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Standard Test Method for Evaluating Growth of Engineered Cartilage Tissue using Magnetic Resonance Imaging
Name übersetzen
NORM herausgegeben am 1.11.2017
Bezeichnung normen: ASTM F3224-17
Ausgabedatum normen: 1.11.2017
SKU: NS-810027
Zahl der Seiten: 10
Gewicht ca.: 30 g (0.07 Pfund)
Land: Amerikanische technische Norm
Kategorie: Technische Normen ASTM
Other standards related to laboratory medicineIT applications in health care technology
Keywords:
biomaterials, cartilage tissue engineering, MRI, MRI assessment of engineered cartilage tissue growth, MRI in tissue engineering, stem cell and regenerative medicine,, ICS Number Code 11.100.99 (Other standards related to laboratory medicine), 35.240.80 (IT applications in health care technology)
Significance and Use |
4.1 Tissue-engineered cartilage is prepared by seeding stem cells or chondrocytes in a three-dimensional biodegradable scaffold under controlled growth conditions. It is expected that the cells will differentiate towards chondrogenic lineage and produce an ample amount of cartilage extracellular matrix proteins, proteoglycans, and collagen type-II. Longitudinal assessment is needed weekly for the first few weeks 4.7.1 The change in calculated relaxation rate, R1.1 This standard is intended as a standard test method for engineered cartilage tissue growth evaluation using MRI. 1.2 This standard is intended for use in the development of tissue engineering regenerative medical products for cartilage damages, such as in knee, hip, or shoulder joints. 1.3 This standard has been prepared for evaluation of engineered cartilage tissue growth at the preclinical stage and summarizes results from tissue growth evaluation of tissue-engineered cartilage in a few notable cases using water spin-spin relaxation time, T2, in vitro and in vivo in small animal models. 1.4 This standard uses the change in mean T1.5 This standard provides a method to remove the scaffold contribution to the tissue growth evaluation. 1.6 Information in this standard is intended to be applicable to most porous natural and synthetic polymers used as a scaffold in engineered cartilage, such as alginate, agarose, collagen, chitosan, and poly-lactic-co-glycolic acid (PLGA). However, some materials (both synthetic and natural) may require unique or varied methods of MRI evaluation that are not covered in this test method. 1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. 1.8 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee. |
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