Multiple pathogen contamination of water, hands, and fomites in rural Nepal and the effect of WaSH interventions.

Water, Sanitation, and Hygiene (WaSH) interventions are the most effective in reducing diarrheal disease severity and prevalence. However, very few studies have investigated the effectiveness of WaSH intervention in reducing pathogen presence and concentration. In this study, we employed a microfluidic PCR approach to quantify twenty bacterial pathogens in water (n = 360), hands (n = 180), and fomite (n = 540) samples collected in rural households of Nepal to assess the pathogen exposures and the effect of WaSH intervention on contamination and exposure rates.

Study on the fluidity of foamed alkali-activated slag cementitious material (AASCM).

This study aims to investigate the evolution patterns of fluidity and rheological properties of AASCM under varying dosages of foaming agent and particle sizes of filling aggregate. The flow characteristics of AASCM are significantly affected by the filling aggregate's size and the foaming agent's dosage. Specifically, an increase in filling aggregate size (D(4,3) ϵ [26 μm, 69 μm]) enhances the fluidity of foamed AASCM, while an increase in foaming agent dosage reduces fluidity.

Experimental Investigation of CO-Induced Silica Gel as the Water Blocking Grout Effect of Aquifer Ions.

This study aimed to prevent water flow in microcracks and simultaneously achieve CO capture during grouting (CCG). Using sodium silicate (SS) as the primary material, the microcracks were grouted by a two-step approach. The low-initial-viscosity (5 mPa s) SS was first saturated within the microcracks followed by CO injection at 2 MPa.

Synthesis and evaluation of inhibitors of Mycobacterium tuberculosis UGM using bioisosteric replacement.

There is a dearth of tuberculosis (TB) drug development activity as current therapeutic treatments are inadequate due to the appearance of drug-resistant TB. The enzyme UDP-galactopyranose mutase (UGM) is involved in the biosynthesis of galactan which is essential for cell wall integrity and bacterial viability. Its inhibition has thus been featured as profitable strategy for anti-TB drug discovery.