I need to test chondrocytes for their in vivo ability to repair articular cartilage defects in rat femoral patellar groove. Need to know the depth of defect I should create.
In my experience this is best achieved with using operating microscope and to check in histology slides in pilot study that all cartilage is removed in the defect area. This is also close to what is done clinically when performing cell transplantation in which you have to trust your surgical skills in order to separate cartilage at the tidmark above the subchondral bone. This is a very important research question and a problem in many of the experimental studies using cartilage defect. All motorozied defect creators would sometimes take to much and other times too little. There is also interindividual differences between the experimental animmals that further make in difficult to define a depth of the defect in articular cartilage.
You are right. I did the procedure on 2 animals but at one depth only which exposed the marrow area. This time I am planning to make three defects in a row of 1mm dia of different depths. It is going to be 0.6mm and upwards. To keep accuracy is a challenge.