Literature DB >> 32240806

Tailored gatifloxacin Pluronic® F-68-loaded contact lens: Addressing the issue of transmittance and swelling.

Furqan A Maulvi1, Riya J Parmar2, Ankita R Desai2, Ditixa M Desai2, Manish R Shukla3, Ketan M Ranch2, Shailesh A Shah2, Dinesh O Shah4.   

Abstract

Loading of gatifloxacin in contact lenses affects critical lens properties (optical and swelling) owing to drug precipitation in the contact lens matrix. The presence of Pluronic® F-68 in the packaging solution creates in-situ micelles in the contact lens to dissolve gatifloxacin precipitates and provide sustained drug release. The micelles further improved the drug uptake from the drug-packaging solution to create an equilibrium of drug between the lens matrix and the packaging solution. In this study, we optimized gatifloxacin-pluronic-loaded contact lenses to achieve the desired optical transmittance, swelling, and gatifloxacin loading capacity as well as sustained drug delivery. Optimization of gatifloxacin-pluronic-loaded contact lens was carried out using a 32 factorial design by tailoring the concentration of Pluronic® F-68 in the packaging solution (X1) and the amount of gatifloxacin in the monomer solution (X2) to achieve the desired lens properties. The optimized batch (X1 = 0.3%w/v and X2 = 0.3%w/v) showed an optical transmittance of 92.84%, swelling of 92.36% and gatifloxacin loading capacity of 92.56 μg. The in vitro flux data of the optimized batch (GT-Pl-CL) showed sustained release up to 72 h, whereas soaked contact lenses (SM-CL) and direct gatifloxacin-loaded contact lenses (DL-CL) showed a sustained release up to 48 h. The in vivo gatifloxacin release data for rabbit tear fluid showed sustained release with a high gatifloxacin level for the GT-Pl-CL lens in comparison to the SM-CL and the eye drop solution. This study demonstrates the application of the 32 full factorial design to optimize gatifloxacin-pluronic-loaded contact lenses to achieve the desired optical transmittance, swelling, and drug loading capacity.
Copyright © 2020 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Animal studies; Contact lens; Critical lens properties; Gatifloxacin; Optimization; Pluronic® F68

Mesh:

Substances:

Year:  2020        PMID: 32240806     DOI: 10.1016/j.ijpharm.2020.119279

Source DB:  PubMed          Journal:  Int J Pharm        ISSN: 0378-5173            Impact factor:   5.875


  4 in total

1.  In vivo drug delivery via contact lenses: The current state of the field from origins to present.

Authors:  Liana D Wuchte; Stephen A DiPasquale; Mark E Byrne
Journal:  J Drug Deliv Sci Technol       Date:  2021-02-18       Impact factor: 5.062

2.  Controllable release of pirfenidone by polyvinyl alcohol film embedded soft contact lenses in vitro and in vivo.

Authors:  Caiqing Wu; Ping Wai Or; Jones Iok Tong Chong; Isuru K K Pathirage Don; Ching Hymn Christopher Lee; Kaili Wu; Minbin Yu; David C C Lam; Yangfan Yang
Journal:  Drug Deliv       Date:  2021-12       Impact factor: 6.419

Review 3.  Considerations for Polymers Used in Ocular Drug Delivery.

Authors:  Megan M Allyn; Richard H Luo; Elle B Hellwarth; Katelyn E Swindle-Reilly
Journal:  Front Med (Lausanne)       Date:  2022-01-28

Review 4.  Flexible polymeric nanosized micelles for ophthalmic drug delivery: research progress in the last three years.

Authors:  Zhiguo Li; Minting Liu; Lingjie Ke; Li-Juan Wang; Caisheng Wu; Cheng Li; Zibiao Li; Yun-Long Wu
Journal:  Nanoscale Adv       Date:  2021-08-10
  4 in total

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