Graduate Program in Health Sciences, State University of Maringá, Avenida Colombo, 5790, Jardim Universitário, Maringá, 87020-900, PR, Brazil.
Health Sciences Center - Department of Clinical Analysis, Federal University of Santa Catarina, Campus Universitário Reitor João David Ferreira Lima, s/n°, Bairro Trindade, Florianópolis, 88040-900, SC, Brazil.
Nanomedicine (Lond). 2021 Jul;16(17):1505-1518. doi: 10.2217/nnm-2021-0119. Epub 2021 Jun 30.
Nanotechnology is a promising strategy to improve existing antileishmanial agents. To explore the evidence of encapsulated meglumine antimoniate for cutaneous leishmaniasis treatment in animal models. The studies were recovered from PubMed, Scopus, EMBASE, LILACS, WoS and Google according to eligibility criteria following Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) and the Population, Intervention, Comparison, Outcomes and Study design (PICOS) strategy. Study appraisal was assessed using the Animal Research Reporting of Experiments, SYstematic Review Centre for Laboratory animal Experimentation (SYRCLE) and Grading of Recommendations Assessment, Development and Evaluation (GRADE) recommendations. Five studies were included. Liposomes, metallic and polymeric nanoparticles were tested in BALB/c mice against , or . Few studies were found to meet the eligibility criteria. All formulations had a significant efficacy, similar to the meglumine antimoniate reference treatment concerning the lesion size and parasite burden. The studies had a high and moderate risk of bias, and the confidence in cumulative evidence was considered low. Therefore, we encourage the development of high-quality preclinical studies. PROSPERO register CRD42020170191.
纳米技术是一种有前途的策略,可以改进现有的抗利什曼原虫药物。 为了探讨囊封葡甲胺锑用于动物模型中皮肤利什曼病治疗的证据。 根据系统评价和荟萃分析(PRISMA)以及人群、干预、比较、结果和研究设计(PICOS)策略,从 PubMed、Scopus、EMBASE、LILACS、WoS 和 Google 中检索研究。使用动物实验报告实验的动物研究报告、系统评价中心的实验室动物实验(SYRCLE)和推荐评估、发展和评估(GRADE)建议评估研究评估。 纳入了 5 项研究。脂质体、金属和聚合物纳米颗粒在 BALB/c 小鼠中针对 、 或 进行了测试。 很少有研究符合入选标准。 所有制剂的疗效均显著,与葡甲胺锑参考治疗相比,在病变大小和寄生虫负荷方面相似。研究存在高风险和中度偏倚,累积证据的可信度被认为较低。因此,我们鼓励开展高质量的临床前研究。 PROSPERO 注册 CRD42020170191。