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Electroforce 3200

Manufactured by TA Instruments
Sourced in United States

The ElectroForce 3200 is a dynamic mechanical analysis (DMA) instrument designed for material characterization. It applies controlled forces or displacements to samples and measures the resulting deformation or force. The ElectroForce 3200 is capable of testing a variety of materials, including polymers, composites, and biological samples.

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37 protocols using electroforce 3200

1

Biomechanical Analysis of Intervertebral Disc Degeneration

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Axial biomechanics are reflective of physiological loading and were used to evaluate NP pressurization, AF tension, and IVD laxity. Creep is known to be sensitive to alterations in short and long-time viscoelastic behaviors. Axial and creep testing used an ElectroForce 3200 instrument (TA Instruments, New Castle, DE). Samples were hydrated in PBS with protease inhibitor tablets (ThermoScientific, Rockford, IL). Motion segments underwent 20 cycles ±8N of tension-compression at 1Hz followed by 60 minutes of compressive creep at −8N and 30 minutes of unloaded rehydration. Compressive stiffness, tensile stiffness, axial range of motion, and axial hysteresis were calculated from the 20th cycle in MATLAB (Figure 3B). Three independent reviewers manually calculated neutral zone (NZ) length and stiffness. Samples with undetectable NZ were excluded from NZ stiffness analysis. Creep was analyzed with MATLAB code measuring total displacement and applying a 5-parameter viscoelastic solid model to calculate elastic response (Se), fast response (τ1 and S1), and slow response (τ2 and S2) time constant and stiffness parameters, respectively (39 (link)) (Figure 3C).
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2

Tibial Compression in C57Bl/6 Mice

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A total of 29 female and 29 male 10 week-old C57Bl/6 mice were obtained from Envigo (Indianapolis, IN). Mice were randomly assigned to experimental groups, and each mouse was subjected to tibial compression using both the prone and supine configurations (described below). Mice were anesthetized via isoflurane inhalation, and tibial compression loading was performed using an electromagnetic materials testing machine (ElectroForce 3200, TA Instruments, New Castle, DE). All mice were euthanized via carbon dioxide inhalation immediately following tibial compression. Mice were maintained and used in accordance with National Institutes of Health guidelines on the care and use of laboratory animals. All procedures were approved by the UC Davis Institutional Animal Care and Use Committee.
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3

CNC-PA6 Nanocomposite Fabrication and Characterization

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The experimental work to validate the model was presented in a previous
study.40 (link) Herein, we summarize the procedure, and readers are encouraged
to see the previous study for detailed information.
PA6 was dissolved in formic acid, and then CNC was added to the suspension based on
the target concentration. The prepared suspension was kept under agitation for
approximately an hour. The prepared suspension was sonicated for 45 min before the
spinning process. 2 mL of the suspension was cast on a rectangular glass substrate,
and the glass substrate was spun at 2000 r/min for 15 s and at 3000 r/min for
30 s.
CNC-PA6 nanocomposite samples were tested using TA Instrument ElectroForce 3200 with
10 N load cells. The elastic modulus of samples was calculated from the linear
region of the stress-strain curve and reported for comparison of the model
predictions and experimental results.
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4

Compression Testing of Composite Hydrogels

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To perform compression testing, biphasic and triphasic composite hydrogels were cut with a mould to obtain 2 mm thick discs of approximately 6 mm diameter. Compression tests were performed with the ElectroForce 3200 (TA instruments, New Castle, DE, USA) using a 1N load cells, applying a maximum displacement of 0.2 mm. For each sample, a load (F) vs displacement (δL) curve was plotted. Stress (σ) and strain (ε) were calculated using equations 1 and 2, respectively, and used to plot the stress vs strain curves, thereby facilitating the calculation of the Young’s modulus (E) using Equation (3), where the stress over strain parameter is determined from the linear fit of the plotted data.
σ=FA(N/m2),
ε=δLL,
E=σε(N/m2),
where A is the cross-sectional area of the sample and L is the initial sample thickness.
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5

Evaluating Fracture Mechanical Properties

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The mechanical properties of the fractures were measured with a standardized four-bending technique. Fractured tibias were dissected 21 days after fracture and loaded into the ElectroForce 3200 (TA Instruments, New Castle, DE) for four-point bending test. The loading rate was set at a constant speed of 5 mm/minute until failure. Force- bending and stress-strain curves were recorded to identify the ultimate bending load (maximum force at failure) and bending stiffness (slope of the linear part of the curve).(58 )
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6

