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1.
Nanoscale ; 15(40): 16371-16380, 2023 Oct 20.
Artigo em Inglês | MEDLINE | ID: mdl-37789717

RESUMO

Atomic force microscopy (AFM) has become indispensable for studying biological and medical samples. More than two decades of experiments have revealed that cancer cells are softer than healthy cells (for measured cells cultured on stiff substrates). The softness or, more precisely, the larger deformability of cancer cells, primarily independent of cancer types, could be used as a sensitive marker of pathological changes. The wide application of biomechanics in clinics would require designing instruments with specific calibration, data collection, and analysis procedures. For these reasons, such development is, at present, still very limited, hampering the clinical exploitation of mechanical measurements. Here, we propose a standardized operational protocol (SOP), developed within the EU ITN network Phys2BioMed, which allows the detection of the biomechanical properties of living cancer cells regardless of the nanoindentation instruments used (AFMs and other indenters) and the laboratory involved in the research. We standardized the cell cultures, AFM calibration, measurements, and data analysis. This effort resulted in a step-by-step SOP for cell cultures, instrument calibration, measurements, and data analysis, leading to the concordance of the results (Young's modulus) measured among the six EU laboratories involved. Our results highlight the importance of the SOP in obtaining a reproducible mechanical characterization of cancer cells and paving the way toward exploiting biomechanics for diagnostic purposes in clinics.


Assuntos
Técnicas de Cultura de Células , Módulo de Elasticidade , Microscopia de Força Atômica/métodos , Fenômenos Biomecânicos
2.
Soft Matter ; 19(4): 615-624, 2023 Jan 25.
Artigo em Inglês | MEDLINE | ID: mdl-36445288

RESUMO

The rheological characterization of soft suspended bodies, such as cells, organoids, or synthetic microstructures, is particularly challenging, even with state-of-the-art methods (e.g. atomic force microscopy, AFM). Providing well-defined boundary conditions for modeling typically requires fixating the sample on a substrate, which is a delicate and time-consuming procedure. Moreover, it needs to be tuned for each chemistry and geometry. Here, we validate a novel technique, called hydraulic force spectroscopy (HFS), against AFM dynamic indentation taken as the gold standard. Combining experimental data with finite element modeling, we show that HFS gives results comparable to AFM microrheology over multiple decades, while obviating any sample preparation requirements.

3.
Commun Biol ; 4(1): 610, 2021 05 21.
Artigo em Inglês | MEDLINE | ID: mdl-34021241

RESUMO

Micropipette aspiration (MPA) is an essential tool in mechanobiology; however, its potential is far from fully exploited. The traditional MPA technique has limited temporal and spatial resolution and requires extensive post processing to obtain the mechanical fingerprints of samples. Here, we develop a MPA system that measures pressure and displacement in real time with sub-nanometer resolution thanks to an interferometric readout. This highly sensitive MPA system enables studying the nanoscale behavior of soft biomaterials under tension and their frequency-dependent viscoelastic response.


Assuntos
Materiais Biocompatíveis/química , Elasticidade , Interferometria/métodos , Nanotecnologia/métodos , Oócitos/citologia , Óptica e Fotônica/métodos , Estresse Mecânico , Animais , Fenômenos Biomecânicos , Bovinos , Teste de Materiais , Modelos Biológicos
4.
IEEE Trans Vis Comput Graph ; 24(4): 1496-1505, 2018 04.
Artigo em Inglês | MEDLINE | ID: mdl-29543167

RESUMO

Today's virtual reality (VR) applications such as gaming, multisensory entertainment, remote dining, and online shopping are mainly based on audio, visual, and touch interactions between humans and virtual worlds. Integrating the sense of taste into VR is difficult since humans are dependent on chemical-based taste delivery systems. This paper presents the 'Thermal Taste Machine', a new digital taste actuation technology that can effectively produce and modify thermal taste sensations on the tongue. It modifies the temperature of the surface of the tongue within a short period of time (from 25°C to 40 °C while heating, and from 25°C to 10 °C while cooling). We tested this device on human subjects and described the experience of thermal taste using 20 known (taste and non-taste) sensations. Our results suggested that rapidly heating the tongue produces sweetness, fatty/oiliness, electric taste, warmness, and reduces the sensibility for metallic taste. Similarly, cooling the tongue produced mint taste, pleasantness, and coldness. By conducting another user study on the perceived sweetness of sucrose solutions after the thermal stimulation, we found that heating the tongue significantly enhances the intensity of sweetness for both thermal tasters and non-thermal tasters. Also, we found that faster temperature rises on the tongue produce more intense sweet sensations for thermal tasters. This technology will be useful in two ways: First, it can produce taste sensations without using chemicals for the individuals who are sensitive to thermal taste. Second, the temperature rise of the device can be used as a way to enhance the intensity of sweetness. We believe that this technology can be used to digitally produce and enhance taste sensations in future virtual reality applications. The key novelties of this paper are as follows: 1. Development of a thermal taste actuation technology for stimulating the human taste receptors, 2. Characterization of the thermal taste produced by the device using taste-related sensations and non-taste related sensations, 3. Research on enhancing the intensity for sucrose solutions using thermal stimulation, 4. Research on how different speeds of heating affect the intensity of sweetness produced by thermal stimulation.


