Rheolution's Resources in Life Sciences
Documents to help you start your Soft Matter Analytics™ Journey
APPLICATION NOTES
Case studies done by Rheolution’s application specialists
APPLICATION NOTES
Case studies done by Rheolution’s application specialists
Poly(glycolic acid) (PGA) is a synthetic aliphatic polyester belonging to the poly(α-hydroxy acid) family. It is produced entirely through industrial chemical synthesis and is characterized by a simple repeating glycolic acid unit linked by ester bonds. PGA is highly crystalline and hydrophilic, features that distinguish it from closely related biodegradable polyesters such as PLA and PLGA.
Poly(ethylene glycol) (PEG) is a synthetic, linear polyether composed of repeating ethylene oxide units. It is produced industrially by the ring-opening polymerization of ethylene oxide, yielding polymers with well-controlled molecular weights and narrow dispersity. PEG is highly hydrophilic, water-soluble, and chemically versatile, making it a foundational material in biomedical polymer science.
Polydimethylsiloxane (PDMS) is a synthetic polysiloxane polymer composed of a flexible inorganic siloxane backbone (–Si–O–Si–) with methyl side groups. This unique inorganic–organic architecture gives PDMS exceptional chain mobility, very low glass transition temperature, and stable elastomeric behavior across a wide temperature range. PDMS is produced exclusively by industrial synthesis, typically involving hydrolysis and condensation of chlorosilanes followed by ring-opening polymerization of cyclic siloxanes.
Poly(lactic acid) (PLA) is a synthetic aliphatic polyester derived from lactic acid monomers. Its chemical structure is based on repeating ester-linked lactic acid units, which can be arranged in different stereochemical configurations depending on the ratio of L- and D-lactic acid. PLA is primarily produced from renewable resources such as corn starch or sugarcane through the fermentation of carbohydrates into lactic acid, followed by polymer synthesis.
Polyurethanes (PUs) are a versatile family of synthetic polymers characterized by the presence of urethane (carbamate) linkages in their backbone. They are industrially synthesized through step-growth polymerization reactions between diisocyanates and polyols, followed by chain extension using low–molecular weight diols or diamines. The resulting macromolecular architecture is typically segmented, consisting of soft segments (derived from polyether, polyester, or polycarbonate polyols) and hard segments (formed from diisocyanates and chain extenders).
Poly(ethylene glycol) diacrylate (PEGDA) hydrogels are synthetic, water-swollen polymer networks formed by chemically crosslinking PEG chains functionalized with acrylate end groups. PEG itself is a hydrophilic, non-ionic polymer produced through industrial polymerization of ethylene oxide, widely used in biomedical applications due to its chemical stability and low toxicity. PEGDA is synthesized by reacting PEG with acrylate-containing reagents, introducing reactive carbon–carbon double bonds at both chain ends.
TECHNICAL NOTES
These articles provide further technical details and specifications about the topic treated in these publications
TECHNICAL NOTES
These articles provide further technical details and specifications about the topic treated in these publications
The μ-volume sample holder was developed as an alternative to the macro-volume sample holder for projects where sample volume is restricted. Due to the non destructive nature of the technology, the sample can be kept in both sample holders and retested multiple times to follow the mechanical profile over time of the sample in controlled environments. One important difference is that the μ-volume sample holder was designed to fit in a 12-well plate for easy sample incubation, and completely autoclavable (made of stainless steel) to better maintain sample sterility cellularized hydrogels ...
The ElastoSens™ Bio is a compact analytical instrument that measures the viscoelastic properties of soft materials following easy and quick steps guided by the Soft Matter Analytics™ App. Prior to testing, the sample to be measured needs to be inserted into the available sample holders specifically designed for the ElastoSens™ Bio. This step plays a key role in ensuring the quality of the data obtained from the instrument. The μ-volume sample holder was developed for applications in which sample volume is limited, such as for natural polymers, blood and plasma ...
TURBIDI.T™ is a technology that accurately measures the turbidity of solutions across a broad spectrum. Its effectiveness has been tested against an established turbidimeter and the results have indicated that both technologies yield consistent measurements for formazin solutions of varying concentrations.
The NEPHEL.O™ nephelometer is a reliable instrument that performs comparably to established and commercially available nephelometers. It provides precise measurements of low turbidity solutions with good repeatability.
