Next Article in Journal
Array of Resonant Electromechanical Nanosystems: A Technological Breakthrough for Uncooled Infrared Imaging
Next Article in Special Issue
Quantification and Imaging of Antigens on Cell Surface with Lipid-Encapsulated Fluorescent Nanodiamonds
Previous Article in Journal
On-Chip Asymmetric Microsupercapacitors Combining Reduced Graphene Oxide and Manganese Oxide for High Energy-Power Tradeoff
Previous Article in Special Issue
The Design and Positioning Method of a Flexible Zoom Artificial Compound Eye
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Micromachines
Volume 9
Issue 8
10.3390/mi9080400
micromachines-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Core-Shell Structures of Upconversion Nanocrystals Coated with Silica for Near Infrared Light Enabled Optical Imaging of Cancer Cells

by
Kumbam Lingeshwar Reddy
1,
Neeraj Prabhakar
2,
Jessica M. Rosenholm
2,* and
Venkata Krishnan
1,*
1
School of Basic Sciences and Advanced Materials Research Center, Indian Institute of Technology Mandi, Kamand, Mandi 175005, Himachal Pradesh, India
2
Pharmaceutical Sciences Laboratory, Faculty of Sciences and Engineering, Åbo Akademi University, 20520 Turku, Finland
*
Authors to whom correspondence should be addressed.
Micromachines 2018, 9(8), 400; https://doi.org/10.3390/mi9080400
Submission received: 3 July 2018 / Revised: 8 August 2018 / Accepted: 9 August 2018 / Published: 14 August 2018
(This article belongs to the Special Issue Nanostructures for Bioimaging)
Browse Figures
Versions Notes

Abstract

:
Optical imaging of cancer cells using near infrared (NIR) light is currently an active area of research, as this spectral region directly corresponds to the therapeutic window of biological tissues. Upconversion nanocrystals are photostable alternatives to conventional fluorophores. In our work, we have prepared upconversion nanocrystals of NaYF4:Yb/Er and encapsulated them in silica to form core-shell structures. The as-prepared core-shell nanostructures have been characterized for their structure, morphology, and optical properties using X-ray diffraction, transmission electron microscopy coupled with elemental mapping, and upconversion luminescence spectroscopy, respectively. The cytotoxicity examined using cell viability assay indicated a low level of toxicity of these core-shell nanostructures. Finally, these core-shell nanostructures have been utilized as photostable probes for NIR light enabled optical imaging of human breast cancer cells. This work paves the way for the development of advanced photostable, biocompatible, low-toxic core-shell nanostructures for potential optical imaging of biological cells and tissues.

1. Introduction

Optical imaging is a useful technique to visualize the structural and functional evolution of biological materials with negligible invasion, and without disturbing the usual metabolic activities [1,2,3]. Luminescent labels are required for optical imaging of biological materials, since most biomolecules do not have measurable fluorescent signals [4,5,6]. In biomedical research there is an enormous demand for fluorescent probes which emit light at particular wavelengths and can be detected under in vivo and in vitro conditions through fluorescence microscopy [7,8]. Despite sensitivity and other benefits, traditional fluorescent molecular probes have a number of limitations, such as low penetration depth of excitation light, high toxicity due to the longer exposure needed at shorter wavelengths, auto-fluorescence and strong light scattering from biological tissues that cause low signal to noise ratio (SNR), and photo-bleaching [9,10]. These undesirable properties of conventional organic fluorophores motivate researchers to look for alternatives in luminescent materials, such as quantum dots, carbon-based nanostructures (e.g., nanodiamonds, carbon dots), and upconverting phosphors. For instance, near infrared (NIR) active inorganic luminescent materials can potentially overcome the limitations of traditional fluorescent molecular probes [11].
In recent years, different research groups have prepared NIR active luminescent nanoparticles and efficiently used them for optical imaging; amongst these, considerable attention has been devoted to upconversion luminescent nanomaterials [12,13,14]. Compared to the emitted light, longer wavelength excitation is required for upconversion photoluminescence. Since this process is quite opposite to Stokes-shift, it is also called anti-Stokes shift [15]. Lately, much interest has especially been directed to lanthanide doped upconversion nanocrystals (UCNC) [16]. Though UCNC have low quantum yield, these nanocrystals have numerous outstanding abilities, for instance: Long Stokes-shift, sharp absorption and emission peaks, extended lifetimes, excessive photostability, no interference with the auto-fluorescence of biological tissues, and minimal photo-toxicity towards biological tissues [17,18,19,20,21,22,23]. The abovementioned advantages make UCNC a fascinating material for most of the applications in various fields including biomedicine [24,25,26]. A further advantage of UCNC is that they can be used as constructs for the easy preparation of bioprobes for imaging applications [27,28,29,30].
Synthesis of monodispersed, single crystal, high quality nanocrystals (NC) with pure crystal phase and well-defined shapes is of utmost importance for successful biomedical applications such as bioimaging, drug delivery, photodynamic therapy, biosensing, etc. [19,31,32,33,34,35,36]. Most of the commonly used UCNC synthesis procedures, such as thermal decomposition [37], high temperature co-precipitation [38,39], solvo/hydrothermal [40], co-precipitation [41], sol-gel methods [42], combustion synthesis [43], microemulsion [44], electrospinning [45], flaming synthesis [46], and microwave synthesis [47], produce hydrophobic surfaced nanostructures. Compared to the abovementioned methods, microwave assisted synthesis procedures are relatively quick, eco-friendly, and energy efficient. Few works have been reported on the preparation of UCNC with microwave assisted technique, for example, the ionic liquid based route was introduced by Chen et al. for the preparation of NaYF4:Yb/Er UCNC with microwave assistance [48]. Wang et al. used air sensitive precursors (such as trifluoroacetates) for the synthesis of Er, Yb doped NaYF4 NC [49].
One of the essential requirements to make use of nanoparticles in biological environments is that the nanoparticles should have a hydrophilic surface [50]. Therefore, a huge variety of surface alteration approaches, such as addition of hydrophilic layers on and/or chemical modification of the surface, have been developed to convert hydrophobic surfaces into hydrophilic surfaces [51,52,53,54]. Among the several methods, growth of a silica shell on UCNC has attracted great interest since they exhibit low cytotoxicity and their chemically active surface can be easily modified to introduce various functional groups, which can satisfy the needs of conjugating biological molecules or functional nanoparticles [55]. Despite the progress achieved in this field, there is still scope for improvement with regard to the synthesis strategies employed for the preparation of upconversion nanostructures, such as post-synthesis surface modification strategies to tune the wettability and consequently biocompatibility, stability, and dispersability behavior of the nanoparticles and in examining the uptake of the nanoparticles by cells for optical imaging applications. Keeping these points in mind, in the present work, we have prepared core-shell nanostructures of lanthanide doped upconversion nanocrystals coated with silica. Silica coatings are a commonly applied strategy to enhance the dispersability of nanoparticles in biological or physiological environments, due to the inherent hydrophobicity of most other inorganic nanoparticles [56]. Deposition of a silica coating further endows the core material (in this case the UCNC) with enhanced colloidal, chemical, photo-, and thermal stability, provides controlled porosity and surface chemistry, easy processing of both coating and any further surface functionalizations, and is optically transparent [57]. The as-prepared core-shell nanostructures have been examined for their cytocompatibility, after which they have been used for cellular labeling and finally utilized as photostable probes for NIR light enabled optical imaging of human breast cancer cells. We anticipate that this work will pave the way for the development of several advanced photostable and biocompatible core-shell nanostructures not only for optical imaging, but also for several other technological applications.

