Aqueous humor concentrations of bimatoprost free acid, bimatoprost and travoprost free acid in cataract surgical patients administered multiple topical ocular doses of LUMIGAN or TRAVATAN
| Autor: | Marlene R. Moster, Cynthia Pailliotet, Kenneth N Sall, Najam A. Sharif, M. Curtis, Kimberly Martens, R. Faulkner, E. Randy Craven, D.C. Dahlin, Jess T. Whitson, Harvey Dubiner, Susan C Orr |
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| Rok vydání: | 2010 |
| Předmět: |
Adult
Male medicine.medical_specialty Free acid medicine.medical_treatment Administration Topical Glaucoma Biological Availability Aqueous humor Cataract Extraction Aqueous Humor Travoprost Bimatoprost Ophthalmic Solution Tandem Mass Spectrometry Ophthalmology medicine Humans Pharmacology (medical) Antihypertensive Agents Intraocular Pressure Aged Pharmacology Aged 80 and over Bimatoprost business.industry Cloprostenol Cataract surgery Middle Aged medicine.disease Amides Female Ocular Hypertension business Glaucoma Open-Angle medicine.drug Surgical patients Chromatography Liquid |
| Zdroj: | Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics. 26(2) |
| ISSN: | 1557-7732 |
| Popis: | To quantify the aqueous humor (AH) concentrations of bimatoprost (amide), travoprost (isopropyl ester), and their hydrolysis products, bimatoprost free acid (BFA) and travoprost free acid (TFA), after multiple topical ocular doses of LUMIGAN and TRAVATAN, respectively, in patients awaiting cataract surgery.In 2 separate open-label, sparse-sampling trials, glaucoma patients with cataracts received LUMIGAN (bimatoprost ophthalmic solution, 0.03%) or TRAVATAN (travoprost ophthalmic solution, 0.004%) bilaterally once daily for at least 21 days prior to cataract surgery. Anterior chamber paracentesis was performed at selected times up to 5 h after the last dose and an AH sample was collected. AH samples were assayed by an independent bioanalytical laboratory using a sensitive and validated tandem LC-MS/MS method. The assay lower limits of quantitation were 0.59 nM for bimatoprost, 0.29 nM for BFA, and 0.44 nM for TFA.AH concentrations of BFA (17-phenyl-trinor PGF(2alpha)) were quantifiable in all but one sample at 0.5 h. The maximum concentration achieved (C(max)) of BFA was 30.9 + or - 16.41 nM (n =5), observed at 2 h postdose. AH concentrations of bimatoprost amide were lower than BFA at all time points, with a C(max) of 6.81 + or - 1.36 nM (n = 7) at 1 h postdose. For TFA, measurable AH concentrations were obtained at all time points with a TFA C(max) of 3.91 + or - 2.27 nM (n = 5), which was observed at 3 h after the dose (all data are mean + or - SEM).Once daily topical ocular administration of LUMIGAN or TRAVATAN for 3 weeks resulted in significant concentrations of BFA and TFA in the AH. Quantifiable levels of bimatoprost amide were also measured. Maximum concentrations of BFA (30.9 nM) and TFA (3.91 nM) in the anterior chamber are sufficient to fully activate the FP prostanoid receptors in the target cells of the ciliary muscle and trabecular meshwork. Both bimatoprost in LUMIGAN and travoprost in TRAVATAN are essentially prodrugs that are rapidly hydrolyzed to their respective free acids that induce the IOP-lowering effect observed with both drugs in vivo. |
| Databáze: | OpenAIRE |
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