Evidence map›Paper›PMID 37219094›Full record

ArticleAnalytical chemistry2023

Reversed Phase-Liquid Chromatography for Recombinant AAV Genome Integrity Assessment.

Christoph Gstöttner, Andrei Hutanu, Sacha Boon, Aurelia Raducanu, Klaus Richter, Markus Haindl, Raphael Ruppert, Elena Domínguez-Vega

Abstract read
In one paragraph

Article in Analytical chemistry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Christoph GstöttnerCenter for Proteomics and Metabolomics, Leiden University Medical Center, 2333ZA Leiden, The Netherlands.
Andrei HutanuPharma Technical Development Analytics, F. Hoffmann-La Roche AG, 4070 Basel, Switzerland.ORCID 0000-0003-0174-5250
Sacha BoonCenter for Proteomics and Metabolomics, Leiden University Medical Center, 2333ZA Leiden, The Netherlands.
Aurelia RaducanuPharma Technical Operation Cell- and Gene Therapy, Roche Diagnostics GmbH, 82377 Penzberg, Germany.
Klaus RichterCoriolis Pharma Research GmbH, 82152 Planegg, Germany.
Markus HaindlPharma Technical Operation Cell- and Gene Therapy, Roche Diagnostics GmbH, 82377 Penzberg, Germany.
Raphael RuppertPharma Technical Operation Cell- and Gene Therapy, Roche Diagnostics GmbH, 82377 Penzberg, Germany.
Elena Domínguez-VegaCenter for Proteomics and Metabolomics, Leiden University Medical Center, 2333ZA Leiden, The Netherlands.ORCID 0000-0002-6394-0783

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

After decades of research, gene therapy products have reached market maturity in recent years. Recombinant adeno-associated viruses (rAAVs) are one of the most promising gene delivery vehicles and are currently under intense scientific investigation. These next-generation medicines remain very challenging when it comes to designing appropriate analytical techniques for quality control. One critical quality attribute is the integrity of ssDNA incorporated in these vectors. The genome is the active compound driving rAAV therapy and therefore requires proper assessment and quality control. Current techniques for rAAV genome characterization include next-generation sequencing, quantitative polymerase chain reaction, analytical ultracentrifugation (AUC), and capillary gel electrophoresis (CGE), yet each of them presents their limitations or lack of user-friendliness. In this work, we demonstrate for the first time the potential of ion pairing-reverse phase-liquid chromatography (IP-RP-LC) to characterize the integrity of rAAV genomes. The obtained results were supported by two orthogonal techniques, AUC and CGE. IP-RP-LC can be performed above DNA melting temperatures, avoiding the detection of secondary DNA isoforms, and does not require the use of dyes due to UV detection. We demonstrate that this technique is suitable for batch comparability, different rAAV serotypes (AAV2 and AAV8), internal vs external (inside vs outside the capsid) DNA analysis, and contaminated samples. Overall, it is exceptionally user-friendly, needs limited sample preparation, has high reproducibility, and permits fractionation for further peak characterization. All of these factors add significant value of IP-RP-LC to the analytical toolbox of rAAV genome assessment.

Indexed as

Genetic VectorsGene Transfer TechniquesChromatography, LiquidDependovirusGenetic TherapyReproducibility of Results

Identifiers

PMID37219094
PMCPMC10248999

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.