Visualization of small lesions in rat cartilage by means of laboratory-based x-ray phase contrast imaging

• Published in: Physics in medicine & biology 2012-12, Vol.57 (24), p.8173-8184
• Main Authors: Marenzana, Massimo, Hagen, Charlotte K, Borges, Patricia Das Neves, Endrizzi, Marco, Szafraniec, Magdalena B, Ignatyev, Konstantin, Olivo, Alessandro
• Format: Article
• Language: English
• Subjects: Animals; cartilage; Cartilage Diseases - diagnostic imaging; Cartilage, Articular - diagnostic imaging; Cost-Benefit Analysis; Laboratories; phase contrast imaging; Rats; Rats, Sprague-Dawley; Tibia - diagnostic imaging; Tomography, X-Ray Computed - economics; Tomography, X-Ray Computed - methods; x-ray imaging
• ISSN: 0031-9155; 1361-6560
• DOI: 10.1088/0031-9155/57/24/8173

Being able to quantitatively assess articular cartilage in three-dimensions (3D) in small rodent animal models, with a simple laboratory set-up, would prove extremely important for the development of pre-clinical research focusing on cartilage pathologies such as osteoarthritis (OA). These models are becoming essential tools for the development of new drugs for OA, a disease affecting up to 1 3 of the population older than 50 years for which there is no cure except prosthetic surgery. However, due to limitations in imaging technology, high-throughput 3D structural imaging has not been achievable in small rodent models, thereby limiting their translational potential and their efficiency as research tools. We show that a simple laboratory system based on coded-aperture x-ray phase contrast imaging (CAXPCi) can correctly visualize the cartilage layer in slices of an excised rat tibia imaged both in air and in saline solution. Moreover, we show that small, surgically induced lesions are also correctly detected by the CAXPCi system, and we support this finding with histopathology examination. Following these successful proof-of-concept results in rat cartilage, we expect that an upgrade of the system to higher resolutions (currently underway) will enable extending the method to the imaging of mouse cartilage as well. From a technological standpoint, by showing the capability of the system to detect cartilage also in water, we demonstrate phase sensitivity comparable to other lab-based phase methods (e.g. grating interferometry). In conclusion, CAXPCi holds a strong potential for being adopted as a routine laboratory tool for non-destructive, high throughput assessment of 3D structural changes in murine articular cartilage, with a possible impact in the field similar to the revolution that conventional microCT brought into bone research.