Adaptation and performance of an immuno-PCR assay for the quantification of Aviscumine in patient plasma samples

Average recovery was found to be 95 ± 19% and the average deviation in precision of the assay was determined to be 9 ± 5%. Data for the quantification of Aviscumine were obtained from all patient samples investigated with the exception of a single patient. The collected data provided the basis for the valid routine quantification of patient samples for the calculation of the pharmacokinetic behaviour of Aviscumine in patient plasma.