» Articles » PMID: 22194895

Intraocular Pressure Changes: an Important Determinant of the Biocompatibility of Intravitreous Implants

Overview
Journal PLoS One
Date 2011 Dec 24
PMID 22194895
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Background: In recent years, research efforts exploring the possibility of using biomaterial nanoparticles for intravitreous drug delivery has increased significantly. However, little is known about the effect of material properties on intravitreous tissue responses.

Principal Findings: To find the answer, nanoparticles made of hyaluronic acid (HA), poly (l-lactic acid) (PLLA), polystyrene (PS), and Poly N-isopropyl acrylamide (PNIPAM) were tested using intravitreous rabbit implantation model. Shortly after implantation, we found that most of the implants accumulated in the trabecular meshwork area followed by clearance from the vitreous. Interestingly, substantial reduction of intraocular pressure (IOP) was observed in eyes implanted with particles made of PS, PNIPAM and PLLA, but not HA nanoparticles and buffered salt solution control. On the other hand, based on histology, we found that the particle implantation had no influence on cornea, iris and even retina. Surprisingly, substantial CD11b+ inflammatory cells were found to accumulate in the trabecular meshwork area in some animals. In addition, there was a good relationship between recruited CD11b+ cells and IOP reduction.

Conclusions: Overall, the results reveal the potential influence of nanoparticle material properties on IOP reduction and inflammatory responses in trabecular meshwork. Such interactions may be critical for the development of future ocular nanodevices with improved safety and perhaps efficacy.

Citing Articles

Emerging trends in long-acting sustained drug delivery for glaucoma management.

So Y, Mishra D, Gite S, Sonawane R, Waite D, Shaikh R Drug Deliv Transl Res. 2025; .

PMID: 39786666 DOI: 10.1007/s13346-024-01779-4.


A Long-Acting Curcumin Nanoparticle/In Situ Hydrogel Composite for the Treatment of Uveal Melanoma.

Xie L, Yue W, Ibrahim K, Shen J Pharmaceutics. 2021; 13(9).

PMID: 34575410 PMC: 8467666. DOI: 10.3390/pharmaceutics13091335.


Targeted Drug Delivery Systems for the Treatment of Glaucoma: Most Advanced Systems Review.

Cegielska O, Sajkiewicz P Polymers (Basel). 2019; 11(11).

PMID: 31652975 PMC: 6918324. DOI: 10.3390/polym11111742.


Gene transfer to the outflow tract.

Dang Y, Loewen R, Parikh H, Roy P, Loewen N Exp Eye Res. 2016; 158:73-84.

PMID: 27131906 PMC: 5083245. DOI: 10.1016/j.exer.2016.04.023.


Silver and gold nanoparticles exposure to in vitro cultured retina--studies on nanoparticle internalization, apoptosis, oxidative stress, glial- and microglial activity.

Soderstjerna E, Bauer P, Cedervall T, Abdshill H, Johansson F, Englund Johansson U PLoS One. 2014; 9(8):e105359.

PMID: 25144684 PMC: 4140780. DOI: 10.1371/journal.pone.0105359.

References
1.
Ohno S, Ichiishi A, Matsuda H . Hypotensive effect of carteolol on intraocular pressure elevation and secondary glaucoma associated with endogenous uveitis. Ophthalmologica. 1989; 199(1):41-5. DOI: 10.1159/000310013. View

2.
Lloyd A, Faragher R, Denyer S . Ocular biomaterials and implants. Biomaterials. 2001; 22(8):769-85. DOI: 10.1016/s0142-9612(00)00237-4. View

3.
Lai J, Ma D, Cheng H, Sun C, Huang S, Li Y . Ocular biocompatibility of carbodiimide cross-linked hyaluronic acid hydrogels for cell sheet delivery carriers. J Biomater Sci Polym Ed. 2010; 21(3):359-76. DOI: 10.1163/156856209X416980. View

4.
Vega E, Egea M, Valls O, Espina M, Garcia M . Flurbiprofen loaded biodegradable nanoparticles for ophtalmic administration. J Pharm Sci. 2006; 95(11):2393-405. DOI: 10.1002/jps.20685. View

5.
Nair A, Zou L, Bhattacharyya D, Timmons R, Tang L . Species and density of implant surface chemistry affect the extent of foreign body reactions. Langmuir. 2008; 24(5):2015-24. PMC: 3230931. DOI: 10.1021/la7025973. View