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

被引:13
作者
Bakker, Noor A. M. [1 ,2 ,3 ,4 ]
de Boer, Renate [1 ,2 ,3 ,4 ]
Marie, Corinne [6 ,7 ,8 ,9 ]
Scherman, Daniel [5 ,7 ,8 ,9 ]
Haanen, John B. A. G. [1 ,2 ,3 ,5 ]
Beijnen, Jos H. [2 ,3 ]
Nuijen, Bastiaan [2 ,3 ]
van den Berg, Joost H. [1 ,2 ,3 ,4 ]
机构
[1] Netherlands Canc Inst Antoni van Leeuwenhoek, Div Immunol, Plesmanslaan 121, NL-1066 CX Amsterdam, Netherlands
[2] Netherlands Canc Inst Antoni van Leeuwenhoek, Div Pharm, Plesmanslaan 121, NL-1066 CX Amsterdam, Netherlands
[3] Netherlands Canc Inst Antoni van Leeuwenhoek, Div Clin Pharmacol, Plesmanslaan 121, NL-1066 CX Amsterdam, Netherlands
[4] Amsterdam Biotherapeut Unit, Louwesweg 6, NL-1066 EC Amsterdam, Netherlands
[5] Netherlands Canc Inst Antoni van Leeuwenhoek, Div Med Oncol, Plesmanslaan 121, NL-1066 CX Amsterdam, Netherlands
[6] CNRS, Unite Technol Chim & Biol Sante UTCBS, UMR 8258, F-75006 Paris, France
[7] INSERM, UTCBS U1022, F-75006 Paris, France
[8] Univ Paris 05, Sorbonne Paris Cite, UTCBS, F-75006 Paris, France
[9] PSL Res Univ, Chim ParisTech, UTCBS, F-75005 Paris, France
关键词
Small scale plasmid production; RNase; GMP; fully disposable; antibiotic-free gene vectors; miniplasmids; PEDF; PURIFICATION;
D O I
10.1016/j.btecx.2019.100007
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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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页数:8
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