Assuntos
Internet , Processamento de Sinais Assistido por Computador , Paladar/fisiologia , Língua/fisiologia , Realidade Virtual , Adulto , Desenho de Equipamento , Feminino , Humanos , Masculino , Temperatura , Interface Usuário-Computador , Adulto Jovem
5.
Tissue Eng Part C Methods ; 22(10): 932-940, 2016 10.
Artigo em Inglês | MEDLINE | ID: mdl-27600722

RESUMO

Engineered heart tissues made from human pluripotent stem cell-derived cardiomyocytes have been used for modeling cardiac pathologies, screening new therapeutics, and providing replacement cardiac tissue. Current methods measure the functional performance of engineered heart tissue by their twitch force and beating frequency, typically obtained by optical measurements. In this article, we describe a novel method for assessing twitch force and beating frequency of engineered heart tissue using magnetic field sensing, which enables multiple tissues to be measured simultaneously. The tissues are formed as thin structures suspended between two silicone posts, where one post is rigid and another is flexible and contains an embedded magnet. When the tissue contracts it causes the flexible post to bend in proportion to its twitch force. We measured the bending of the post using giant magnetoresistive (GMR) sensors located underneath a 24-well plate containing the tissues. We validated the accuracy of the readings from the GMR sensors against optical measurements. We demonstrated the utility and sensitivity of our approach by testing the effects of three concentrations of isoproterenol and verapamil on twitch force and beating frequency in real-time, parallel experiments. This system should be scalable beyond the 24-well format, enabling greater automation in assessing the contractile function of cardiomyocytes in a tissue-engineered environment.


Assuntos
Técnicas Biossensoriais/métodos , Células-Tronco Pluripotentes Induzidas/citologia , Campos Magnéticos , Contração Miocárdica/efeitos dos fármacos , Miócitos Cardíacos/fisiologia , Engenharia Tecidual/métodos , Antiarrítmicos/farmacologia , Cardiotônicos/farmacologia , Diferenciação Celular/efeitos dos fármacos , Células Cultivadas , Humanos , Isoproterenol/farmacologia , Fenômenos Mecânicos , Miócitos Cardíacos/citologia , Miócitos Cardíacos/efeitos dos fármacos , Verapamil/farmacologia
6.
Lab Chip ; 13(14): 2773-84, 2013 Jul 21.
Artigo em Inglês | MEDLINE | ID: mdl-23670166

RESUMO

In this work, we introduce a simple solvent-assisted micromolding technique for the fabrication of high-fidelity styrene-ethylene/butylene-styrene (SEBS) microfluidic devices with high polystyrene (PS) content (42 wt% PS, SEBS42). SEBS triblock copolymers are styrenic thermoplastic elastomers that exhibit both glassy thermoplastic and elastomeric properties resulting from their respective hard PS and rubbery ethylene/butylene segments. The PS fraction gives SEBS microdevices many of the appealing properties of pure PS devices, while the elastomeric properties simplify fabrication of the devices, similar to PDMS. SEBS42 devices have wettable, stable surfaces (both contact angle and zeta potential) that support cell attachment and proliferation consistent with tissue culture dish substrates, do not adsorb hydrophobic molecules, and have high bond strength to wide range of substrates (glass, PS, SEBS). Furthermore, SEBS42 devices are mechanically robust, thermally stable, as well as exhibit low auto-fluorescence and high transmissivity. We characterize SEBS42 surface properties by contact angle measurements, cell culture studies, zeta potential measurements, and the adsorption of hydrophobic molecules. The PS surface composition of SEBS microdevices cast on different substrates is determined by time-of-flight secondary ion mass spectrometry (ToF-SIMS). The attractive SEBS42 material properties, coupled with the simple fabrication method, make SEBS42 a quality substrate for microfluidic applications where the properties of PS are desired but the ease of PDMS micromolding is favoured.


Assuntos
Materiais Biocompatíveis/química , Técnicas de Cultura de Células/métodos , Elastômeros/química , Técnicas Analíticas Microfluídicas/métodos , Polietilenos/química , Poliestirenos/química , Animais , Bovinos , Técnicas de Cultura de Células/instrumentação , Meios de Cultura , Células Endoteliais/citologia , Desenho de Equipamento , Fibroblastos/citologia , Humanos , Teste de Materiais , Camundongos , Técnicas Analíticas Microfluídicas/instrumentação , Células NIH 3T3 , Espectrometria de Massa de Íon Secundário , Espectroscopia de Luz Próxima ao Infravermelho , Molhabilidade
7.
Biophys J ; 103(4): 640-8, 2012 Aug 22.
Artigo em Inglês | MEDLINE | ID: mdl-22947925

RESUMO

Mechanical cues can influence the manner in which cells generate traction forces and form focal adhesions. The stiffness of a cell's substrate and the available area on which it can spread can influence its generation of traction forces, but to what extent these factors are intertwined is unclear. In this study, we used microcontact printing and micropost arrays to control cell spreading, substrate stiffness, and post density to assess their effect on traction forces and focal adhesions. We find that both the spread area and the substrate stiffness influence traction forces in an independent manner, but these factors have opposite effects: cells on stiffer substrates produce higher average forces, whereas cells with larger spread areas generate lower average forces. We show that post density influences the generation of traction forces in a manner that is more dominant than the effect of spread area. Additionally, we observe that focal adhesions respond to spread area, substrate stiffness, and post density in a manner that closely matches the trends seen for traction forces. This work supports the notion that traction forces and focal adhesions have a close relationship in their response to mechanical cues.


Assuntos
Adesões Focais/metabolismo , Fenômenos Mecânicos , Microtecnologia/métodos , Fenômenos Biomecânicos , Células Endoteliais/citologia , Humanos
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