Small-scale GMP production of plasmid DNA using a simplified and fully disposable production method.

J Biotechnol

Divisions of Immunology, Pharmacy & Clinical Pharmacology, The Netherlands Cancer Institute - Antoni van Leeuwenhoek, Plesmanslaan 121, 1066 CX, Amsterdam, the Netherlands; Amsterdam Biotherapeutics Unit, Louwesweg 6, 1066 EC, Amsterdam, the Netherlands. Electronic address:

Published: May 2019

AI Article Synopsis

  • There has been increasing demand for small batches of clinical-grade plasmid DNA, prompting the creation of a scaled-down Good Manufacturing Practices (GMP) production method suitable for producing 1-4 mg batches.
  • The new method utilizes simple, disposable materials, making it easy to implement and streamline the production process, with successful production demonstrated for two different plasmids.
  • Quality control tests confirmed the method's effectiveness, revealing that the final formulation remains stable for at least two years and is intended for use in a phase I/II clinical trial for treating Age Related Macular Degeneration.

Article Abstract

In the past years, the demand for small batches of clinical grade plasmid DNA has been growing. For that purpose, we designed and qualified a scaled-down Good Manufacturing Practices (GMP) production method, able to produce small batches (1-4 mg) of plasmid. The developed method does not require any complex production equipment and utilizes only disposable production materials, which makes it easy to implement and simplifies line-clearance. We have successfully used this method to produce several small batches of two different plasmids. The produced plasmids, both formulated in an Electroporation Buffer, are mixed and filled into small, single-use, aliquots. Quality control confirmed the robustness of the developed method and a stability study showed that the final formulation is stable for at least two years. The final patient formulation will be subsequently used in a phase I/II clinical trial in which retina cells of patients with Age Related Macular Degeneration, are transfected. The presented production method can be generically used for other plasmid constructs and final formulation designs.

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Source
http://dx.doi.org/10.1016/j.btecx.2019.100007DOI Listing

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