Preparation method of decellularized amnion intrauterine scaffold carrying estradiol microspheres
An estradiol-loaded, decellularized technology, applied in the field of biomedical equipment preparation, can solve the problems of high recurrence rate and poor treatment effect of intrauterine adhesions
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Embodiment 1
[0028] A. Preparation of acellular amnion matrix:
[0029] (1) Take amniotic membrane tissue: take the placenta negative for hepatitis B, hepatitis C, AIDS, and syphilis under sterile conditions, bluntly separate the amniotic membrane about 10cm×10cm, remove the chorionic membrane tissue, and use 50mg / ml penicillin, 50mg / ml streptomycin Stored after washing with phosphate buffered saline (pH 7.2-7.4).
[0030] (2) Preparation of acellular amniotic matrix: the amniotic membrane was washed repeatedly with normal saline, soaked in the volume fraction polyethylene glycol octylphenyl ether (TritonX-100) solution, placed in a constant temperature incubator at 37°C and shaken overnight, and taken out Then rinse with normal saline, add 25g / L trypsin and 0.2g / L ethylenediaminetetraacetic acid (EDTA), fully shake, and incubate at 37°C for 4h. After taking it out, rinse it repeatedly with normal saline, then place the amniotic membrane tissue in 8.8% sodium chloride solution, incubate a...
Embodiment 2
[0050] A. Preparation of acellular amnion matrix:
[0051] (1) Take amniotic membrane tissue: take the placenta negative for hepatitis B, hepatitis C, AIDS, and syphilis under sterile conditions, bluntly separate the amniotic membrane about 10cm×10cm, remove the chorionic membrane tissue, and use 50mg / ml penicillin, 50mg / ml streptomycin Stored after washing with phosphate buffered saline (pH 7.2-7.4).
[0052] (2) Preparation of acellular amnion matrix: the amnion was rinsed repeatedly with normal saline, soaked in 0.1% TritonX-100 solution by volume fraction, placed in a constant temperature incubator at 37°C and shaken overnight, rinsed with normal saline after taking it out, and added 25g / L trypsin and 0.2g / L EDTA, shake well, and incubate at 37°C for 4h. After taking it out, rinse it repeatedly with physiological saline, then place the amnion tissue in 8.8% sodium chloride solution, incubate at room temperature for 4 hours, take it out, wash it repeatedly with 0.01M phos...
Embodiment 3
[0075] A. Preparation of acellular amnion matrix:
[0076] (1) Take amniotic membrane tissue: take the placenta negative for hepatitis B, hepatitis C, AIDS, and syphilis under sterile conditions, bluntly separate the amniotic membrane about 10cm×10cm, remove the chorionic membrane tissue, and use 50mg / ml penicillin, 50mg / ml streptomycin Stored after washing with phosphate buffered saline (pH 7.2-7.4).
[0077] (2) Preparation of acellular amnion matrix: the amnion was rinsed repeatedly with normal saline, soaked in 0.1% TritonX-100 solution by volume fraction, placed in a constant temperature incubator at 37°C and shaken overnight, rinsed with normal saline after taking it out, and added 25g / L trypsin and 0.2g / L EDTA, shake well, and incubate at 37°C for 4h. After taking it out, rinse it repeatedly with physiological saline, then place the amnion tissue in 8.8% sodium chloride solution, incubate at room temperature for 4 hours, take it out, wash it repeatedly with 0.01M phos...
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