Skip to main content

2018 | OriginalPaper | Buchkapitel

Fully Disposable Manufacturing Concepts for Clinical and Commercial Manufacturing and Ballroom Concepts

Aktivieren Sie unsere intelligente Suche, um passende Fachinhalte oder Patente zu finden.

search-config
loading …

Abstract

The availability and use of pre-sterilized disposables has greatly changed the methods used in biopharmaceuticals development and production, particularly from mammalian cell culture. Nowadays, almost all process steps from cell expansion, fermentation, cell removal, and purification to formulation and storage of drug substances can be carried out in disposables, although there are still limitations with single-use technologies, particularly in the areas of pretesting and quality control of disposables, bag and connections standardization and qualification, extractables and leachables (E/L) validation, and dependency on individual vendors. The current status of single-use technologies is summarized for all process unit operations using a standard mAb process as an example. In addition, current pros and cons of using disposables are addressed in a comparative way, including quality control and E/L validation.
The continuing progress in developing single-use technologies has an important impact on manufacturing facilities, resulting in much faster, less expensive and simpler plant design, start-up, and operation, because cell culture process steps are no longer performed in hard-piped unit operations. This leads to simpler operations in a lab-like environment. Overall it enriches the current landscape of available facilities from standard hard-piped to hard-piped/disposables hybrid to completely single-use-based production plants using the current segregation and containment concept. At the top, disposables in combination with completely and functionally closed systems facilitate a new, revolutionary design of ballroom facilities without or with much less segregation, which enables us to perform good manufacturing practice manufacturing of different products simultaneously in unclassified but controlled areas.
Finally, single-use processing in lab-like shell facilities is a big enabler of transferring and establishing production in emergent countries, and this is described in more detail in 7.

Sie haben noch keine Lizenz? Dann Informieren Sie sich jetzt über unsere Produkte:

Springer Professional "Wirtschaft+Technik"

Online-Abonnement

Mit Springer Professional "Wirtschaft+Technik" erhalten Sie Zugriff auf:

  • über 102.000 Bücher
  • über 537 Zeitschriften

aus folgenden Fachgebieten:

  • Automobil + Motoren
  • Bauwesen + Immobilien
  • Business IT + Informatik
  • Elektrotechnik + Elektronik
  • Energie + Nachhaltigkeit
  • Finance + Banking
  • Management + Führung
  • Marketing + Vertrieb
  • Maschinenbau + Werkstoffe
  • Versicherung + Risiko

Jetzt Wissensvorsprung sichern!

Springer Professional "Technik"

Online-Abonnement

Mit Springer Professional "Technik" erhalten Sie Zugriff auf:

  • über 67.000 Bücher
  • über 390 Zeitschriften

aus folgenden Fachgebieten:

  • Automobil + Motoren
  • Bauwesen + Immobilien
  • Business IT + Informatik
  • Elektrotechnik + Elektronik
  • Energie + Nachhaltigkeit
  • Maschinenbau + Werkstoffe




 

Jetzt Wissensvorsprung sichern!

