Core point pixel-level localization by fingerprint features in spatial domain.

Singular point detection is a primary step in fingerprint recognition, especially for fingerprint alignment and classification. But in present there are still some problems and challenges such as more false-positive singular points or inaccurate reference point localization. This paper proposes an accurate core point localization method based on spatial domain features of fingerprint images from a completely different viewpoint to improve the fingerprint core point displacement problem of singular point detection.

Open set recognition algorithm based on Conditional Gaussian Encoder.

For the existing Closed Set Recognition (CSR) methods mistakenly identify unknown jamming signals as a known class, a Conditional Gaussian Encoder (CG-Encoder) for 1-dimensional signal Open Set Recognition (OSR) is designed. The network retains the original form of the signal as much as possible and deep neural network is used to extract useful information. CG-Encoder adopts residual network structure and a new Kullback-Leibler (KL) divergence is defined.

Preparation, characterization and in vitro and in vivo evaluation of a solid dispersion of Naringin.

Naringin (NA) is one of typical flavanone glycosides widely distributed in nature and possesses several biological activities including antioxidant, anti-inflammatory, and antiapoptotic. The aim of this study was to develop solid dispersion (SD) and to improve the dissolution rate and oral bioavailability of NA. NA-SD was prepared by the traditional preparation methods using PEG6000, F68, or PVP K30 as carrier at different drug to carrier ratios.

[The effect of morin on activation, proliferation and cell-cycle of murine T lymphocytes in vitro].

Aim: To discover the effects of morin on the activation, proliferation and cell-cycle of murine T lymphocytes in vitro.

Methods: Murine lymph node-derived T lymphocytes were separated and stimulated with concanavalin A (ConA) and different experimental groups were set by co-cultured with morin of different final concentration. Flow cytometry (FCM) was used to detect the activation, proliferation [carboxylfluorescein diacetate, succinimide ester (CFDA-SE) staining] and cell-cycle [propidium iodide(PI) staining] of T cells.