Evidence map›Paper›PMID 40038316›Full record

ArticleScientific reports2025

Machine learning aided UV absorbance spectroscopy for microbial contamination in cell therapy products.

Shruthi Pandi Chelvam, Alice Jie Ying Ng, Jiayi Huang, Elizabeth Lee, Maciej Baranski, Derrick Yong, Rohan B H Williams, Stacy L Springs, Rajeev J Ram

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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.

Shruthi Pandi ChelvamCritical Analytics for Manufacturing Personalized Medicine (CAMP), Singapore-MIT Alliance for Research and Technology Centre, Singapore, Singapore.
Alice Jie Ying NgCritical Analytics for Manufacturing Personalized Medicine (CAMP), Singapore-MIT Alliance for Research and Technology Centre, Singapore, Singapore.
Jiayi HuangCritical Analytics for Manufacturing Personalized Medicine (CAMP), Singapore-MIT Alliance for Research and Technology Centre, Singapore, Singapore.
Elizabeth LeeCritical Analytics for Manufacturing Personalized Medicine (CAMP), Singapore-MIT Alliance for Research and Technology Centre, Singapore, Singapore.
Maciej BaranskiCritical Analytics for Manufacturing Personalized Medicine (CAMP), Singapore-MIT Alliance for Research and Technology Centre, Singapore, Singapore.
Derrick YongCritical Analytics for Manufacturing Personalized Medicine (CAMP), Singapore-MIT Alliance for Research and Technology Centre, Singapore, Singapore.
Rohan B H WilliamsCritical Analytics for Manufacturing Personalized Medicine (CAMP), Singapore-MIT Alliance for Research and Technology Centre, Singapore, Singapore.
Stacy L SpringsCritical Analytics for Manufacturing Personalized Medicine (CAMP), Singapore-MIT Alliance for Research and Technology Centre, Singapore, Singapore.
Rajeev J RamCritical Analytics for Manufacturing Personalized Medicine (CAMP), Singapore-MIT Alliance for Research and Technology Centre, Singapore, Singapore. rajeev@mit.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We demonstrate the feasibility of machine-learning aided UV absorbance spectroscopy for in-process microbial contamination detection during cell therapy product (CTP) manufacturing. This method leverages a one-class support vector machine to analyse the absorbance spectra of cell cultures and predict if a sample is sterile or contaminated. This label-free technique provides a rapid output (< 30 minutes) with minimal sample preparation and volume (< 1 mL). Spiking of 7 microbial organisms into mesenchymal stromal cells supernatant aliquots from 6 commercial donors showed that contamination events could be detected at low inoculums of 10 CFUs with mean true positive and negative rates of 92.7% and 77.7% respectively. The true negative rate further improved to 92% after excluding samples from a single donor with anomalously high nicotinic acid. In cells spiked with 10 CFUs of E. coli, contamination was detected at the 21-hour timepoint, demonstrating comparable sensitivity to compendial USP < 71 > test (~ 24 hours). We hypothesize that spectral differences between nicotinic acid and nicotinamide in the UV region are the underlying mechanisms for contamination detection. This approach can be deployed as a preliminary test during different CTP manufacturing stages, for real-time, continuous culture monitoring enabling early detection of microbial contamination, assuring safety of CTP.

Indexed as

Cell- and Tissue-Based TherapyDrug ContaminationMachine LearningEscherichia coliHumansMesenchymal Stem CellsSpectrophotometry, Ultraviolet

Identifiers

PMID40038316
PMCPMC11880552

What OpenQuestion holds

Textmetadata
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.