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A two-beam second-harmonic generation technique is developed to calibrate the magnitude of the second-order nonlinear optical susceptibility components of surface and bulk (multipolar origin) of isotropic materials. The values obtained for fused silica calibrated against ChiXXX of crystalline quartz are chi parallel parallel perpendicular = 7.9(4), chi perpendicular parallel parallel (+)gamma = 3.8(4), parallel perpendicular perpendicular perpendicular(+)gamma = 59(4), and delta' = 7.8(4) in units of 10(-22) m(2)/V. Similar values are obtained for BK7 glass. An alternative way of calibration against ChiXYZ of quartz is demonstrated. The technique could also be extended to characterize the susceptibility tensor of crystals as a convenient alternative to the Maker-fringe technique.

We use two-beam second-harmonic generation to perform a quantitative tensor analysis of the effective dipolar surface nonlinearity and the separable multipolar bulk nonlinearity for BK7 glass. The most straightforward, self-consistent interpretation of the results is obtained when the effective surface response is assumed to have approximate Kleinman symmetry and the bulk contribution is dominated by magnetic, rather than quadrupole, effects.

We show that nonlinear optical signals generated by non-phase-matched interactions are strongly suppressed when the interaction volume is finite and localized deep inside the bulk of a homogeneous material, as opposed to the case where the interaction volume extends across a boundary of the material. The suppression in the bulk originates from destructive interference between the signals generated in the two regions where the interaction is gradually turned on and off and depends on the ratio of the coherence length to the characteristic length of the interaction volume.

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Background:Hepatocellular carcinoma (HCC) is one of the most important health problems in China.Objectives:This study analyzed expression of high-mobility group protein B1 (HMGB1) and inhibitor of apoptosis protein-2 (c-IAP2) proteins in HCC compared to paired para-tumor tissue samples to assess the association with HCC pathogenesis and progression.Materials and Methods:Sixty-eight HCC and para-tumor tissue samples were collected for Western blot, qRT-PCR and immunohistochemical analyses of HMGB1 and c-IAP2.Results:HMGB1 and c-IAP2 proteins were highly expressed in HCC tissue samples [85.3% (58/68) and 82.4% (56/68), respectively] compared to para-tumor tissue samples [32.3% and 27.9%, respectively]. Furthermore, expression of HMGB1 was significantly associated with enhanced c-IAP2 expression in HCC tissue samples (r = 0.878, P < 0.01). Expression of HMGB1 was associated with tumor multiplicity and size, alpha-fetoprotein (AFP) level and advanced TNM stage, while expression of c-IAP2 was associated with tumor size, AFP level and advanced TNM stage.Conclusions:Expression of HMGB1 and c-IAP2 proteins was associated with HCC development and progression, and the expression of HMGB1 and c-IAP2 proteins in HCC were significantly associated with each other. Additionally, these proteins may show promise as biomarkers to predict HCC progression.

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