Reduction of Recombinant Adeno-Associated Virus Vector Adsorption on Solid Surfaces by Polyionic Hydrophilic Complex Coating

Recombinant adeno-associated virus (rAAV) vectors have proven efficacy as gene therapy vehicles. However, non-specific adsorption of these vectors on solid surfaces is encountered during production, storage, and administration, as well as in quantification processes. Such adsorption has been reporte...

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Published inJournal of pharmaceutical sciences Vol. 111; no. 3; pp. 663 - 671
Main Authors Ramy, Salama, Ueda, Yuki, Nakajima, Hiroyuki, Hiroi, Miya, Hiroi, Yoshiomi, Torisu, Tetsuo, Uchiyama, Susumu
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.03.2022
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Abstract Recombinant adeno-associated virus (rAAV) vectors have proven efficacy as gene therapy vehicles. However, non-specific adsorption of these vectors on solid surfaces is encountered during production, storage, and administration, as well as in quantification processes. Such adsorption has been reported to result in the loss of up to 90% of vector particles and can also result in high variability in vector genome quantification. In this study, we demonstrate the effective decrease of recombinant adeno-associated virus vector adsorption by application of a polyionic hydrophilic complex polymer coating on the surfaces of the tools used in viral vector quantification analyses [i.e., pipette tips, cryotube vials, and quantitative polymerase chain reaction (qPCR) plates]. qPCR analyses showed efficient recovery of vector particles from tools with this coating, with up to 95% of vector particle loss being prevented, leading to a higher transduction efficiency in vitro. Thus, the tested coating has the potential to be widely used in material processing in the gene therapy field.
AbstractList Recombinant adeno-associated virus (rAAV) vectors have proven efficacy as gene therapy vehicles. However, non-specific adsorption of these vectors on solid surfaces is encountered during production, storage, and administration, as well as in quantification processes. Such adsorption has been reported to result in the loss of up to 90% of vector particles and can also result in high variability in vector genome quantification. In this study, we demonstrate the effective decrease of recombinant adeno-associated virus vector adsorption by application of a polyionic hydrophilic complex polymer coating on the surfaces of the tools used in viral vector quantification analyses [i.e., pipette tips, cryotube vials, and quantitative polymerase chain reaction (qPCR) plates]. qPCR analyses showed efficient recovery of vector particles from tools with this coating, with up to 95% of vector particle loss being prevented, leading to a higher transduction efficiency in vitro. Thus, the tested coating has the potential to be widely used in material processing in the gene therapy field.
Author Hiroi, Yoshiomi
Ramy, Salama
Torisu, Tetsuo
Hiroi, Miya
Ueda, Yuki
Uchiyama, Susumu
Nakajima, Hiroyuki
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  email: suchi@bio.eng.osaka-u.ac.jp
  organization: Department of Biotechnology, Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871, Japan
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Issue 3
Keywords Adeno-associated virus (AAV)
PBS
FDA
Viral vector
COP
Polymer
PHC
Contact angle
Surfactant
D-PBS (–)
rAAV
GFP
ddPCR
VG
Surface binding
RSS
Adsorption
F/T cycles
AAV
qPCR
Coating
zwitterion
Gene therapy
Language English
License This is an open access article under the CC BY license.
Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.
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Snippet Recombinant adeno-associated virus (rAAV) vectors have proven efficacy as gene therapy vehicles. However, non-specific adsorption of these vectors on solid...
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SubjectTerms Adeno-associated virus (AAV)
Adsorption
Coating
Contact angle
Dependovirus - genetics
Gene therapy
Genetic Therapy
Genetic Vectors
Polymer
Surface binding
Surfactant
Viral vector
zwitterion
Title Reduction of Recombinant Adeno-Associated Virus Vector Adsorption on Solid Surfaces by Polyionic Hydrophilic Complex Coating
URI https://dx.doi.org/10.1016/j.xphs.2021.10.022
https://www.ncbi.nlm.nih.gov/pubmed/34706282
https://search.proquest.com/docview/2587755161
Volume 111
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