The microvascular images allow the identification of several vessel patterns, including the episcleral veins distribution.
Methods: analysis was made of sapheno-femoral junction (SFJ) incompetence, non-SFJ incompetence, segmental and perforating vein incompetence, distribution of varicosities, deep venous insufficiency, and short saphenous incompetence.
In the same vein, the gender distribution of the sample did not influence the results, not supporting our hypothesis.
After injection into the dorsal tail vein, the average distribution was higher in blood and in the heart.
In order to test the feasibility of C labeled thymidine as the potential tracker for MSCs tracking and to investigate the bio-distribution of PDB-MSCs after implantation, PDB-MSCs was labeled with C-TdR and then injected into the nude mice via the caudal vein for bio-distribution study.
Thus, a pseudo-elliptical sampling model is proposed to retain the spatial distribution of vein patterns, to reduce the redundant information in finger images, and to reduce differences.
The results demonstrated that the interconnectivity of pores allowed for uniform human umbilical vein endothelial cells (HUVECs) distribution and proliferation in the scaffolds, leading to high cell density and confluency at the end of the culture period.
NIR-dye-conjugated HAssLG nanoparticles were administered intravenously via the tail vein of mice, and distribution of nanoparticles in mice was observed with NIR imaging equipment as shown in Fig. 6.
Twenty minutes after insulin injection, mice were injected with 2-[F]fluoro-2-deoxyglucose (FDG) (4.1 MBq) via the tail vein, and whole-body distribution of FDG was monitored by positron emission tomography (PET) using a microPET R4 tomograph (Concorde Microsystems, Knoxville, TN, USA).
