2019
DOI: 10.1089/adt.2018.911
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Micro/Nanoparticle Delivery Systems for Ocular Diseases

Abstract: Micro-(MPs) and nanoparticles (NPs) have been recently studied for their application in ophthalmic drug delivery. These drug delivery systems are able to circumvent the ocular barriers that currently limit the efficacy of conventional treatments, as well as provide a more sustained release of drug, reducing the frequency of administration and increasing patient compliance. This review summarizes the recent trends in ophthalmic research from conventional treatment to the utilization of MPs and NPs as drug carri… Show more

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Cited by 15 publications
(8 citation statements)
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References 88 publications
(105 reference statements)
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“…Conversely, it blocks the passage of hydrophilic drugs that would enter through the paracellular pathway due to the presence of tight junctions (zonula occludens) [ 27 , 28 ]. The conjunctiva, which is the thin and transparent structure composed of a mucous epithelial, adenoids and fibrous layer covering one-third of the eyeball [ 29 ], increases the protective function and corresponds to the second static anterior barrier. One of its main functions is the formation of the tear film by producing electrolytes, fluid and mucins, but in contrast to the cornea, the conjunctiva has demonstrated lipophilic affinity to drugs [ 30 ] due to its increased paracellular spaces (230 times greater) and higher pore density (16 times higher) [ 31 ].…”
Section: Ocular Drug Barriersmentioning
confidence: 99%
“…Conversely, it blocks the passage of hydrophilic drugs that would enter through the paracellular pathway due to the presence of tight junctions (zonula occludens) [ 27 , 28 ]. The conjunctiva, which is the thin and transparent structure composed of a mucous epithelial, adenoids and fibrous layer covering one-third of the eyeball [ 29 ], increases the protective function and corresponds to the second static anterior barrier. One of its main functions is the formation of the tear film by producing electrolytes, fluid and mucins, but in contrast to the cornea, the conjunctiva has demonstrated lipophilic affinity to drugs [ 30 ] due to its increased paracellular spaces (230 times greater) and higher pore density (16 times higher) [ 31 ].…”
Section: Ocular Drug Barriersmentioning
confidence: 99%
“…Microparticles have been evaluated for ocular drug delivery for decades, and typically demonstrate higher drug loading capacity and release duration than nanoparticles due to the larger size of the particles, but a balance between drug loading and size considerations for injectability must be established. Several articles have focused on microparticles in the range of 1-50 µm for intravitreal injection to balance these considerations (144). It has been recently proposed to use nanoparticles embedded in microparticles to overcome some of these challenges (145).…”
Section: Micro-and Nano-scale Technologiesmentioning
confidence: 99%
“…Some reports show that polymeric materials of nanospheres and nanocapsules can interact with cell surface receptors, mitochondrial enzymes, and cytoplasmic proteins, which can cause stress responses and alteration of metabolic processes. Although polymers of nanospheres and nanocapsules are generally non-toxic to the ocular surface, the molecules may cause irritation and immune reactions, especially when applied in intraocular tissues [ 104 , 105 ]. Poly(lactic- co -glycolic acid) (PLGA) nanocapsules have been found to cause cytoplasmic vacuole formation in rabbits [ 106 ].…”
Section: Innovations That Increase Intraocular Bioavailability Of Topical Drugsmentioning
confidence: 99%