Compositions and methods for treating and repairing tendons
a technology of tendons and compositions, applied in the field of compositions and methods for repairing tendons, can solve the problems of rupture or torn tendons, and the healing of tendons can take several years
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example 1
[0042]A skin biopsy from the occipital area of the scalp is obtained from a subject as follows. Briefly, once an appropriate area of the scalp has been selected, it is shaved with hair clippers, ensuring some stubble remains. The biopsy area is then thoroughly disinfected and anaesthetized. Once anesthesia has taken effect, a 4-10 mm deep punch biopsy is gently removed from the biopsy site and the incision closed with sutures which can be removed 12-14 days later. The skin biopsy is then packaged under aseptic conditions into a pre-labelled biopsy tube containing biopsy transport medium, composed of DMEM / Hams F12 with antibiotics.
example 2
Isolation and Cultivation of NBDS Cells
[0043]A sterility test is performed on the medium in which the biopsy has been transported to ensure the sample is free from contamination, or alternatively, if the sample is contaminated to ensure that medium with antibiotics is subsequently utilized. The biopsy is then washed several times to remove the biopsy transportation medium and any debris to prepare the tissue for subsequent processing. Hair follicles are processed in Hams F10 by cutting away the skin epithelium with a sterile scalpel and “plucking” or dissecting the whole hair follicle unit from the surrounding dermal tissue using sterile forceps. The hair follicle is gripped with a forceps as close as possible to the skin surface and the follicle exposed by pulling up on the hair in the hair follicle unit. Follicles in the anagen phase (growing phase of the hair cycle, indicated by the visible outer root sheath, and DSC of the hair bulb) are selected for further processing.
[0044]NBD...
example 3
Preparation and Administration of NBDS Cells into a Tendon
[0047]Cells are prepared for use in two-chambered syringe. The first chamber contains approximately 20 million cells suspended in 1 ml of total volume. The second chamber contains 1.5 ml of autologous plasma from the patient (prepared separately before this procedure).
[0048]The two-chambered syringe is utilized to inject cells (under ultrasound guidance) into multiple locations of the tendon to be repaired.
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