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technique of direct powder compression
相关语句
  粉末直接压片工艺
     Study on the technique of direct powder compression of Captopril Tablets
     卡托普利全粉末直接压片工艺研究
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  “technique of direct powder compression”译为未确定词的双语例句
     Conclusion: The technique of direct powder compression is simple and useful, and the prep ared sustained-release tablets release well during 12 hours in vitro.
     结论:粉末直接压片法工艺简单可行,骨架片体外释放效果良好。
短句来源
     Method The technique of direct powder compression was adopted using compressible starch as the main excipient.
     方法采用可压性淀粉为主辅料,粉末直接压片。
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  相似匹配句对
     Study on the technique of direct powder compression of Captopril Tablets
     卡托普利全粉末直接压片工艺研究
短句来源
     Preparation of Dosmalfate Dispersible Tablets by Direct Powder Compression Technique
     粉末直接压片法制备多司马酯分散片
短句来源
     Objective:To prepare dosmalfate dispersible tablets by direct powder compression technique.
     目的:采用粉末直接压片工艺制备多司马酯分散片。
短句来源
     Study on direct powder compression of Naoan tablet
     脑安片粉末直接压片新工艺研究
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     Study on direct powder compression of aspirin tablet
     阿司匹林片剂粉末直接压片新工艺研究
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Objective: To prepare the tetramethylpyrazine ph osphate tablet that can release constantly for 12 hours. Methods: According to the preliminary experiments, the optimization prescription de sign and technique were obtained by orthogonal design. Based on the method in Ch inese Pharmacopoeia(2000), the release rates of the prepared sustained-release t ablets were tested in vitro. Results: An ideal tablet model was obtained by direct powder compression. The release rate in vitro was about 2 5% at 1 hour and more...

Objective: To prepare the tetramethylpyrazine ph osphate tablet that can release constantly for 12 hours. Methods: According to the preliminary experiments, the optimization prescription de sign and technique were obtained by orthogonal design. Based on the method in Ch inese Pharmacopoeia(2000), the release rates of the prepared sustained-release t ablets were tested in vitro. Results: An ideal tablet model was obtained by direct powder compression. The release rate in vitro was about 2 5% at 1 hour and more than 90% at 12 hours. The release characteristics during 1 2 hours were correspondent with Higuchi equation. Conclusion: The technique of direct powder compression is simple and useful, and the prep ared sustained-release tablets release well during 12 hours in vitro.

 目的:研制持续释药12 h的磷酸川芎嗪骨架片。方法:根据预实验结果,采用正交设计进行处方设计和工艺优化,并用中国药典(2000年版)释放度测定方法测定骨架片的体外释放度。结果:直接压片可得到理想的片型,缓释片体外释药1 h释放度为25 0%左右,12 h在90. 0%以上。12 h内释药特性符合Higuchi方程。结论:粉末直接压片法工艺简单可行,骨架片体外释放效果良好。

Objective To solve the problem that the content of bisulfide in captopril is easily higher than limit. Method The technique of direct powder compression was adopted using compressible starch as the main excipient. Results All the results of tests were consistent with the requirment of Chp. 2000.Conclusion The optimized process can avoid the oxidation of captopril, and it is a simple, stable and efficient method.

目的解决卡托普利片剂中二硫化物易超标的问题。方法采用可压性淀粉为主辅料,粉末直接压片。结果产品质量符合中国药典2000版二部标准。结论粉末直接压片可避免湿颗粒在干燥过程中因高温及水分造成卡托普利氧化,导致二硫化物超标。

 
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