Tensile Characterization of Biomimetic Patches

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Tensile tests were carried out on patches with 6 × 6 repeat units in both 1- and 2-directions of the patch (directions annotated in Figure 1A). Precise length and width measurements were known from the fabrication technique. Thickness was determined by scanning electron microscopy, operated at 10 kV (Figure S6, Supporting Information, 29.12 ± 6.8 μm, N = 3, n = 5). Patches were wetted with deionized water and mounted using custom made stainless steel grips on an Electroforce 3200 mechanical tester with a 250 g load cell (TA Instruments, New Castle, DE) controlled by WinTest software (Ver. 7). Patches were strained to failure at a rate of 0.1% strain s−1, assuming quasi-static loading. The effective stiffnesses (E) were determined by taking the slope of a regression within the initial linear region of the stress–strain curve up to 10% strain. The anisotropic ratio of effective stiffnesses (E1/E2) was calculated by dividing the mean of E1 (N = 10) by the mean of E2 (N = 10). UTS was measured as the maximum stress reached and the strain-at-failure was taken as the strain at the UTS point.
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7

Murine Tibial Biomechanical Evaluation

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Both tibiae from twelve mice per group were randomly selected for four-point bend tests to failure (lower support span at 9 mm, upper loading span at 3 mm), with the medial surface in tension (TA Instruments ElectroForce 3200). The bones were loaded at a displacement control rate of 0.025 mm/s while the sample remained hydrated with phosphate buffered saline (PBS). Cross-sectional cortical properties at the center of the load span were obtained from μCT images as described above. These properties were used to map load-displacement data into stress-strain data using standard engineering equations as previously reported to estimate tissue level properties. [27 (link)] Two bones in the standard control group and one bone from the thermoneutral control group were removed from analysis due to abnormal mechanical curves caused by rotation during testing. Contralateral limbs were also removed from the analysis.
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8

Tibial Compression Overload in Aging Mice

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Right knee joints of 10-week-old and 62-week-old C57BL/6J mice (Jackson Laboratory, Bar Harbor, ME, USA; Stock No: 000664) received a single non-invasive tibial compression overload at 1 mm/s displacement rate until ACL rupture using an electromagnetic material testing system (ElectroForce 3200, TA Instruments, New Castle, DE, USA), as previously described [8 (link),10 (link),19 (link)]. Buprenorphine was administered immediately post-injury (0.01 mg/kg) for pain relief. All animal experimental procedures were completed in accordance with the Institutional Animal Care and Use Committee (IACUC) guidance at Lawrence Livermore National Laboratory and the University of California, Davis in AAALAC-accredited facilities under protocol 168 approved in February 2019.
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9

Mechanical Stimulation of Cartilage Explants

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Cartilage explants, immersed in culture media, were subjected to a range of loading regimes (2.5 MPa, 5 MPa or 8 MPa at 1 or 4 Hz, 15 min) using the ElectroForce® 3200 (TA Instruments, Delaware, USA), and gene expression either analysed directly post-cessation of load or 24 h post-load. Chondrocytes were subjected to a physiological tensile strain (7.5% elongation, 1 Hz) for 30 min using the Flexcell FX-3000 system (Flexcell International Corp, Hillsborough, NC, USA)12 (link), 13 (link), 14 (link), and cells processed four hours post-cessation of load to analyse gene expression. Duplicate cultures of explants or cells, devoid of mechanical stimulation, were set up as controls. Cartilage explants were snap frozen and remained in liquid nitrogen until the RNA extraction. Isolated chondrocytes were lysed directly in TRIzol® (1 ml per well) and stored at −80°C until processed for RNA extraction.
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10

Murine ACL Rupture Protocol

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Mice were anaesthetized with isoflurane and custom built cups21 used to hold the right ankle and knee in flexion with a 30 degree offset prior to the application of a 0.5N pre‐load (ElectroForce® 3200, TA Instruments, Elstree, UK). A single 12N load at a velocity of 1.4 mm/s was then applied resulting in ACL rupture. These parameters were chosen based upon prior experiments showing that 12N was a threshold force in these mice where a mid‐substance tear of the ligament would occur immediately on application of one load cycle at 1.4 mm/s. ACL rupture was identified through the waveform as a continued increase in displacement following release of the applied compressive force with an audible “popping” sound. To determine whether contralateral knees could serve as unloaded controls, they were compared with the right and left knees of naïve mice which were not subjected to anaesthetic or load.22 Mice were culled by cervical dislocation at multiple time points to assess for the presence of an inflammatory response and joint degeneration.
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