Evidence map›Paper›PMID 42375310›Full record

ArticleOpen veterinary journal2026

Optimization and validation of the real-time polymerase chain reaction protocol for porcine gelatin detection in processed food and cosmetic products.

Rumiyati Rumiyati, Miftiana Nugraha Sari, Hazza' Hammam Nawwaruddin, Marlyn Dian Laksitorini, Abdul Rohman

Abstract readValidation Study
In one paragraph

Article in Open veterinary journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Rumiyati RumiyatiFaculty of Pharmacy, Universitas Gadjah Mada, Yogyakarta, Indonesia.
Miftiana Nugraha SariFaculty of Pharmacy, Universitas Gadjah Mada, Yogyakarta, Indonesia.
Hazza' Hammam NawwaruddinFaculty of Pharmacy, Universitas Gadjah Mada, Yogyakarta, Indonesia.
Marlyn Dian LaksitoriniFaculty of Pharmacy, Universitas Gadjah Mada, Yogyakarta, Indonesia.
Abdul RohmanFaculty of Pharmacy, Universitas Gadjah Mada, Yogyakarta, Indonesia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Processed food and cosmetic products are integral to modern life, and technological advances have enabled the creation of increasingly complex formulations. Many of these products contain animal-derived ingredients, such as gelatin, whose source must be verified due to religious, health, and ethical concerns. Porcine is one of the primary sources of gelatin production, which has become a major concern. Its detection in complex matrices, such as processed food and cosmetics, is challenging, as gelatin itself undergoes extensive production processes. Real-time polymerase chain reaction (PCR) is widely recognized as one of the analytical methods of choice for species determination; however, its application to gelatin source identification in complex samples remains limited. Aim: This study aimed to develop and optimize a real-time PCR protocol for identifying porcine gelatin contamination in highly processed matrix samples (processed foods and cosmetics) for halal authentication. Methods: This study was established through the following steps: DNA extraction, post-isolation DNA analysis, annealing temperature and primer concentration optimization, specificity assay, amplification efficiency trial, sensitivity test, repeatability examination, and marketed sample analysis. Results: The developed method demonstrated good specificity under optimized conditions (annealing temperature of 58.4°C and primer concentration of 0.2 µM). It achieved a good amplification efficiency of 101.2% with an Conclusion: The real-time PCR method meets the validation criteria for qualitative analysis, including specificity, amplification efficiency, sensitivity, and repeatability. This method provides a valuable foundation for advancing halal authentication, particularly for detecting porcine gelatin contamination in processed food and cosmetic products.

Indexed as

CosmeticsFood ContaminationGelatinReal-Time Polymerase Chain ReactionAnimalsReproducibility of ResultsSensitivity and SpecificitySwineCosmeticsGelatinCosmeticHalalProcessed foodReal-time PCR

Identifiers

PMID42375310
PMCPMC13313944

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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.