Detail-enhanced exposure fusion.

In a typical processing chain of image enhancement, an exposure fusion scheme can be used to synthesize a more detailed low dynamic range (LDR) image directly from a set of differently exposed LDR images, without generation of an intermediate high dynamic range image. In this brief, we introduce a new quadratic optimization-based method to extract fine details from a vector field. The new method extracts fine details from a set of differently exposed LDR images simultaneously. The extracted fine details are then added to an intermediate LDR image which is fused by simply using an existing exposure fusion scheme. With this, the proposed scheme can enhance fine details to produce sharper images.

Wear of opposing teeth by posterior composite resins--evaluation of newly developed wear test methods.

In the present study, enamel wear against indirect composite resins was evaluated using two newly designed wear test methods: a rotating sliding wear test and a buff wear test. For the composite resins investigated in this study, their surface morphologies were examined using a scanning probe microscope after buff-polishing. After the wear tests, enamel was worn down by hard fillers that protruded from the abraded resin matrices. Notably, enamel wear was induced by composite materials with a Vickers hardness number (VHN) greater than 45 and that the amount of enamel wear increased with increasing hardness of the composite material. Therefore, 45 VHN was the critical hardness value for composite resins at which antagonistic enamel wear would occur. Besides, the D-value obtained from the buff wear test indicated not only the relative wear resistance of the composite resin itself, but also its potential risk to induce antagonistic enamel wear.

[Lung metastasis of human choriocarcinoma in mice: establishment of experimental metastatic model and its biological characteristics].

OBJECTIVE: To establish a satisfactory lung metastasis model of human choriocarcinoma using severe combined immunodeficient (SCID) mice and explore the appropriate cell concentration for the model. METHODS: Forty SCID mice aged between 5 - 6 weeks were randomly divided into four groups. 1 × 10(7) cells/ml × 0.1 ml, 5 × 10(6) cells/ml × 0.2 ml and 1 × 10(6) cells/ml × 0.1 ml of human choriocarcinoma cells JEG-3 were respectively injected in SCID mice of experimental groups by lateral tail vein, the remain group was assigned to the control group. The status and weight of mice were observed every three days. When these mice were being dying, the size and the number of the lesions of lung metastasis in every mouse were inspected with Micro CT. After Micro CT inspection, the SCID mice were executed dissected to note whether there were tumors on all organ surfaces with naked eyes, then made pathological sections from the metastatic foci of fresh lung tissues, and cultured primarily cells and purified cells and passaged cells isolated from the same metastastic foci. The pathological sections were observed under the microscope. The special antigen human chorionic gonadotropin-beta subunit (ß-hCG) of the choriocarcinoma cells was immunohistochemically detected in the pathological sections and the cells out of cultured primarily cells. The chromosomes of the cells out of cultured primarily cells were analysed. RESULTS: Of the group inoculated 1 × 10(7) cells/ml × 0.1 ml, all mice died when inoculating. In the group of 5 × 10(6) cells/ml × 0.2 ml, when inoculating, 3 mice died; the remain 7 mice were being dying on (18.0 ± 2.0) days after injection. 5 of them, there were 1 - 3 lesions of lung metastasis after Micro CT inspection in each mice, and the diameter of the tumors lesions reached 1.5 - 3.5 mm, which was choriocarcinoma confirmed by pathological sections. The special antigen ß-hCG was detected by immunohistochemical method in the pathological sections of pulmonary tissue with tumor and in the cells, which were purified and passaged from being cultured primarily cells isolated from metastastic foci of fresh lung tissues from the SCID mice. The chromosome numbers of these cells out of cultured primarily cells were variety from 19 to 128, and modal numbers were variety from 70 to 79. CONCLUSIONS: We successfully established the lung metastatic model of human choriocarcinoma in SCID mice by injecting JEG-3 cells into lateral tail vein, of which 5 × 10(6) cells/ml × 0.2 ml is the suitable concentration and volume for the model.

[Monitoring of methotrexate concentrations in lung and other tissues of rat through internal iliac artery infusion].

OBJECTIVE: To establish the high-performance liquid chromatography (HPLC) method for measuring concentrations of methotrexate (MTX) in rat lung and some other tissues through internal iliac artery infusion. METHODS: Fifty female Sprague-Dawley rats were included in this study. The rats were randomly assigned to two groups. Methotrexate was injected to group one through internal iliac artery, and was injected to group two through femoral vein. Blood and tissues were collected in each group at 15, 30, 60, 90 and 120 minutes for detection of the drug concentrations with HPLC. RESULTS: The area under the concentration time curve (AUC) in rat lung, ovary and uterus in the artery group were separately (3.77 +/- 0.28), (4.40 +/- 0.40), (9.97 +/- 0.89) microgxh(-1)xg(-1), which were significantly different from those of the vein group [(2.31 +/- 0.25), (3.91 +/- 0.19), (7.65 +/- 1.54) microgxh(-1)xg(-1); P < 0.05]. The AUC in the rat plasma, heart, kidney, liver and spleen in the artery group were separately (6.13 +/- 0.53), (1.90 +/- 0.11), (5.32 +/- 0.89), (14.16 +/- 1.96), (0.76 +/- 0.20) microgxh(-1)xg(-1). There were no significant differences from the vein group [(5.79 +/- 0.71), (1.64 +/- 0.29), (5.15 +/- 1.69), (14.29 +/- 3.47), (0.76 +/- 0.13) microgxh(-1)xg(-1); P > 0.05]. CONCLUSIONS: Through internal iliac artery infusion, there are higher drug concentrations in lung, uterus and ovarian compared to venous injection. The internal-arterial chemotherapy may be used to treat pulmonary metastasis of gynecological tumor.