Emilie Darrigues

Dr. Emilie Darrigues

orcid

Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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9 November 2019 in Nanoscale Horizons
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Journal Article
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EDEmilie Darrigues
Emilie Darrigues
ZNZeid Nima
Zeid Nima
RGRobert Griffin
Robert Griffin
JAJames M. Anderson
James M. Anderson
ABAlexandru Biris
Alexandru Biris
ARAnaliz Rodriguez
Analiz Rodriguez
Photothermal therapy (PTT) is one of the most promising techniques for cancer tumor ablation. Nanoparticles are increasingly being investigated for use with PTT and can serve as theranostic agents. Based on the ability of near-infrared nano-photo-absorbers to generate heat under laser irradiation, PTT could prove advantageous in certain situations over more classical cancer therapies. To analyze the efficacy of nanoparticle-based PTT, preclinical in vitro studies typically use 2D cultures, but this method cannot completely mimic the complex tumor organization, bioactivity, and physiology that all control the complex penetration depth, biodistribution, and tissue diffusion parameters of nanomaterials in vivo. To fill this knowledge gap, 3D culture systems have been explored for PTT analysis. These models provide more realistic microenvironments that allow spatiotemporal oxygen gradients and cancer cell adaptations to be considered. This review highlights the work that has been done to advance 3D models for cancer microenvironment modeling, specifically in the context of advanced, functionalized nanoparticle-directed PTT.

4 September 2016 in Journal of Applied Toxicology
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Journal Article
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WMWaqar Majeed
Waqar Majeed
SBShawn Bourdo
Shawn Bourdo
DPDayton M. Petibone
Dayton M. Petibone
VSViney Saini
Viney Saini
KVKieng Bao Vang
Kieng Bao Vang
ABAlexandru S. Biris
Alexandru S. Biris

25 February 2020 in Scientific Reports
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Journal Article
Open access
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EDEmilie Darrigues
Emilie Darrigues
ZNZeid A. Nima
Zeid A. Nima
DNDmitry A. Nedosekin
Dmitry A. Nedosekin
FWFumiya Watanabe
Fumiya Watanabe
KAKarrer M. Alghazali
Karrer M. Alghazali
ABAlexandru Biris
Alexandru Biris
Pancreatic cancer is one of the most complex types of cancers to detect, diagnose, and treat. However, the field of nanomedicine has strong potential to address such challenges. When evaluating the diffusion and penetration of theranostic nanoparticles, the extracellular matrix (ECM) is of crucial importance because it acts as a barrier to the tumor microenvironment. In the present study, the penetration of functionalized, fluorescent gold nanorods into large (>500 μm) multicellular 3D tissue spheroids was studied using a multimodal imaging approach. The spheroids were generated by co-culturing pancreatic cancer cells and pancreatic stellate cells in multiple ratios to mimic variable tumor-stromal compositions and to investigate nanoparticle penetration. Fluorescence live imaging, photothermal, and photoacoustic analysis were utilized to examine nanoparticle behavior in the spheroids. Uniquely, the nanorods are intrinsically photoacoustic and photothermal, enabling multi-imaging detection even when fluorescence tracking is not possible or ideal.

Verified
Journal Article
Open access
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EDEmilie Darrigues
Emilie Darrigues
EZEdward H. Zhao
Edward H. Zhao
ALAnnick De Loose
Annick De Loose
MLMadison P. Lee
Madison P. Lee
MBMichael J. Borrelli
Michael J. Borrelli
ARAnaliz Rodriguez
Analiz Rodriguez
Glioblastoma (GBM) is highly resistant to treatment and invasion into the surrounding brain is a cancer hallmark that leads to recurrence despite surgical resection. With the emergence of precision medicine, patient-derived 3D systems are considered potentially robust GBM preclinical models. In this study, we screened a library of 22 anti-invasive compounds (i.e., NF-kB, GSK-3-B, COX-2, and tubulin inhibitors) using glioblastoma U-251 MG cell spheroids. We evaluated toxicity and invasion inhibition using a 3D Matrigel invasion assay. We next selected three compounds that inhibited invasion and screened them in patient-derived glioblastoma organoids (GBOs). We developed a platform using available macros for FIJI/ImageJ to quantify invasion from the outer margin of organoids. Our data demonstrated that a high-throughput invasion screening can be done using both an established cell line and patient-derived 3D model systems. Tubulin inhibitor compounds had the best efficacy with U-251 MG cells, however, in ex vivo patient organoids the results were highly variable. Our results indicate that the efficacy of compounds is highly related to patient intra and inter-tumor heterogeneity. These results indicate that such models can be used to evaluate personal oncology therapeutic strategies.

14 July 2017 in Scientific Reports
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Journal Article
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KVKieng Bao Vang
Kieng Bao Vang
ISIngrid Safina
Ingrid Safina
EDEmilie Darrigues
Emilie Darrigues
DNDmitry Nedosekin
Dmitry Nedosekin
ZNZeid Nima
Zeid Nima
ABAlexandru S. Biris
Alexandru S. Biris
Dendritic cells (DCs) can acquire, process, and present antigens to T-cells to induce an immune response. For this reason, targeting cancer antigens to DCs in order to cause an immune response against cancer is an emerging area of nanomedicine that has the potential to redefine the way certain cancers are treated. The use of plasmonically active silver-coated gold nanorods (henceforth referred to as plasmonic nano vectors (PNVs)) as potential carriers for DC tumor vaccines has not been presented before. Effective carriers must be able to be phagocytized by DCs, present low toxicity, and induce the maturation of DCs—an early indication of an immune response. When we treated DCs with the PNVs, we found that the cell viability of DCs was unaffected, up to 200 μg/ml. Additionally, the PNVs associated with the DCs as they were phagocytized and they were found to reside within intracellular compartments such as endosomes. More importantly, the PNVs were able to induce expression of surface markers indicative of DC activation and maturation, i.e. CD40, CD86, and MHC class II. These results provide the first evidence that PNVs are promising carriers for DC-based vaccines and warrant further investigating for clinical use.

3 April 2017 in Drug Metabolism Reviews
Verified
Journal Article
Closed access
EDEmilie Darrigues
Emilie Darrigues
VDVijayalakshmi Dantuluri
Vijayalakshmi Dantuluri
ZNZeid Nima
Zeid Nima
KVKieng Bao Vang-Dings
Kieng Bao Vang-Dings
RGRobert Griffin
Robert Griffin
ABAlexandru S. Biris
Alexandru S. Biris
Raman spectroscopy and surface-enhanced raman scattering (SERS) have the potential to improve the detection and monitoring of various diseases, particularly cancer, with or without the support of multifunctional active nanosystems. This review is focused on the recent advances that have made Raman a major tool for treatment guidance for surgical tumor resection or for analytical monitoring of various therapies, such as photodynamic therapy, photothermal therapy, and drug delivery. The potential of Raman spectroscopy and nanosytems to further improve cancer treatments is also discussed.