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Updated: Apr 12, 2026

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Alternative Developmental Toxicity Screening Methods Using Chick Embryo-Based Models.

Jeong Hwan Kim1, Cheoljin Park1, Donghee Kim1

  • 1Laboratory Animal Medicine, College of Veterinary Medicine, Chungnam National University, Daejeon, Republic of Korea.

Journal of Applied Toxicology : JAT
|April 10, 2026
PubMed
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Chick embryo models offer a cost-effective and ethically considerate alternative for developmental toxicity studies. These models can supplement traditional animal testing and bridge the gap between in vitro and in vivo research.

Area of Science:

  • Toxicology
  • Developmental Biology
  • Animal Alternatives

Background:

  • Nonclinical developmental toxicity studies assess drug/chemical effects on embryonic and fetal development.
  • Current mammalian models (rats, rabbits) face ethical concerns, high costs, and lengthy durations.
  • Existing alternatives (cell cultures, organoids, zebrafish) struggle with whole-body physiological complexity.

Purpose of the Study:

  • To review chick embryo-based models for developmental toxicity screening.
  • To evaluate their potential to overcome limitations of other alternative models.
  • To discuss advantages, limitations, and future directions.

Main Methods:

  • Literature review of chick embryo applications in developmental toxicity.
  • Analysis of chick embryo models' developmental relevance, cost-effectiveness, and ethical aspects.
Keywords:
3Rsfertilized eggnonclinical developmental toxicityrelative replacement

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  • Comparison with mammalian and other alternative models.
  • Main Results:

    • Chick embryos have demonstrated utility in cardiovascular development, cancer, and vaccine research.
    • Advantages include developmental relevance, cost-efficiency, and ethical benefits.
    • Limitations involve challenges in replicating whole-body homeostasis and the need for protocol standardization.

    Conclusions:

    • Chick embryo models show promise as a complementary approach to mammalian studies.
    • They can bridge the gap between in vitro and in vivo research systems.
    • Further standardization, validation, and technological integration are crucial for practical application.