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dc.contributor.authorChuang, Kuo-Hsiangen_US
dc.contributor.authorKao, Chien-Hanen_US
dc.contributor.authorRoffler, Steve R.en_US
dc.contributor.authorLu, Ssu-Jungen_US
dc.contributor.authorCheng, Ta-Chunen_US
dc.contributor.authorWang, Yun-Mingen_US
dc.contributor.authorChuang, Chih-Hungen_US
dc.contributor.authorHsieh, Yuan-Chinen_US
dc.contributor.authorWang, Yeng-Tsengen_US
dc.contributor.authorWang, Jaw-Yuanen_US
dc.contributor.authorWeng, Kuo-Yien_US
dc.contributor.authorCheng, Tian-Luen_US
dc.date.accessioned2014-12-08T15:36:56Z-
dc.date.available2014-12-08T15:36:56Z-
dc.date.issued2014-10-14en_US
dc.identifier.issn0024-9297en_US
dc.identifier.urihttp://dx.doi.org/10.1021/ma501156ren_US
dc.identifier.urihttp://hdl.handle.net/11536/25331-
dc.description.abstractQuantitative pharmacokinetic analysis of methoxy-poly(ethylene glycol) (mPEG) and mPEGylated molecules is important for clinical drug development. Here we developed sensitive sandwich and competitive ELISAs by expressing an anti-mPEG antibody on the surface of fibroblasts for effective capture of mPEG molecules in biological samples. alpha-mPEG sandwich ELISA could quantify the higher-molecular-weight of mPEG (2, 5, and 20 kDa) and mPEGylated molecules. alpha-mPEG cell-based competitive ELISA was developed to measure the lower-molecular-weight of mPEG molecules (559, 750, and 1000 Da) at nanomolar levels. In addition, alpha-mPEG cell-based ELISA was unaffected by the presence of 10% human serum or murine serum. We further demonstrate that the alpha-mPEG cell-based ELISA determined similar pharmacokinetics of mPEG(5K) as traditional gamma counting of I-131-mPEG(5K). The alpha-mPEG cell-based ELISA may provide an accurate, high sensitivity and easy-to-use tool for directly measuring mPEG and mPEGylated molecules in complex biological samples to accelerate the clinical development of mPEG drugs.en_US
dc.language.isoen_USen_US
dc.titleDevelopment of an Anti-Methoxy Poly(ethylene glycol) (alpha-mPEG) Cell-Based Capture System to Measure mPEG and mPEGylated Moleculesen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/ma501156ren_US
dc.identifier.journalMACROMOLECULESen_US
dc.citation.volume47en_US
dc.citation.issue19en_US
dc.citation.spage6880en_US
dc.citation.epage6888en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.identifier.wosnumberWOS:000343196200039-
dc.citation.woscount0-
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