Freeze-drying is a common method to produce porous scaffolds from a hydrogel composed of natural or synthetic polymers. In a number of cases, the polymeric solution is crosslinked (bonds or interactions are established among the polymeric chains) and the hydrogel is then freeze-dried to obtain the porous and dried scaffold (1-3).
ElastoSens™ Bio is a compact instrument adept at measuring the viscoelastic properties of soft materials. Its patented Viscoelasticity Testing of Bilayered Materials (VeTBiM) technology relies on a bi-layered system, including a sample and a flexible membrane, that responds to induced vibrations. This cutting-edge tool allows for precise analysis of resonance properties, sample height, and temperature, providing comprehensive data on a material's viscoelastic characteristics. Its non-destructive method ensures samples can be reused for subsequent tests or other purposes.
ELASTOSENS™ BIO HOW TO SERIES
ELASTOSENS™ BIO HOW TO SERIES
01. Installation of the ElastoSens™ Bio
02. Daily Vibration Calibration for ElastoSens™ Bio
03. Configure a Test on the ElastoSens™ Bio
04. Build Test Sequences with ElastoSens™ Bio
05. Data Visualisation on the ElastoSens™ Bio App
06. Export ElastoSens™ Bio’s data to Excel
07. Retest a sample using the ElastoSens™ Bio
08. Create custom fields on the ElastoSens™ Bio
09. Create custom buttons on the ElastoSens™ Bio
10. How to clean the ElastoSens™ Bio
11 .Calibrate the temperature of the ElastoSens™ Bio
12. Calibrate the height of the ElastoSens™ Bio
13. How to use the µ-volume sample holder for ElastoSens™ Bio?
14. How to use the Membrane Sample Holder for ElastoSens™ Bio?
RHEOLUTION ARTICLES
Original articles prepared by our application specialists commenting on topics of interest to our community
RHEOLUTION ARTICLES
Original articles prepared by our application specialists commenting on topics of interest to our community
Hemostatic agents (HAs) can be absorbable, biological, or synthetic. Absorbable HAs, like gelatin or oxidized cellulose, speed up clotting and are naturally absorbed by the body. Biological HAs include thrombin, fibrinogen, and platelets which are key to blood clotting. Synthetic HAs, such as polyethylene glycol, form strong sealant matrices. The choice of HA depends on the type of bleeding, tissue interaction, and patient's coagulation profile. Instruments like the ElastoSens™ Bio provide valuable data on HA efficacy by measuring blood absorption and coagulation kinetics.
In January 2022, we studied alginate hydrogels in tissue engineering and drug delivery. Alginate, often used as a bioink in 3D bioprinting, forms hydrogels with tunable properties. We examined the effects of varying CaCl2 concentration on alginate crosslinking, crucial for 3D printing. Due to alginate's low viscosity, printing methods include pre-crosslinking with CaCl2, using a coaxial needle for immediate crosslinking, or mixing alginate with other biomaterials to improve printability.
Decellularization is a process that removes cellular components from organs, leaving behind the extracellular matrix (ECM). This ECM, composed of proteins, proteoglycans, and glycoproteins, serves as a natural scaffold for tissue engineering applications. Decellularization can be achieved through chemical, physical, or biological methods. The resulting decellularized ECM, known as dECM, can be utilized to create hydrogels, bioinks, or coatings for enhancing cell adhesion and tissue regeneration.
In October, our focus was on the mechanical characterization of soft organs. Understanding the mechanical properties of tissues is crucial for advancements in tissue engineering and regenerative medicine. However, measuring the mechanical properties of soft tissues is not straightforward and often involves customized approaches. Standardized and reproducible methods are needed to accurately characterize the mechanical properties of soft organs. By establishing consistent measurement techniques, researchers can gain a deeper understanding of tissue mechanics and develop effective treatments and therapies.
In September, we explored the applications of photostimulation in hydrogels. Light-induced reactions are commonly used in various fields, including dentistry, coatings, and beauty salons. In biomedical research, natural components like collagen and hyaluronic acid have been modified to react to light exposure. These modifications, along with the use of photoinitiators, allow for better control over the processability and viscoelastic properties of hydrogels. This control is essential for applications such as in vivo injection, 3D bioprinting, and matching the mechanical behavior of implantation sites.
