Albuminated PLGA nanoparticles containing bevacizumab intended for ocular neovascularization treatment

Abstract

Bevacizumab, an anti-VEGF antibody, has demonstrated trustworthy effects in treatment of retinal and choroidal neovascularization that both are crucial sight threatening conditions. However, the weak point is the short half-life of the drug in vitreous which necessitates frequent intravitreal injections. Accordingly employing controlled-release drug delivery systems such as polymeric nanoparticles (NPs) has been suggested. In this study albuminated-PLGA-NPs containing bevacizumab were prepared and studied intended for reducing the number of injections. NPs were formulated by double-emulsion method and a single dose of NPs was intravitreally injected to rabbits. The drug concentrations in vitreous and aqueous humor were assayed in different time intervals using ELISA and intraocular pharmacokinetic parameters were calculated. Moreover, coumarin-6 loaded albuminated-PLGA-NPs were employed to evaluate the distribution and persistence of the NPs in the posterior segment. Results revealed that the bevacizumab vitreous concentration maintained above 500 ng mL(-1) for about 8 weeks and 3.3 times elevation was observed in the drug vitreous MRT compared with the control. According to coumarin-6 NP tests, fluorescence emissions in posterior tissues were observed for 56 days which confirmed the nanoparticles persistence in ocular tissues during the test span. Therefore our prepared formulation may offer improvements in treatment of eye posterior segment neovascularization.

Investigation of antitumor activities of trastuzumab delivered by PLGA nanoparticles

“…One possible strategy to overcome these problems resides in the antibody encapsulation into biodegradable and biocompatible polymers creating a tailorable nanosystem. [15][16][17] In this way, the loaded antibody is protected from degradation and from interaction with the immune system and can be released in a controlled manner. Poly(lactic-co-glycolic) acid (PLGA) is an excellent candidate, as it has been approved by FDA for human use because of its biodegradability and low systemic toxicity.…”

Use of biomaterials for sustained delivery of anti-VEGF to treat retinal diseases

“…Many of the studies have demonstrated that sustained release for anti-VEGF molecules can be achieved for more than 1 month in in vitro and in vivo models [58,[60][61][62][63][64]. However, data regarding the bioactivity exerted by the anti-VEGF loaded particles in reducing retinal neovascularisation in vivo remains limited [58].…”

Therapeutic use of monoclonal antibodies: general aspects and challenges for drug delivery

“…They found that the vitreous concentration of bevacizumab was sustained for about 8 weeks at values greater than 500 ng mL −1 and that the nanoparticles presented a drug vitreous medium retention time (MRT) 3.3 times higher than the control. In addition, it was confirmed the nanoparticles persistence in ocular tissues for 56 days (Varshochian et al, 2013(Varshochian et al, , 2015.…”