Massage is widely used to help improve the intake of colonization: Collegian spong helps in the treatment of inflammation and inflammation, and the scaped-like implant is used to repair the bone. However, over time, the repair process of tissues changes, so scientists are developing biometrics that interact with tissue with therapeutics.
Now, Dr. Ben Alamquist and his team have built a new nuclear at Imperial College London that can replace traditional material with the body as it can work. Traction is known as Force-enabled payloads (tramps), their method allows the body to talk to the body's natural repair systems to run the body.
Researchers have said that the inclusion of tramps in existing medical material can revolutionize injuries as they are treated. Dr. Bioengineering Department of Imperial Division Alamquist said: "Our technology can help create new content that actively works with tissues to run healing."
These findings are published today Advanced Content.
Cellular Call for Action
After injury, Collagen & # 39; Scaffolds & # 39; Cells & # 39; Crawl & # 39; Are found in wounds, such as the spying species navigating. As they move forward, they pull the scaffold, which activates the hidden therapy proteins that begin to repair the injured tissues.
Researchers have designed the trays as a way to rebuild this natural therapy. They combined DNA segments into three-dimensional shapes, which are called proteins as tightly adept athletes. Then, before adding an end to the scaffolds like Collagen, a custom & # 39; handle & # 39; Join that cells can hold on one side.
During their laboratory testing laboratory, they found that when they cry by collagen scaffolds, the cells are stretched onto the trays. Pulling makes the trumps open to open the shells and activate healing proteins. This protein suggests to increase and multiply healing cells.
Researchers also found that the cellular 'handle' By replacing, they can change what type of cell can hold and pull, allowing a specific cellular protein to be adapted to the trumps. By doing so, TRAPs make content that can interact with the right cell at the right time during repair.
This is the first time scientists have activated healing proteins using different types of cells in human content. This nature mimics the therapeutic practices in nature. Dr. Almakvist said: "To activate healing, the use of cell movement is found in marine sponges to human beings. Our approach imitates them and actively works with different cells that reach our damaged tissues with time to promote therapeutic . "
From lab to human
This approach is acceptable for different types of cells, so that various injuries such as fractured bones, skirts after heart attack, and damage to the infection are damaged. Current technologies, such as diabetes foot ulcers, which are the leading cause of non-traumatic lower foot decomposition, are still needed for new techniques to treat nerves.
It is relatively easy to make trumps and is completely human-made, which means that they are easily rebuilt in different labs and can be extended to industrial quantities. Their adaptability also means that they can help scientists create new methods for the study of diseases, stem cells, and tissue development laboratory.
Apatars are currently being used as drugs, which means they have already been proved safe and have been optimized for medical use. Because the Traps take advantage of the Aptus, which is currently optimized for use in humans, it can take a short route to the clinic than the ground zero methods.
Dr. Alamquist said: "Trap technique provides a flexible mechanism for creating content that actively interacts with wounds and provides major instructions when needed and where necessary. Such intelligent, dynamic healing healing process Useful in each stage. The potential to increase your chances of recovering the body, and many different types of wounds. It uses II. To work with the technology as a potential treatment for TB kandarela time to orbit various cells with the potential to serve as a conductor. "
This research was funded by the Engineering and Physical Sciences Research Council and Wellcome Trust.
Content provided by Imperial College London. Written by Original Caroline Brongen. Note: Content can be edited for style and length.