Oligosaccharide profiles of Asian commercial honeys

As part of the development of a method to detect honey in imported materials, a database of the oligosaccharide composition of a range of Asian commercial honeys has been prepared. Low maltose contents were detected compared with literature values for honey from Europe, North Africa and South America; with this exception oligosaccharide contents were similar to those in the literature. Moisture contents were slightly high compared with literature values for Europe and North America but comparable with literature values for Asia. Moisture, monosaccharide and sucrose contents were generally within the limits applied by the Codex. Four honeys were apparently adulterated

Efficient routes to epimerically-pure side-chain derivatives of lanosterol

A technically simple route is described to individual epimers of side-chain derivatives of lanosterol (3-hydroxy-5-lanosta-8,24-diene). Epimerically pure 24,25-epoxy-, 24,25-dihydroxy- and 24-bromo-25-hydroxy-lanosterol have been prepared in good yield from commercial (50-60%) lanosterol. Hypophosphorous acid was used as a catalyst for the cohalogenation of the 24(25) bond and also for the efficient conversion of 24,25-epoxy- and 24-bromo-25-hydroxylanosterol to epimerically pure 24(R) or 24(S)-24,25-dihydroxylanosterols

Determination of total potentially available nucleosides in bovine milk

Bovine colostrum and milk samples were collected from two herds over the course of the first month post-partum, pooled for each herd by stage of lactation and total potentially available nucleosides were determined. Sample analysis consisted of parallel enzymatic treatments, phenylboronate clean-up, and liquid chromatography to quantify contributions of nucleosides, monomeric nucleotides, nucleotide adducts, and polymeric nucleotides to the available nucleosides pool. Bovine colostrum contained high levels of nucleosides and monomeric nucleotides, which rapidly decreased as lactation progressed into transitional milk. Mature milk was relatively consistent in nucleoside and monomeric nucleotide concentrations from approximately the tenth day post-partum. Differences in concentrations between summer-milk and winter-milk herds were largely attributable to variability in uridine and monomeric nucleotide concentrations

A low-toxicity method for the separation of lanosterol and dihydrolanosterol from commercial mixtures

We describe an inexpensive, low-toxicity and high-yielding method for the production of pure lanosterol and dihydrolanosterol from the commercially available mixture. Optimum conditions are presented for the one-pot production of the intermediate 24,25 vicinal diol of lanosterol acetate (via either epoxidation or hydroxyhalogenation) which is readily separated from the unreacted dihydrolanosterol acetate. The lanosterol diol can then be converted to pure (>97%) lanosterol. Hypophosphorous acid was used for both the conversion of the epoxide to the diol, and as a catalyst for the hydroxyhalogenation by N-halosuccinimides of the olefinic bond

Carbonisation of biomass-derived chars and the thermal reduction of a graphene oxide sample studied using Raman spectroscopy

Chars and carbonised chars were produced from three different oxygen-rich precursors (Pinus radiata wood, Phormium tenax leaf fibres, and sucrose crystals). These non-graphitisable carbons were analysed with Raman spectroscopy in order to study the nanostructural development which occurs with increasingly severe heat treatments up to approximately 1000 °C. The thermal reduction of a graphene oxide sample was similarly studied, as this is considered to involve the development of nanometre-scale graphene-like domains within a different oxygen-rich precursor. Increasing the heat treatment temperatures used in the charring and carbonisation processes, led to significant changes in a number of parameters measured in the Raman spectra. Correlations based on these parameter changes could have future applications in evaluating various char samples and estimating the heat treatment temperatures employed during their manufacture. After production heat treatment temperatures exceeded 700 °C, the Raman spectra of the carbonised chars appeared to be largely precursor independent. The spectra of these carbonised chars were similar to the spectra obtained from thermally-reduced graphene oxides, especially when compared to a wide range of other carbonaceous materials analysed using this particular methodology. Partial reduction of a graphene oxide sample due to reasonably mild laser exposures during Raman analysis was also observed

Sorption of sulfamethoxazole, sulfachloropyridazine and sulfamethazine onto six New Zealand dairy farm soils

We have investigated the sorption potential of three sulfonamides (SAs) in six New Zealand dairy farming soils using a modified batch equilibrium method employing 0.005 M CaCl₂ as background solution. Both liquid and solid phases were extracted to analyse for the antibiotic concentrations in order to avoid underestimation that may arise a result of photolysis or biotic degradation. The experimental data were later used to construct Freundlich isotherms to determine the effective distribution coefficients. Low log Koc value for all SAs suggests considerable leaching potential for SAs under conditions that are conducive for leaching. The sorption affinity for all soils followed the trend SCP>SMZ>SMO

