Rapid automated process development of a continuous capsule-filling process

被引:7
作者
Wagner, Bernhard [1 ,2 ,4 ]
Brinz, Thomas [1 ]
Otterbach, Stephanie [1 ,4 ]
Khinast, Johannes [2 ,3 ]
机构
[1] Robert Bosch Packaging Technol GmbH, Waiblingen, Germany
[2] Graz Univ Technol, Inst Particle & Proc Engn, Graz, Austria
[3] Res Ctr Pharmaceut Engn, Graz, Austria
[4] Robert Bosch Packaging Technol GmbH, Engn Pharma Serv PA PH EPS Wa, Postfach 11 27, D-71301 Waiblingen, Germany
关键词
Rapid automated process development; Continuous capsule filling; Automated capsule filling; Design of experiments; Process modeling; Optimized process; FORMULATIONS; DOSATOR; MACHINE;
D O I
10.1016/j.ijpharm.2018.05.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This paper introduces a rapid automated process-development approach for a continuous capsule-filling process. In our proposed method, both the material attributes and the critical process parameters were varied to understand and to optimize the overall process. Using our approach a statistical process model can be generated with unprecedented speed (2 days), which is the prerequisite for effectively developing and operating continuous process platforms. In a first set of experiments a process model was developed using different mixture compositions of ascorbic acid, lactose and magnesium stearate while changing simultaneously the critical process parameters of the capsule filler (speed, pressure, immersion depth and powder bed height). Targets of the model were the mean fill weight and the relative standard deviation of the produced capsules. In a second experimental set the model was tested, i.e., the goal was to predict the behavior of the system at different set points in order to predict weight and relative standard deviation for predefined targets. Predictions were very good, thus validating our approach. The combination of the rapid automated process development approach and the continuous capsule-filling process resulted in a new strategy for the development and manufacture of pharmaceutical dosage forms.
引用
收藏
页码:154 / 165
页数:12
相关论文
共 20 条
  • [1] Bauer-Brandl A., 2012, TABLETTE HDB ENTWICK, P586
  • [2] Carr R.L., 1965, Chem. Eng, V72, P163, DOI DOI 10.1016/J.JAEROSCI.2007.10.003
  • [3] Council of Europe, 2013, EUROPEAN PHARMACOPOE, V1, P357
  • [4] Council of Europe, 2013, EUROPEAN PHARMACOPOE, V1, P297
  • [5] Eriksson L, 2000, DESIGN EXPT PRINCIPL, P213
  • [6] Eriksson L., 2000, DESIGN EXPT PRINCIPL, P87
  • [7] FDA, 2004, pharmaceutical CGMPS for the 21 st century-a risk-based approach final report
  • [8] Rational design of powder formulations for tamp filling processes
    Hardy, IJ
    Fitzpatrick, S
    Booth, SW
    [J]. JOURNAL OF PHARMACY AND PHARMACOLOGY, 2003, 55 (12) : 1593 - 1599
  • [9] HAUER B, 1993, PHARM IND, V55, P780
  • [10] Heda PK, 2002, AAPS PHARMSCI, V4