Anticancer slow release agent of nimustine and its progression agent
A nimustine 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 complications, and reduce costs
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Embodiment 1
[0127] Put 90 mg of polylactic acid (PLA) with a molecular weight of 20,000-40,000 as a pharmaceutical excipient into a container, add 100 ml of organic solvent dichloromethane to dissolve and mix well, add 10 mg of nimustine, shake well, and then vacuum dry to remove the organic solvent . Shake again and dry in vacuo to remove the organic solvent. The dried drug-containing solid composition is frozen and pulverized to make a micropowder containing 10% by weight of nimustine, and then suspended in physiological saline containing 1.5% sodium carboxymethylcellulose to obtain the corresponding suspension Type sustained-release injection, the viscosity is 360cp-480cp (at 25°C-30°C). The subcutaneous release time is 25-30 days.
Embodiment 2
[0129] Put 75 mg of polylactic acid (PLA) with a molecular weight of 30,000-50,000 as a pharmaceutical excipient into a container, add 100 ml of organic solvent dichloromethane to dissolve and mix well, add 25 mg of nimustine, re-shake, and then vacuum dry to remove the organic solvent . The dried solid composition is shaped immediately, subpackaged and then sterilized by radiation to obtain an anti-cancer in vivo implant containing 25% by weight of nimustine for treating solid tumors. The subcutaneous release time is 35-40 days.
Embodiment 3
[0131] Put 95 mg of polylactic acid (PLA) with a molecular weight of 25,000-40,000 as a pharmaceutical excipient into a container, add 100 ml of organic solvent dichloromethane to dissolve and mix well, add 5 mg of nimustine, re-shake, and then vacuum dry to remove the organic solvent . The dried solid composition is shaped immediately, subpackaged and then sterilized by radiation to obtain an anticancer implant in vivo containing 5% by weight of nimustine for treating solid tumors. The subcutaneous release time is 30-40 days.
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