Editorial: Emerging Advances in Bio-Nano Engineered Approaches Toward Intelligent Nanomedicine

Editorial on the Research Topic
Emerging Advances in Bio-Nano Engineered Approaches Toward Intelligent Nanomedicine

In the past two decades, nanomedicine has made tremendous progress in the fields of diagnosis, treatment, and prevention of diseases. With the continuous deepening of the knowledge in nanobiology, nanomedicine has rapidly evolved from the early stage of classic functional nanoparticles (e.g., liposomes, iron oxide nanoparticles, semiconductor/graphene quantum dots, colloidal gold nanoparticles, etc.) to a variety of bio-nano fusion systems with the “intelligent” use of nano-biological effects. This paradigm shift will bring about fundamental changes in drug delivery strategies (Zhang et al., 2018), companion diagnostics (Cai et al., 2018; Liu et al., 2021), synchronous therapy (Shi et al., 2020), as well as in the way of manipulating bio-nano interactions for medical applications (Tao et al., 2019). In this Research Topic, we present six representative original articles highlighting the recent research advances in design and concepts of novel bio-nano engineered approaches that cover multiple applications, including polymer-lipid hybrid nanovaccine for anti-tumor therapy, differently charged super-paramagnetic iron oxide nanoparticles (SPIONs) for M2 to M1 macrophages polarization, immuno-inert nanoMOFs for cancer therapy, self-driven photodynamic therapy (PDT), exosomes-based osteoporosis therapy, and nanomedicine for chronic pain relief.

Wang et al. described an effective prophylactic anti-cancer nanovaccine approached by co-encapsulation of lipidated TLR7/8 agonists and ovalbumin-derived peptide (SIINFEKL) in core-shell polymer–lipid hybrid nanoparticles (PLNs). This research attempts to address the major limitations of conventional vaccine formulation, including the poor tolerability profile of adjuvants, instability of peptide antigens, insufficient cellular uptake, rapid diffusion from post-injection, and systemic adverse effects. They have demonstrated that lipidation of adjuvant and peptide epitope following PLN encapsulation can largely improve anti-tumor immune responses and achieve desired in vivo prophylactic efficacy. In comparison to aluminum-contained vaccine formulation, PLN vaccine exhibited minimally systemic exposure, enhanced encapsulation efficacy, persistent antigen-presenting cellular uptake, and prolonged immune surveillance effect. The integration of lipidation modification and the PLN approach developed by the authors could be an important concept to direct the future success of anti-cancer nanovaccines.

Understanding the interactions between biological systems and nanoscale entities play a crucial role in the development of the biomedical application of nanomedicine (Liu et al., 2021). In this research topic, Zhang et al. presented a hypothesis that differently charged SPIONs would exhibit variable abilities to induce the conversion of the macrophage phenotype. The authors designed three different charged SPIONs (i.e., S+ positive, SN neutral, and S– negative) and investigated their intrinsic re-polarization effect on tumor-associated macrophages (TAMs), as well as their influence on tumor growth rate. They found that both S+ and S– could effectively reprogram TAMs from an M2 to an M1 phenotype at cellular level. This is possibly due to their high cellular uptake. To further study the in vivo antitumor activity, the authors co-injected the TAMs (pre-treated with SPIONs) with the tumor cells to establish a tumor xenograft. The tumor growth was significantly attenuated by S+ and S–, but S– exhibited enhanced cytotoxicity at higher concentrations. They concluded that S+ may be considered for further clinical anti-tumoral evaluation.

In another original work, Li et al. designed a “stealth” nanoMOFs for safe and efficient anti-cancer therapy. They engineered the MIL-100(Fe) nanoMOF via a step approach. Initially, the drug molecules (Gem-MP) were loaded into the pores and on the surfaces of the nanoMOF through the impregnation in aqueous solutions; then, the Gem-MP-loaded nanoMOF was further modified by the surface coating of DOPC and DSPE-PEG 2000 in alcoholic solution. This work showed that the PEGylation of drug-loaded MIL-100(Fe) can not only influence the drug release rate but also regulate the degradation process. The authors showed that PEGylation of NanoMOFs can significantly reduce the human serum albumin adsorption, macrophage uptake, and exhibited notable in vitro anticancer activity. However, a further in vivo study is encouraged to explore their therapeutic potential.

In a review article, Xie et al. highlighted the important role of exosomes in the pathogenesis of age-related osteoporosis. They initially introduced the basic characteristics of exosomes, followed by the discussion of regulatory pathways in mesenchymal stem cells (MSCs) differentiation mediated by exosomes. Then, they summarized the recent findings regarding osteoblast proliferation and osteoclastogenesis effects stimulated by exosomes. They also pointed out the negative regulatory effects of exosomes on osteoclast differentiation. In the end, the authors commented on the opportunities and challenges of clinical translation on utilizing exosomes for treating osteoporosis. In another mini-review, Chen et al. briefly introduced the latest nanotechnological approaches for managing chronic pain. The application of Liposomes, PLGA nanoparticles, carbon-based, and other inorganic nanomaterials for the targeted/non-targeted neuropathic pain relief were highlighted. Moreover, the authors provided a detailed discussion in considerations of nanomaterial design for chronic pain relief and exemplified future strategies that can be explored, such as oral, inhalation, sprayable nanomaterials, electrical stimulation, microneedles, targeted delivery, etc. In another mini-review, Blum et al. introduced the concept of self-exciting photodynamic therapy (auto-PDT) to overcome the major limitation of conventional PDT, which is the insufficient tissue penetration depth of light. The auto-PDT nanoplatforms can drive the PDT process without the presence of an external light source. However, these platforms are usually designed in response to oxidative chemical excitation in the manner of chemiluminescence or Cherenkov luminescence (radiological excitation). The authors critically reviewed the design strategies, mechanisms of excitation, and the therapeutic effect of auto-PDT nanoplatforms with state-of-the-art researches. In addition, the authors also provided a detailed discussion of the recent studies of auto-PDT nanotherapeutics concerning design strategy, challenges, and themes in their synthesis and application.

Overall, this collection of articles contributes to the research topic with innovative designs and concepts in intelligent nanomedicine. The bio-nano engineered approach is not only the key strategy to overcome the intrinsic limitations of nanomaterials but also opening doors to new opportunities for patients. The fast pace and emerging breakthroughs in bio-nanotechnology will motivate and inspire both research and industry to accelerate these interdisciplinary translations to clinical applications.

Author Contributions

All authors listed have made a substantial, direct and intellectual contribution to the work, and approved it for publication.

Funding

This work was financially supported in part by the National Natural Science Foundation of China (82001887, 81925019, and U1705281), the Major State Basic Research Development Program of China (2017YFA0205201), and the Program for New Century Excellent Talents in University, China (NCET-13-0502). JW was also supported by a grant from the Hundred Talents Program (75110-18841227) from Sun Yat-sen University and the Guangdong Basic and Applied Basic Research Foundation (2019A1515110326).

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

We thank the support of the National Natural Science Foundation of China.

References

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