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Record W2791780371 · doi:10.1149/ma2018-01/42/2441

Comparison of Ex-Situ and In-Situ Nano Plasmonic Platforms for Capture and Detection of Exosomes

2018· article· en· W2791780371 on OpenAlexaff
R. Duraichelvan, B. Srinivas, Simona Bǎdilescu, Anirban Ghosh, Muthukumaran Packirisamy

Bibliographic record

VenueECS Meeting Abstracts · 2018
Typearticle
Languageen
FieldMaterials Science
TopicGold and Silver Nanoparticles Synthesis and Applications
Canadian institutionsAtlantic Cancer Research InstituteConcordia University
Fundersnot available
KeywordsMicrovesiclesNanotechnologyPlasmonMaterials scienceBiosensorNanomedicineNanoparticleExtracellular vesiclesComputer scienceChemistrymicroRNABiologyCell biologyOptoelectronics

Abstract

fetched live from OpenAlex

Over the past few decades, in the field of sensing, the fabrication of the optimal nanostructures for detecting specific bio-entities remained an active area of research. It is well-known that the structure and the plasmonic properties of noble metal nanoparticles can be customized for specific applications such as biosensing, diagnosis, imaging, etc. by tuning the size and shape of the nanoparticles. Thus, by using the plasmonic property of noble metals, the detection at the nano-scale is possible by monitoring the shift of the local resonance band with respect to the changes in refractive index of the surrounding medium. The present study is aimed at comparing the quality and performance of two nano plasmonic platforms for the capture and detection of exosomes. Exosomes are nanoscale heterogeneous vesicles that are released by different cells. These vesicles plays significant role in intercellular communications, transport of proteins, RNA, and other molecular informations. In the last decade, researchers have shown substantial interest in this field as there is a lack of specific methodology to isolate and detect them. Currently, the exact science behind the major standard techniques of isolation of exosomes is not clearly understood. Thus, limitations with low yield and poor quality exosomes compromise further molecular analysis for diagnosis. The ultracentrifugation method of isolation of exosomes is time consuming, laborious, infrastructure intensive and may lack specificity. Therefore, a lot of challenges are existing in this field in order to develop next generation affinity-based technologies to capture the exosomes selectively and use them for further diagnosis at the clinical level. The two different sensing platforms, developed and tested for sensing of exosomes are the ex-situ gold (Au) nano-islands on glass substrates and the in-situ prepared silver (Ag) - polydimethylsiloxane (PDMS) nano-composite. The gold platform is fabricated by depositing colloidal gold on glass by the thermal convection method, followed by morphology tuning of the formed nanoparticles by annealing. The second is the nano-composite platform developed by the in-situ synthesis of silver ions present in the silver nitrate solution and the curing agent present in the PDMS polymer. In both cases, the capture and detection of exosomes is based on the strong affinity of heat shock proteins contained by exosomes and a polypeptide called Vn96, specially synthesized for this purpose. The Vn96 peptide targets canonical heat shock proteins that are present on the surface of exosomes. The Vn96 - based exosomes-capture method is further validated for downstream analyses, clinical compatibility, and liquid biopsy assays (biomarker and mutation detection) and platform-versatility using cell-culture conditioned media and human body fluids as sources of exosomes. Vn96 provides multiple advantages over currently-available methods for exosomes isolation: the scalability, quality, platform versatility, and cost-effectiveness. By using the gold platform, biotinylated Vn96 peptide is bound onto the streptavidin-coated Au nano-islands, and the subsequent steps of binding of nano-sized vesicles (exosomes) are monitored through the localized surface plasmon resonance (LSPR) band of Au. The sensing process was modelled, taking into account the characteristics of the nano-island structure. It is found that the results of the sensing process depend on the two major steps: the molar ratios of streptavidin to biotin-PEG-Vn96 and, the final step, the capture of exosomes by the biotin-PEG-Vn96 complex. The Ag-PDMS platform is used in a similar way and the shift of the Ag LSPR band is monitored after each sensing step. It is found that the bio sensitivity of the ex-situ synthesized gold/glass platform is considerably higher than that of the in-situ synthesized Ag-PDMS nanocomposite and, consequently, this platform is much more performant for the sensing of exosomes. Two principal reasons were identified in order to account for this difference. It is thought that, because of the low temperature of annealing of Ag-PDMS, contrary to the nano-islands of gold, a non-suitable morphology is formed. It has been demonstrated that nano-island structures have a higher sensitivity due to their morphological characteristics. On the other hand, due to the in-situ formation mechanism, a large proportion of the surface Ag particles will diffuse inside the polymer layer, that is, they will not be available anymore for sensing. The morphology of Au nano-islands and Ag-PDMS composite were investigated by SEM and the LSPR techniques are discussed in the paper.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.001
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.001
Threshold uncertainty score0.007

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.001
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0000.001
Bibliometrics0.0010.000
Science and technology studies0.0000.000
Scholarly communication0.0010.001
Open science0.0010.001
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0010.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.025
GPT teacher head0.276
Teacher spread0.251 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2018
Admission routes1
Has abstractyes

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