Taipei Medical University

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Sheu MT, Ho HO, Wang PY, Liou YB, and Wu AB*
------>authors3_c=None
------>paper_class1=1
------>Impact_Factor=None
------>paper_class3=2
------>paper_class2=1
------>vol=41
------>confirm_bywho=kyhsu
------>insert_bywho=anbangwu
------>Jurnal_Rank=None
------>authors4_c=None
------>comm_author=1
------>patent_EDate=None
------>authors5_c=None
------>publish_day=None
------>paper_class2Letter=None
------>page2=204
------>medlineContent=
------>unit=G0400
------>insert_date=20030912
------>iam=5
------>update_date=
------>author=???
------>change_event=5
------>ISSN=None
------>authors_c=None
------>score=500
------>journal_name=J. Chromatogr. Sci.
------>paper_name=Photolysis of NSAIDS. I. Photodegradation Products of Carprofen determined by LC-ESI-MS
------>confirm_date=20031020
------>tch_id=065001
------>pmid=12803808
------>page1=200
------>fullAbstract=A solution of carprofen in methanol at a concentration of 2.74 x 10(-2) mg/mL is subjected to photoirradiation using a Hanovia 200-W high-pressure Hg lamp for 9 h. In total, seven photodegradation products are separated, and their quasimolecular ions are subsequently determined online using a liquid chromatography (LC)-electrospray ionization (ESI)-mass spectrometry (MS) method. The high-performance LC consists of an Inertsil 5 ODS-80A (2.1- x 150-mm) column. The mobile phase is initially CH(3)CN. NH(4)OAc (20mM in de-ionized H(2)O) is 43:57 (v/v), and after 14 min it is CH(3)CN. NH(4)OAc (20mM in de-ionized H2O) is 54: 46 (v/v). The UV detector was set at 260 nm. The parameters of LC-MS for mass determination involves an atmospheric pressure ionization electron spray interface with a negative mode of polarity (ESI(-)). The chemical structures of the degradants are elucidated based on the mass-to-charge ratio of the quasimolecular ions and the molecular weight changes by comparison with the parent drug (carprofen). The degradation proceeds via an initial dechlorination. A dechlorination or esterification reaction is competed with decarboxylation. This finding is in accordance with our previously reported result of first order photodecomposition kinetics for carprofen.
------>tmu_sno=None
------>sno=7545
------>authors2=None
------>authors3=None
------>authors4=None
------>authors5=None
------>authors6=None
------>authors6_c=None
------>authors=Sheu MT, Ho HO, Wang PY, Liou YB, and Wu AB*
------>delete_flag=0
------>SCI_JNo=None
------>authors2_c=None
------>publish_area=None
------>updateTitle=Photolysis of NSAIDs. I. photodegradation products of carprofen determined by LC-ESI-MS.
------>language=2
------>check_flag=
------>submit_date=
------>country=None
------>no=4
------>patent_SDate=None
------>update_bywho=
------>publish_year=2003
------>submit_flag=
------>publish_month=None
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z