Evidence map›Paper›PMID 27450412›Full record

ArticlePharmaceutical research2016

Optimization of Spray Drying Conditions for Yield, Particle Size and Biological Activity of Thermally Stable Viral Vectors.

Daniel A LeClair, Emily D Cranston, Zhou Xing, Michael R Thompson

Abstract read
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In one paragraph

Article in Pharmaceutical research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Review
  2. Article
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  5. Article
  6. Review
  7. Article
  8. Evaluation of the microencapsulation process of conidia of Trichoderma asperellum by spray drying.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2022
    Article
  9. Article
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  11. Article
  12. Review
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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

4 authors.

Daniel A LeClairDepartment of Chemical Engineering, McMaster University, Hamilton, Ontario, Canada, L8S 4 L7.
Emily D CranstonDepartment of Chemical Engineering, McMaster University, Hamilton, Ontario, Canada, L8S 4 L7.
Zhou XingMcMaster Immunology Research Centre & Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, Canada, L8S 4 L7.
Michael R ThompsonDepartment of Chemical Engineering, McMaster University, Hamilton, Ontario, Canada, L8S 4 L7. mthomps@mcmaster.ca.

Funding

CIHR
6 · The paper itself

Abstract

purposeThis work examines the relevance of viral activity in the optimization of spray drying process parameters for the development of thermally stable vaccine powders. In some instances, the actual active pharmaceutical ingredient (API) is not included in the process optimization as it is deemed too costly to use until the final selection of operating conditions, however, that approach is inappropriate for highly labile biopharmaceutics. We investigate the effects of spray drying parameters on i) yield, ii) particle size and iii) viral vector activity of a mannitol/dextran encapsulated recombinant human type 5 adenoviral vector vaccine, to demonstrate the effects and magnitude of each effect on the three responses, and further show that the API must be included earlier in the optimization.

methodsA design of experiments approach was used with response surface methodology (RSM) to optimize parameters including inlet temperature, spray gas flow rate, liquid feed rate and solute concentration in the feed.

resultsIn general, good conditions for maintaining viral activity led to reduced yield and fewer particles of the desired size. Within the range of parameters tested, the yield varied from 50 to 90%, the percentage of ideally size particles was 10-50%, and the viral vector titre loss was 0.25-4.0 log loss.

conclusionsRSM indicates that the most significant spray drying parameters are the inlet temperature and spray gas flow rate. It was not possible to optimize all three output variables with one set of parameters, indicating that there will only be one dominant criteria for processing which in the case of viral vaccines will likely be viral vector activity.

Indexed as

Genetic VectorsA549 CellsAdenoviridaeDesiccationDextransDrug CompoundingDrug StabilityHumansMannitolParticle SizePowdersTemperatureVaccinesDextransMannitolPowdersVaccinesadenovirusoptimizationparticle sizeprocess parametersspray drysurface response methodologytitreviral vectoryield

Identifiers

What OpenQuestion holds

Textmetadata
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.