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The Chick Chorioallantoic Membrane In Vivo Model to Assess Perineural Invasion in Head and Neck Cancer
Published on: June 21, 2019
The gelatin sponge-chorioallantoic membrane assay.
Domenico Ribatti1, Beatrice Nico, Angelo Vacca
1Department of Human Anatomy and Histology, University of Bari Medical School, Piazza Giulio Cesare 11, Policlinico, 70124 Bari, Italy. ribatti@anatomia.uniba.it
This study introduces a simple, cost-effective method to quantify angiogenesis and antiangiogenesis using a gelatin sponge on the chick embryo chorioallantoic membrane (CAM). This technique is suitable for large-scale screening of blood vessel formation.
Area of Science:
- Vascular Biology
- Developmental Biology
- Pharmacology
Background:
- Angiogenesis, the formation of new blood vessels, is crucial for development and disease.
- Quantifying angiogenesis and antiangiogenesis is essential for drug discovery and understanding vascular diseases.
- Existing methods may have limitations in terms of cost, complexity, or scalability.
Purpose of the Study:
- To present a novel method for quantifying angiogenesis and antiangiogenesis.
- To establish a simple, inexpensive, and scalable assay using the chick embryo chorioallantoic membrane (CAM).
Main Methods:
- Implantation of a gelatin sponge onto the CAM of chick embryos on day 8.
- Treatment of the sponge with angiogenesis stimulators and/or inhibitors.
- Macroscopic and microscopic quantification of blood vessel growth into the sponge on day 12.
Main Results:
- The gelatin sponge-CAM assay allows for the quantification of both pro-angiogenic and anti-angiogenic effects.
- The assay is estimated to take 10 days to complete.
- While requiring careful analysis to distinguish new from existing vessels, the method is suitable for large-scale screening.
Conclusions:
- The gelatin sponge-CAM assay provides a practical and economical approach for studying angiogenesis and antiangiogenesis.
- This method is advantageous for high-throughput screening in drug discovery and research.
- It offers a valuable alternative to other angiogenesis assays, despite some analytical considerations.
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