Given the sub-wavelength trapping challenges in the optical tweezers, the plasmonic tweezers serve as a bridge by breaking the diffraction limit. Hence, the development of plasmonic tweezers can open up many potential applications in biology, medicine, and chemistry. In this paper, using localized surface plasmons (LSPs) of graphene nanodisk with a resonance frequency of 20 THz, we design a lab-on-a-chip optophoresis system, which can be utilized to effectively trap the nanoparticles. The LSPs of graphene nanodisk generate a large field gradient in the deep sub-wavelength area around the resonance frequency. We show that by an appropriate choice of chemical potentials of the graphene nanodisks, the strong optical near-field forces desired for trapping can be generated under the illumination of the THz source when the polystyrene (PS) nanoparticles are located in the vicinity of graphene nanodisks. Numerical simulations show that the designed system with graphene nanodisks of 250 nm in diameter and chemical potentials of µ c = 0.6 eV can trap the PS nanoparticles of 12 nm in diameter and larger with a THz source intensity of 19 mW/µm 2 , demonstrating acceptable sensitivities for variations in the nanoparticle diameter and refractive index. Moreover, at the same source intensity, the graphene nanodisks with µ c = 0.7 eV can trap the PS nanoparticle as small as 9.5 nm in diameter.
We take advantage of graphene nano-taper plasmons to design tunable plasmonic tweezers for neuroblastoma extracellular vesicles manipulation. It consists of Si/SiO2/Graphene stack topped by a microfluidic chamber. Using plasmons of isosceles-triangle-shaped graphene nano-taper with a resonance frequency of 6.25 THz, the proposed device can efficiently trap the nanoparticles. The plasmons of graphene nano-taper generate a large field intensity in the deep sub-wavelength area around the vertices of the triangle. We show that by engineering the dimensions of the graphene nano-taper and an appropriate choice of its Fermi energy, the desired near-field gradient force for trapping can be generated under relatively low-intensity illumination of the THz source when the nanoparticles are placed near the front vertex of the nano-taper. Our results show that the designed system with graphene nano-taper of L = 1200 nm length and W = 600 nm base size and THz source intensity of I = 2 mW/µm2, can trap polystyrene nanoparticles with diameters of D = 140, 73, and 54 nm, and with trap stiffnesses of ky = 9.9 fN/nm, ky = 23.77 fN/nm, and ky = 35.51 fN/nm at Fermi energies of Ef = 0.4, 0.5, and 0.6 eV, respectively. It is well known that the plasmonic tweezer as a high-precision and non-contact means of control has potential applications in biology. Our investigations demonstrate that the proposed tweezing device with L = 1200 nm, W = 600 nm, and Ef = 0.6 eV can be utilized to manipulate the nano-bio-specimens. So that, at the given source intensity, it can trap the neuroblastoma extracellular vesicles, which are released by neuroblastoma cells and play an important role in modulating the function of neuroblastoma cells and other cell populations, as small as 88 nm at the front tip of isosceles-triangle-shaped graphene nano-taper. The trap stiffness for the given neuroblastoma extracellular vesicle is obtained as ky = 17.92 fN/nm.
Epimorphic regeneration in New Zealand rabbit ear is an interesting example of mammalian wound healing in which blastema formation is involved in replacement of injured tissues. It has been suggested that isolated cells from regenerating rabbit ear possess stem-like properties. In this study, we aimed to determine the expression of stemness markers, OCT4 and SOX2 proteins, in regenerating rabbit tissues by immunohistochemistry. Results indicated that both proteins could be detected in epithelial cells, hair follicle cells and perichondrium cells. Expression pattern analysis of OCT4 and SOX2 proteins showed no clear differences between regenerative and non-regenerative control tissues. According to several reports of OCT4 and SOX2 proteins expression in adult stem cells, it could be proposed that OCT4 and SOX2 expressing cells in regenerating rabbit ear tissues are progenitor/adult stem cells which are resident in these tissues, and other markers should be used for detection of blastema cells.
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