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Postural effects on peritoneal transport and systemic uptake of radiolabeled monoclonal antibodies

dc.contributor.authorWahl, Richard L.en_US
dc.contributor.authorBarrett, Jeffrey S.en_US
dc.contributor.authorFisher, Susan J.en_US
dc.date.accessioned2006-09-08T19:57:08Z
dc.date.available2006-09-08T19:57:08Z
dc.date.issued1997-06en_US
dc.identifier.citationBarrett, Jeffrey S.; Fisher, Susan J.; Wahl, R. L.; (1997). "Postural effects on peritoneal transport and systemic uptake of radiolabeled monoclonal antibodies." Cancer Immunology, Immunotherapy 44(3): 173-178. <http://hdl.handle.net/2027.42/42083>en_US
dc.identifier.issn0340-7004en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/42083
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=9191877&dopt=citationen_US
dc.description.abstract To optimize the regional delivery advantage with i. p. administration of monoclonal antibody (mAb) for radioimmunotherapy, it may be possible to delay the rate and extent of mAb absorption from the peritoneal cavity by simply altering the position of a patient after radioantibody administration. It has been shown that the hydrostatic pressure against the diaphragm plays a major role in the rate of egress of radioantibodies from the peritoneal cavity and that fluid removal from the peritoneal cavity can be altered by posture. The current study examined postural effects in normal rats following the i. p. injection of 125 I-5G6.4 murine IgG2a anticarcinoma antibody (45 μCi). A 10-ml injection volume of the radioantibody solution was administered to rats restrained in either a supine or inclined (reverse Trendelenburg; feet down at a 45° angle) position. Pharmacokinetic analysis confirmed that the appearance of the radioantibody into the systemic circulation was delayed in the inclined group. The time to peak blood concentration was prolonged from 14.7 (supine) to 19.2 (inclined) hours ( P = 0.005). All other pharmacokinetic parameters were equivalent across the treatment groups. The mean half-life of 166 h, mean blood clearance of 9 ml/min, and mean steady-state volume of distribution of 36 ml were consistent with previous experience with this radioantibody in the rat. The intrinsic absorption profile indicated that the mean percentage absorption from the peritoneal cavity to the blood stream was greater in the supine animals from 4 h after i. p. injection until absorption was complete. By 10 h after injection, absorption from the peritoneal cavity was essentially complete in the supine-dosed animals, while those restrained in an inclined position had cleared only 50% of the total absorbed dose. Hence, the regional delivery advantage afforded by intraperitoneal administration of the radioantibody may be further exploited by maintaining an inclined position throughout the absorption phase, a strategy that may be applicable to radioimmunotherapy of patients.en_US
dc.format.extent161917 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlag; Springer-Verlag Berlin Heidelbergen_US
dc.subject.otherPharmacokineticsen_US
dc.subject.otherPostureen_US
dc.subject.otherKey Words Monoclonal Antibodiesen_US
dc.subject.otherLegacyen_US
dc.subject.otherIntraperitonealen_US
dc.titlePostural effects on peritoneal transport and systemic uptake of radiolabeled monoclonal antibodiesen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelMicrobiology and Immunologyen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDivision of Nuclear Medicine, Box 0028, Department of Internal Medicine and Department of Radiology, University of Michigan Medical Center, 1500 East Medical Center Drive Ann Arbor, MI 48109-0028, USA, USen_US
dc.contributor.affiliationumDivision of Nuclear Medicine, Box 0028, Department of Internal Medicine and Department of Radiology, University of Michigan Medical Center, 1500 East Medical Center Drive Ann Arbor, MI 48109-0028, USA, USen_US
dc.contributor.affiliationotherDuPont Merck Pharmaceuticals, Department of Drug Metabolism and Pharmacokinetics, Newark, Del., USA, USen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid9191877en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/42083/1/262-44-3-173_70440173.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/s002620050370en_US
dc.identifier.sourceCancer Immunology, Immunotherapyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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