Considering the extremely large effect size of the CCEP, we recommend that this program be used in the correction of postural hyper-kyphosis deformity in future.

The two enantiomers (mirror images) of a biomolecule can show drastically different behaviors, requiring the development of sensitive approaches for their identification and separation. Plasmonic nanostructures have shown promise for enhancing the sensitivities of chiral spectroscopies, but the generation of chiral near fields with a specific handedness in the spatial domain surrounding the plasmonic structures remains a challenge. Here we demonstrate that achiral bianisotropic structures, which couple the electric and magnetic fields, can achieve high enhancements of optical chirality in an extended spatial region. Magneto-electric coupling in such structures facilitates electrically excited magnetic resonances in the near IR and optical regimes, which in turn can result in highly enhanced optical chirality in an extended region of space. We apply this concept to achiral double split ring resonators (DSRRs) and demonstrate their potential in generating enhanced chiral fields and forces. Also, the behavior of optical chirality density gradient and chirality flux in such structures is examined, and it is shown that plasmonically generated chiral forces may pave the way to a new class of chiral biosensors.

Recently the new concepts of transverse spin angular momentum and Belinfante spin momentum of evanescent waves have drawn considerable attention. Here, we investigate these novel physical properties of electromagnetic fields in the context of locally excited surface plasmon polaritons. We demonstrate, both analytically and numerically, that locally excited surface plasmon polaritons possess transverse spin angular momentum and Belinfante momentum with rich and non-trivial characteristics. We also show that the transverse spin angular momentum of locally excited surface plasmon polaritons leads to the emergence of transverse chiral forces in opposite directions for chiral objects of different handedness. The magnitude of such a transverse force is comparable to the optical gradient force and scattering forces. This finding may pave the way for realization of optical separation of chiral biomolecules

Femtosecond (fs) pulsed laser irradiation techniques have attracted interest as a photonic approach for the selective inactivation of virus contaminations in biological samples. Conventional pulsed laser approaches require, however, relatively long irradiation times to achieve a significant inactivation of virus. In this study, we investigate the enhancement of the photonic inactivation of Murine Leukemia Virus (MLV) via 805 nm femtosecond pulses through gold nanorods whose localized surface plasmon resonance overlaps with the excitation laser. We report a plasmonically enhanced virus inactivation, with greater than 3.7-log reduction measured by virus infectivity assays. Reliable virus inactivation was obtained for 10 s laser exposure with incident laser powers ≥0.3 W. Importantly, the fs-pulse induced inactivation was selective to the virus and did not induce any measurable damage to co-incubated antibodies. The loss in viral infection was associated with reduced viral fusion, linking the loss in infectivity with a perturbation of the viral envelope. Based on the observations that physical contact between nanorods and virus particles was not required for viral inactivation and that reactive oxygen species (ROS) did not participate in the detected viral inactivation, a model of virus inactivation based on plasmon enhanced shockwave generation is proposed.

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