2. Materials and Methods

2.1. Materials

Yttrium trichloride hexahydrate (YCl3·6H2O), ytterbium trichloride hexahydrate (YbCl3·6H2O), erbium trichloride hexahydrate (ErCl3·6H2O), sodium hydroxide (NaOH), ammonium fluoride (NH4F), acetic acid, ethanol, dimethyl sulfoxide (DMSO), 4′,6-diamidino-2-phenylindole (DAPI), TritonX-100, tetraethyl orthosilicate (TEOS), (3-aminopropyl)triethoxysilane (APTES), 2-(4-iodophenyl)-3-(4-nitrophenyl)-5-(2,4-disulfophenyl)-2H-tetrazolium, monosodium salt (WST-1), and ammonium hydroxide (NH4OH) were procured from Sigma-Aldrich, India. All the chemicals received from the vendor were used as they were, without any extra purification. All the experiments were performed with Milli-Q (18.2 MΩ-cm) water.

2.2. Synthesis

2.2.1. NaYF4:Yb/Er Nanocrystals

Lanthanide (Yb and Er) doped NaYF4 nanocrystals were prepared through a microwave assisted synthesis route as earlier reported by our group [58]. In the typical synthesis procedure, YCl3 (0.8 mmol), YbCl3 (0.18 mmol) and ErCl3 (0.02 mmol) were mixed with a solution mixture of 8 mL of ethanol (EtOH), NaOH (7.5 mmol) dissolved in 2 mL of water, 2 mL acetic acid (AcOH) under constant magnetic stirring at room temperature (RT). Lastly, 2 mL water containing 4 mmol of NH4F was added drop wise to the above solution mixture. After 30 min of stirring at room temperature, the entire reaction mixture was moved to a microwave reaction vessel (20 mL) and tightly sealed to heat for 3 h at 150 °C with continuous stirring of 600 rpm. Then the complete system was allowed to cool to 40 °C. Last, of all, the products were rinsed with ethanol and water (7:3 v/v) mixture three times and collected through centrifugation to eliminate any unreacted leftover precursors. Then the UCNC were dried in vacuum at 60 °C.

2.2.2. UCNC@SiO2 Core-Shell Nanostructures

UCNC@SiO2 core-shell nanostructures synthesis was carried out as per a previous report with some modifications [59]. In brief, 20 mg of UCNC were properly dispersed in 20 mL ethanol and 2 mL of TritonX-100 was added to the above solution while stirring. Stirring was continued for 30 min, then 0.42 mL of NH4OH was added and allowed to stir for another 30 min. Lastly, 0.051 mL of tetraethyl orthosilicate (TEOS) was added and allowed it to stir for 6 h. Then silica coated UCNC core-shell nanostructures were collected through centrifugation. Finally, the obtained core-shell nanostructures were dispersed in ethanol and kept at 4 °C in refrigerator for future use.

2.3. Instrumentation

NaYF4:Yb/Er UCNC synthesis was done by using Anton Paar Monowave 300′ microwave synthesizer (New Delhi, India). For the collection of powder X-ray diffraction data, Rigaku Smart Lab 9 KW powder X-ray diffractometer (PXRD, New Delhi, India) was used. The transmission electron microscope (TEM) of FEI Tecnai G2 20 S-twin (New Delhi, India) operating at 200 kV was used to acquire the morphology of the nanostructures. Energy dispersive X-ray analysis (EDAX) and elemental mapping were also performed using the same TEM instrument. For upconversion luminescence (UCL) measurements, 980 nm laser diode (CW, 500 mW, purchased from Optochem International, New Delhi, India) equipped Cary Eclipse fluorescence spectrophotometer was used. For UCL measurements, 1 mg of samples (UCNC and UCNC@SiO2) was dispersed in 1 mL of Milli-Q water, followed by 5 min of sonication. Subsequently, the sample was transferred to a 1 mL cuvette and measurements were performed. Leica SP5 STED/MP microscope (New Delhi, India) was used for cell imaging, wherein for excitation, a Ti:sapphire femtosecond pulse laser (Chameleon Ulta, Coherent Inc., Santa Clara, CA, USA) at 980 nm was used. In this case, a standard PMT detector and a 63× oil immersion objective (Leica) was used for imaging the cells.

2.4. Cell Viability Assessment

2-(4-iodophenyl)-3-(4-nitrophenyl)-5-(2,4-disulfophenyl)-2H-tetrazolium monosodium salt (WST-1) cell viability assay was used to measure cell toxicity. MDA-MB-231, Human breast cancer cells, were developed in a 96 well microplate (7000 cells/well) in cell growth medium (DMEM) and then incubated at 37 °C, 5% CO2 for 24 h. From each well, the growth medium was replaced with the addition of UCNC and UCNC@SiO2, which was prepared in 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid) (HEPES) buffer (pH 7.4). Next, 5, 10, 25 µg mL−1 concentration of particles were added to the cell media and incubated for 48 h. Then 10 µL of WST-1 was added to each well and incubated again for 2 h at 37 °C, 5% CO2. After the incubation, the 96 well plate was read by a Varioskan Flash Multimode Reader (Thermo Scientific Inc., Waltham, MA, USA) to get the absorbance at 440 nm. Averaged absorbance readings were plotted and the viable cells were correlated with the absorbance of each concentration of particles.

