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11. |
Pharmacokinetics of Cyclosporine A After Intravenous and Oral Administration in Liver Transplant Patients Measured with High‐Performance Liquid Chromatography |
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Therapeutic Drug Monitoring,
Volume 15,
Issue 1,
1993,
Page 60-64
I. Klompmaker,
J. Wierda,
W. Sluiter,
D. Uges,
E. Haagsma,
R. Verwer,
M. Slooff,
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摘要:
Cyclosporine A (CsA) bioavailability after i.v. and oral administration was studied in six stable liver transplant patients with open and clamped bile drain. CsA levels were determined by the high-performance liquid chromatography method (HPLC). External bile drainage decreased CsA absorption considerably. Clamping the bile drain resulted in higher and earlier peak CsA levels. Clamping the bile drain increased the bioavailability (9.6% vs. 7%,p< 0.05), but even then it was considerably lower than the value of ∼30% generally reported in literature. It is recommended to continue i.v. CsA administration to obtain therapeutic plasma concentrations. Early bile drain clamping or bile refeeding will improve CsA absorption and may also result in continuously therapeutic CsA levels.
ISSN:0163-4356
出版商:OVID
年代:1993
数据来源: OVID
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12. |
A Reliable High‐Performance Liquid Chromatography Assay for High‐Throughput Routine Cyclosporin A Monitoring in Whole Blood |
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Therapeutic Drug Monitoring,
Volume 15,
Issue 1,
1993,
Page 65-69
P. Salm,
R. Norris,
P. Taylor,
D. Davis,
P. Ravenscroft,
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PDF (368KB)
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摘要:
We report here a reliable high-performance liquid chromatography-ultraviolet assay for routine assay of cyclosporin A (CsA) in whole blood using solid-phase extraction. This assay is linear, between 20 and 2,000 μg/L, with correlation coefficients >0.998 for five consecutive standard curves. All coefficients of variation (CV) were <8% at CsA concentrations of 45, 480, and 1,800 μg/L, with the exception of the between-day CV at 45 μg/L, which was <15%. The relative accuracy of the method is >94% at 45, 480, and 1,800 μg/L. The mean recoveries for CsA and cyclosporin D (internal standard) were 38.2 ± 4.8% (n = 45) and 40.1 ± 6.7% (n = 45), respectively. This method has proven to be reliable and robust in a high-throughput therapeutic drug monitoring laboratory.
ISSN:0163-4356
出版商:OVID
年代:1993
数据来源: OVID
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13. |
Announcements |
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Therapeutic Drug Monitoring,
Volume 15,
Issue 1,
1993,
Page 70-70
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PDF (24KB)
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ISSN:0163-4356
出版商:OVID
年代:1993
数据来源: OVID
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