Anticancer slow release agent of nimustine and its progression agent
A slow-release agent and synergist technology, applied in the field of anti-cancer sustained-release agents, can solve problems such as unclear effects, achieve the effects of convenient drug injection, reduce toxicity, and increase drug concentration
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Embodiment 1
[0127] Put 90mg of polylactic acid (PLA) with a molecular weight of 20000-40000 as pharmaceutical excipients into the container, add 100ml of organic solvent to dissolve it in dichloromethane, add 10mg of Nimustine, shake again and vacuum dry to remove the organic solvent . Shake well and vacuum dry to remove organic solvents. The dried drug-containing solid composition was freeze-pulverized into a micropowder containing 10% by weight nimustine, and then suspended in physiological saline containing 1.5% sodium carboxymethyl cellulose to prepare the corresponding suspension Type sustained-release injection, viscosity is 360cp-480cp (at 25℃-30℃). The subcutaneous release time is 25-30 days.
Embodiment 2
[0129] Put 75mg of polylactic acid (PLA) with a molecular weight of 30000-50000 as pharmaceutical excipients into the container, add 100ml of organic solvent to dissolve it in dichloromethane, add 25mg of Nimustine, shake again and vacuum dry to remove the organic solvent . The dried solid composition is immediately shaped, and after packaging, it is ray sterilized to obtain an anti-cancer in vivo implant containing 25% by weight of nimustine for curing solid tumors. The subcutaneous release time is 35-40 days.
Embodiment 3
[0131] Put 95mg of polylactic acid (PLA) with a molecular weight of 25000-40000 as pharmaceutical excipients into the container, add 100ml of organic solvent to dissolve in dichloromethane, add 5mg of Nimustine, shake again and vacuum dry to remove the organic solvent . The dried solid composition is immediately shaped, and then ray sterilized after being dispensed to obtain an anti-cancer in vivo implant containing 5% by weight nimustine for curing solid tumors. The subcutaneous release time is 30-40 days.
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