Evidence map›Paper›PMID 40342498›Full record

ArticleFrontiers in public health2025

Development of real-time PCR methods for quality control detection of pathogenic bacteria in cosmetic preparations.

Veronica Bolzon, Michela Bulfoni, Alessandro Nencioni, Emanuele Nencioni

Abstract read
In one paragraph

Article in Frontiers in public health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Molecular identification ofOpen veterinary journal · 2026
    Article
  3. Article
  4. 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

4 authors.

Veronica BolzonBiofarma Group Srl., Udine, Italy.
Michela BulfoniDepartment of Medicine, University of Udine, Udine, Italy.
Alessandro NencioniIBSA Institut Biochimique SA, Lugano, Switzerland.
Emanuele NencioniBiofarma Group Srl., Udine, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The preservation of microbial safety in cosmetic products is essential for consumer health and requires rapid and accurate detection strategies… Traditional detection methods, such as quantitative and qualitative tests, are effective but often time-consuming and labor-intensive. Moreover, plate count methods fail to detect viable but non-cultivable cells, which remain alive but cannot grow under standard laboratory conditions. To address these limitations, molecular techniques like PCR, particularly real-time PCR (rt-PCR), multiplex rt-PCR, and viability PCR assays, as well as flow cytometry, have enhanced microbiological analysis by improving detection sensitivity, accuracy, and enabling rapid pathogen identification. ISO standards offer guidelines for reliable and consistent microbial detection methods, to guarantee the effectiveness of traditional and molecular techniques in food and cosmetic safety testing. Methods: This study evaluates real-time PCR (rt-PCR) as an alternative to the traditional plate-based method for the detection of Results and discussion: rt-PCR consistently demonstrated superior sensitivity and reliability, particularly in detecting pathogens at low inoculum levels and within complex matrices. For all pathogens, rt-PCR achieved a 100% detection rate across all replicates, reaching the same or superior results than the classical plate method. rt-PCR's ability to directly target DNA overcomes issues related to colony morphology and microbial competition. The study highlights the necessity of standardized rt-PCR protocols aligned with international ISO guidelines to enhance its applicability in routine quality control programs. In conclusion, rt-PCR represents a significant advancement in microbial safety for food and cosmetics, offering a rapid, sensitive, and reliable alternative to conventional methods. By integrating enrichment strategies, rt-PCR ensures higher accuracy in pathogen detection, reinforcing product safety and regulatory compliance in the cosmetics industry.

Indexed as

BacteriaCosmeticsReal-Time Polymerase Chain ReactionCandida albicansEscherichia coliHumansPseudomonas aeruginosaQuality ControlReproducibility of ResultsSensitivity and SpecificityCosmeticscosmeticsDNAISO standardsmethod verificationpathogenic bacteriaquality controlreal-time PCR (rt-PCR)

Identifiers

PMID40342498
PMCPMC12058689

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Registered trials

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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.