2.5. Cancer Cell Imaging

The MDA-MB-231 cells were plated over glass coverslips using cell media (DMEM) at 5% CO2 and 37 °C. Cells (7 × 104 cells mL−1) were placed on a fresh coverslip and left to stick for 24 h. Later the cells were cleaned with phosphate buffer solution (PBS) then incubated with UCNC and UCNC@SiO2 (5 µg mL−1 dispersed in DMEM) for 48 h at 5% CO2 and 37 °C. Then 4% paraformaldehyde was used to fix the cells and cell sample was mounted using VECTASHIELD® with DAPI for optical microscopy. TCS SP5 MP (Multi-photon, Leica microsystems), HyD detectors, 100× (HCX PL APO CS 100.0×/1.40 OIL) oil objective and LASAF software (Leica application suite) consisting multi-photon microscopy setup was used for imaging. For excitation, Ti-sapphire femtosecond pulse at 980 nm (1.07 W) was used while performing multi-photon microscopy. The green and red emissions were collected in 520–570 nm and 630–680 nm, respectively.

3. Results and Discussion

The synthesis of UCNC@SiO2 and their application in cancer cell imaging is schematically demonstrated in Scheme 1.
To study structural and phase properties, UCNC and UCNC@SiO2 were characterized using X-ray diffraction technique and the obtained patterns are shown in Figure 1. The diffraction peaks displayed at 2θ = 28.1°, 32.5°, 46.8°, 55.5°, 58.1°, 68.4°, 75.5°, and 77.8° could be attributed to (111), (200), (220), (311), (222), (400), (331), and (420) Miller indices, respectively. The XRD pattern of UCNC is exactly matching with prior reported data of cubic phase (JCPDS No. 77-2042) [60]. UCNC@SiO2 diffraction peaks were also obtained at the same 2θ position where the core (UCNCs) peaks were evidenced without any additional peaks, indicating that the formation of core-shell nanostructures does not alter the crystallinity of the core UCNC, and also do not lead to the formation of any additional compounds. In accordance with the amorphous nature of the silica shell around UCNC, the peaks corresponding to SiO2 could not be evidenced.
To investigate the morphology and size of the UCNC and core-shell nanostructures, TEM images were acquired (shown in Figure 2). Figure 2a shows the TEM image of microwave assisted synthesized NaYF4:Yb/Er nanocrystals. These particles are of spherical shape with an average size of approximately 25 nm. Figure 2b shows a high-resolution TEM (HRTEM) image of UCNC, which reveals the cubic phase of NaYF4 with lattice distance of 0.19 nm, also confirming the d-spacing for (220) Miller indices of the material. The selected area electron diffraction (SAED) patterns presented in Figure 2c clearly shows the diffraction rings corresponding to the cubic NaYF4 lattice. The thin silica layer coated on the UCNC to form core-shell nanostructures can be clearly seen in Figure 2d. The energy dispersive X-ray analysis (EDAX) of the core-shell nanostructures shown in Figure 2e clearly indicates the existence of all the constituent elements. In addition, the existence of all integral elements such as, sodium (Na), ytterbium (Yb), yttrium (Y), erbium (Er), fluoride (F), silicon (Si), and oxygen (O) was confirmed by TEM elemental mapping of UCNC@SiO2 core-shell nanostructures and is presented in Figure 3.
Upconversion luminescence (UCL) of UCNC@SiO2 core-shell nanostructures was measured at room temperature by excitation at 980 nm wavelength through infrared continuous laser. Two bands have been observed in the UCL spectra of UCNC@SiO2 at 658 nm and 544 nm, which is shown in Figure 4a. These upconversion emissions are the results of Er3+ ions electronic transitions from 4F9/2 → 4I15/2 and 4S3/2 → 4I15/2, respectively, and the transitions are schematically shown in Figure 4b [61].
Before performing cell imaging studies, cytotoxicity experiments were performed using a cell proliferation assay (WST-1). The cell toxicity induced by nanoparticulate imaging probes is mainly associated with their concentration and their surface functionalization [62,63]. In our cell viability experiment, DMSO was used as a positive control, as it is a known cell growth inhibitor and thus behaves like an effective toxin. Therefore, DMSO (10%) was mixed with the DMEM (cell growth media) as a toxin (positive control), while as a negative control, untreated cells (merely DMEM) were used. The untreated UCNC@SiO2 core-shell nanostructures were measured in variable concentrations up to 25 μg mL−1. The cell proliferation assay was used to evaluate the effect of UCNC@SiO2 core-shell nanostructures on the proliferation of human breast cancer cells (MDA-MB-231) after 48 h. The cell viability data is shown in Figure 5. The cell proliferation with UCNC@SiO2 did not induce significant toxicity at lower concentrations, and the proliferation of untreated cells is comparable. Nevertheless, a reduction in cell proliferation was noticed with the regular augmentation of UCNC@SiO2 nanostructure concentrations in cell growth media.
Based on optical properties and cell toxicity investigations of UCNC@SiO2, in vitro imaging of human breast cancer cells was performed by incubating them with 10 μg mL−1 UCNC@SiO2 core-shell nanostructures for 48 h, and the resulting images are presented in Figure 6. To investigate the intracellular location of UCNC in the cancer cells, their nucleus was stained with DAPI (Figure 6a). It can clearly be seen (Figure 6b,c) that a cluster of cells displayed bright signal in both the green and red channels, upon an excitation with 980 nm multi-photon excitation, which demonstrates that the UCNC@SiO2 core-shell nanostructures are capable of internalization into the human breast cancer cells. UCL emission of core-shell nanostructures was mainly localized in the cytoplasm of the cells, and we did not observe luminescence in the nucleus. The overlay image is presented in Figure 6d. The UCNC@SiO2 core-shell nanostructures showed sufficiently good cell viability and efficacy of cellular labeling for optical imaging applications even without further surface functionalization, which could be readily applied on to the silica coating for promoting further cellular uptake or other functions [64]. Importantly, auto-fluorescence of MDA-MB-231 cells can be removed by excitation at longer wavelengths, i.e., 980 nm laser. Consequently, UCNC@SiO2 is capable of multi-photon excitation with longer wavelengths, which, in turn, allows less scattering, deep penetration, low tissue absorption, and low autofluorescence for imaging of biological samples [65,66].