The use of 3D printers to produce organs holds great potential for improving medical treatments. Hydrogels, which closely resemble the properties of tissue matrix, are used as the "ink" in this process. Human cells are incorporated into the hydrogel to provide functionality. The bioink is loaded into the printer and shaped according to a computer-aided design (CAD) model. However, there are several challenges to overcome in this process. One key challenge is ensuring the appropriate viscoelastic properties of the bioink and the final construct. Researchers are actively working on addressing these challenges to make extrusion-based 3D printing a viable option in medical care.
ARTICLES OF THE MONTH
Each month, a published scientific article that covers a theme of interest to our community is summarized and commented by our application specialists
ARTICLES OF THE MONTH
Each month, a published scientific article that covers a theme of interest to our community is summarized and commented by our application specialists
Dr. Daniel J. Kelly and his team at Trinity College Dublin researched how changing the formulation of an alginate bioink can alter the mechanical properties of a 3D printed scaffold. Like preparing a sauce, the consistency of a bioink can be adjusted by changing the concentration of its ingredients. However, it's more complex in biomedical research and requires analytical tools for quantification. Alginate, a natural biomaterial from algae, can quickly crosslink in the presence of ions (like Ca2+), forming a cohesive hydrogel with tunable properties. This makes it an ideal bioink for 3D bioprinting in tissue engineering and drug delivery.
During this last month, we explored the use of decellularized extracellular matrices (dECM) in tissue engineering and cell culture. dECM provides a natural scaffold for cells, containing the necessary biochemical cues and structural support to mimic native tissues. In one study, researchers from Trinity College Dublin investigated how the formulation of an alginate bioink can modulate the mechanical properties of 3D printed scaffolds. Alginate, a natural biomaterial derived from algae, is commonly used as a bioink due to its viscosifying, gelling, and biocompatible properties. The researchers examined different formulations of the bioink, varying the degree of polymerization and the type of divalent cations used for crosslinking. They evaluated the mechanical properties of the resulting scaffolds and assessed their suitability for tissue engineering applications. This work highlights the importance of optimizing bioink formulations to achieve desired mechanical properties in 3D printed constructs.
Mechanical testing of soft tissues and organs is crucial for biomaterial development. A study from the University of Massachusetts compared different testing techniques and evaluated the impact of sample freezing on lung tissue. The findings highlighted variations in mechanical properties depending on the technique used and showed a slight difference between fresh and frozen samples. Standardized testing methods are necessary for reliable measurements and advancements in tissue engineering.
In the context of dental treatments and other applications like surface coatings and 3D printing, the use of light to transform deformable resins into rigid materials is well-known. Similarly, in biomedical applications, photostimulation is used to modify the mechanical properties of hydrogels. Natural hydrogels have been chemically modified to allow precise control over their viscoelastic properties through light exposure. These photosensitive hydrogels can transition from a liquid to a gel state with varying levels of firmness based on formulation, light intensity, and exposure time. Matching the viscoelasticity of the hydrogel to the target organ is crucial in tissue engineering and regenerative medicine.
In a recent study, researchers from the University of California at Davis investigated the impact of the viscoelasticity of the cell's environment on bone formation by mesenchymal stromal cells (MSCs). They prepared alginate hydrogels with different mechanical properties and loaded them with MSC aggregates. The results showed that while both hydrogels supported high cell viability, the viscoelastic hydrogel promoted significantly higher calcium production by the cells compared to the elastic hydrogel. Calcium is an essential component for bone regeneration. These findings emphasize the importance of the cell's external environment, specifically its viscoelastic properties, in influencing cellular behavior and tissue regeneration.
A research study conducted by the University of Delaware explored whether the physiological differences in the maturation of specific brain regions could explain the increased risk-taking tendencies during adolescence. The study, titled "Viscoelasticity of reward and control systems in adolescent risk-taking" and published in the Neuroimage Journal, proposed that risk-taking behaviors are influenced by two opposing brain systems: the reward system (socioemotional system) and the cognitive control system, responsible for regulating impulsive responses. Due to the chronological development of these systems, an imbalance may occur, potentially making adolescents more prone to engaging in risky activities.
SCIENTIFIC PUBLICATIONS
Published scientific articles using Rheolution’s instruments
SCIENTIFIC PUBLICATIONS
Published scientific articles using Rheolution’s instruments
EXPERT CORNER
EXPERT CORNER