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3D bioprinting is revolutionizing the fields of personalized and precision medicine by enabling the manufacturing of bioartificial implants that recapitulate the structural and functional characteristics of native tissues. However, the lack of quantitative and noninvasive techniques to longitudinally track the function of implants has hampered clinical applications of bioprinted scaffolds. In this study, multimaterial 3D bioprinting, engineered nanoparticles (NPs), and spectral photon-counting computed tomography (PCCT) technologies are integrated for the aim of developing a new precision medicine approach to custom-engineer scaffolds with traceability. Multiple CT-visible hydrogel-based bioinks, containing distinct molecular (iodine and gadolinium) and NP (iodine-loaded liposome, gold, methacrylated gold (AuMA), and Gd O ) contrast agents, are used to bioprint scaffolds with varying geometries at adequate fidelity levels. In vitro release studies, together with printing fidelity, mechanical, and biocompatibility tests identified AuMA and Gd O NPs as optimal reagents to track bioprinted constructs. Spectral PCCT imaging of scaffolds in vitro and subcutaneous implants in mice enabled noninvasive material discrimination and contrast agent quantification. Together, these results establish a novel theranostic platform with high precision, tunability, throughput, and reproducibility and open new prospects for a broad range of applications in the field of precision and personalized regenerative medicine.
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http://dx.doi.org/10.1002/adhm.202302271 | DOI Listing |
Anal Chim Acta
November 2025
Institute of Materials Science, Vietnam Academy of Science and Technology, Hanoi, 10000, Viet Nam. Electronic address:
Background: Recent advancements in cancer therapeutics have catalyzed the development of noninvasive treatment modalities, including the utilization of fluorescent chemotherapeutic agents. These agents offer dual functionality, enabling targeted drug delivery, real-time tumor imaging, and personalized therapy monitoring. Such capabilities are instrumental in the progression toward more precise and effective cancer interventions.
View Article and Find Full Text PDFPhotochem Photobiol
September 2025
Department of Chemistry, Case Western Reserve University, Cleveland, Ohio, USA.
The development of biocompatible organic photosensitizers remains an important challenge for advancing image-guided photodynamic therapy. Specifically, photosensitizers that combine strong photodynamic activity, fluorescence emission for bioimaging, decrease or stop the proliferation of cancer cells, and allow synthetic accessibility are in high demand. Herein, we report the synthesis and characterization of a new class of alloxazine-based photosensitizers (ANOMe, A8OMe and A7OMe).
View Article and Find Full Text PDFActa Oncol
September 2025
Department of Oncology, Copenhagen University Hospital - Herlev and Gentofte, Herlev, Denmark.
Background And Purpose: Photon-counting computed tomography (PCCT) offers enhanced image quality, including improvements in contrast, spatial resolution, and noise reduction. In radiotherapy (RT), optimal image quality is critical for accurate tumor and organ-at-risk delineation. However, reconstruction parameter selection often relies on subjective assessment.
View Article and Find Full Text PDFIEEE Trans Med Imaging
September 2025
Photon-counting computed tomography (PCCT) based on photon-counting detectors (PCDs) represents a cutting-edge CT technology, offering higher spatial resolution, reduced radiation dose, and advanced material decomposition capabilities. Accurately modeling complex and nonlinear PCDs under limited calibration data becomes one of the challenges hindering the widespread accessibility of PCCT. This paper introduces a physics-ASIC architecture-driven deep learning detector model for PCDs.
View Article and Find Full Text PDFRadiographics
October 2025
Mallinckrodt Institute of Radiology, Washington University School of Medicine, 510 S Kingshighway Blvd, CB 8131, St Louis, MO 63110.
CT angiography (CTA) of the aortoiliofemoral (AIF) arteries in the abdomen, pelvis, and lower extremities has become an invaluable tool in assessment of patients with peripheral arterial disease (PAD) and lower extremity trauma. AIF CTA provides rapid and comprehensive assessment of arterial inflow and outflow, guiding management of patients with chronic claudication and those with more acute manifestations, including atherothrombotic occlusion, embolic disease, or thrombosis of prior interventions such as bypass graft or stent placement. Careful attention to technique is critical in performing diagnostic AIF CTA, as pitfalls related to imaging too early or too late relative to the arrival of contrast material in the legs can lead to misdiagnosis or diagnostic uncertainty.
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