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Nanostructure of DiR-Loaded Solid Lipid Nanoparticles with Potential Bioimaging Functions

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Abstract

The fluorescence dye-loaded nanoparticles are widely used as bioimaging agents in the field of nanotheranostics. However, the nanoparticles for nanotheranostics usually consist of synthetic materials, such as metal, silica, and organic polymers, which are often biologically incompatible and may arouse toxicity issues. Herein, the potential of near-infrared probe DiR-containing solid lipid nanoparticle suspensions (DiR-SLNS) as the bioimaging agent, which was prepared by lipids and surfactants with excellent biocompatibility, was investigated in this study. The nanostructure of DIR-SLNS system and the distribution of DiR were studied by dissipative particle dynamics (DPD) simulations. The stability of physicochemical properties and fluorescence spectra of DIR-SLNS system were investigated using dynamic laser scattering (DLS), nanoparticle tracking analysis (NTA), and fluorescence spectra. The fluorescence intensity-concentration correlation of DIR-SLNS was also evaluated. As a result, DiR-SLNS demonstrated a “core-shell”-like nanostructure and DiR was mainly distributed in the cetyl palmitate (CP) core rather than the surface of SLNS, which was beneficial to its potential applications in bioimaging. DiR-SLNS exhibited remarkable physicochemical stability as the nanoparticles maintained ~ 90% fluorescence intensity during the 10-day storage time. The correlation between fluorescence intensity and concentration was established and validated using a linear regression model. This study proposed a type of promising candidates in nano-scale with higher safety and fluorescence stability for bioimaging.

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References

  1. Chen HM, Zhang WZ, Zhu GZ, Xie J, Chen XY. Rethinking cancer nanotheranostics. Nat Rev Mater. 2017;2(7).

  2. Trofymchuk K, Valanciunaite J, Andreiuk B, Reisch A, Collot M, Klymchenko AS. BODIPY-loaded polymer nanoparticles: chemical structure of cargo defines leakage from nanocarrier in living cells. J Mater Chem B. 2019;7(34):5199–210.

    Article  CAS  Google Scholar 

  3. Sancho-Albero M, Encabo-Berzosa MD, Beltran-Visiedo M, Fernandez-Messina L, Sebastian V, Sanchez-Madrid F, et al. Efficient encapsulation of theranostic nanoparticles in cell-derived exosomes: leveraging the exosomal biogenesis pathway to obtain hollow gold nanoparticle-hybrids. Nanoscale. 2019;11(40):18825–36.

    Article  CAS  Google Scholar 

  4. Kharin AY, Lysenko VV, Rogov A, Ryabchikov YV, Geloen A, Tishchenko I, et al. Bi-modal nonlinear optical contrast from Si nanoparticles for cancer theranostics. Adv Opt Mater. 2019;7(13).

  5. Sierra-Martin B, Fernandez-Barbero A. Multifunctional hybrid nanogels for theranostic applications. Soft Matter. 2015;11(42):8205–16.

    Article  CAS  Google Scholar 

  6. Carvalho IPS, Miranda MA, Silva LB, Chrysostomo-Massaro TN, Paschoal JAR, Bastos JK, et al. In vitro anticancer activity and physicochemical properties of solanum lycocarpum alkaloidic extract loaded in natural lipid-based nanoparticles. Colloid Interfac Sci. 2019;28:5–14.

    Article  CAS  Google Scholar 

  7. Xie B, Wan J, Chen X, Han W, Wang H. Preclinical evaluation of a cabazitaxel prodrug using nanoparticle delivery for the treatment of taxane-resistant malignancies. Mol Cancer Ther. 2020;19(3):822–34.

    Article  CAS  Google Scholar 

  8. Han Y, Chu XY, Cui L, Fu SY, Gao CS, Li Y, et al. Neuronal mitochondria-targeted therapy for Alzheimer's disease by systemic delivery of resveratrol using dual-modified novel biomimetic nanosystems. Drug Deliv. 2020;27(1):502–18.

    Article  CAS  Google Scholar 

  9. Dal Magro R, Albertini B, Beretta S, Rigolio R, Donzelli E, Chiorazzi A, et al. Artificial apolipoprotein corona enables nanoparticle brain targeting. Nanomed-Nanotechnol Biol Med. 2018;14(2):429–38.

    Article  CAS  Google Scholar 

  10. Wu L, Zhang F, Chen X, Wan J, Wang Y, Li T, et al. Self-assembled gemcitabine Prodrug nanoparticles show enhanced efficacy against patient-derived pancreatic ductal adenocarcinoma. ACS Appl Mater Interfaces. 2020;12(3):3327–40.

    Article  CAS  Google Scholar 

  11. Zhou L, Xie H, Chen X, Wan J, Xu S, Han Y, et al. Dimerization-induced self-assembly of a redox-responsive prodrug into nanoparticles for improved therapeutic index. Acta Biomater. 2020;113:464–77.

    Article  CAS  Google Scholar 

  12. Han W, Shi L, Xie B, Wan J, Ren L, Wang Y, et al. Supramolecular engineering of molecular inhibitors in an adaptive cytotoxic nanoparticle for synergistic cancer therapy. ACS Appl Mater Interfaces. 2020;12(1):1707–20.

