可使细胞因子(TNF-α、IL-1β)和一氧化氮的产生抑制约 50%。在急性角叉菜胶诱导的大鼠模型中进行的体内试验观察到了显著的抗炎作用。
我们的初步研究结果表明,纳米技术在应用天然前药物质生产新型安全、有效和负担得起的抗病毒药物方面具有潜力。