4. Conclusions

In summary, we have synthesized NaYF4:Yb/Er upconversion nanocrystals and coated them with silica to procedure core-shell nanostructures. Powder X-ray diffraction pattern of UCNC@SiO2 core-shell structures confirms that the core UCNC are in cubic phase. TEM images show that the core-shell nanostructures are predominantly spherical in shape comprising a thin silica shell around the UCNC core of about 25 nm size. The presence of all the constituent elements was confirmed through EDAX and elemental mapping studies. Upconversion photoluminescence measurements proved that the UCNC@SiO2 core-shell nanostructures display very good upconversion luminescence. Cell viability experiments through MTT assay shows low cytotoxicity of the nanostructure. Finally, we have demonstrated the bioimaging capability of the UCNC@SiO2 core-shell nanostructures through NIR light enabled optical imaging of breast cancer cells. This work opens the way for the development of low-toxic photostable alternatives to traditional fluorophores for bioimaging applications.

Author Contributions

K.L.R., N.P., J.M.R. and V.K. conceived and designed the experiments, K.L.R. and N.P. performed the experiments, analyzed the data, and wrote the initial draft of the manuscript, and all authors cross-checked the data, read and approved the final version of the manuscript.

Funding

This research was funded by Academy of Finland (projects 284542 and 309374).

