Nimustine slow release injection for treating noumenal tumour
A technology for sustained-release injections and sustained-release implants, which is used in antitumor drugs, liquid delivery, emulsion delivery, etc., can solve problems such as unclear effects, and achieve the effects of facilitating drug injection, reducing toxicity, and improving drug concentration.
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Embodiment 1
[0117] Put 90 mg of polylactic acid (PLA) with a molecular weight of 10,000 as pharmaceutical excipients into a container, add 100 ml of organic solvent to dissolve and mix with dichloromethane, add 10 mg 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 Sustained release injection, viscosity is 380cp-460cp (at 25℃-30℃). The subcutaneous release time is 30-35 days.
Embodiment 2
[0119] Put 75 mg of polylactic acid (PLA) with a molecular weight of 20,000 as pharmaceutical excipients into a container, add 100 ml of organic solvent to dissolve and mix with dichloromethane, add 25 mg of nimustine, shake again, and vacuum dry to remove the organic solvent. The dried solid composition is immediately shaped, and then irradiated to sterilize the dried solid composition to obtain an anti-cancer body implant containing 25% by weight of nimustine for curing solid tumors. The subcutaneous release time is 35-40 days.
Embodiment 3
[0121] Put 95 mg of polylactic acid (PLA) with a molecular weight of 40,000 as pharmaceutical excipients into a container, add 100 ml of methylene chloride as an organic solvent to dissolve and mix well, add 5 mg of Nimustine, shake again, and vacuum dry to remove the organic solvent. The dried solid composition is immediately shaped, and after being dispensed, it is ray sterilized to obtain an anti-cancer in vivo implant containing 100% by weight nimustine for curing solid tumors. The subcutaneous release time is 30-40 days.
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