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A universal mechanism for the action of general anesthetics (GA) is not yet available. In this study, we investigated the interaction between halothane and 1,2-dipalmitoyl-sn-3-glycero-3-phosphocholine (DPPC) and 1,2-dioleoyl-sn-3-glycero-3-phosphocholine (DOPC) bilayers labeled with Laurdan, Prodan, and NBD-C6-PC as the reporter probes using steady-state fluorescence spectroscopy. We have evidence that halothane is located on the acyl chain side, near the headgroup region of the bilayer. Additionally, we find that halothane may be inhomogeneously distributed within DOPC and DPPC bilayers. We also show data that indicate halothane increases the free volume available to fluorescent probes. Differential scanning calorimetry and UV scanning calorimetry experiments were implemented to further observe the effects of halothane addition to the DPPC lipid bilayer. A significant shift of the phase-transition temperature of the DPPC system was observed. Our findings suggest that general anesthetic – lipid bilayer interactions may play a significant role in the overall mechanism of anesthetic action, and these effects should not be ignored when interactions between membrane proteins and anesthetics are considered.Key words: liposomes, anesthesia, fluorescence, phase transition, phospholipid bilayers.

The known thermal and hydrolytic stability of bismuth-sulfur bonds indicates that biological targets for bismuth likely involve thiol or thiolate functionalities, such as in L-cysteine. Complexes of bismuth with cysteine or other thiol-carboxylic acid ligands have been isolated and characterized providing a preliminary view of the potential participation of these functional groups in the biochemical mechanisms involving bismuth. A broader assessment of bismuth-thiolate interactions has been possible using electrospray ionization mass spectrometry (ESI-MS). A wide range of complexes has been observed containing mercaptosuccinic acid, 2-mercaptopropionic acid, 3-mercaptopropionic acid, and/or 2-amino-3-mercaptopropionic acid (cysteine). The identification of various multibismuth multiligand cluster ions defines new chemistry for bismuth.

Chemistry students are often introduced to the concept of reaction rates through demonstrations or laboratory activities involving the well-known iodine clock reaction. For example, a laboratory experiment involving thiosulfate as an iodine scavenger is part of the first-year general chemistry laboratory curriculum at Dalhousie University. With the necessary materials, expertise, and laboratory space readily available, this undergraduate clock reaction experiment was modified to make it accessible to grade 9 students. The revised, qualitative experiment has been performed as an on-campus outreach initiative with eight grade 9 classes, reaching a total of 250 students, teachers, parents, and aides. The activity was facilitated by graduate student volunteers, who assisted the grade 9 students as they were exposed to a colorful adventure involving kinetics, chemical reactions, and catalysis. In general, adapting undergraduate experiments offers researchers and educators a positive and efficient way to introduce younger students to a university chemistry laboratory.

Recent studies of attraction to sodium chloride baits suggest that diverse ant species forage for salt. We used experimental presentations of salt baits to test whether leaf cutter ants (Atta cephalotes) are attracted to and harvest salt-treated paper baits that offer no other resources. Atta foragers were most attracted to sucrose baits (positive control), but more foragers touched and cut salt-treated baits than water-treated baits (negative control). Furthermore, the ants removed more paper from the salt baits than from water-treated baits. We conclude that leaf cutter ants expend time and energy to harvest salt in the absence of other rewards. Salt could be harvested for the workers' consumption, or it could be fed to the fungus gardens in the ants' nest.