MFMarcos Vilas Boas Filho

Marcos Vilas Boas Filho

*This is an algorithmically generated author record based on publicly available information.

Current Organizations / Institutes

The organizations/institutes from the scholar's latest article


Marcos Vilas Boas Filho has a total of 7 co-authors. Here are the top co-authors by number of shared publications:


Latest Publications

  • Open Access

    Recent Advances in Nanomaterials for Enhanced Colorimetric Detection of Viruses and Bacteria

    by Caroline R. Basso, Marcos V. B. Filho, Victoria D. Gavioli, Joao P. R. L. L. Parra, Gustavo R. Castro, Valber A. Pedrosa

    The increasing prevalence of pathogen outbreaks underscores the urgent need for rapid, accurate, and cost-effective diagnostic tools. Colorimetric detection has gained significant attention among the available techniques due to its simplicity, portability, and potential for point-of-care applications. The nanomaterial-based colorimetric detection field continues to evolve, with innovations focusing on improving sensitivity, specificity, robustness, cost-effectiveness, and friendly analysis. Additionally, efforts to address limitations, such as stability and environmental impact, pave the way for more sustainable and reliable diagnostic solutions. This review highlights recent advances in nanomaterials for colorimetric pathogen detection in the last five years.


  • Open Access

    Rapid Isolation of Circulating Tumor Cells from Glioblastoma Patients Using a Lateral Filter Array Microfluidic Device

    by Victória D’amario Gavioli, Marcos Vilas Boas Filho, Gustavo R. Castro, Pedro Tadao Hamamoto Filho, Adriana Camargo Ferrasi, Valber A. Pedrosa

    Glioblastoma is the most common form of brain cancer in adults, representing 35–40% of all malignant brain tumors. This highly aggressive malignancy originates in the central nervous system, and despite notable advancements in treatment strategies, it continues to be an incurable disease. The isolation of circulating tumor cells (CTC) at an early stage is challenging due to the low probability of their presence in peripheral blood. Detection and enumeration as early as possible can reportedly lead to more effective treatment. This study proposes a novel label-free, rapid, and continuous CTC separation device based on a lateral filter array microfluidic device for the highly efficient immunoaffinity isolation of CTCs. Our methodology successfully captured and isolated circulating tumor cells (CTCs) from the whole blood of glioblastoma (GBM) patients prior to surgery, achieving over 90% capture efficiency in under 40 min of analysis. These findings highlight the potential of this technology to enhance our understanding of the clinical significance of CTCs in the management of GBM in future research.