4.7 Review

Designing Functional Bionanoconstructs for Effective In Vivo Targeting

期刊

BIOCONJUGATE CHEMISTRY
卷 33, 期 3, 页码 429-443

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.bioconjchem.1c00546

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资金

  1. Science Foundation Ireland [17/NSFC/4898, 17/ERCD/4962, 15/SIRG/3423, 16/ENM-ERA/3457]
  2. Irish Research Council [GOIPD/2020/434]
  3. Celtic Advanced Life Science Innovation Network (CALIN), an Ireland-Wales INTERREG project
  4. European Regional Development Fund through the Welsh Government [80885]
  5. Chinese Scholarship Council [201806220054]
  6. Science Foundation Ireland (SFI) [17/ERCD/4962, 17/NSFC/4898, 16/ENM-ERA/3457, 15/SIRG/3423] Funding Source: Science Foundation Ireland (SFI)

向作者/读者索取更多资源

This review discusses the fundamental obstacles in designing successful bionanoconstructs and emphasizes the importance of surface architecture and thorough characterization of engineered bionanoconstructs, as well as the significance of population heterogeneity in interpreting in vitro and in vivo results.
The progress achieved over the last three decades in the field of bioconjugation has enabled the preparation of sophisticated nanomaterial-biomolecule conjugates, referred to herein as bionanoconstructs, for a multitude of applications including biosensing, diagnostics, and therapeutics. However, the development of bionanoconstructs for the active targeting of cells and cellular compartments, both in vitro and in vivo, is challenged by the lack of understanding of the mechanisms governing nanoscale recognition. In this review, we highlight fundamental obstacles in designing a successful bionanoconstruct, considering findings in the field of bionanointeractions. We argue that the biological recognition of bionanoconstructs is modulated not only by their molecular composition but also by the collective architecture presented upon their surface, and we discuss fundamental aspects of this surface architecture that are central to successful recognition, such as the mode of biomolecule conjugation and nanomaterial passivation. We also emphasize the need for thorough characterization of engineered bionanoconstructs and highlight the significance of population heterogeneity, which too presents a in the interpretation of in vitro and in vivo results. Consideration of such issues together will better define bioconjugation, in the future, will deliver functional and clinically relevant bionanoconstructs.

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