Tuan Vo-Dinh

Overview:

Dr. Tuan Vo-Dinh is R. Eugene and Susie E. Goodson Distinguished Professor of Biomedical Engineering, Professor of Chemistry, and Director of The Fitzpatrick Institute for Photonics.

Dr. Vo-Dinh’s research activities and interests involve biophotonics, nanophotonics, plasmonics, laser-excited luminescence spectroscopy, room temperature phosphorimetry, synchronous luminescence spectroscopy, and surface-enhanced Raman spectroscopy for multi-modality bioimaging, and theranostics (diagnostics and therapy) of diseases such as cancer and infectious diseases.

We have pioneered the development of a new generation of gene biosensing probes using surface-enhanced Raman scattering (SERS) detection with “Molecular Sentinels” and Plasmonic Coupling Interference (PCI) molecular probes for multiplex and label-free detection of nucleic acid biomarkers (DNA, mRNA, microRNA) in early detection of a wide variety of diseases.

In genomic and precision medicine, nucleic acid-based molecular diagnosis is of paramount importance with many advantages such as high specificity, high sensitivity, serotyping capability, and mutation detection. Using SERS-based plasmonic nanobiosensors and nanochips, we are developing novel nucleic acid detection methods that can be integrated into lab-on-a-chip systems for point-of-care diagnosis  (e.g., breast, GI cancer) and global health applications (e.g., detection of malaria and dengue).

In bioimaging, we are developing a novel multifunctional gold nanostar (GNS) probe for use in multi-modality bioimaging in pre-operative scans with PET, MRI and CT, intraoperative margin delineation with optical imaging, SERS and two-photon luminescence (TPL). The GNS can be used also for cancer treatment with plasmonics enhanced photothermal therapy (PTT), thus providing an excellent platform for seamless diagnostics and therapy (i.e., theranostics). Preclinical studies have shown its great potential for cancer diagnostics and therapeutics for future clinical translation.

For fundamental studies, various nanobiosensors are being developed for monitoring intracellular parameters (e.g., pH) and biomolecular processes (e.g., apoptosis, caspases), opening the possibility for fundamental molecular biological research as well as biomedical applications (e.g., drug discovery) at the single cell level in a systems biology approach. For point of care diagnostics, nanoprobes and nanochips with highly multiplex SERS detection and imaging use artificial intelligence and machine learning for data analysis.

Our research activities in immunotherapy involve unique plasmonics-active gold “nanostars.” These star-shaped nanobodies made of gold work like “lightning rods,” concentrating the electromagnetic energy at their tips and allowing them to capture photon energy more efficiently when irradiated by laser light. Teaming with medical collaborators, we have developed a novel cancer treatment modality, called synergistic immuno photothermal nanotherapy (SYMPHONY), which combines immune-checkpoint inhibition and gold nanostar–mediated photothermal immunotherapy that can unleash the immunotherapeutic efficacy of checkpoint inhibitors. This combination treatment can eradicate the primary tumors as well as distant “untreated” tumors, and induce immunologic memory like a “anti-cancer vaccine” effect in murine model.

Positions:

R. Eugene and Susie E. Goodson Distinguished Professor of Biomedical Engineering

Biomedical Engineering
Pratt School of Engineering

Professor of Biomedical Engineering

Biomedical Engineering
Pratt School of Engineering

Professor in the Department of Chemistry

Chemistry
Trinity College of Arts & Sciences

Faculty Network Member of The Energy Initiative

Nicholas Institute for Energy, Environment & Sustainability
Institutes and Provost's Academic Units

Member of the Duke Cancer Institute

Duke Cancer Institute
School of Medicine

Education:

B.S. 1971

Swiss Federal Institute of Technology-EPFL Lausanne (Switzerland)

Ph.D. 1975

Swiss Federal Institute of Technology-ETH Zurich (Switzerland)

Grants:

Nanoplasmonics-based molecular analysis tool for molecular biomarkers of cancer

Administered By
Biomedical Engineering
Awarded By
National Institutes of Health
Role
Principal Investigator
Start Date
End Date

Plasmonics-Active SERS Nanoplatforms for In Vivo Diagnostics

Administered By
Biomedical Engineering
Awarded By
Defense Advanced Research Projects Agency
Role
Principal Investigator
Start Date
End Date

Nanoplatform for Tracking Adipose-Derived Stem Cell Migration

Awarded By
Southeastern Society of Plastic and Reconstructive Surgeons
Role
Collaborator
Start Date
End Date

Plasmonic nanoparticle-mediated immunotherapy to treat metastatic cancer

Administered By
Biomedical Engineering
Awarded By
National Institutes of Health
Role
Principal Investigator
Start Date
End Date

Does Cytoplasmic PELP1 Predict Resistance To Tamoxifen Chemoprevention?

Administered By
Medicine, Medical Oncology
Awarded By
National Institutes of Health
Role
Co-Mentor
Start Date
End Date

Publications:

Xenorecognition and costimulation of porcine endothelium-derived extracellular vesicles in initiating human porcine-specific T cell immune responses.

