Even the best-maintained water distribution network (WDN) might suffer pipe bursts occasionally, and the utility company must reconstruct the damaged sections of the system. The affected area must be segregated by closing the corresponding isolation valves; as a result, the required amount of drinking water might not be available. This paper explores the behaviour and topology of segments, especially their criticality from the viewpoint of the whole system. A novel, objective, dimensionless, segment-based quantity is proposed to evaluate the vulnerability of both the segments and the whole WDN against a single, incidental pipe break, computed as the product of the probability of failure within the segment and the amount of unserved consumption. 27 comprehensive real-life WDNs have been examined by means of the new metric and with the help of complex network theory, exploiting the concept of the degree distribution and topology-based structural properties (e.g. network diameter, clustering coefficient). It was found that metrics based purely on topology suggest different network behaviour as vulnerability analysis, which also includes the hydraulics. The investigation of the global network vulnerabilities has revealed several critically exposed systems, and the local distributions unveiled new properties of WDNs in the case of a random pipe break.

Cell adhesion is a fundamental phenomenon vital for all multicellular organisms. Recognition of and adhesion to specific macromolecules is a crucial task of leukocytes to initiate the immune response. To gain statistically reliable information of cell adhesion, large numbers of cells should be measured. However, direct measurement of the adhesion force of single cells is still challenging and today’s techniques typically have an extremely low throughput (5–10 cells per day). Here, we introduce a computer controlled micropipette mounted onto a normal inverted microscope for probing single cell interactions with specific macromolecules. We calculated the estimated hydrodynamic lifting force acting on target cells by the numerical simulation of the flow at the micropipette tip. The adhesion force of surface attached cells could be accurately probed by repeating the pick-up process with increasing vacuum applied in the pipette positioned above the cell under investigation. Using the introduced methodology hundreds of cells adhered to specific macromolecules were measured one by one in a relatively short period of time (∼30 min). We blocked nonspecific cell adhesion by the protein non-adhesive PLL-g-PEG polymer. We found that human primary monocytes are less adherent to fibrinogen than their in vitro differentiated descendants: macrophages and dendritic cells, the latter producing the highest average adhesion force. Validation of the here introduced method was achieved by the hydrostatic step-pressure micropipette manipulation technique. Additionally the result was reinforced in standard microfluidic shear stress channels. Nevertheless, automated micropipette gave higher sensitivity and less side-effect than the shear stress channel. Using our technique, the probed single cells can be easily picked up and further investigated by other techniques; a definite advantage of the computer controlled micropipette. Our experiments revealed the existence of a sub-population of strongly fibrinogen adherent cells appearing in macrophages and highly represented in dendritic cells, but not observed in monocytes.