Platelet-rich plasma tissue engineering scaffold and preparation method thereof
A tissue engineering scaffold and bone scaffold technology, applied in the field of biomedicine, can solve the problems of not effectively promoting rapid and high-quality healing of patients, poor recovery of motor function, unsatisfactory healing effect, etc., and achieve high-quality rapid healing , excellent sustained release effect, excellent sustained release and accelerated healing effect
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Embodiment 1
[0056] Embodiment 1 PRP-loaded tissue engineering scaffold of icariin and preparation method thereof (1)
[0057] 1. Preparation of concentrated PRP
[0058] 20 mL of autologous blood was taken from the rabbit's ear vein, and the red blood cells were removed by gradient centrifugation (differential speed centrifugation), firstly at 300 g x 10 min. Then 800g×10min, take 2.4mL of the lower layer, and discard the remaining upper layer liquid; shake well and shake for 30s to prepare concentrated PRP.
[0059] 2. Preparation of PRP-loaded icariin tissue engineering scaffold
[0060] Dissolve icariin in DMSO to prepare a DMSO solution (ICA-DMSO solution) containing 50 mM icariin, take 10 μL ICA-DMSO solution and 0.1 mL of mass concentration 10% calcium chloride solution (solvent is 0.1M PBS solution) and 1.0 mL of concentrated PRP were mixed to obtain a PRP-loaded icariin gel. After lyophilization in a vacuum freeze dryer and ethylene oxide gas sterilization, the tissue engineeri...
Embodiment 3
[0068] Example 3 Test of Icariin Sustained Release Effect in Tissue Engineering Scaffold
[0069] The stents prepared in Example 1 and Comparative Example 3 were immersed in 1 mL of sterile PBS solution in the centrifuge tube at room temperature, and kept stirring gently. At the time points of 4d, 5d, 6d, and 7d, take 0.6 mL of incubation solution each, and add a new equal volume of PBS liquid to the centrifuge tube at the same time after the liquid. Use high-performance liquid chromatography (HPLC) to detect the corresponding peak area of ICA in the sample to be tested, and calculate the corresponding ICA concentration in the sample to be tested according to the standard curve, thereby quantifying the in vitro release curve of icariin , the results are shown in Table 1, 2 and figure 2 shown.
[0070] Table 1 Cumulative release rate of ICA in PRP loaded ICA scaffold (%)
[0071] Bracket category 0h 1h 2h 4h 8h 16h 1d 2d 3d 4d 5d 6d 7d freeze-d...
Embodiment 5
[0075] Example 5 Tissue Engineering Scaffold Treatment Effect Test
[0076] 1. Establishment and grouping of animal models
[0077] Select 48 healthy adult New Zealand white rabbits, male or female, body weight (3.0±0.5) kg, rabbits fed with common feed, 24h cycle light, free to eat and drink, all animals have no trauma, infection and deformity in the operation area, and no For other systemic diseases, all operating procedures complied with the guidelines for animal experiments.
[0078] 48 white rabbits were randomly divided into 3 groups according to the commonly used grouping method in animal experiment scientific research design (random number table method), 16 in each group. They were patellar injury group (control group-CLT); freeze-dried PRP scaffold group (FD-PRP); freeze-dried PRP-loaded ICA scaffold group (FD-PRP / ICA).
[0079] Animals were anesthetized with Sumianxin, disinfected, and draped. An incision was made on the medial side of the patellar tendon of the ri...
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