A composite gel system for promoting wound healing and its preparation method and application
A compound gel and wound healing technology, which is applied in the fields of pharmaceutical formulation, medical science, drug delivery, etc., can solve the problems of poor automatic disintegration performance, achieve good biocompatibility, good therapeutic effect, and shorten the healing time
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Embodiment 1
[0025] The preparation of embodiment 1 composite gel GSNO / GG-cl-Im-Ba
[0026] Prepare Im-Ba solution: weigh Im-Ba dry sample, prepare Im-Ba solution with a concentration of 1% m / v, and adjust to pH 8-9 with 1M NaOH solution;
[0027] Configuration of guar gum / GSNO solution: add 850 μL deionized water to a round bottom flask, vacuumize, fill with nitrogen, under nitrogen protection, add 36 mg guar gum powder and 0.9 mg GSNO, stir with 500 g magnetic force until completely dissolved, Get guar gum / GSNO solution;
[0028] Take 300 μL of guar gum / GSNO solution, add 150 μL of Im-Ba solution, and stir magnetically for 30 s under the protection of nitrogen to obtain the ROS-sensitive composite gel GSNO / GG-cl-Im-Ba loaded with GSNO.
Embodiment 2
[0029] Example 2 Preparation of composite gel GSNO / tEVs / GG-cl-Im-Ba
[0030] Prepare Im-Ba solution: weigh the dried Im-Ba sample, prepare Im-Ba solution with a concentration of 1% m / v, and adjust the pH to 8-9 with 1M NaOH solution;
[0031] Preparation of tEVs suspension: Exosomal tEVs were extracted from 80ml 4T1 cell culture supernatant by ultracentrifugation, and dissolved in 200μL PBS buffer solution to make the concentration of tEVs 1.19×10 10 Each / ml tEVs suspension was stored at 4°C for later use;
[0032] Configuration of guar gum / GSNO solution: add 850 μL deionized water to a round bottom flask, vacuumize, fill with nitrogen, under nitrogen protection, add 36 mg guar gum powder and 0.9 mg GSNO, stir with 500 g magnetic force until completely dissolved, Get guar gum / GSNO solution;
[0033] Take 300 μL of guar gum / GSNO solution, add 200 μL of step-tEVs suspension, under nitrogen protection, magnetically stir and mix to obtain a mixed solution; then add 150 μL of Im-...
Embodiment 3
[0034] Example 3 Biocompatibility Evaluation of New Composite Gel GSNO / tEVs / GG-cl-Im-Ba Material
[0035] 4-week-old male C57BL / 6 (C57) mice were divided into three groups of parallel controls, 3 mice in each group, and 0.5ml of compound gel GSNO / tEVs / GG-cl-Im- Ba, 4 days later, tissue sections around the subcutaneous injection of the legs were taken, and the biocompatibility of the GSNO / tEVs / GG-cl-Im-Ba hydrogel in vivo was evaluated by hematoxylin-eosin (HE) staining.
[0036] The results of HE staining showed that there were no inflammatory cells in the leg muscles of mice injected with the composite gel GSNO / tEVs / GG-cl-Im-Ba, indicating that the composite gel GSNO / tEVs / GG-cl-Im-Ba Low immunogenicity and high safety.
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