Porcine vascular endothelial cells (PECs) form a mechanistic centerpiece of xenograft rejection. Here, we determined that resting PECs release swine leukocyte antigen class I (SLA-I) but not swine leukocyte antigen class-II DR (SLA-DR) expressing extracellular vesicles (EVs) and investigated whether these EVs proficiently initiate xenoreactive T cell responses via direct xenorecognition and costimulation. Human T cells acquired SLA-I+ EVs with or without direct contact to PECs, and these EVs colocalized with T cell receptors. Although interferon gamma-activated PECs released SLA-DR+ EVs, the binding of SLA-DR+ EVs to T cells was sparse. Human T cells demonstrated low levels of proliferation without direct contact to PECs, but marked T cell proliferation was induced following exposure to EVs. EV-induced proliferation proceeded independent of monocytes/macrophages, suggesting that EVs delivered both a T cell receptor signal and costimulation. Costimulation blockade targeting B7, CD40L, or CD11a significantly reduced T cell proliferation to PEC-derived EVs. These findings indicate that endothelial-derived EVs can directly initiate T cell-mediated immune responses, and suggest that inhibiting the release of SLA-I EVs from organ xenografts has the potential to modify the xenograft rejection. We propose a secondary-direct pathway for T cell activation via xenoantigen recognition/costimulation by endothelial-derived EVs.
Authors
Li, S; Anwar, IJ; Canning, AJ; Vo-Dinh, T; Kirk, AD; Xu, H
MLA Citation
Li, Shu, et al. “Xenorecognition and costimulation of porcine endothelium-derived extracellular vesicles in initiating human porcine-specific T cell immune responses.Am J Transplant, vol. 23, no. 7, July 2023, pp. 904–19. Pubmed, doi:10.1016/j.ajt.2023.04.006.
URI
https://scholars.duke.edu/individual/pub1571822
PMID
37054891
Source
pubmed
Published In
Am J Transplant
Volume
23
Published Date
Start Page
904
End Page
919
DOI
10.1016/j.ajt.2023.04.006

Ultra-trace SERS detection of cocaine and heroin using bimetallic gold-silver nanostars (BGNS-Ag).

A rapid, in-field, and reliable method for the detection of illegal drugs of abuse in biological fluids without any sample pretreatment would potentially be helpful for law enforcement, drug control officials, and public healthcare. In this study, we presented a cost-effective and highly reproducible solution-based surface-enhanced Raman scattering (SERS) platform utilizing a portable Raman instrument for fast sensitive SERS detection of illegal drugs, such as cocaine, and heroin in human urine without any sample preprocessing. The SERS platform was constructed for the first time by combining the superior SERS enhancement properties of bimetallic silver-coated gold nanostars (BGNS-Ag) and the advantages of suitable alkaline metal salts such as NaI for SERS signal amplification. The effects of the silver thickness of BGNS-Ag and alkaline salts on the SERS performance were investigated in detail; we observed that the maximum SERS enhancement was obtained for BGNS-Ag with the maximum silver thickness (54 ± 5 nm) in presence of NaI salt. Our SERS platform shows ultra-high sensitivity of cocaine and heroin with a limit of detection (LOD) as low as 10 pg/mL for cocaine and 100 pg/mL for heroin, which was 100 times lower than that of the traditional silver nanoparticle-based illegal drug detection. As a demonstration, the platform was further applied to detect cocaine and heroin spiked in human urine without any sample preprocessing achieving a LOD of 100 pg/mL for cocaine and 1 ng/mL for heroin. Overall, our SERS detection platform shows potential for rapid, onsite, ultra-low-cost portable applications for trace detection of illegal drugs and biomarkers.
Authors
Atta, S; Vo-Dinh, T
MLA Citation
Atta, Supriya, and Tuan Vo-Dinh. “Ultra-trace SERS detection of cocaine and heroin using bimetallic gold-silver nanostars (BGNS-Ag).Analytica Chimica Acta, vol. 1251, Apr. 2023, p. 340956. Epmc, doi:10.1016/j.aca.2023.340956.
URI
https://scholars.duke.edu/individual/pub1567036
PMID
36925275
Source
epmc
Published In
Analytica Chimica Acta
Volume
1251
Published Date
Start Page
340956
DOI
10.1016/j.aca.2023.340956

A hybrid plasmonic nanoprobe using polyvinylpyrrolidone-capped bimetallic silver-gold nanostars for highly sensitive and reproducible solution-based SERS sensing.