Studying carbonisation with raman spectroscopy

Raman spectroscopy can provide fast and non-destructive analysis of carbonaceous materials. As it is able to detect nanometre-sized structural features, Raman spectroscopy is widely used in the study of carbon nanotubes, fullerenes, graphenes, and many other carbon-rich materials. Raman analysis has previously shown potential for estimating the heat treatment temperatures (HTT) employed in the preparation of Japanese cedar charcoals which suggested future usefulness in quality control . In the current work, Raman spectroscopy was used to investigate the nanostructural development which had occurred within various chars prepared and carbonised at a range of heat treatment temperatures between ≈ 340°C and 1000°C. Chars were produced from sucrose sugar as standard precursor of high purity and two sources of biomass common in New Zealand (Radiata pine wood and Harakeke leaf fibres). In chars produced at lower HTTs, signals could be detected which were interpreted as representing hydrogen-rich amorphous carbon structures. In contrast, the Raman spectra of well-carbonised chars produced at higher HTTs featured signals consistent with graphene-like structures with coherent domains limited in size to below a few nanometres across. Measurement of such signals provides the ability to evaluate the extent of nanostructural development, identify char samples which are ‘undercooked’ when compared to other char samples, and estimate effective HTTs used in the production of a given char sample. More detailed Raman analysis of Radiata-derived chars was carried out, including analysis of chars produced from carbonising pyrolysis tars. Results of Raman analysis were correlated to H/C atom ratios obtained through elemental analysis for these chars produced from Radiata pine

Decolouring bloodmeal: Consumption and potential recycling of peracetic acid

A method of deodorizing and decolouring bloodmeal using an equilibrium mixture of peracetic acid, hydrogen peroxide, acetic acid and water has been developed to improve its marketability as a source of protein for bioplastics. The objective of this study was to determine what quantity of peracetic acid is required to give reasonable bleaching of the bloodmeal and determine whether there is potential for the wastewater to be recycled. This was carried out by measuring the quantity of chemical species in the initial equilibrium mixture and the resulting wastewater upon bleaching using volumetric analysis. Bleaching efficacy was determined after exposing 100 g bloodmeal to 1.1, 2.5, 3.6, 4.5 and 5.6 wt% peracetic acid solutions as either 300 g total solution or a constant molar equivalent of 2.2 mmol peracetic acid/g bloodmeal and using a chromameter to measure colour change. Addition of 300 g 5.6 wt% peracetic acid solution resulted in effective bleaching. This represented a ratio of 2.20 mmol peracetic acid/g bloodmeal of which 1.4 mmol peracetic acid/g bloodmeal was consumed (63%). If 300 g 300 g of <2.5 wt% solution is added such that there is still 2.2 mmol peracetic acid/g bloodmeal, bleaching is still insufficient. These results suggest that an excess of peracetic is required for bleaching to occur, and that its concentration is paramount to bleaching efficacy. Due to the excess of peracetic acid used in the bleaching process, there is potential for wastewater recycling to be carried out provided that the wastewater is not diluted

An investigation by LA-ICP-MS of possum tooth enamel as a model for identifying childhood geographical locations of historical and archaeological human from New Zealand

LA -IC P-MS (laser ablation-inductively coupled plasma-mass spectrometry) has been used to analyse enamel from the teeth of brushtail possum (Trichosurus vulpecula) in order to model a method for identifying the childhood geographical origin of human remains within New Zealand. The model application of the method is promising for establishing locations of historical and archaeological human remains, including preserved heads, upoko tuhi

Analysis of the flavonoid component of bioactive New Zealand mānuka (Leptospermum scoparium) honey and the isolation, characterisation and synthesis of an unusual pyrrole

The flavonoid components of New Zealand mānuka (Leptospermum scoparium) honey have been quantified in a series of 31 honeys of varying non-peroxide antibacterial activity to clarify discrepancies between previous studies reported in the literature. Total flavonoid content was 1.16 mg/100 g honey. The principal flavonoids present were pinobanksin, pinocembrin, luteolin and chrysin and together these represented 61% of the total flavonoid content. 1, 2-formyl-5-(2-methoxyphenyl)-pyrrole, which was weakly correlated with the non-peroxide antibacterial activity, was isolated from the flavonoid fraction and separately synthesised. 1 did not display inhibitory activity against Staphylococcus aureus in vitro and thus the origin of the correlation, which is still unknown, is not a direct contribution