Serum protein binding of lerisetron, a novel specific 5HT3 antagonist, in patients with cancer
| Autor: | Elena Suarez, Ma Luisa Lucero, Ana Gonzalo, Ewa Raczka, Ignacio F. Trocóniz, Rosario Calvo, Aurelio Orjales, R.M. Jiménez |
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| Rok vydání: | 1998 |
| Předmět: |
Adult
Male Cancer Research medicine.medical_specialty medicine.drug_class Lerisetron Serum albumin Orosomucoid Toxicology Pharmacokinetics Piperidines Internal medicine Neoplasms medicine Antiemetic Humans Pharmacology (medical) Carbon Radioisotopes Serum Albumin Pharmacology biology business.industry Antagonist Middle Aged Receptor antagonist Human serum albumin Endocrinology Oncology Receptors Serotonin biology.protein Antiemetics Benzimidazoles Female Serotonin Antagonists Receptors Serotonin 5-HT3 business medicine.drug Protein Binding |
| Zdroj: | Cancer chemotherapy and pharmacology. 42(5) |
| ISSN: | 0344-5704 |
| Popis: | The aim of this study was, (1) to characterize the serum protein binding of lerisetron, a new 5-hydroxytryptamine (5-HT3) receptor antagonist under investigation as an antiemetic agent, and (2) to measure the percentage of unbound lerisetron in cancer patients. The binding parameters were determined in human serum albumin (HSA), alpha1-acid glycoprotein (AAG) and in pooled serum from six healthy volunteers. Concentrations of lerisetron ranging from 50 ng/ml to 2 microg/ml were used. The serum protein binding of 14C-lerisetron (2 microg/ml) was determined by ultrafiltration in three groups of individuals. Group I comprised healthy subjects (n = 11), group II comprised cancer patients undergoing radiotherapy (n = 9), and group III comprised cancer patients receiving chemotherapy (n = 18). The unbound concentration of lerisetron was measured in all samples by liquid scintillation counting. Concentrations of both AAG and HSA were also measured in all serum samples. The drug was extensively bound in pooled serum, involving a nonsaturated process. In HSA, lerisetron was also highly bound (4.04+/-0.8% unbound) and the protein binding was essentially unchanged within the studied concentration range of lerisetron. The extent of binding to AAG was high but significantly lower than in serum and in HSA and was also independent of lerisetron concentration. The unbound lerisetron was significantly decreased in group II cancer patients when compared with group I subjects (2.38+/-0.64% vs 3.70+/-0.70%; P0.001). No significant changes in lerisetron binding were observed in group III patients. HSA was diminished in both groups of patients and AAG was only significantly increased in group II. Unbound lerisetron was correlated with AAG in group II and with HSA in group III. |
| Databáze: | OpenAIRE |
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