A kind of in situ gel for subcutaneous injection for treating osteosarcoma
A technology of subcutaneous injection and in situ gel, applied in the field of medicine, can solve the problems of inconvenient life of patients and less than 20% survival rate
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Embodiment 1
[0023] Example 1 Preparation of in situ gel for subcutaneous injection for the treatment of osteosarcoma
[0024] 1) Take 280 g of doxorubicin hydrochloride and 20 g of HIV-1-TAT protein 47-57 polypeptide fragments, add deionized water to make a solution A, and the concentration of doxorubicin in the solution A is 10 mg / ml;
[0025] 2) Add poloxamer P407, poloxamer P188, and hydroxypropyl methylcellulose K4M to the preparation A in sequence, stir well, and disperse evenly to obtain the preparation B. The amount of poloxamer P407 in the preparation B is The weight percentage is 20%, the weight percentage of poloxamer P188 is 1.2%, and the weight percentage of hydroxypropyl methylcellulose K4M is 0.3%;
[0026] 3) Swell the solution B at 4°C for 24 hours, pass it through a 0.22 μm microporous membrane, and dispense it.
Embodiment 2
[0027] Example 2 Preparation of in situ gel for subcutaneous injection for the treatment of osteosarcoma
[0028] 1) Take 480 g of doxorubicin hydrochloride and 30 g of HIV-1-TAT protein 47-57 polypeptide fragments, add deionized water to make preparation A, and the concentration of doxorubicin in preparation A is 10 mg / ml;
[0029] 2) Add poloxamer P407, poloxamer P188, and hydroxypropyl methylcellulose K4M to the preparation A in sequence, stir well, and disperse evenly to obtain the preparation B. The amount of poloxamer P407 in the preparation B is The weight percentage is 20%, the weight percentage of poloxamer P188 is 1.2%, and the weight percentage of hydroxypropyl methylcellulose K4M is 0.3%;
[0030] 3) Swell the solution B at 4°C for 24 hours, pass it through a 0.22 μm microporous membrane, and dispense it.
Embodiment 3
[0031] Example 3 Preparation of in situ gel for subcutaneous injection for the treatment of osteosarcoma
[0032] 1) Take 340 g of doxorubicin hydrochloride and 20 g of HIV-1-TAT protein 47-57 polypeptide fragments, add deionized water to make a solution A, and the concentration of doxorubicin in the solution A is 10 mg / ml;
[0033] 2) Add poloxamer P407, poloxamer P188, and hydroxypropyl methylcellulose K4M to the preparation A in sequence, stir well, and disperse evenly to obtain the preparation B. The amount of poloxamer P407 in the preparation B is The weight percentage is 20%, the weight percentage of poloxamer P188 is 1.2%, and the weight percentage of hydroxypropyl methylcellulose K4M is 0.3%;
[0034] 3) Swell the solution B at 4°C for 24 hours, pass it through a 0.22 μm microporous membrane, and dispense it.
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Abstract
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