Acknowledgment

We are thankful to Advanced Materials Research Centre (AMRC), IIT Mandi for laboratory and the characterization facilities. K.L.R. is thankful to Ministry of Human Resource Development (MHRD), India for research fellowship and Center for International Mobility (CIMO), Finland for doctoral exchange fellowship. N.P. acknowledges the Doctoral Network for Materials Research at Åbo Akademi University.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Ntziachristos, V. Going deeper than microscopy: The optical imaging frontier in biology. Nat. Methods 2010, 7, 603–614. [Google Scholar] [CrossRef] [PubMed]
  2. Weissleder, R.; Pittet, M.J. Imaging in the era of molecular oncology. Nature 2008, 452, 580–589. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Li, Z.; Zhang, Y.; Jiang, S. Multicolor core/shell-structured upconversion fluorescent nanoparticles. Adv. Mater. 2008, 20, 4765–4769. [Google Scholar] [CrossRef]
  4. Terai, T.; Nagano, T. Fluorescent probes for bioimaging applications. Curr. Opin.Chem. Biol. 2008, 12, 515–521. [Google Scholar] [CrossRef] [PubMed]
  5. Kamiya, M.; Kobayashi, H.; Hama, Y.; Koyama, Y.; Bernardo, M.; Nagano, T.; Choyke, P.L.; Urano, Y. An enzymatically activated fluorescence probe for targeted tumor imaging. J. Am. Chem. Soc. 2007, 129, 3918–3929. [Google Scholar] [CrossRef] [PubMed]
  6. Johnson, I. Review: Fluorescent probes for living cells. Histochem. J. 1998, 30, 123–140. [Google Scholar] [CrossRef] [PubMed]
  7. Dean, K.M.; Palmer, A.E. Advances in fluorescence labeling strategies for dynamic cellular imaging. Nat. Chem. Biol. 2014, 10, 512–523. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  8. Jańczewski, D.; Zhang, Y.; Das, G.K.; Yi, D.K.; Padmanabhan, P.; Bhakoo, K.K.; Tan, T.T.Y.; Selvan, S.T. Bimodal magnetic–fluorescent probes for bioimaging. Microsc. Res. Tech. 2011, 74, 563–576. [Google Scholar] [CrossRef] [PubMed]
  9. Chen, G.; Qiu, H.; Prasad, P.N.; Chen, X. Upconversion nanoparticles: Design, nanochemistry, and applications in theranostics. Chem. Rev. 2014, 114, 5161–5214. [Google Scholar] [CrossRef] [PubMed]
  10. Wang, F.; Liu, X. Recent advances in the chemistry of lanthanide-doped upconversion nanocrystals. Chem. Soc. Rev. 2009, 38, 976–989. [Google Scholar] [CrossRef] [PubMed]
  11. Dong, N.N.; Pedroni, M.; Piccinelli, F.; Conti, G.; Sbarbati, A.; Ramirez-Hernandez, J.E.; Maestro, L.M.; Iglesias-de la Cruz, M.C.; Sanz-Rodriguez, F.; Juarranz, A.; et al. Nir-to-nir two-photon excited caf2:Tm3+,yb3+ nanoparticles: Multifunctional nanoprobes for highly penetrating fluorescence bio-imaging. ACS Nano 2011, 5, 8665–8671. [Google Scholar] [CrossRef] [PubMed]
  12. Peng, J.; Xu, W.; Teoh, C.L.; Han, S.; Kim, B.; Samanta, A.; Er, J.C.; Wang, L.; Yuan, L.; Liu, X.; et al. High-efficiency in vitro and in vivo detection of zn2+ by dye-assembled upconversion nanoparticles. J. Am. Chem. Soc. 2015, 137, 2336–2342. [Google Scholar] [CrossRef] [PubMed]
  13. Valero, E.; Fiorini, S.; Tambalo, S.; Busquier, H.; Callejas-Fernández, J.; Marzola, P.; Gálvez, N.; Domínguez-Vera, J.M. In vivo long-term magnetic resonance imaging activity of ferritin-based magnetic nanoparticles versus a standard contrast agent. J. Med. Chem. 2014, 57, 5686–5692. [Google Scholar] [CrossRef] [PubMed]
  14. Min, Y.; Li, J.; Liu, F.; Padmanabhan, P.; Yeow, E.; Xing, B. Recent advance of biological molecular imaging based on lanthanide-doped upconversion-luminescent nanomaterials. Nanomaterials 2014, 4, 129–154. [Google Scholar] [CrossRef] [PubMed]
  15. Auzel, F. Upconversion and anti-stokes processes with f and d ions in solids. Chem. Rev. 2004, 104, 139–174. [Google Scholar] [CrossRef] [PubMed]
  16. Reddy, K.L.; Rai, M.; Prabhakar, N.; Arppe, R.; Rai, S.B.; Singh, S.K.; Rosenholm, J.M.; Krishnan, V. Controlled synthesis, bioimaging and toxicity assessments in strong red emitting mn2+ doped nayf4:Yb3+/ho3+ nanophosphors. RSC Adv. 2016, 6, 53698–53704. [Google Scholar] [CrossRef]
  17. Yan, C.; Dadvand, A.; Rosei, F.; Perepichka, D.F. Near-ir photoresponse in new up-converting cdse/nayf4:Yb,er nanoheterostructures. J. Am. Chem. Soc. 2010, 132, 8868–8869. [Google Scholar] [CrossRef] [PubMed]
  18. Boyer, J.-C.; Cuccia, L.A.; Capobianco, J.A. Synthesis of colloidal upconverting nayf4:  Er3+/yb3+ and tm3+/yb3+ monodisperse nanocrystals. Nano Lett. 2007, 7, 847–852. [Google Scholar] [CrossRef] [PubMed]
  19. Wang, F.; Han, Y.; Lim, C.S.; Lu, Y.; Wang, J.; Xu, J.; Chen, H.; Zhang, C.; Hong, M.; Liu, X. Simultaneous phase and size control of upconversion nanocrystals through lanthanide doping. Nature 2010, 463, 1061. [Google Scholar] [CrossRef] [PubMed]
  20. Boyer, J.-C.; Carling, C.-J.; Gates, B.D.; Branda, N.R. Two-way photoswitching using one type of near-infrared light, upconverting nanoparticles, and changing only the light intensity. J. Am. Chem. Soc. 2010, 132, 15766–15772. [Google Scholar] [CrossRef] [PubMed]
  21. Bogdan, N.; Vetrone, F.; Ozin, G.A.; Capobianco, J.A. Synthesis of ligand-free colloidally stable water dispersible brightly luminescent lanthanide-doped upconverting nanoparticles. Nano Lett. 2011, 11, 835–840. [Google Scholar] [CrossRef] [PubMed]
  22. Zhou, L.; Li, Z.; Liu, Z.; Yin, M.; Ren, J.; Qu, X. One-step nucleotide-programmed growth of porous upconversion nanoparticles: Application to cell labeling and drug delivery. Nanoscale 2014, 6, 1445–1452. [Google Scholar] [CrossRef] [PubMed]
  23. Chien, Y.-H.; Chou, Y.-L.; Wang, S.-W.; Hung, S.-T.; Liau, M.-C.; Chao, Y.-J.; Su, C.-H.; Yeh, C.-S. Near-infrared light photocontrolled targeting, bioimaging, and chemotherapy with caged upconversion nanoparticles in vitro and in vivo. ACS Nano 2013, 7, 8516–8528. [Google Scholar] [CrossRef] [PubMed]
