TY - GEN
T1 - Novel Cleaning-in-Place Strategies for Pharmaceutical Hot Melt Extrusion
AU - Spoerk, Martin
AU - Koutsamanis, Ioannis
AU - Matic, Josip
AU - Eder, Simone
AU - Zuniga, Carolina Patricia Alva
AU - Poms, Johannes
AU - Urich, Jesus Alberto Afonso
AU - Garcia, Raymar Andreina Lara
AU - Nickisch, Klaus
AU - Eggenreich, Karin
AU - Berghaus, Andreas
AU - Reusch, Kathrin
AU - Relle, Yorick
AU - Khinast, Johannes
AU - Paudel, Amrit
PY - 2020/6
Y1 - 2020/6
N2 - To avoid any type of cross-contamination, residue-free production equipment is of utmost importance in the pharmaceutical industry. The equipment cleaning for continuous processes such as hot melt extrusion (HME), which has recently gained popularity in pharmaceutical applications, necessitates extensive manual labour and costs. The present work tackles the HME cleaning issue by investigating two cleaning strategies following the extrusion of polymeric formulations of a hormonal drug and for a sustained release formulation of a poorly soluble drug. First, an in-line quantification by means of UV–Vis spectroscopy was successfully implemented to assess very low active pharmaceutical ingredient (API) concentrations in the extrudates during a cleaning procedure for the first time. Secondly, a novel in-situ solvent-based cleaning approach was developed and its usability was evaluated and compared to a polymer-based cleaning sequence. Comparing the in-line data to typical swab and rinse tests of the process equipment indicated that inaccessible parts of the equipment were still contaminated after the polymer-based cleaning procedure, although no API was detected in the extrudate. Nevertheless, the novel solvent-based cleaning approach proved to be suitable for removing API residue from the majority of problematic equipment parts and can potentially enable a full API cleaning-in-place of a pharmaceutical extruder for the first time.
AB - To avoid any type of cross-contamination, residue-free production equipment is of utmost importance in the pharmaceutical industry. The equipment cleaning for continuous processes such as hot melt extrusion (HME), which has recently gained popularity in pharmaceutical applications, necessitates extensive manual labour and costs. The present work tackles the HME cleaning issue by investigating two cleaning strategies following the extrusion of polymeric formulations of a hormonal drug and for a sustained release formulation of a poorly soluble drug. First, an in-line quantification by means of UV–Vis spectroscopy was successfully implemented to assess very low active pharmaceutical ingredient (API) concentrations in the extrudates during a cleaning procedure for the first time. Secondly, a novel in-situ solvent-based cleaning approach was developed and its usability was evaluated and compared to a polymer-based cleaning sequence. Comparing the in-line data to typical swab and rinse tests of the process equipment indicated that inaccessible parts of the equipment were still contaminated after the polymer-based cleaning procedure, although no API was detected in the extrudate. Nevertheless, the novel solvent-based cleaning approach proved to be suitable for removing API residue from the majority of problematic equipment parts and can potentially enable a full API cleaning-in-place of a pharmaceutical extruder for the first time.
KW - cleaning verification
KW - cleaning-in-place
KW - hot melt extrusion
KW - API contamination
KW - UV-Vis spectroscopy
KW - process analytical technology
KW - swab and rinse tests
KW - estradiol
KW - estriol
KW - ibuprofen
KW - Hot melt extrusion
KW - Cleaning verification
KW - Estradiol
KW - Process analytical technology
KW - Ibuprofen
KW - Swab and rinse tests
KW - Cleaning-in-place
KW - Estriol
KW - UV–Vis spectroscopy
UR - http://www.scopus.com/inward/record.url?scp=85086838146&partnerID=8YFLogxK
U2 - 10.3390/pharmaceutics12060588
DO - 10.3390/pharmaceutics12060588
M3 - Other contribution
VL - 12
T3 - Pharmaceutics
ER -