Zolinza sustained-release implant treating for solid tumor
A technology of slow-release implants and slow-release modulators, which can be used in antineoplastic drugs, pharmaceutical formulations, active ingredients of amides, etc., and can solve problems such as systemic toxic and side effects that limit clinical application
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Embodiment 1
[0082] Put the weighed (90 mg) sustained-release excipient (polylactic acid (PLA) with a molecular weight of 10000-20000) into a container, add a certain amount of organic solvent to dissolve and mix (subject to full dissolution), and then add 10 mg of Zhuo Linzer, re-shake well and vacuum-dry to remove organic solvents. The dried solid composition is shaped immediately, subpackaged and sterilized by radiation to obtain a slow-release implant containing 10% Zolinze. The release time of the sustained-release implant in physiological saline in vitro is 18-24 days, and the release time in mouse subcutaneous is 25-32 days.
Embodiment 2
[0084] Sustained-release implants were made according to the method described in Example 1, but the anti-cancer active ingredients contained were one of the following:
[0085] (A) 1% Zhuo Linze and 99% polylactic acid;
[0086] (B) 5% Zhuo Linze and 95% polylactic acid;
[0087] (C) 10% Zhuo Linze and 90% polylactic acid;
[0088] (D) 15% Zhuo Linze and 85% polylactic acid;
[0089] (E) 20% Zhuo Linze and 80% polylactic acid.
Embodiment 3
[0091] Put the weighed (85mg) sustained-release excipient (PLGA with a molecular weight of 15000-30000, 50:50) into the container, add a certain amount of organic solvent to dissolve and mix (subject to full dissolution), then add 15mg of Zolin Shake, re-shake and vacuum-dry to remove organic solvents. The dried solid composition is shaped immediately, subpackaged and then sterilized by radiation to obtain a sustained-release implant containing 15% Zolinze. The release time of the sustained-release implant in physiological saline in vitro is 14-24 days, and the release time in mouse subcutaneous is 20-28 days.
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