Literatur
1.
Zurück zum Zitat Mahajan E, Dent K, Chan E, Hudson T (2014) UNICAN: dual capability in single use bioreactors, Cell Culture Engineering XIV, April 2014, Quebec, Canada Mahajan E, Dent K, Chan E, Hudson T (2014) UNICAN: dual capability in single use bioreactors, Cell Culture Engineering XIV, April 2014, Quebec, Canada
2.
Zurück zum Zitat Gikanga B et al. (2015) Mixing monoclonal antibody formulations using bottom-mounted mixers: impact of mechanism and design on drug product quality. PDA J Pharma Sci Technol 69:284–296CrossRef Gikanga B et al. (2015) Mixing monoclonal antibody formulations using bottom-mounted mixers: impact of mechanism and design on drug product quality. PDA J Pharma Sci Technol 69:284–296CrossRef
3.
Zurück zum Zitat Goldstein A (2015) Pharmaceutical engineering, vol 35. ISPE, Bethesda Goldstein A (2015) Pharmaceutical engineering, vol 35. ISPE, Bethesda
4.
Zurück zum Zitat Samavedam R, Goldstein A, Schieche D (2006) Implementation of disposables: validation and other considerations. Am Pharm Rev 9(5):46–51 Samavedam R, Goldstein A, Schieche D (2006) Implementation of disposables: validation and other considerations. Am Pharm Rev 9(5):46–51
5.
Zurück zum Zitat Goldstein A, Pohlscheidt M (2012) Disposable freeze systems in the pharmaceutical industry. Am Pharm Rev 15, 53–58 Goldstein A, Pohlscheidt M (2012) Disposable freeze systems in the pharmaceutical industry. Am Pharm Rev 15, 53–58
6.
Zurück zum Zitat Boedeker B (2012) Improving biologic manufacturing operations and plant design through single-use technologies applications. Pharm Outsourcing 13:12–17 Boedeker B (2012) Improving biologic manufacturing operations and plant design through single-use technologies applications. Pharm Outsourcing 13:12–17
7.
Zurück zum Zitat Boedeker B (2013) Assessing possibilities and preventing the risk of using disposables. BioPharma Asia Vol 2(2) March/April 2013, 38–45 Boedeker B (2013) Assessing possibilities and preventing the risk of using disposables. BioPharma Asia Vol 2(2) March/April 2013, 38–45
8.
Zurück zum Zitat Leveen L (2009) Single use technology and its carbon and water footprints, part 2. Am Pharm Rev 13:50–56 Leveen L (2009) Single use technology and its carbon and water footprints, part 2. Am Pharm Rev 13:50–56
9.
Zurück zum Zitat Ding W et al. (2014) Standardized extractables testing protocol for single use systems in biomanufacturing. Pharm Eng 34(6), 1–11 Ding W et al. (2014) Standardized extractables testing protocol for single use systems in biomanufacturing. Pharm Eng 34(6), 1–11
10.
Zurück zum Zitat Boedeker B (2014) Facility of the future: effect of disposables and continuous processing on plant design. BioPharma Asia Vol 4(3) May/June 2014, 24–27 Boedeker B (2014) Facility of the future: effect of disposables and continuous processing on plant design. BioPharma Asia Vol 4(3) May/June 2014, 24–27
11.
Zurück zum Zitat Chalk S et al. (2011) Challenging the cleanroom paradigm for biopharmaceutical manufacturing of bulk drug substance. BioPharm Int Aug 2011:1–13 Chalk S et al. (2011) Challenging the cleanroom paradigm for biopharmaceutical manufacturing of bulk drug substance. BioPharm Int Aug 2011:1–13
12.
Zurück zum Zitat Mahajan E (2011) Microline: a fully disposable manufacturing facility. In: ISPE Annual Conference, Nov 2011 Mahajan E (2011) Microline: a fully disposable manufacturing facility. In: ISPE Annual Conference, Nov 2011
13.
Zurück zum Zitat Hudson T (2014) Evaluating where single-use technology provides the most value for a company with well established manufacturing infrastructure. 247th ACS National Meeting and Exposition, March 16–20, 2014, Dallas, Texas Chemistry and Materials for Energy Hudson T (2014) Evaluating where single-use technology provides the most value for a company with well established manufacturing infrastructure. 247th ACS National Meeting and Exposition, March 16–20, 2014, Dallas, Texas Chemistry and Materials for Energy
Metadaten
Titel
Fully Disposable Manufacturing Concepts for Clinical and Commercial Manufacturing and Ballroom Concepts
verfasst von
Berthold Boedeker
Adam Goldstein
Ekta Mahajan
Copyright-Jahr
2018
DOI
https://doi.org/10.1007/10_2017_19

    Marktübersichten

    Die im Laufe eines Jahres in der „adhäsion“ veröffentlichten Marktübersichten helfen Anwendern verschiedenster Branchen, sich einen gezielten Überblick über Lieferantenangebote zu verschaffen.