Evidence map›Paper›PMID 40074162›Full record

ArticleInternational journal of pharmaceutics2025

Scale-up of a low-temperature spray-drying process for a tuberculosis vaccine candidate using lab-scale equipment.

Maximilian Aisenstat, Joseph McCollum, Mani Ordoubadi, Hui Wang, Zahra Minootan, Alana Gerhardt, Andrew R Martin, Christopher B Fox, Reinhard Vehring

Abstract read
In one paragraph

Article in International journal of pharmaceutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

9 authors.

Maximilian AisenstatDepartment of Mechanical Engineering, University of Alberta, Edmonton, AB, Canada.
Joseph McCollumAccess to Advanced Health Institute (AAHI), Seattle, WA, United States.
Mani OrdoubadiDepartment of Mechanical Engineering, University of Alberta, Edmonton, AB, Canada.
Hui WangDepartment of Mechanical Engineering, University of Alberta, Edmonton, AB, Canada.
Zahra MinootanDepartment of Mechanical Engineering, University of Alberta, Edmonton, AB, Canada.
Alana GerhardtAccess to Advanced Health Institute (AAHI), Seattle, WA, United States.
Andrew R MartinDepartment of Mechanical Engineering, University of Alberta, Edmonton, AB, Canada. Electronic address: armartin@ualberta.ca.
Christopher B FoxAccess to Advanced Health Institute (AAHI), Seattle, WA, United States.
Reinhard VehringDepartment of Mechanical Engineering, University of Alberta, Edmonton, AB, Canada.

Funding

NIAID NIH HHS HHSN272201400041C
6 · The paper itself

Abstract

Laboratory-scale spray drying can be a useful tool in developing new dry powder formulations for the delivery of biologics such as therapeutic proteins or vaccines. Low-temperature drying is often used in these processes to prevent the exposure of biologics to harsh conditions that could potentially lead to degradation or instability of the final product. However, low-temperature drying on small-scale equipment can result in very low production rates that may not be practical for generating sufficient material for studies requiring larger sample quantities, such as key preclinical or toxicology studies. This study demonstrates a scale-up effort for a spray dried adjuvanted protein tuberculosis (TB) vaccine candidate using a custom lab-scale spray dryer. To achieve higher throughput without compromising the stability of the powder and biologic material, a process model for the spray dryer was used to determine optimal processing parameters and establish general vaccine powder manufacturing guidelines, such as minimizing exposure to high temperatures and relative humidity during drying. Maximizing dryer throughput and increasing overall feed concentration resulted in a tenfold increase in production rate using lab-scale equipment, such that 97.6 g of powder (the equivalent of about 5,000 human doses) could be produced using a lab-scale spray dryer in a single 6-hour spray drying run.

Indexed as

Spray DryingTechnology, PharmaceuticalTuberculosis VaccinesChemistry, PharmaceuticalDesiccationDrug CompoundingDrug StabilityHumansPowdersTemperaturePowdersTuberculosis VaccinesGlass StabilizationParticle EngineeringScale-UpSpray dryingTuberculosis Vaccine

Identifiers

PMID40074162
PMCPMC12005957

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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.