Low-Force Testing of Tissues and Biomaterials In Vitro
Testing of soft tissues and biomaterials presents many unique challenges for those in the biomedical field. Many soft tissues, such as skin or collagen, are delicate specimens with low ultimate strength values, requiring a testing system that is highly sensitive to low force measurements and small displacements in tension, compression, flexure, and fatigue. Gripping solutions for tissues can be extremely problematic due to their size, fragile nature and that typically testing must be conducted under simulated in-vivo conditions. Testing in-vitro ensures that the mechanical properties of natural tissues are maintained and that bio-engineered tissues are tested in their working environment.
Our temperature-controlled Bath has a pneumatic lifting and lowering mechanism that allows easy specimen loading in the grips and prevents spilling of solution in the test space. The Submersible Pneumatic Grips are operated with a footswitch, providing you “hands-free” operation for easy loading of soft, compliant specimens. You are also able to adjust the grip pressure to accommodate a wide variety of specimens with a single set of grips. For example, hydrogels and soft tissues require a lower gripping pressure than rigid plastics or metal wire to prevent tearing and consequently failure in the grips. Finally, pneumatic grips provide a constant grip pressure throughout the test to prevent or minimize specimen slipping.
The grips can be removed from the submersible pull-rods and allow for attachment of a wide variety of additional submersible fixtures - compression platens, flexure fixtures or your own custom fixture designed for your specific testing needs.
Records management compliance with FDA 21 CFR § 11 is non-negotiable for many Medical Device and Pharmaceutical companies. ComplianceBuilder™ (CB) is a stand-alone, add-on compliance solution that can be integrated with Instron's Software®Bluehill, providing features necessary to meet the latest FDA 21 CFR § 11 regulations.
The BioPuls submersible pneumatic side action grips and temperature-controlled bath with pneumatic lifting and lowering mechanism is the ideal testing solution for a wide variety of biomedical testing applications.
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5900 Universal Testing Systems are engineered for precision, built for durability, and offer the flexibility for changing requirements. They are designed with standard and optional features that increase testing efficiency and improve the testing experience for the operator. A wide range of models are available for testing capacities from < 100N up to 600kN.
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For Medical Device and Pharmaceutical companies, records management compliance with FDA 21 CFR § 11 is non-negotiable. ComplianceBuilder™ (CB) is a stand-alone, add-on compliance solution that can be integrated with Instron’s Bluehill® Software to provide features necessary to meet the latest FDA 21 CFR § 11 regulations.
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