Practical solution-based assays using surface-enhanced Raman spectroscopy (SERS) with portable instrumentation are currently of particular interest for rapid, efficient, and low-cost detection of analytes. However, current assays still have limited applicability due to their poor sensitivity and reproducibility. Herein, we demonstrate highly stable polyvinylpyrrolidone (PVP)-capped bimetallic silver-coated gold nanostars (BGNS-Ag-PVP) as a solution-based SERS nanoprobe that is capable of producing a strong, uniform, and reproducible SERS signal using a portable Raman instrument. The developed hybrid BGNS-Ag-PVP nanostructure shows tunable optical properties with improved SERS sensitivity and reproducibility as compared to gold nanostars. We have synthesized bimetallic nanoprobes BGNS-Ag-PVP having three different silvers, referred to as BGNS-Ag-PVP-1, BGNS-Ag-PVP-2, and BGNS-Ag-PVP-3. The SERS performance of BGNS-Ag-PVP was studied using methylene blue (Meb) as a probe molecule, and we achieved a detection limit of up to 10 nM indicating the high sensitivity of the solution-based SERS platform. The application of such bimetallic nanoparticles is demonstrated <i>via</i> the sensitive detection of the antithyroid drug methimazole (Mz) used as a model analyte system. We have achieved a detection limit of 1 nM for Mz spiked with human urine indicating three orders of magnitude lower than previously reported solution-based SERS detection methods. Furthermore, the SERS performance was reproducible over 3 months indicating excellent stability and repeatability. The result illustrates the potential of this solution-based SERS detection platform as a promising sensing tool for analytes such as illicit drugs, and biomarkers that have affinity to bind on nanoprobes.
Authors
Atta, S; Vo-Dinh, T
MLA Citation
Atta, Supriya, and Tuan Vo-Dinh. “A hybrid plasmonic nanoprobe using polyvinylpyrrolidone-capped bimetallic silver-gold nanostars for highly sensitive and reproducible solution-based SERS sensing.The Analyst, vol. 148, no. 8, Apr. 2023, pp. 1786–96. Epmc, doi:10.1039/d2an01876d.
URI
https://scholars.duke.edu/individual/pub1569385
PMID
36920068
Source
epmc
Published In
The Analyst
Volume
148
Published Date
Start Page
1786
End Page
1796
DOI
10.1039/d2an01876d

Sharp Branched Gold Nanostar-Based Lateral-Flow Immunoassay for Detection of Yersinia pestis

Over the past few decades, colorimetric paper-based lateral flow immunoassay (LFIA) has emerged as a versatile analytical tool for rapid point-of-care detection of infectious diseases with high simplicity and flexibility. The LFIA sensitivity is based on color visualization of the antibody-labeled nanoparticles bound with the target analytes at the test line. Therefore, the nanoparticle design is crucial for LFIA sensitivity. The traditional LFIA is based on spherical gold nanoparticles, which usually suffer from poor sensitivity because of very low optical contrast at the test line. To improve the LFIA sensitivity, we have developed an LFIA based on gold nanostars (GNSs) with different branch lengths and sharpness (GNS-1, GNS-2, and GNS-3), which possess higher optical contrast than conventional gold nanospheres (GNSPs). We have selected the bacterium Yersinia pestis as a model analyte system. The effective affinity of GNSPs and GNSs with the Y. pestis fraction 1 (F1) protein was quantitively investigated by colorimetric and optical density measurements of the test line. The results show that GNS-3, which has maximum spike length and branch sharpness, exhibits the highest analytical sensitivity based on the limit of detection of the LFIA readout compared to other GNSs and GNSPs. The detection limit of the Y. pestis F1 antigen was achieved up to 0.1 ng/mL for GNS-3, which is 100 times lower than that for the GNSP at a 1 pmol/L concentration and 10 times lower than that for the reported procedure based on traditional gold nanoparticles. Overall, our prototype LFIA platform based on a highly spiked GNS (GNS-3) exhibits high analytical sensitivity, indicating it to be a promising candidate for routine LFIA application to detect infectious diseases.
Authors
Atta, S; Canning, AJ; Odion, R; Wang, HN; Hau, D; Devadhasan, JP; Summers, AJ; Gates-Hollingsworth, MA; Pflughoeft, KJ; Gu, J; Montgomery, DC; AuCoin, DP; Zenhausern, F; Vo-Dinh, T
MLA Citation
Atta, S., et al. “Sharp Branched Gold Nanostar-Based Lateral-Flow Immunoassay for Detection of Yersinia pestis.” Acs Applied Nano Materials, vol. 6, no. 5, Mar. 2023, pp. 3884–92. Scopus, doi:10.1021/acsanm.2c05557.
URI
https://scholars.duke.edu/individual/pub1568262
Source
scopus
Published In
Acs Applied Nano Materials
Volume
6
Published Date
Start Page
3884
End Page
3892
DOI
10.1021/acsanm.2c05557

Development of Gold Nanostars for Photothermal and Immunotherapy Applications

Authors
Liu, Y; Indrasekara, S; Vo-Dinh, T
MLA Citation
Liu, Y., et al. “Development of Gold Nanostars for Photothermal and Immunotherapy Applications.” World Scientific Series in Nanoscience and Nanotechnology, vol. 22, 2022, pp. 555–75. Scopus, doi:10.1142/9789811235252_0014.
URI
https://scholars.duke.edu/individual/pub1571567
Source
scopus
Volume
22
Published Date
Start Page
555
End Page
575
DOI
10.1142/9789811235252_0014