{"id":31497,"date":"2025-04-15T15:27:46","date_gmt":"2025-04-15T15:27:46","guid":{"rendered":"https:\/\/amelie-project.eu\/?post_type=publication&#038;p=31497"},"modified":"2025-12-17T16:46:58","modified_gmt":"2025-12-17T16:46:58","slug":"des-microspheres-visibles-au-ct-permettent-le-suivi-in-vivo-du-corps-entier-des-echafaudages-injectables-dingenierie-tissulaire","status":"publish","type":"publication","link":"https:\/\/amelie-project.eu\/fr\/publication\/des-microspheres-visibles-au-ct-permettent-le-suivi-in-vivo-du-corps-entier-des-echafaudages-injectables-dingenierie-tissulaire\/","title":{"rendered":"Des microsph\u00e8res visibles par tomodensitom\u00e9trie permettent le suivi in vivo du corps entier des \u00e9chafaudages injectables d'ing\u00e9nierie tissulaire"},"content":{"rendered":"<p>[et_pb_section fb_built=&#8221;1&#8243; admin_label=&#8221;section&#8221; _builder_version=&#8221;4.16&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_row admin_label=&#8221;row&#8221; _builder_version=&#8221;4.21.0&#8243; background_size=&#8221;initial&#8221; background_position=&#8221;top_left&#8221; background_repeat=&#8221;repeat&#8221; width=&#8221;100%&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column type=&#8221;4_4&#8243; _builder_version=&#8221;4.16&#8243; custom_padding=&#8221;|||&#8221; global_colors_info=&#8221;{}&#8221; custom_padding__hover=&#8221;|||&#8221;][et_pb_text admin_label=&#8221;Text&#8221; _builder_version=&#8221;4.21.0&#8243; background_size=&#8221;initial&#8221; background_position=&#8221;top_left&#8221; background_repeat=&#8221;repeat&#8221; global_colors_info=&#8221;{}&#8221;]<!-- divi:paragraph --><\/p>\n<p><strong>Annalisa Bettini, Peter Stephen Patrick, Richard M. Day, Daniel J. Stuckey.<\/strong><\/p>\n<p>Advanced Healthcare Materials. 2024;13(17).<\/p>\n<p><em>Summary<\/em><\/p>\n<p>This study developed tiny sponge-like beads (called microcarriers) that can carry therapeutic cells and, importantly, can be seen clearly on medical imaging scans. The researchers added a harmless contrast material, barium sulphate, so the beads show up on computed tomography (CT) scans after they are injected into the body. This makes it possible for doctors to track where the implanted material goes, how long it stays in place, and whether the transplanted cells remain alive. In laboratory tests and in animal studies, the beads were safe, allowed cells to grow on them, and stayed visible on scans for at least two weeks. The microspheres could also be delivered through minimally invasive injections, including into the heart. Overall, this technology could help improve regenerative therapies by ensuring that implanted cell-carrying scaffolds reach the right location and stay there \u2013 while giving doctors a way to monitor the treatment in real time.<\/p>\n<p><em>Abstract<\/em><\/p>\n<p><span style=\"font-size: 18px;\">Targeted delivery and retention are essential requirements for implantable tissue-engineered products. Non-invasive imaging methods that can confirm location, retention, and biodistribution of transplanted cells attached to implanted tissue engineering scaffolds will be invaluable for the optimization and enhancement of regenerative therapies. To address this need, an injectable tissue engineering scaffold consisting of highly porous microspheres compatible with transplantation of cells is modified to contain the computed tomography (CT) contrast agent barium sulphate (BaSO4). The trackable microspheres show high x-ray absorption, with contrast permitting whole-body tracking. The microspheres are cellularized with GFP+ Luciferase+ mesenchymal stem cells and show in vitro biocompatibility. In vivo, cellularized BaSO4-loaded microspheres are delivered into the hindlimb of mice where they remain viable for 14 days. Co-registration of 3D-bioluminescent imaging and \u00b5CT reconstructions enable the assessment of scaffold material and cell co-localization. The trackable microspheres are also compatible with minimally-invasive delivery by ultrasound-guided transthoracic intramyocardial injections in rats. These findings suggest that BaSO4-loaded microspheres can be used as a novel tool for optimizing delivery techniques and tracking persistence and distribution of implanted scaffold materials. Additionally, the microspheres can be cellularized and have the potential to be developed into an injectable tissue-engineered combination product for cardiac regeneration.<\/span><\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p><!-- \/divi:paragraph --><\/p>\n<p>Access the full paper here:<\/p>\n<p><a href=\"https:\/\/advanced.onlinelibrary.wiley.com\/doi\/full\/10.1002\/adhm.202303588\">https:\/\/advanced.onlinelibrary.wiley.com\/doi\/full\/10.1002\/adhm.202303588<\/a>\u00a0<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p><!