AI Article Synopsis

  • - Dermal fibroblasts are essential for skin wound healing, but in diabetic foot ulcers, their migration and proliferation are hindered by harmful substances and inflammation.
  • - A new drug delivery system using magnetic gelatin-hesperidin microrobots was created to enhance fibroblast activity while addressing the issues caused by high glucose levels.
  • - These microrobots showed fast, controllable movement (up to 9.237 μm/s), and effectively released about 78% of the drug in 30 minutes, resulting in improved fibroblast proliferation and migration, making it a promising solution for diabetic wound healing.

Article Abstract

Dermal fibroblasts play a crucial role in the formation of granulation tissue in skin wounds. Consequently, the differentiation, migration, and proliferation of dermal fibroblasts are considered key factors in the skin wound healing process. However, in patients with diabetic foot ulcers, the proliferation and migration of fibroblasts are impaired by reactive oxygen species and inflammatory factors impair. Therefore, a novel magnetic gelatin-hesperidin microrobots drug delivery system was developed using microfluidics. The morphology, motility characteristics, and drug release of the microrobot were assessed, along with its impact on the proliferation and migration of human dermal fibroblasts under high-glucose conditions. Subjected to a rotating magnetic field, the microrobots exhibit precise, controllable, and flexible autonomous motion, achieving a maximum speed of 9.237 μm/s. drug release experiments revealed that approximately 78% of the drug was released within 30 min. It was demonstrated through cellular experiments that the proliferation of human dermal fibroblasts was actively promoted by the nanorobot, the migration ability of fibroblasts in a high-glucose state was enhanced, and good biocompatibility was exhibited. Hence, our study may provide a novel drug delivery system with significant potential for promoting the healing of diabetic foot wounds.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11499193PMC
http://dx.doi.org/10.3389/fchem.2024.1478338DOI Listing

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