Evidence map›Paper›PMID 40231435›Full record

ArticleBiotechnology progress

Continuous purification of a parvovirus using two aqueous two-phase extraction steps.

Natalie M Nold, Sheridan Waldack, Grace James, Trisha Colling, Lynn Manchester, Taravat Sarvari, Amanda Bekkala, Seth A Kriz, Madison Baldwin, Emily Agustin-Mazariegos and 2 more

Abstract read
In one paragraph

Article in Biotechnology progress. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
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

12 authors.

Natalie M NoldDepartment of Chemical Engineering, Michigan Technological University, Houghton, Michigan, USA.
Sheridan WaldackDepartment of Chemical Engineering, Michigan Technological University, Houghton, Michigan, USA.
Grace JamesDepartment of Chemical Engineering, Michigan Technological University, Houghton, Michigan, USA.
Trisha CollingHealth Research Institute, Michigan Technological University, Houghton, Michigan, USA.
Lynn ManchesterDepartment of Chemical Engineering, Michigan Technological University, Houghton, Michigan, USA.
Taravat SarvariDepartment of Chemical Engineering, Michigan Technological University, Houghton, Michigan, USA.
Amanda BekkalaDepartment of Chemical Engineering, Michigan Technological University, Houghton, Michigan, USA.
Seth A KrizDepartment of Chemical Engineering, Michigan Technological University, Houghton, Michigan, USA.
Madison BaldwinDepartment of Chemical Engineering, Michigan Technological University, Houghton, Michigan, USA.
Emily Agustin-MazariegosDepartment of Chemical Engineering, Michigan Technological University, Houghton, Michigan, USA.
Michael J BetenbaughDepartment of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, Maryland, USA.
Caryn L HeldtDepartment of Chemical Engineering, Michigan Technological University, Houghton, Michigan, USA.ORCID 0000-0002-0776-8763

Funding

FDA HHS R01 FD007461FDA HHS R01FD007461National Science Foundation GRFP-2034833
6 · The paper itself

Abstract

Aqueous two-phase systems (ATPS) are a liquid-liquid extraction method that offers low-cost, continuous-adaptable virus purification. A two-step ATPS using polyethylene glycol (PEG) and sodium citrate that recovered 66% of infectious porcine parvovirus with 2.0 logs of protein removal and 1.0 logs of DNA removal in batch has now been run continuously. The continuous system output of <10 ng/mL DNA regardless of starting DNA titer agreed with batch studies. However, the continuous system had a five-fold higher contaminating protein titer than batch studies, likely because of incomplete mixing or settling. Turbidity was tested as a measure of mixing and settling efficiency. Monitoring in-line absorbance at 880 nm directly after mixing and before collection in the settling reservoir could track both mixing and settling during operation. Settling time was reduced by changing the settling line material from PVC to PTFE, which is more hydrophobic. A flow-through AEX filter tested to make impurity removal more robust recovered 90% of PPV and removed an additional 87% of host cell DNA. The filter did not add any additional protein removal. In the future, in-line absorbance sensors could be implemented along with conductivity sensors to measure salt concentration, refractive index sensors to track the PEG-citrate interface, and scales to track mixer and reservoir volumes to enable automated, continuous ATPS. Our vision is to integrate continuous ATPS into a fully continuous end-to-end production for viral vectors.

Indexed as

Liquid-Liquid ExtractionParvovirus, PorcineAnimalsCitratesDNA, ViralPolyethylene GlycolsSodium CitrateSwineCitratesDNA, ViralPolyethylene GlycolsSodium CitrateAAVchromatographyprocess intensificationvaccine manufacturing

Identifiers

PMID40231435
PMCPMC12531933

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.