PubMed Health⌕ Search

Biomedical subjects

W Lund

Publications and source records attributed to W Lund.

12 recordsLinked to original sources
PubMed2003

Kidney transplantation without calcineurin inhibitors using sirolimus.

INTRODUCTION: With the introduction of new immunosuppressive medicines, it has become possible to determine the extent to which nephrotoxic medicines contribute to CAN. The aim of this study is to compare the safety and efficacy of calcineurin inhibitor (CI) free immunosuppression in a prospective, randomized trial comparing sirolimus-mycophenolate mofetil (MMF)-prednisone to tacrolimus- MMF-prednisone. METHODS: Patients are randomized at the time of transplant to receive either tacrolimus (target level 12 to 15 ng/mL in the first month) or sirolimus (target level 12 to 18 ng/mL in the first month). All patients also receive MMF (750 mg bid) and prednisone tapered to 10 mg/d by 3 months and thymoglobulin induction (1.5 mg/kg/d on days 0, 1, 2, 4 and 6). RESULTS: At this point we have 4-month follow-up in 85 patients. The acute rejection rate is 7.5% (3/40) in the tacrolimus group and 6.7% (3/45) in the sirolimus group. We have discontinued sirolimus in eight patients so far, with wound complications being the most common indication. Renal function appears to be better in the sirolimus group at 1 month after transplantation, but the difference is not statistically significant. CONCLUSIONS: While longer follow-up is needed, these results demonstrate that total avoidance of CI can be achieved with extremely low acute cellular rejection rates using sirolimus-based immunosuppression in combination with thymoglobulin, MMF, and prednisone.

Calcineurin Inhibitors↗
PubMed2000

Capillary electrophoresis-inductively coupled plasma mass spectrometry interface with minimised dead volume for high separation efficiency.

A modified microconcentric nebulizer (MCN-100) has been used to construct an improved interface with minimised liquid and gas phase dead volumes for the coupling of capillary electrophoresis (CE) and inductively coupled plasma mass spectrometry (ICP-MS). A plate number of 3.6 x 10(6) plates m(-1) has been achieved. This is an order of magnitude better than the results previously reported for CE-ICP-MS. The separation efficiency of the system is demonstrated by the baseline separation of eight rare earth metals within a time span of 14.6 s. The system was used to control the purity of vitamin B12 and glutaredoxin 2 from Escherichia coli.

Electrophoresis, Capillary↗
PubMed1997

Speciation of aluminium in tea infusions studied by size exclusion chromatography with detection by post-column reaction.

Aluminium-organic species in tea infusions were studied by size exclusion chromatography, using a Superose 12 HR column, a mobile phase of 0.12 mol l-1 tris(hydroxymethyl)aminomethane adjusted to pH 5.5 and detection by UV-visible spectrophotometry. Aluminium was detected after post-column reaction with pyrocatechol violet at 585 nm and the organic material was detected at 280 nm. Teas of different origin were analyzed; the results indicate that aluminium is bound to the same relatively narrow size-range of large organic molecules in the tea infusions, irrespective of the origin of the tea.

Aluminum↗
PubMed1995

Determination of aluminium in liver from reindeer, moose and sheep by electrothermal atomic absorption spectrometry.

Aluminium in liver from reindeer, moose and sheep from the northeast part of Norway was determined by graphite furnace atomic absorption spectrometry following digestion of the samples with nitric acid. The concentration of aluminium in the liver was markedly higher for reindeer than for moose and sheep; the median values obtained were 0.56 microgram g-1 Al (wet wt.) for 101 reindeer, 0.06 microgram g-1 Al for 72 moose and 0.09 microgram g-1 Al for 40 sheep. The detection limit of the method was 0.01 microgram g-1 Al. The NIST SRM 1577a Bovine Liver was also analyzed.

Aluminum↗
PubMed1976

Automated adsorption isotherm device.

A device is described for the automated determination of the water adsorption isotherms of biological materials. The vapor pressure and weight of the adsorbate are measured directly with appropriate transducers, and equilibrium is defined on the basis of constant pressure. The accuracy of the device, determined on two samples with well-known water binding properties, is +/- 5%. Automation is achieved by electronic control.

Adsorption↗
PubMedDate not supplied

Determination of arsenic by inductively coupled plasma mass spectrometry--comparison of sample introduction techniques.

A comparison is made of four sample introduction techniques for the determination of As by inductively coupled plasma mass spectrometry. The techniques studied were 1) flow injection with pneumatic nebulization (FIA-PN), 2) direct electrothermal vaporization (ETV), 3) continuous hydride generation (HG) and 4) hydride generation with in situ trapping followed by electrothermal vaporization (HG-ETV). It was found that FIA-PN and ETV gave similar detection limits in concentration units (about 20 pg mL(-1)), although ETV had a much lower absolute detection limit (0.2 pg). Sample introduction by hydride generation gave an inferior detection limit (100-200 pg mL(-1)), also in combination with in situ trapping and ETV, owing to the blank signal from traces of As in NaBH4 which is difficult to eliminate. The results indicate that the more elaborate sample introduction techniques based on ETV and HG may not offer significant advantages compared to normal solution nebulization for the determination of As in simple sample matrices such as natural fresh waters, where matrix removal is not required.

Journal Article↗