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Janus base nanotubes (JBNTs), also known as Rosette nanotubes, are synthesized from DNA-inspired base molecular monomers and show promise for biomedical applications. However, their clinical translation has been hindered by a lack of comprehensive biocompatibility and biodistribution studies. In this study, we evaluated the in vitro and in vivo biocompatibility of JBNTs and their biodistribution following intravenous and knee intra-articular injections. Within the concentration range of 40 μg/mL, JBNTs supported excellent cell growth with no significant inflammatory response, and even at a concentration of 100 μg/mL, no noticeable erythrocyte hemolysis was observed. In vivo biocompatibility assessment revealed that intravenous injection of 30 μg and 150 μg of JBNTs did not result in significant abnormalities in routine blood tests, inflammatory responses, or organ damage within 7 days. JBNTs were primarily metabolized by the liver and kidneys, with excretion occurring via urine and feces. Notably, we observed that JBNTs extended the retention time of macromolecular substances within the knee joint cavity. While Cy7 alone remained in the joint for approximately 3 days, JBNTs-Cy7 persisted for more than 21 days. This study underscores the safety, efficacy, and transformative potential of JBNTs for clinical applications in targeted drug delivery and tissue regeneration.
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http://dx.doi.org/10.1016/j.ijbiomac.2025.144010 | DOI Listing |
J Control Release
August 2025
Department of Biomedical Engineering, University of Connecticut, Storrs, CT 06269, United States of America. Electronic address:
Various nanomaterials have been developed for drug delivery, but the vast majority are spherical nanoparticles (50-500 nm in diameter). This limits their ability to target and infiltrate hard-to-penetrate tissues, such as certain solid tumors with a dense extracellular matrix (ECM). To investigate how the key physical parameter of shape influences tumor targeting, we developed Janus base nanoparticles (JBNps), a family of rod-shaped delivery vehicles that self-assemble into nanotube bundles with encapsulated drug cargos.
View Article and Find Full Text PDFJ Bone Miner Res
August 2025
Centre for Metabolic Bone Diseases, University of Sheffield, Sheffield, United Kingdom.
The aim of this international meta-analysis was to quantify the predictive value of body mass index (BMI) for incident fracture and relationship of this risk with age, sex, follow-up time and bone mineral density (BMD). 1 667 922 men and women from 32 countries (63 cohorts), followed for a total of 16.0 million person-years were studied.
View Article and Find Full Text PDFAdv Healthc Mater
July 2025
School of Chemistry and Pharmaceutical Engineering, Medical Science and Technology Innovation Center, Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan, Shandong Province, 250117, P. R. China.
Wound dressings equipped with disinfection and wound tissue regeneration capabilities demonstrate significant potential in chronic wound management. However, current multifunctional dressings can rarely accommodate multiple repair processes accurately due to the time-dependent variational wound microenvironment. Herein, a Janus wound dressing is developed based on electrospun nanofibrous scaffold featuring programmed drug release performance and asymmetrical wettability.
View Article and Find Full Text PDFOff-label use of biologic therapies in patients with pediatric inflammatory bowel disease (IBD) has seen an increase in utilization. In this paper, we review the current state of off-label therapies in the pediatric IBD population. Real-world use of ustekinumab (UST), vedolizumab (VDZ), upadacitinib (UPA), tofacitinib, and ozanimod in the adult population could prove positive outcomes in the pediatric population.
View Article and Find Full Text PDFBioact Mater
September 2025
Key Laboratory for Ultrafine Materials of Ministry of Education, Frontiers Science Center for Materiobiology and Dynamic Chemistry, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai, 200237, China.
Corneal transplantation presents an urgent demand for artificial cornea stromal substitutes (ACSs) with comprehensive functional design, spanning from material biology to clinical application. Here, we report the use of an engineering integration strategy to develop Janus ACSs with collagen-based multiscale biomimetic skeletons and tissue-adhesion. Specifically, the electro-assembly of collagen is employed to construct the skeleton of Janus ACS that mimics the microstructure and macroscopic morphology of native corneal stroma, ensuring the desired transparency, refractive power and adaptable shape.
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