Development and validation for the determination of olopatadine in human plasma by liquid chromatography–tandem mass spectrometry: application to a bioequivalence study of Ilhwa Allotadine tablet (olopatadine HCl 5 mg)-Reference-Cited by-同舟云学术

Development and validation for the determination of olopatadine in human plasma by liquid chromatography–tandem mass spectrometry: application to a bioequivalence study of Ilhwa Allotadine tablet (olopatadine HCl 5 mg)

Published:2015-01-25 Issue:3 Volume:45 Page:285-292
ISSN:2093-5552
Container-title:Journal of Pharmaceutical Investigation
language:en
Short-container-title:Journal of Pharmaceutical Investigation

Author:

Choi Soo-Wan,Ryu Ju-Hee,Park Ji-Sun,Lee Myung-Jae,Yim Sung-Vin,Lee Kyung-Tae

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology, Toxicology and Pharmaceutics (miscellaneous),Pharmaceutical Science

Link

http://link.springer.com/content/pdf/10.1007/s40005-015-0175-2.pdf

Reference13 articles.

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3. Chu NN, Chen WL, Xu HR, Li XN (2009) Pharmacokinetics of orally administered single—and multiple-dose olopatadine in healthy Chinese subjects: an open-label study. Clin Drug Investig 29(7):451–457

4. Fujimaki K, Lee XP, Kumazawa T, Sato J, Sato K (2006) Determination of some antiallergic drugs in human plasma by direct-injection high-performance liquid chromatography-tandem mass spectrometry. Forensic Toxicol 24:8–16

5. Fujita K, Magara H, Kobayashi H (1999) Determination of olopatadine, a new antiallergic agent, and its metabolites in human plasma by high-performance liquid chromatography with electrospray ionization tandem mass spectrometry. J Chromatogr B 731:345–352

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