Exploration of Synthesis Pathways for Multifunctional Nanobiomaterials Based on Biomedical Demands
DOI:
https://doi.org/10.61173/keympg60Keywords:
multifunctional nanobiomaterials, biomimetic coating, DNA origami, biocompatibility, targeted delivery, clinical translationAbstract
Recent progress in multifunctional nanobiomaterials has paved novel avenues for precision medicine. These materials enable the integration of targeted delivery, imaging, and therapeutic functionalities within a single system. They include chemical ways like coordination self-assembly and polymerization, biomimetic methods such as cell membrane coating and biotemplate synthesis, and nucleic acid scaffold methods like DNA origami. We evaluate the performance of these methods in physiological environments. For example, carbon nanotubes with branched PEG have a longer blood half-life of about 22.1 hours, while those without PEG last only 5.4 hours. Also, nanocarriers coated with red blood cell membranes exhibit robust immune evasion capabilities in animal models. We discuss how cross-linking, multilayer coating, and dynamic shielding can improve biocompatibility, and how to design materials that respond to outside signals. At the end, we look at problems like reproducibility, scale-up, and clinical translation, and suggest future directions. This review aims to provide a comprehensive overview for the rational design of clinically applicable nanobiomaterials.
References
[1] Kyriakides, T. R., et al. (2021). Biocompatibility of nanomaterials and their immunological responses. Frontiers in Nanotechnology.
[2] Altammar, K. A., et al. (2023). A review on nanoparticles: characteristics, synthesis, and biomimetic approaches. Frontiers in Microbiology.
[3] Low, S. S., et al. (2021). Sonoproduction of nanobiomaterials: a critical review. PMC.
[4] “In situ small-angle X-ray scattering reveals strong condensation of DNA origami during silicification.“ (2022). Journal/ source.
[5] Nagime, P. V., et al. (2024). A comprehensive review of nanomaterials synthesis. Elsevier.
[6] Prencipe, G., Tabakman, S. M., Welsher, K., Liu, Z., Goodwin, A. P., Zhang, L., & Dai, H. (2009). PEG branched polymer for functionalization of nanomaterials with ultralong blood circulation. arXiv.
[7] Haroon, H. B., et al. (2022). A brief history of long circulating nanoparticles. Journal of Colloid and Interface Science.
[8] Mitchell, M. J., et al. (2020). Engineering precision nanoparticles for drug delivery. Nature Reviews Materials. Dean&Francis ISSN 2959-6157
[9] Hoshyar, N., Gray, S., Han, H., & Bao, G. (2016). The effect of nanoparticle size on in vivo pharmacokinetics and cellular interaction. ACS Nano / PMC.
[10] Yusuf, A., et al. (2023). Nanoparticles as drug delivery systems: a review of the biological, physicochemical, and toxicity aspects. MDPI.
[11] Hou, X., Zaks, T., Langer, R., & Dong, Y. (2021). Lipid nanoparticles for mRNA delivery. Nature Reviews Materials.
[12] Yang, R. X., et al. (2022). Big Data in a Nano World: A Review on Computational, Data-Driven Research. ACS Nano.
[13] Noah, N., & Ndangili, P. (2021). Green synthesis of nanomaterials from sustainable materials for biosensors and drug delivery. arXiv.
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2026 by the authors.

This work is licensed under a Creative Commons Attribution 4.0 International License.