  24. Wang, B.-Y.; Liao, M.-L.; Hong, G.-C.; Chang, W.-W.; Chu, C.-C. Near-infrared-triggered photodynamic therapy toward breast cancer cells using dendrimer-functionalized upconversion nanoparticles. Nanomaterials 2017, 7, 269. [Google Scholar] [CrossRef] [PubMed]
  25. Zheng, W.; Zhou, S.; Chen, Z.; Hu, P.; Liu, Y.; Tu, D.; Zhu, H.; Li, R.; Huang, M.; Chen, X. Sub-10 nm lanthanide-doped caf2 nanoprobes for time-resolved luminescent biodetection. Angew. Chem. Int. Ed. 2013, 52, 6671–6676. [Google Scholar] [CrossRef] [PubMed]
  26. Zhou, J.; Yu, M.; Sun, Y.; Zhang, X.; Zhu, X.; Wu, Z.; Wu, D.; Li, F. Fluorine-18-labeled gd3+/yb3+/er3+ co-doped nayf4 nanophosphors for multimodality pet/mr/ucl imaging. Biomaterials 2011, 32, 1148–1156. [Google Scholar] [CrossRef] [PubMed]
  27. Ge, X.; Sun, L.; Ma, B.; Jin, D.; Dong, L.; Shi, L.; Li, N.; Chen, H.; Huang, W. Simultaneous realization of hg2+ sensing, magnetic resonance imaging and upconversion luminescence in vitro and in vivo bioimaging based on hollow mesoporous silica coated ucnps and ruthenium complex. Nanoscale 2015, 7, 13877–13887. [Google Scholar] [CrossRef] [PubMed]
  28. Wang, L.; Liu, J.; Dai, Y.; Yang, Q.; Zhang, Y.; Yang, P.; Cheng, Z.; Lian, H.; Li, C.; Hou, Z.; et al. Efficient gene delivery and multimodal imaging by lanthanide-based upconversion nanoparticles. Langmuir 2014, 30, 13042–13051. [Google Scholar] [CrossRef] [PubMed]
  29. Zhai, X.; Lei, P.; Zhang, P.; Wang, Z.; Song, S.; Xu, X.; Liu, X.; Feng, J.; Zhang, H. Growth of lanthanide-doped ligdf4 nanoparticles induced by liluf4 core as tri-modal imaging bioprobes. Biomaterials 2015, 65, 115–123. [Google Scholar] [CrossRef] [PubMed]
  30. Li, Z.; Zhang, Y.; La, H.; Zhu, R.; El-Banna, G.; Wei, Y.; Han, G. Upconverting nir photons for bioimaging. Nanomaterials 2015, 5, 2148. [Google Scholar] [CrossRef] [PubMed]
  31. Tee, S.Y.; Teng, C.P.; Ye, E. Metal nanostructures for non-enzymatic glucose sensing. Mate. Sci. Eng. C 2017, 70, 1018–1030. [Google Scholar] [CrossRef] [PubMed]
  32. Ye, E.; Zhang, S.Y.; Lim, S.H.; Bosman, M.; Zhang, Z.; Win, K.Y.; Han, M.Y. Ternary cobalt–iron phosphide nanocrystals with controlled compositions, properties, and morphologies from nanorods and nanorice to split nanostructures. Chem. Eur. J. 2011, 17, 5982–5988. [Google Scholar] [CrossRef] [PubMed]
  33. Ye, E.; Tan, H.; Li, S.; Fan, W.Y. Self-organization of spherical, core–shell palladium aggregates by laser-induced and thermal decomposition of [pd (pph3) 4]. Angew. Chem. Int. Ed. 2006, 45, 1120–1123. [Google Scholar] [CrossRef] [PubMed]
  34. Liu, S.-H.; Gao, H.; Ye, E.; Low, M.; Lim, S.H.; Zhang, S.-Y.; Lieu, X.; Tripathy, S.; Tremel, W.; Han, M.-Y. Graphitically encapsulated cobalt nanocrystal assemblies. Chem. Commun. 2010, 46, 4749–4751. [Google Scholar] [CrossRef] [PubMed]
  35. Ye, E.; Zhang, S.-Y.; Lim, S.H.; Liu, S.; Han, M.-Y. Morphological tuning, self-assembly and optical properties of indium oxide nanocrystals. Phys. Chem. Chem. Phys. 2010, 12, 11923–11929. [Google Scholar] [CrossRef] [PubMed]
  36. Lingeshwar Reddy, K.; Balaji, R.; Kumar, A.; Krishnan, V. Lanthanide doped near infrared active upconversion nanophosphors: Fundamental concepts, synthesis strategies, and technological applications. Small 2018, 1801304. [Google Scholar] [CrossRef] [PubMed]
  37. Ehlert, O.; Thomann, R.; Darbandi, M.; Nann, T. A four-color colloidal multiplexing nanoparticle system. ACS Nano 2008, 2, 120–124. [Google Scholar] [CrossRef] [PubMed]
  38. Chan, Y.-C.; Chen, C.-W.; Chan, M.-H.; Chang, Y.-C.; Chang, W.-M.; Chi, L.-H.; Yu, H.-M.; Lin, Y.-F.; Tsai, D.P.; Liu, R.-S.; et al. Mmp2-sensing up-conversion nanoparticle for fluorescence biosensing in head and neck cancer cells. Biosens. Bioelectron. 2016, 80, 131–139. [Google Scholar] [CrossRef] [PubMed]
  39. Li, Z.; Zhang, Y. An efficient and user-friendly method for the synthesis of hexagonal-phase nayf4: Yb, er/tm nanocrystals with controllable shape and upconversion fluorescence. Nanotechnology 2008, 19, 345606. [Google Scholar] [CrossRef] [PubMed]
  40. Yajuan, S.; Yue, C.; Lijin, T.; Yi, Y.; Xianggui, K.; Junwei, Z.; Hong, Z. Controlled synthesis and morphology dependent upconversion luminescence of nayf 4:Yb, er nanocrystals. Nanotechnology 2007, 18, 275609. [Google Scholar]
  41. Yi, G.; Lu, H.; Zhao, S.; Ge, Y.; Yang, W.; Chen, D.; Guo, L.-H. Synthesis, characterization, and biological application of size-controlled nanocrystalline nayf4:Yb,er infrared-to-visible up-conversion phosphors. Nano Lett. 2004, 4, 2191–2196. [Google Scholar] [CrossRef]
  42. Zhu, Y.; Sun, Z.; Yin, Z.; Song, H.; Xu, W.; Wang, Y.; Zhang, L.; Zhang, H. Self-assembly, highly modified spontaneous emission and energy transfer properties of lapo4:Ce3+, tb3+ inverse opals. Dalton Trans. 2013, 42, 8049–8057. [Google Scholar] [CrossRef] [PubMed]
  43. Luo, X.-x.; Cao, W.-h. Ethanol-assistant solution combustion method to prepare la2o2s:Yb,pr nanometer phosphor. J. Alloys Compd. 2008, 460, 529–534. [Google Scholar] [CrossRef]
  44. Wang, G.; Qin, W.; Wei, G.; Wang, L.; Zhu, P.; Kim, R.; Zhang, D.; Ding, F.; Zheng, K. Synthesis and upconversion luminescence properties of yf3:Yb3+/tm3+ octahedral nanocrystals. J. Fluorine Chem. 2009, 130, 158–161. [Google Scholar] [CrossRef]
  45. Dong, B.; Song, H.; Yu, H.; Zhang, H.; Qin, R.; Bai, X.; Pan, G.; Lu, S.; Wang, F.; Fan, L.; et al. Upconversion properties of ln3+ doped nayf4/polymer composite fibers prepared by electrospinning. J. Phys. Chem. C 2008, 112, 1435–1440. [Google Scholar] [CrossRef]