    Article  CAS  Google Scholar 

  13. Wan J, Qiao Y, Chen X, Wu J, Zhou L, Zhang J, et al. Structure-guided engineering of cytotoxic cabazitaxel for an adaptive nanoparticle formulation: enhancing the drug safety and therapeutic efficacy. Adv Funct Mater. 2018;28(52):1804229.

    Article  Google Scholar 

  14. Wang H, Zhou L, Xie K, Wu J, Song P, Xie H, et al. Polylactide-tethered prodrugs in polymeric nanoparticles as reliable nanomedicines for the efficient eradication of patient-derived hepatocellular carcinoma. Theranostics. 2018;8(14):3949–63.

    Article  CAS  Google Scholar 

  15. Liu D, Wan B, Qi J, Dong X, Zhao W, Wu W, et al. Permeation into but not across the cornea: bioimaging of intact nanoemulsions and nanosuspensions using aggregation-caused quenching probes. Chin Chem Lett. 2018;29(12):1834–8.

    Article  CAS  Google Scholar 

  16. Zhuang J, Wang D, Li D, Yang Y, Lu Y, Wu W, et al. The influence of nanoparticle shape on bilateral exocytosis from Caco-2 cells. Chin Chem Lett. 2018;29(12):1815–8.

    Article  CAS  Google Scholar 

  17. Huang ZW, Huang Y, Wang WH, Fu FQ, Wang WH, Dang SS, et al. Relationship between particle size and lung retention time of intact solid lipid nanoparticle suspensions after pulmonary delivery. J Control Release. 2020;325:206–22.

    Article  CAS  Google Scholar 

  18. Shi L, Wang Y, Wang Q, Jiang Z, Ren L, Yan Y, et al. Transforming a toxic drug into an efficacious nanomedicine using a lipoprodrug strategy for the treatment of patient-derived melanoma xenografts. J Control Release. 2020;324:289–302.

    Article  CAS  Google Scholar 

  19. Bagde A, Patel K, Kutlehria S, Chowdhury N, Singh M. Formulation of topical ibuprofen solid lipid nanoparticle (SLN) gel using hot melt extrusion technique (HME) and determining its anti-inflammatory strength. Drug Deliv Transl Res. 2019;9(4):816–27.

    Article  CAS  Google Scholar 

  20. Srinivasan RC, Kannisto K, Strom SC, Gramignoli R. Evaluation of different routes of administration and biodistribution of human amnion epithelial cells in mice. Cytotherapy. 2019;21(1):113–24.

    Article  CAS  Google Scholar 

  21. Qi J, Hu X, Dong X, Lu Y, Lu H, Zhao W, et al. Towards more accurate bioimaging of drug nanocarriers: turning aggregation-caused quenching into a useful tool. Adv Drug Deliv Rev. 2019;143:206–25.

    Article  CAS  Google Scholar 

  22. Gao JB, Wang P, Wang ZK, Li CL, Sun SQ, Hu SQ. Self-assembly of DCPD-loaded cross-linked micelle from triblock copolymers and its pH-responsive behavior: a dissipative particle dynamics study. Chem Eng Sci. 2019;195:325–34.

    Article  CAS  Google Scholar 

  23. Tallury SS, Spontak RJ, Pasquinelli MA. Dissipative particle dynamics of triblock copolymer melts: a midblock conformational study at moderate segregation. J Chem Phys. 2014;141(24):244911.

    Article  Google Scholar 

  24. Wang C, Paddison SJ. Mesoscale modeling of hydrated morphologies of sulfonated polysulfone ionomers. Soft Matter. 2014;10(6):819–30.

    Article  CAS  Google Scholar 

  25. Muntimadugu E, Dhommati R, Jain A, Gopala V, Challa S, Shaheen M, et al. Intranasal delivery of nanoparticle encapsulated tarenflurbil: a potential brain targeting strategy for Alzheimer's disease. Eur J Pharm Sci. 2016;92:224–34.

    Article  CAS  Google Scholar 

  26. Maiolo D, Colombo J, Beretta J, Malloggi C, Candiani G, Bombelli FB. The polyplex, protein corona, cell interplay: tips and drawbacks. Colloid Surface B. 2018;168:60–7.

    Article  CAS  Google Scholar 

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Acknowledgments

We are thankful for the financial support from the National Science Foundation of China (Grant No. 81703431 and 81673375).

Funding

This study received financial support from the National Science Foundation of China (Grant No. 81703431 and 81673375).

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Authors and Affiliations

Authors

Contributions

L. Shu performed part of tests and wrote the manuscript. F. Fu analyzed the data and participate in part of experiments. Y. Huang designed the experimental details, check the data and polished the manuscript. P. Hu performed critical reading and helped to improve the language. Z. Huang and X. Pan determined the research framework and supervised the study, manuscript preparation and submission.

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Correspondence to Zhengwei Huang or Xin Pan.

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The authors declare that they have no conflict of interest.

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Lei Shu and Fangqin Fu are regarded as co-first authors.

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Shu, L., Fu, F., Huang, Z. et al. Nanostructure of DiR-Loaded Solid Lipid Nanoparticles with Potential Bioimaging Functions. AAPS PharmSciTech 21, 321 (2020). https://doi.org/10.1208/s12249-020-01847-1

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