In this work, we study the mechanical properties of sodium dodecyl sulfate (SDS) and dodecylamine hydrochloride (DAH) micellar films at a graphite surface via atomic force microscopy (AFM). Breakthrough forces for these films were measured using silicon nitride cantilevers and were found to be 1.1 ± 0.1 nN for a 10 mM DAH film and 3.0 ± 0.3 nN for a 10 mM SDS film. For 10 mM SDS films, it was found that the addition of 1.5 mM of NaCl, Na₂SO₄, or MgCl₂ produced a 50-70% increase in the measured breakthrough force. Similar results were found for 10 mM DAH films when NaCl and MgCl₂ were added. A model was developed on the basis of previous work on lipid films and CMC data gathered via spectrofluorometry measurements to predict the change in normalized breakthrough forces with added salt concentrations for SDS and DAH films. Using this model, it was found that the activation volume required to initiate the breakthrough was roughly 0.4 nm³ for SDS and 0.3 nm³ for DAH, roughly the volume of a single molecule. Normalized breakthrough force data for SDS films with added MgCl₂ showed an unexpected dip at low added salt concentrations. The model was adapted to account for changing activation volumes, and a curve of activation volume versus magnesium concentration was obtained, showing a minimum volume of 0.21 nm³. The addition of 0.2 mM SDS to a 10 mM DAH solution was found to double the measured breakthrough force of the film. Images taken of the surface showed a phase change from cylindrical hemimicelles to a planar film that may have produced the observed differences. The pH of the bulk solution was varied for both 10 mM SDS and DAH films and was found to have little effect on the breakthrough force.

Physalis pubescens L. plant produces nutritious and healthy fruits, called husk tomato or hairy ground cherry. However, its bioactive components are largely unknown. Four new withanolide steroids (1-4) together with one known withanolide (5) were isolated from the extract of P. pubescens L. and their chemical structures were established by extensive spectroscopic analyses. Compounds 1, 3 and 5 showed potent growth inhibitory effects against four human renal cell carcinoma (RCC) cell lines (i.e. 786-O, A-498, Caki-2 and ACHN). Among them, compound 1 was the most potent one with IC₅₀s ranged from 0.30 to 0.77 μM. Further experiment showed that 1 sensitized human RCC cells 786-O to the tumor necrosis factor related apoptosis ligand (TRAIL)-induced apoptosis and increased the expression of C/EBP-homologous protein (CHOP) and death receptor-5 (DR5), leading to activation of the DR5 and caspase-8/3 mediated apoptosis pathway. Molecular docking analysis revealed that compound 1 could bind stably to the TRAIL/DR5 complex through hydrogen bonds. These results suggest that the new withanolide (1) is a lead anti-cancer compound existing in P. pubescens L. and deserves further investigation for RCC prevention and treatment.