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不同制备工艺对奈拉滨注射液稳定性的影响 被引量:1

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摘要 目的:制备奈拉滨注射液,并考察其稳定性。方法:通过性状、pH、有关物质检查等考察,拟定处方组成与制备工艺。采用低温冻融试验、长期留样、加速试验考察其稳定性。结果:按优化的最佳处方及工艺制备的3批中试样品均合格。结论:该制剂处方工艺合理可行,质量可控。
出处 《中国药师》 CAS 2011年第7期1062-1063,共2页 China Pharmacist
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