A control strategy for bioavailability enhancement by size reduction: Effect of micronization conditions on the bulk, surface and blending characteristics of an active pharmaceutical ingredient

作者：Olusanmi Dolapo^*; Jayawickrama Dimuthu; Bu Dongsheng; McGeorge Gary; Sailes Helen; Kelleher Joanne; Gamble John F; Shah Umang V; Tobyn Mike

来源：Powder Technology, 2014, 258: 222-233.

DOI：10.1016/j.powtec.2014.03.032

• Micronization
• Milling
• QbD
• Blending
• Surface energy
• Surface area
• Cohesion

In a Quality by Design (QbD) development environment the effect of early process parameters on downstream manufacturing parameters, and the ultimate effect on drug product quality, need to be understood. For poorly soluble drugs, size reduction is frequently employed to obtain consistent in-vivo exposures. As a result, micronization is a key early stage processing step for many active pharmaceutical ingredients (APIs). This paper demonstrates the effect of varying micronization conditions on an API for which micronization is deemed necessary to ensure consistent drug delivery after human administration. Material micronized to different extents are confirmed as different by surface area, surface energy, particle size analysis, bulk density and surface adhesion measurements.
These material characteristics can be correlated with the outcomes from a key processing step, blending. The evolution of the blending process is followed using PAT techniques, so that an overall understanding of the relationship between particle properties and blend uniformity can be demonstrated. Execution of such a study during drug development can enable selection of the appropriate control strategy to ensure production of API in the desired range where consistent optimal bioavailability and downstream processability are achieved.

• 出版日期2014-5