Asepsis patch for postoperative wound pain relieving
A technology of patch and wound, applied in the field of patch, can solve the problems of organ tissue toxicity, high cost of pain relief pump, inconvenience of life, etc., and achieve the effect of slow release
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Embodiment 1
[0012] A sterile patch for postoperative wound pain relief, which is composed of an anti-adhesion layer, a drug storage layer and a backing layer. The drug storage layer is composed of a framework material of polyvinyl alcohol and microspheres carrying Lidocaine. Each square centimeter of the membrane contains 5 mg of lidoca.
[0013] Lidocaine-loaded microspheres are prepared by a conventional spray drying method. The drug-loaded microspheres prepared by using polylactic acid and lidocaine are uniformly mixed with the framework material polyvinyl alcohol, coated on the backing layer and then covered with an anti-adhesive layer. The preparation process is carried out under aseptic conditions.
[0014] Before use, peel off the anti-adhesive layer, stick the medicine storage layer with the backing layer directly on the wound after suture treatment, then peel off the backing layer, and finally wrap the wound with sterile gauze.
Embodiment 2
[0016] A sterile patch used for postoperative wound pain relief, which is composed of an anti-adhesion layer, a drug storage layer and a backing layer. The drug storage layer is composed of a framework material chitosan and microspheres loaded with tetracaine. Each square centimeter of the membrane contains 1 mg of Dinka.
[0017] The microspheres loaded with tetracaine are prepared by the emulsification-solvent volatilization method. Polylactic acid-glycolic acid and tetracaine are used to prepare drug-loaded microspheres, which are then uniformly mixed with chitosan as the framework material, and then coated on the backing layer and covered with an anti-adhesion layer. The preparation process is carried out under aseptic conditions.
Embodiment 3
[0019] A sterile patch for postoperative wound pain relief, which is composed of an anti-adhesion layer, a drug storage layer and a backing layer. The drug storage layer is composed of a skeleton material polyvinylpyrrolidone and procaine-loaded microspheres . Each square centimeter of the membrane contains 3 mg of proca.
[0020] Procaine-loaded microspheres are prepared by the emulsification-solvent evaporation method. Chitosan and procaine are used to prepare drug-loaded microspheres, which are then uniformly mixed with the framework material polyvinylpyrrolidone, coated on the backing layer and then covered with an anti-adhesive layer.
[0021] The preparation process is carried out under aseptic conditions.
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