» Articles » PMID: 18547433

Comparative Study of the Stability of Bimatoprost 0.03% and Latanoprost 0.005%: a Patient-use Study

Overview
Journal BMC Ophthalmol
Publisher Biomed Central
Specialty Ophthalmology
Date 2008 Jun 13
PMID 18547433
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Background: The stability of ophthalmic preparations in multidose containers is influenced by the preservative as well as the stability of the active ingredient. Unstable drugs may require refrigeration to preserve their active ingredient level and they are more likely to degrade over time, therefore becoming more susceptible to degradation based on patient mishandling. The purpose of this study was to determine the degree of molecular degradation that occurs in bimatoprost and latanoprost in a patient-use setting.

Methods: This was an open-label, laboratory evaluation of the relative stability of bimatoprost and latanoprost. Patients presently using bimatoprost (n = 31) or latanoprost (n = 34) were identified at 2 clinical sites in Brazil. Patients were instructed to use and store their drops as usual and return all used medication bottles between day 28 and day 34 after opening.

Results: Bimatoprost demonstrated no degradation, but latanoprost degraded at various levels. The mean age of bimatoprost was 43.0 +/- 3.4 days and the mean age of latanoprost was 43.9 +/- 2.8 days (P = .072). The mean percentage of labeled concentration was 103.7% in the bimatoprost bottles and 88.1% in the latanoprost bottles (P < 001).

Conclusion: This study showed that bimatoprost maintained > or =100% concentration throughout the study period while latanoprost did not.

Citing Articles

Evaluation of Physical Properties of Generic and Branded Travoprost Formulations.

Wadhwani M, Mishra S, Angmo D, Velpandian T, Sihota R, Kotnala A J Curr Glaucoma Pract. 2016; 10(2):49-55.

PMID: 27536047 PMC: 4981658. DOI: 10.5005/jp-journals-10008-1201.


Evaluation of physical properties and dose equivalency of generic versus branded latanoprost formulations.

Angmo D, Wadhwani M, Velpandian T, Kotnal A, Sihota R, Dada T Int Ophthalmol. 2016; 37(2):423-428.

PMID: 27334605 DOI: 10.1007/s10792-016-0280-x.


Thermal stability of bimatoprost, latanoprost, and travoprost under simulated daily use.

Johnson T, Gupta P, Vudathala D, Blair I, Tanna A J Ocul Pharmacol Ther. 2010; 27(1):51-9.

PMID: 21117945 PMC: 3038126. DOI: 10.1089/jop.2010.0115.


Bimatoprost: a review of its use in open-angle glaucoma and ocular hypertension.

Curran M Drugs Aging. 2009; 26(12):1049-71.

PMID: 19929032 DOI: 10.2165/11203210-000000000-00000.

References
1.
Alm A, Widengard I, Kjellgren D, Soderstrom M, Fristrom B, Heijl A . Latanoprost administered once daily caused a maintained reduction of intraocular pressure in glaucoma patients treated concomitantly with timolol. Br J Ophthalmol. 1995; 79(1):12-6. PMC: 505011. DOI: 10.1136/bjo.79.1.12. View

2.
DuBiner H, Cooke D, Dirks M, Stewart W, VanDenburgh A, Felix C . Efficacy and safety of bimatoprost in patients with elevated intraocular pressure: a 30-day comparison with latanoprost. Surv Ophthalmol. 2001; 45 Suppl 4:S353-60. DOI: 10.1016/s0039-6257(01)00212-0. View

3.
Varma R, Winarko J, Kiat-Winarko T, Winarko B . Concentration of latanoprost ophthalmic solution after 4 to 6 weeks' use in an eye clinic setting. Invest Ophthalmol Vis Sci. 2005; 47(1):222-5. DOI: 10.1167/iovs.04-1367. View

4.
Laibovitz R, VanDenburgh A, Felix C, David R, Batoosingh A, Rosenthal A . Comparison of the ocular hypotensive lipid AGN 192024 with timolol: dosing, efficacy, and safety evaluation of a novel compound for glaucoma management. Arch Ophthalmol. 2001; 119(7):994-1000. DOI: 10.1001/archopht.119.7.994. View

5.
Asrani S, Zeimer R, Wilensky J, Gieser D, Vitale S, Lindenmuth K . Large diurnal fluctuations in intraocular pressure are an independent risk factor in patients with glaucoma. J Glaucoma. 2000; 9(2):134-42. DOI: 10.1097/00061198-200004000-00002. View