  46. Qin, X.; Yokomori, T.; Ju, Y. Flame synthesis and characterization of rare-earth (er3+, ho3+, and tm3+) doped upconversion nanophosphors. Appl. Phys. Lett. 2007, 90, 073104. [Google Scholar] [CrossRef]
  47. Chan, E.M. Combinatorial approaches for developing upconverting nanomaterials: High-throughput screening, modeling, and applications. Chem. Soc. Rev. 2015, 44, 1653–1679. [Google Scholar] [CrossRef] [PubMed]
  48. Chen, C.; Sun, L.-D.; Li, Z.-X.; Li, L.-L.; Zhang, J.; Zhang, Y.-W.; Yan, C.-H. Ionic liquid-based route to spherical nayf4 nanoclusters with the assistance of microwave radiation and their multicolor upconversion luminescence. Langmuir 2010, 26, 8797–8803. [Google Scholar] [CrossRef] [PubMed]
  49. Wang, H.-Q.; Nann, T. Monodisperse upconverting nanocrystals by microwave-assisted synthesis. ACS Nano 2009, 3, 3804–3808. [Google Scholar] [CrossRef] [PubMed]
  50. Erathodiyil, N.; Ying, J.Y. Functionalization of inorganic nanoparticles for bioimaging applications. Acc. Chem. Res. 2011, 44, 925–935. [Google Scholar] [CrossRef] [PubMed]
  51. Muhr, V.; Wilhelm, S.; Hirsch, T.; Wolfbeis, O.S. Upconversion nanoparticles: From hydrophobic to hydrophilic surfaces. Acc. Chem. Res. 2014, 47, 3481–3493. [Google Scholar] [CrossRef] [PubMed]
  52. Chang, H.; Xie, J.; Zhao, B.; Liu, B.; Xu, S.; Ren, N.; Xie, X.; Huang, L.; Huang, W. Rare earth ion-doped upconversion nanocrystals: Synthesis and surface modification. Nanomaterials 2015, 5, 1. [Google Scholar] [CrossRef] [PubMed]
  53. Von Haartman, E.; Jiang, H.; Khomich, A.A.; Zhang, J.; Burikov, S.A.; Dolenko, T.A.; Ruokolainen, J.; Gu, H.; Shenderova, O.A.; Vlasov, I.I.; et al. Core-shell designs of photoluminescent nanodiamonds with porous silica coatings for bioimaging and drug delivery i: Fabrication. J. Mater. Chem. B 2013, 1, 2358–2366. [Google Scholar] [CrossRef]
  54. Li, Z.; Zhang, Y. Monodisperse silica-coated polyvinylpyrrolidone/nayf4 nanocrystals with multicolor upconversion fluorescence emission. Angew. Chem. 2006, 118, 7896–7899. [Google Scholar] [CrossRef]
  55. Liu, J.-N.; Bu, W.-B.; Shi, J.-L. Silica coated upconversion nanoparticles: A versatile platform for the development of efficient theranostics. Acc. Chem. Res. 2015, 48, 1797–1805. [Google Scholar] [CrossRef] [PubMed]
  56. Ghosh Chaudhuri, R.; Paria, S. Core/shell nanoparticles: Classes, properties, synthesis mechanisms, characterization, and applications. Chem. Rev. 2011, 112, 2373–2433. [Google Scholar] [CrossRef] [PubMed]
  57. Karaman, D.Ş.; Sarparanta, M.P.; Rosenholm, J.M.; Airaksinen, A.J. Multimodality imaging of silica and silicon materials in vivo. Adv. Mater. 2018, 1703651. [Google Scholar] [CrossRef] [PubMed]
  58. Reddy, K.L.; Prabhakar, N.; Arppe, R.; Rosenholm, J.M.; Krishnan, V. Microwave-assisted one-step synthesis of acetate-capped nayf4:Yb/er upconversion nanocrystals and their application in bioimaging. J. Mater. Sci. 2017, 52, 5738–5750. [Google Scholar] [CrossRef]
  59. Guerrero-Martínez, A.; Pérez-Juste, J.; Liz-Marzán, L.M. Recent progress on silica coating of nanoparticles and related nanomaterials. Adv. Mater. 2010, 22, 1182–1195. [Google Scholar] [CrossRef] [PubMed]
  60. Tian, G.; Gu, Z.; Zhou, L.; Yin, W.; Liu, X.; Yan, L.; Jin, S.; Ren, W.; Xing, G.; Li, S.; et al. Mn2+ dopant-controlled synthesis of nayf4:Yb/er upconversion nanoparticles for in vivo imaging and drug delivery. Adv. Mater. 2012, 24, 1226–1231. [Google Scholar] [CrossRef] [PubMed]
  61. Han, Y.; Gai, S.; Ma, P.a.; Wang, L.; Zhang, M.; Huang, S.; Yang, P. Highly uniform α-nayf4:Yb/er hollow microspheres and their application as drug carrier. Inorg. Chem. 2013, 52, 9184–9191. [Google Scholar] [CrossRef] [PubMed]
  62. Desai, D.; Karaman Didem, S.; Prabhakar, N.; Tadayon, S.; Duchanoy, A.; Toivola Diana, M.; Rajput, S.; Näreoja, T.; Rosenholm Jessica, M. Design considerations for mesoporous silica nanoparticulate systems in facilitating biomedical applications. Open Mater. Sci. 2014, 1, 1. [Google Scholar] [CrossRef]
  63. Paatero, I.; Casals, E.; Niemi, R.; Özliseli, E.; Rosenholm, J.M.; Sahlgren, C. Analyses in zebrafish embryos reveal that nanotoxicity profiles are dependent on surface-functionalization controlled penetrance of biological membranes. Sci. Rep. 2017, 7, 8423. [Google Scholar] [CrossRef] [PubMed]
  64. Gulin-Sarfraz, T.; Sarfraz, J.; Karaman, D.Ş.; Zhang, J.; Oetken-Lindholm, C.; Duchanoy, A.; Rosenholm, J.M.; Abankwa, D. Fret-reporter nanoparticles to monitor redox-induced intracellular delivery of active compounds. RSC Adv. 2014, 4, 16429–16437. [Google Scholar] [CrossRef]
  65. Svoboda, K.; Yasuda, R. Principles of two-photon excitation microscopy and its applications to neuroscience. Neuron 2006, 50, 823–839. [Google Scholar] [CrossRef] [PubMed]
  66. Helmchen, F.; Denk, W. Deep tissue two-photon microscopy. Nat Methods 2005, 2, 932–940. [Google Scholar] [CrossRef] [PubMed]
Micromachines 09 00400 sch001 550
Scheme 1. Schematic illustration of upconversion nanocrystals (UCNC)@SiO2 synthesis and their application in cancer cell imaging.
Scheme 1. Schematic illustration of upconversion nanocrystals (UCNC)@SiO2 synthesis and their application in cancer cell imaging.
Micromachines 09 00400 sch001
Micromachines 09 00400 g001 550
Figure 1. Powder X-ray diffraction pattern of upconversion nanocrystals (UCNC) and UCNC@SiO2.
Figure 1. Powder X-ray diffraction pattern of upconversion nanocrystals (UCNC) and UCNC@SiO2.
Micromachines 09 00400 g001
Micromachines 09 00400 g002 550
