【24h】

Compatibility of the antitumoral beta-lapachone with different solid dosage forms excipients.

机译:抗肿瘤β-拉帕酮与不同固体剂型赋形剂的相容性。

获取原文
获取原文并翻译 | 示例
           

摘要

The objective of the present study was to evaluate the compatibility of the beta-lapachone (betaLAP), an antitumoral drug in clinical phase, with pharmaceutical excipients of common use including diluents, binders, disintegrants, lubricants and solubilising agents. Differential scanning calorimetry (DSC) was used for a first screening to find small variations in peak temperatures and/or their associated enthalpy for six drug/excipient combinations (magnesium stearate, sodium estearyl fumarate, dicalcium phosphate dihydrate, mannitol, randomized methyl-beta-cyclodextrin and hydroxypropyl-beta-cyclodextrin), which indicate some degree of interaction. Additional studies using Fourier transformed infrared spectroscopy (FTIR), optical microscopy (OM) and heating-cooling DSC (HC-DSC) confirmed the incompatibility of betaLAP with magnesium stearate and dicalcium phosphate dihydrate. Those excipients should be avoided in the development of solid dosage forms.
机译:本研究的目的是评估临床阶段的抗肿瘤药物β-拉帕酮(betaLAP)与常用的药物赋形剂(包括稀释剂,粘合剂,崩解剂,润滑剂和增溶剂)的相容性。差示扫描量热法(DSC)用于首次筛选,以发现六种药物/赋形剂组合(硬脂酸镁,十八烷基富马酸硬脂酯,二水合磷酸二钙,甘露醇,随机甲基-β-环糊精和羟丙基-β-环糊精),它们之间存在一定程度的相互作用。使用傅里叶变换红外光谱(FTIR),光学显微镜(OM)和加热冷却DSC(HC-DSC)进行的其他研究证实了betaLAP与硬脂酸镁和二水合磷酸二钙的不相容性。在开发固体剂型时应避免使用这些赋形剂。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号