Current trends in separation of plasmid DNA vaccines: A review

被引:67
作者
Ghanem, Ashraf [1 ]
Healey, Robert [1 ]
Adly, Frady G. [1 ]
机构
[1] Univ Canberra, Chiral Grp, Fac Appl Sci, Canberra, ACT 2617, Australia
关键词
Plasmids; Vaccine; pDNA; Separation; Purification; Chromatography; Monolith; PERFORMANCE LIQUID-CHROMATOGRAPHY; TANGENTIAL FLOW FILTRATION; LARGE-SCALE PURIFICATION; GENE-THERAPY; AFFINITY-CHROMATOGRAPHY; DIFFERENTIAL INTERACTIONS; EXCHANGE CHROMATOGRAPHY; STATIONARY-PHASE; GENOMIC DNA; DESIGN;
D O I
10.1016/j.aca.2012.11.006
中图分类号
O65 [分析化学];
学科分类号
070302 [分析化学];
摘要
Plasmid DNA (pDNA)-based vaccines offer more rapid avenues for development and production if compared to those of conventional virus-based vaccines. They do not rely on time- or labour-intensive cell culture processes and allow greater flexibility in shipping and storage. Stimulating antibodies and cell-mediated components of the immune system are considered as some of the major advantages associated with the use of pDNA vaccines. This review summarizes the current trends in the purification of pDNA vaccines for practical and analytical applications. Special attention is paid to chromatographic techniques aimed at reducing the steps of final purification, post primary isolation and intermediate recovery, in order to reduce the number of steps necessary to reach a purified end product from the crude plasmid. Crown Copyright (C) 2012 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 15
页数:15
相关论文
共 88 条
[1]
Ali I., 2009, LC GC, V27, P22
[2]
[Anonymous], 2005, GUID CONS PLASM DNA
[3]
Biotechnology applications of amino acids in protein purification and formulations [J].
Arakawa, T. ;
Tsumoto, K. ;
Kita, Y. ;
Chang, B. ;
Ejima, D. .
AMINO ACIDS, 2007, 33 (04) :587-605
[4]
Suppression of protein interactions by arginine: A proposed mechanism of the arginine effects [J].
Arakawa, Tsutomu ;
Ejima, Daisuke ;
Tsumoto, Kouhei ;
Obeyama, Noriyuki ;
Tanaka, Yoshikazu ;
Kita, Yoshiko ;
Timasheff, Serge N. .
BIOPHYSICAL CHEMISTRY, 2007, 127 (1-2) :1-8
[5]
Methacrylate-based short monolithic columns: Enabling tools for rapid and efficient analyses of biomolecules and nanoparticles [J].
Barut, Milos ;
Podgornik, Ales ;
Urbas, Lidija ;
Gabor, Bostjan ;
Brne, Peter ;
Vidic, Jana ;
Plevak, Saso ;
Strancar, Ales .
JOURNAL OF SEPARATION SCIENCE, 2008, 31 (11) :1867-1880
[6]
MODELING OF LIQUID-CHROMATOGRAPHY EQUILIBRIA [J].
BELLOT, JC ;
CONDORET, JS .
PROCESS BIOCHEMISTRY, 1993, 28 (06) :365-376
[7]
Influence of the methacrylate monolith structure on genomic DNA mechanical degradation, enzymes activity and clogging [J].
Bencina, Katja ;
Bencina, Mojca ;
Podgornik, Ales ;
Strancar, Ales .
JOURNAL OF CHROMATOGRAPHY A, 2007, 1160 (1-2) :176-183
[8]
Twenty-five years of immobilized metal ion affinity chromatography: past, present and future [J].
Chaga, GS .
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS, 2001, 49 (1-3) :313-334
[9]
LARGE-SCALE PURIFICATION OF PLASMID DNA BY FAST PROTEIN LIQUID-CHROMATOGRAPHY USING A HI-LOAD Q-SEPHAROSE COLUMN [J].
CHANDRA, G ;
PATEL, P ;
KOST, TA ;
GRAY, JG .
ANALYTICAL BIOCHEMISTRY, 1992, 203 (01) :169-172
[10]
ANALYSIS AND PURIFICATION OF PLASMID DNA BY REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
COLOTE, S ;
FERRAZ, C ;
LIAUTARD, JP .
ANALYTICAL BIOCHEMISTRY, 1986, 154 (01) :15-20