Figure 2. Transmission electron microscope (TEM) image of (a) NaYF4:Yb/Er UCNC, (b) High-resolution TEM image of NaYF4:Yb/Er UCNC, (c) selected area electron diffraction (SAED) patterns of NaYF4:Yb/Er UCNC, (d) UCNC@SiO2, and (e) energy dispersive X-ray analysis (EDAX) of UCNC@SiO2.
Figure 2. Transmission electron microscope (TEM) image of (a) NaYF4:Yb/Er UCNC, (b) High-resolution TEM image of NaYF4:Yb/Er UCNC, (c) selected area electron diffraction (SAED) patterns of NaYF4:Yb/Er UCNC, (d) UCNC@SiO2, and (e) energy dispersive X-ray analysis (EDAX) of UCNC@SiO2.
Micromachines 09 00400 g002
Micromachines 09 00400 g003 550
Figure 3. (a) STEM-HAADF image of UCNC@SiO2 core-shell nanostructures with associated (b) sodium (Na), (c) yttrium (Y), (d) fluoride (F), (e) ytterbium (Yb), (f) erbium (Er), (g) silicon (Si), and (h) oxygen (O) elemental mapping.
Figure 3. (a) STEM-HAADF image of UCNC@SiO2 core-shell nanostructures with associated (b) sodium (Na), (c) yttrium (Y), (d) fluoride (F), (e) ytterbium (Yb), (f) erbium (Er), (g) silicon (Si), and (h) oxygen (O) elemental mapping.
Micromachines 09 00400 g003
Micromachines 09 00400 g004 550
Figure 4. Upconversion luminescence spectra of (a) NaYF4:Yb/Er and silica-coated excited at 980nm and (b) Schematic illustration of lanthanide ions (Yb3+, Er3+) energy transitions in NaYF4:Yb/Er nanocrystals.
Figure 4. Upconversion luminescence spectra of (a) NaYF4:Yb/Er and silica-coated excited at 980nm and (b) Schematic illustration of lanthanide ions (Yb3+, Er3+) energy transitions in NaYF4:Yb/Er nanocrystals.
Micromachines 09 00400 g004
Micromachines 09 00400 g005 550
Figure 5. MDA-MB-231 cell viability was assessed by cell proliferation assay (WST-1) on incubation of UCNC@SiO2 for 48 h. The cell viability was assessed with positive (DMSO) and negative (media only) controls. The cells incubated with 10% DMSO (toxin), showed efficient toxicity with comparatively lowest cell survival or proliferation. However, the negative control cells have approximately 100% cell proliferation. The UCNC@SiO2 treated cells have shown concentration-dependent cell proliferation i.e. the higher the particle concentration, the lower the cell proliferation. The measured cell viability for 5 μg mL−1, 10 μg mL−1, and 25 μg mL−1 UCNC@SiO2 treated cells were approximately 90%, 80%, and 70%, respectively.
Figure 5. MDA-MB-231 cell viability was assessed by cell proliferation assay (WST-1) on incubation of UCNC@SiO2 for 48 h. The cell viability was assessed with positive (DMSO) and negative (media only) controls. The cells incubated with 10% DMSO (toxin), showed efficient toxicity with comparatively lowest cell survival or proliferation. However, the negative control cells have approximately 100% cell proliferation. The UCNC@SiO2 treated cells have shown concentration-dependent cell proliferation i.e. the higher the particle concentration, the lower the cell proliferation. The measured cell viability for 5 μg mL−1, 10 μg mL−1, and 25 μg mL−1 UCNC@SiO2 treated cells were approximately 90%, 80%, and 70%, respectively.
Micromachines 09 00400 g005
Micromachines 09 00400 g006 550
Figure 6. The imaging potential of developed UCNC@SiO2 was demonstrated by performing in vitro imaging of MDA-MB-231 cells by multi-photon excitation (980 nm laser excitation). The developed UCNC@SiO2 has bright, dual color emission in both green and red channels. The UCNC@SiO2 imaging further demonstrated that particles are localized in the cytoplasmic space after uptake. (a) Cell nuclei were visualized by 4′,6-diamidino-2-phenylindole (DAPI) staining, (b) The UCNC@SiO2 can be seen as localized spots inside cells. The green emission form UCNC@SiO2 was detected in 520–570 nm range. (c) The red emission from UCNC@SiO2 can be seen again as localized spots in cells. The red emission from UCNC@SiO2 was detected in 630–680 nm range. (d) Overlay image of (a–c) with bright-field.
Figure 6. The imaging potential of developed UCNC@SiO2 was demonstrated by performing in vitro imaging of MDA-MB-231 cells by multi-photon excitation (980 nm laser excitation). The developed UCNC@SiO2 has bright, dual color emission in both green and red channels. The UCNC@SiO2 imaging further demonstrated that particles are localized in the cytoplasmic space after uptake. (a) Cell nuclei were visualized by 4′,6-diamidino-2-phenylindole (DAPI) staining, (b) The UCNC@SiO2 can be seen as localized spots inside cells. The green emission form UCNC@SiO2 was detected in 520–570 nm range. (c) The red emission from UCNC@SiO2 can be seen again as localized spots in cells. The red emission from UCNC@SiO2 was detected in 630–680 nm range. (d) Overlay image of (a–c) with bright-field.
Micromachines 09 00400 g006

Share and Cite

MDPI and ACS Style

Lingeshwar Reddy, K.; Prabhakar, N.; Rosenholm, J.M.; Krishnan, V. Core-Shell Structures of Upconversion Nanocrystals Coated with Silica for Near Infrared Light Enabled Optical Imaging of Cancer Cells. Micromachines 2018, 9, 400. https://doi.org/10.3390/mi9080400

AMA Style

Lingeshwar Reddy K, Prabhakar N, Rosenholm JM, Krishnan V. Core-Shell Structures of Upconversion Nanocrystals Coated with Silica for Near Infrared Light Enabled Optical Imaging of Cancer Cells. Micromachines. 2018; 9(8):400. https://doi.org/10.3390/mi9080400

Chicago/Turabian Style

Lingeshwar Reddy, Kumbam, Neeraj Prabhakar, Jessica M. Rosenholm, and Venkata Krishnan. 2018. "Core-Shell Structures of Upconversion Nanocrystals Coated with Silica for Near Infrared Light Enabled Optical Imaging of Cancer Cells" Micromachines 9, no. 8: 400. https://doi.org/10.3390/mi9080400

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop