2021
DOI: 10.1016/j.ijpharm.2021.120910
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Monitoring of high-load dose formulations based on co-processed and non co-processed excipients

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Cited by 7 publications
(2 citation statements)
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“…The development of these co-processed excipients often involved fluid-bed granulation and spray drying, among others [ 44 , 46 ]. In the earlier studies, the aim of co-processed pharmaceutical excipients is to acquire a new composite excipient with better functional properties than the raw excipient [ 46 , 47 ]. The co-processed excipients are also popular in direct compaction since they have excellent key direct compaction properties that could effectively improve the direct compaction properties of drug powders.…”
Section: Introductionmentioning
confidence: 99%
“…The development of these co-processed excipients often involved fluid-bed granulation and spray drying, among others [ 44 , 46 ]. In the earlier studies, the aim of co-processed pharmaceutical excipients is to acquire a new composite excipient with better functional properties than the raw excipient [ 46 , 47 ]. The co-processed excipients are also popular in direct compaction since they have excellent key direct compaction properties that could effectively improve the direct compaction properties of drug powders.…”
Section: Introductionmentioning
confidence: 99%
“…In recent years, NIR and Raman spectroscopy have been used to monitor drug concentrations at the feed frame, immediately before tablets are compressed. [8][9][10] The feed frame, and a stream sampler currently under development, are the main agents for meeting the Fundamental Sampling Principle (FSP) in which all parts of a moving lot must have the same opportunity of being sampled for analysis. 11 NIR and Raman spectroscopic methods are essential parts of real-time monitoring and control approaches within the field of PAT.…”
Section: Sampling Special Section Sampling Special Sectionmentioning
confidence: 99%