Brinzolamide nanocrystal formulations for ophthalmic delivery: Reduction of elevated intraocular pressure in vivo

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• 作者：Annika Tuomela^a ; ¹ ; ^{annika.tuomela@helsinki.fi" class="auth_mail} ; Peng Liu^a ; ¹ ; Jooseppi Puranen^b ; ¹ ; Seppo Rö ; nkkö ; ^c ; Timo Laaksonen^a ; Giedrius Kalesnykas^b ; ^d ; Olli Oksala^e ; Jukka Ilkka^f ; Johanna Laru^g ; Kristiina Jä ; rvinen^c ; Jouni Hirvonen^a ; Leena Peltonen^a
• 关键词：Brinzolamide ; Glaucoma ; Intraocular pressure ; Nanocrystal suspension ; Ophthalmic delivery
• 刊名：International Journal of Pharmaceutics
• 出版年：5 June 2014
• 年：2014
• 卷：467
• 期：1-2
• 页码：34-41
• 全文大小：975 K

文摘

Nanocrystal-based drug delivery systems provide important tools for ocular formulation development, especially when considering poorly soluble drugs. The objective of the study was to formulate ophthalmic, intraocular pressure (IOP) reducing, nanocrystal suspensions from a poorly soluble drug, brinzolamide (BRA), using a rapid wet milling technique, and to investigate their IOP reducing effect in vivo. Different stabilizers for the nanocrystals were screened (hydroxypropyl methylcellulose (HPMC), poloxamer F127 and F68, polysorbate 80) and HPMC was found to be the only successful stabilizer. In order to investigate both the effect of an added absorption enhancer (polysorbate 80) and the impact of the free drug in the nanocrystal suspension, formulations in phosphate buffered saline (PBS) at pH 7.4 and pH 4.5 were prepared. Particle size, polydispersity (PI), solid state (DSC), morphology (SEM) as well as dissolution behavior and the uniformity of the formulations were characterized. There was rapid dissolution of BRA (in PBS pH 7.4) from all the nanocrystal formulations; after 1 min 100% of the drug was fully dissolved. The effect was significantly pronounced at pH 4.5, where the dissolved fraction of drug was the highest. The cytotoxicity of nanocrystal formulations to human corneal epithelial cell (HCE-T) viability was tested. The effects of the nanocrystal formulations and the commercial product on the cell viability were comparable. The intraocular pressure (IOP) lowering effect was investigated in vivo using a modern rat ocular hypertensive model and elevated IOP reduction was seen in vivo with all the formulations. Notably, the reduction achieved in experimentally elevated IOP was comparable to that obtained with a marketed product. In conclusion, various BRA nanocrystal formulations, which all showed advantageous dissolution and absorption behavior, were successfully formulated.