Bioavailability of Ruminally or Abomasally Infused L-carnitine in Holstein Heifers

This study evaluated the relative bioavailability of carnitine delivered by different methods in dairy cattle. Four Holstein heifers were used in a split-plot design to compare ruminally or abomasally infused L-carnitine. The study included 2 main-plot periods, with infusion routes allocated in a crossover design. Within main-plot periods, each of 3 subplot periods consisted of 4-d infusions separated with 4-d rest periods. Subplot treatments were infusion of 1, 3, and 6 g L-carnitine daily. Doses were increased within a period to minimize carryover. Treatments were delivered in two 10-h infusions daily. Blood was collected before the start of infusions and on day 4 of each infusion to obtain baseline and treatment carnitine concentrations. There was a dose × route interaction (P \u3c 0.05) and route effect (P \u3c 0.01) for increases in plasma carnitine above baseline, with increases above baseline being greater across all dose levels when infused abomasally compared to ruminally. Results demonstrated superior bioavailability of carnitine when ruminal exposure was physically bypassed

Bioavailability of Rumen-Protected Carnitine in Lactating Dairy Cows

For this study, 56 lactating Holstein cows (143 ± 72 days in milk) were used in a randomized complete block design to evaluate 2 rumen-protected products compared to crystalline carnitine. Treatments were a) control, b) 3 grams/day crystalline L-carnitine (raw), c) 6 grams/day raw, d) 5 grams/day 40COAT (40% coating, 60% L-carnitine), e) 10 grams/day 40COAT, f) 7.5 grams/day 60COAT (60% coating, 40% L-carnitine), and g) 15 grams/day 60COAT. Treatments were top-dressed to diets twice daily. The 14-day experiment included a 6-day baseline-measurement period with the final 2 days used for data and sample collection and an 8-day treatment period with the final 2 days used for data and sample collection. Plasma, urine, and milk samples were analyzed for L-carnitine. Crystalline (P \u3c 0.001) and 40COAT (P = 0.01) linearly increased plasma L-carnitine, and 60COAT tended to linearly increase plasma L-carnitine (P = 0.08). Total daily excretion (milk + urine) of L-carnitine averaged 1.52 ± 0.04 grams in controls, increased linearly with crystalline and 40COAT, and increased quadratically with 60COAT (all P \u3c 0.05). Crystalline increased plasma L-carnitine and milk + urine L-carnitine more than 40COAT and 60COAT (all P \u3c 0.05). Carnitine supplementation increased carnitine concentrations in plasma, milk, and urine; however, the rumen protection did not provide additional increases in concentration

Synthesis of carboxylated derivatives of poly(isobutylene-co-isoprene) by azide–alkyne “click” chemistry

The final publication is available at Springer via https://dx.doi.org/10.1038/s41428-018-0130-yThe synthesis of carboxylated derivatives of poly(isobutylene-co-isoprene) (isobutylene–isoprene rubber, IIR) with substitution levels ranging from 1 to 4 mol% and different spacer lengths was accomplished through azide–alkyne Huisgen cycloaddition. Azido-functionalized IIR was first prepared by reacting brominated IIR with sodium azide to full conversion in a 90:10 tetrahydrofuran/N,N-dimethylacetamide mixture. The click reaction of azido-functionalized IIR with acetylenic acids, which was carried out using the copper(I) bromide/N,N,N′,N″,N″-pentamethyldiethylenetriamine catalyst system in tetrahydrofuran, yielded carboxylated IIRs. The products were characterized by 1H NMR and FT-IR spectroscopy, and their molecular weight was determined by size exclusion chromatography analysis. The conversion to carboxylated groups reached up to 100% as determined by NMR spectroscopy but was highly dependent on the type of solvent and the amounts of catalysts and reactants used in the procedures.ARLANXEO Canada Inc.Natural Sciences and Engineering Research Council (NSERC) of Canad