-- \/divi:paragraph -->[\/et_pb_text][\/et_pb_column][\/et_pb_row][\/et_pb_section]<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Annalisa Bettini, Peter Stephen Patrick, Richard M. Day, Daniel J. Stuckey. Advanced Healthcare Materials. 2024;13(17). Summary This study developed tiny sponge-like beads (called microcarriers) that can carry therapeutic cells and, importantly, can be seen clearly on medical imaging scans. The researchers added a harmless contrast material, barium sulphate, so the beads show up on computed tomography (CT) scans after they are injected into the body. This makes it possible for doctors to track where the implanted material goes, how long it stays in place, and whether the transplanted cells remain alive. In laboratory tests and in animal studies, the beads were safe, allowed cells to grow on them, and stayed visible on scans for at least two weeks. The microspheres could also be delivered through minimally invasive injections, including into the heart. Overall, this technology could help improve regenerative therapies by ensuring that implanted cell-carrying scaffolds reach the right location and stay there \u2013 while giving doctors a way to monitor the treatment in real time. Abstract Targeted delivery and retention are essential requirements for implantable tissue-engineered products. Non-invasive imaging methods that can confirm location, retention, and biodistribution of transplanted cells attached to implanted tissue engineering scaffolds will be invaluable [&hellip;]<\/p>\n","protected":false},"featured_media":31499,"template":"","meta":{"_et_pb_use_builder":"on","_et_pb_old_content":"<!-- wp:paragraph -->\n<p>Charlotte Desprez, Davide Danovi, Charles H Knowles and Richard M Day.<\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>J. Tissue Eng. 2023;14:1\u201318.<\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p><em>Abstract<\/em><\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>Skeletal muscle-derived cells (SMDC) hold tremendous potential for replenishing dysfunctional muscle lost due to disease or trauma. Current therapeutic usage of SMDC relies on harvesting autologous cells from muscle biopsies that are subsequently expanded in vitro before re-implantation into the patient. Heterogeneity can arise from multiple factors including quality of the starting biopsy, age and comorbidity affecting the processed SMDC. Quality attributes intended for clinical use often focus on minimum levels of myogenic cell marker expression. Such approaches do not evaluate the likelihood of SMDC to differentiate and form myofibres when implanted in vivo, which ultimately determines the likelihood of muscle regeneration. Predicting the therapeutic potency of SMDC in vitro prior to implantation is key to developing successful therapeutics in regenerative medicine and reducing implementation costs. Here, we report on the development of a novel SMDC profiling tool to examine populations of cells in vitro derived from different donors. We developed an image-based pipeline to quantify morphological features and extracted cell shape descriptors. We investigated whether these could predict heterogeneity in the formation of myotubes and correlate with the myogenic fusion index. Several of the early cell shape characteristics were found to negatively correlate with the fusion index. These included total area occupied by cells, area shape, bounding box area, compactness, equivalent diameter, minimum ferret diameter, minor axis length and perimeter of SMDC at 24 h after initiating culture. The information extracted with our approach indicates live cell imaging can detect a range of cell phenotypes based on cell-shape alone and preserving cell integrity could be used to predict propensity to form myotubes in vitro and functional tissue in vivo.<\/p>\n<!-- \/wp:paragraph -->\n\n<!-- wp:paragraph -->\n<p>Access the full paper here:&nbsp;<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/36949843\/\">https:\/\/pubmed.ncbi.nlm.nih.gov\/36949843\/<\/a><\/p>\n<!-- \/wp:paragraph -->","_et_gb_content_width":"","_coblocks_attr":"","_coblocks_dimensions":"","_coblocks_responsive_height":"","_coblocks_accordion_ie_support":"","_links_to":"","_links_to_target":""},"categories":[43],"class_list":["post-31497","publication","type-publication","status-publish","has-post-thumbnail","hentry","category-publication"],"_links":{"self":[{"href":"https:\/\/amelie-project.eu\/fr\/wp-json\/wp\/v2\/publication\/31497","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/amelie-project.eu\/fr\/wp-json\/wp\/v2\/publication"}],"about":[{"href":"https:\/\/amelie-project.eu\/fr\/wp-json\/wp\/v2\/types\/publication"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/amelie-project.eu\/fr\/wp-json\/wp\/v2\/media\/31499"}],"wp:attachment":[{"href":"https:\/\/amelie-project.eu\/fr\/wp-json\/wp\/v2\/media?parent=31497"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/amelie-project.eu\/fr\/wp-json\/wp\/v2\/categories?post=31497"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}