98%
921
2 minutes
20
Microfabricated devices have been introduced as a promising approach to overcome some of the challenges related to oral administration of drugs and, thereby, improve their oral bioavailability. In this study, we fabricate biodegradable microcontainers with different polymers, namely poly-ɛ-caprolactone (PCL), poly(lactic-co-glycolic acid) (PLGA) 50:50 and PLGA 75:25 by hot punching. The mucoadhesion of the microcontainers is assessed with an retention model on porcine intestinal tissue. Finally, degradation studies of the biodegradable microcontainers are completed for six weeks in simulated intestinal medium with the addition of pancreatic enzymes. Through SEM inspection, the PLGA 50:50 microcontainers show the first signs of degradation already after two weeks and complete degradation within four weeks, while the other polymers slowly degrade in the medium over several weeks.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6918296 | PMC |
http://dx.doi.org/10.3390/polym11111828 | DOI Listing |
Acta Biotheor
July 2025
Life Sciences Center, Institute of Biochemistry, Vilnius University, Saulėtekio al. 7, LT-10257, Vilnius, Lithuania.
This paper deals with the computational modelling of the bioluminescence pattern formation in suspensions of luminous Escherichia coli bacteria. The aim of this work is to improve the reaction-diffusion-chemotaxis model by introducing modulation functions applied to the rates of the bacterial growth, the chemoattractant production and the oxygen consumption as well as to investigate the influence of the function form on the spatiotemporal pattern formation in an E. coli colony.
View Article and Find Full Text PDFACS Nano
July 2025
Central European Institute of Technology, Brno University of Technology, Purkyňova 123, Brno 61200, Czech Republic.
Inspired by Richard Feynman's 1959 lecture and the 1966 film , the field of micro/nanorobots has evolved from science fiction to reality, with significant advancements in biomedical and environmental applications. Despite the rapid progress, the deployment of functional micro/nanorobots remains limited. This review of the technology roadmap identifies key challenges hindering their widespread use, focusing on propulsion mechanisms, fundamental theoretical aspects, collective behavior, material design, and embodied intelligence.
View Article and Find Full Text PDFAnal Chem
April 2025
Center for Intelligent Drug Delivery and Sensing Using Microcontainers and Nanomechanics (IDUN), Department of Health Technology, Technical University of Denmark, Lyngby, Kongens 2800, Denmark.
Infections are the leading causes of death, especially in intensive care units (ICUs), necessitating immediate and optimal antibiotic treatment with proper monitoring of the drug dosage. Present analytical techniques measuring antibiotic levels result in a long lag time for dose adjustments. Therefore, introducing versatile techniques that quickly quantify antibiotic levels in a patient's blood is essential.
View Article and Find Full Text PDFGigascience
January 2024
Department of Health Technology, Technical University of Denmark, Kongens Lyngby 2800, Denmark.
Background: Corneocyte surface nanoscale topography (nanotexture) has recently emerged as a potential biomarker for inflammatory skin diseases, such as atopic dermatitis (AD). This assessment method involves quantifying circular nano-size objects (CNOs) in corneocyte nanotexture images, enabling noninvasive analysis via stratum corneum (SC) tape stripping. Current approaches for identifying CNOs rely on computer vision techniques with specific geometric criteria, resulting in inaccuracies due to the susceptibility of nano-imaging techniques to environmental noise and structural occlusion on the corneocyte.
View Article and Find Full Text PDFPLoS Pathog
December 2024
Department of Biotechnology and Biomedicine, Technical University of Denmark, Kgs. Lyngby, Denmark.
Evolution of the highly successful and multidrug resistant clone ST111 in Pseudomonas aeruginosa involves serotype switching from O-antigen O4 to O12. How expression of a different O-antigen serotype alters pathogen physiology to enable global dissemination of this high-risk clone-type is not understood. Here, we engineered isogenic laboratory and clinical P.
View Article and Find Full Text PDF