Department of Biology, São Paulo State University-UNESP, Rua Cristóvão Colombo, São José do Rio Preto, Brazil.
Laboratory of Bioactive Compounds and Nanobiotechnology (LBCNano), University of Brasilia, Campus Universitário - Centro Metropolitano, Ceilândia Sul, Brasília, Federal District, Brazil.
PLoS One. 2023 Sep 7;18(9):e0283817. doi: 10.1371/journal.pone.0283817. eCollection 2023.
Zika virus (ZIKV) has spread all over the world since its major outbreak in 2015. This infection has been recognized as a major global health issue due to the neurological complications related to ZIKV infection, such as Guillain-Barré Syndrome and Zika virus Congenital Syndrome. Currently, there are no vaccines or specific treatments for ZIKV infection, which makes the development of specific therapies for its treatment very important. Several studies have been developed to analyze the potential of compounds against ZIKV, with the aim of finding new promising treatments. Herein, we evaluate the ability of a copaiba (Copaifera officinalis) oil nanoemulsion (CNE) to inhibit ZIKV. First, the highest non-cytotoxic concentration of 180 μg/mL was chosen since this concentration maintains 80% cell viability up to 96h after treatment with CNE in VERO cells resulted from MTT assay. The intracellular uptake assay was performed, and confirmed the internalization of the nanoemulsion in cells at all times analyzed. VERO cells were infected with ZIKV and simultaneously treated with CNE and the nanoformulation without oil (ENE) at the highest non-toxic concentration. The results evaluated by plaque assay revealed a viral inhibition of 80% for CNE and 70% for ENE. A dose-dependence assay revealed that the CNE treatment demonstrated a dose-dependent response in the viral RNA levels, whereas all ENE tested concentrations exhibited a similar degree of reduction. Taken together, our results suggest CNE as a promising nano-sized platform to be further studied for antiviral treatments.
寨卡病毒(ZIKV)自 2015 年大规模爆发以来已在全球范围内传播。由于与 ZIKV 感染相关的神经并发症,如格林-巴利综合征和寨卡病毒先天综合征,该感染已被认为是一个主要的全球健康问题。目前,尚无针对 ZIKV 感染的疫苗或特定治疗方法,这使得开发针对其治疗的特定疗法非常重要。已经开展了几项研究来分析针对 ZIKV 的化合物的潜力,旨在寻找新的有前途的治疗方法。在此,我们评估了 copaiba(Copaifera officinalis)油纳米乳液(CNE)抑制 ZIKV 的能力。首先,选择了最高非细胞毒性浓度 180μg/mL,因为该浓度在 MTT 测定中用 CNE 处理 VERO 细胞 96 小时后保持 80%的细胞活力。进行了细胞内摄取测定,并证实了纳米乳液在所有分析时间都在细胞内内化。用 ZIKV 感染 VERO 细胞,并同时用 CNE 和最高非毒性浓度的无油纳米制剂(ENE)处理。通过蚀斑测定评估的结果显示,CNE 对病毒的抑制率为 80%,ENE 为 70%。剂量依赖性测定显示,CNE 处理在病毒 RNA 水平上表现出剂量依赖性反应,而测试的所有 ENE 浓度均表现出相似程度的降低。总之,我们的结果表明 CNE 是一种很有前途的纳米级平台,可进一步研究用于抗病毒治疗。