International Journal of World Medicine, 2026, 7(1); doi: 10.38007/IJWM.2026.070105.
Zhiyuan Qu
Bioengineering, School of Engineering, Boston, 02120, MA, USA
Advances in nanotechnology and biomedical engineering have significantly enhanced the potential of drug delivery systems for nanomedicines, offering improved drug solubility, extended intracellular residence times, optimized targeting, and controlled release. However, the micron-sized particles and large surface areas of nanomaterials may raise safety concerns, including unpredictable distribution within the body, heightened immune responses, difficulties in degradation and metabolism, and long-term accumulation. This paper reviews the literature and conducts structural analysis to examine various material types, biocompatibility evaluation, and safety factors in nanomedicine drug delivery systems. The results indicate that assessing the safety of such systems requires consideration of aspects such as cytotoxicity, hematological compatibility, immunological compatibility, local tissue response, and in vivo safety. Additionally, factors such as particle size, morphology, surface charge, material composition, administration method, release pattern, and exposure duration also influence safety. Future research should focus on selecting biodegradable materials, modifying surfaces, controlling release processes, and developing standardized evaluation systems to improve the design of nanomedicine delivery systems and enhance safety, stability, and controllability in biomedical applications.
Nanopharmaceutical delivery systems, biocompatibility, safety assessment, biomedical engineering, nanomaterials
Zhiyuan Qu. Biocompatibility Evaluation of Nanomedicine Delivery Systems and Their Safety Research in Biomedical Engineering. International Journal of World Medicine (2026), Vol. 7, Issue 1: 42-51. https://doi.org/10.38007/IJWM.2026.070105.
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