| Literature DB >> 28836212 |
João Quintas Coentro1,2, Héctor Capella-Monsonís1,2, Valeria Graceffa1,2, Zhuning Wu1,2, Anne Maria Mullen3, Michael Raghunath4, Dimitrios I Zeugolis5,6.
Abstract
Collagen is the major extracellular protein in mammals. Accurate quantification of collagen is essential in the biomaterials (e.g., reproducible collagen scaffold fabrication), drug discovery (e.g., assessment of collagen in pathophysiologies, such as fibrosis), and tissue engineering (e.g., quantification of cell-synthesized collagen) fields. Although measuring hydroxyproline content is the most widely used method to quantify collagen in biological specimens, the process is very laborious. To this end, the Sircol™ Collagen Assay is widely used due to its inherent simplicity and convenience. However, this method leads to overestimation of collagen content due to the interaction of Sirius red with basic amino acids of non-collagenous proteins. Herein, we describe the addition of an ultrafiltration purification step in the process to accurately determine collagen content in tissues.Entities:
Keywords: Biological specimens; Collagen quantification; Colorimetric assay; Sirius red; Ultrafiltration purification
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Year: 2017 PMID: 28836212 DOI: 10.1007/978-1-4939-7113-8_22
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745