ABSTRACT
In this research, some physical properties such as the density, specific heat capacity, and micro-hardness of galena ore lumps purchased from the public market were determined. The microscopic study, using the scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS), confirmed that the as-received galena ore was mostly lead sulfide (PbS). The XRD pattern of the galena powder also elucidated that all the peaks were assigned to PbS. In addition, the as-received galena was roughly crushed, and fine-milled using a high-vibration milling machine with tungsten carbide rings. Nanoscale particles of about 90 nm were produced in a very short milling time of around 15 min. The obtained nanoscale powder was well investigated in the SEM at low and high magnifications to assess the exact range of particle size. Meanwhile, the SEM was employed to investigate the microstructure of sintered samples, where a part of the milled galena powder was compacted and sintered at 700 °C for 2 h. Again, the result of this investigation proved the formation of PbS with even smaller grain size compared with the grain size of the starting galena ore. A high relative sinter density of approximately 97% for galena powder was achieved by sintering under vacuum.
ABSTRACT
Biliary atresia (BA) is the most frequent indication for paediatric liver transplantation. We tested the hypothesis of a viral aetiology of this disease by screening liver samples of a large number of BA patients for the common human hepatotropic viruses. Moreover, we correlated our findings to the expression of Mx protein, which has been shown to be significantly up-regulated during viral infections. Seventy-four liver biopsies (taken during Kasai portoenterostomy) were tested by polymerase chain reaction (PCR) for DNA viruses (herpes simplex virus [HSV], Epstein-Barr virus [EBV], varicella zoster virus [VZV], cytomegalovirus [CMV], adenovirus, parvovirus B19 and polyoma BK) and RNA viruses (enteroviruses, rotavirus and reovirus 3). Mx protein expression was assessed by immunohistochemistry. Virus DNA/RNA was found in less than half of the biopsies (8/74 CMV, 1/74 adenovirus; 21/64 reovirus, 1/64 enterovirus). A limited number presented with double infection. Patients that had detectable viral RNA/DNA in their liver biopsies were significantly older than virus-free patients (P = 0.037). The majority (54/59) of the liver biopsies showed expression of Mx proteins in hepatocytes, bile ducts and epithelium. Our data suggest that the known hepatotropic viruses do not play a major role in the aetiology and progression of BA. Their incidence appears to be, rather, a secondary phenomenon. Nonetheless, the inflammatory response in the livers of BA patients mimics that observed during viral infections.
