Evidence map›Paper›PMID 30295090›Full record

ArticleCurrent eye research2019

Biodegradable Microsphere-Hydrogel Ocular Drug Delivery System for Controlled and Extended Release of Bioactive Aflibercept In Vitro.

Wenqiang Liu, Bao-Shiang Lee, William F Mieler, Jennifer J Kang-Mieler

Abstract readValidation Study
In one paragraph

Article in Current eye research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

39 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Wenqiang Liua Biomedical Engineering , Illinois Institute of Technology , Chicago , Illinois , USA.
Bao-Shiang Leeb Research Resource Center , University of Illinois at Chicago , Chicago , Illinois , USA.
William F Mielerc Ophthalmology and Visual Sciences , University of Illinois at Chicago , Chicago , Illinois , USA.
Jennifer J Kang-Mielera Biomedical Engineering , Illinois Institute of Technology , Chicago , Illinois , USA.

Funding

Efficacy of the Microsphere-Thermo-Responsive Hydrogel Ocular Drug Delivery SystemR15EY025434 · NEI · ILLINOIS INSTITUTE OF TECHNOLOGY · PI KANG-MIELER, JENNIFER J · 2016 to 2016
$420k
NEI NIH HHS R15 EY025434
6 · The paper itself

Abstract

purposeCurrent standard of care for neovascular eye diseases require repeated intravitreal bolus injections of anti-vascular endothelial growth factors (anti-VEGFs). The purpose of this study was to validate a degradable microsphere-thermoresponsive hydrogel drug delivery system (DDS) capable of releasing bioactive aflibercept in a controlled and extended manner for 6 months. MATERIALS AND

methodsThe DDS was fabricated by suspending aflibercept-loaded poly(lactic-co-glycolic acid) microspheres within a biodegradable poly(ethylene glycol)-co-(l-lactic acid) diacrylate/N-isopropylacrylamide (PEG-PLLA-DA/NIPAAm) thermoresponsive hydrogel. Encapsulation efficiency of DDSs and in vitro release profiles were characterized by iodine-125 radiolabeled aflibercept. The degradation of hydrogel was determined by dry weight changes. The cytotoxicity from degraded DDS byproducts was investigated by quantifying cell viability using LIVE/DEAD® assay. In addition, dot blot and enzyme-linked immunosorbent assay were used to determine the bioactivity of released drug. Finally, morphology of microspheres and hydrogel were investigated by cryo-scanning electron microscopy before and after thermal transformation.

resultsThe microsphere-hydrogel DDS was capable of releasing bioactive aflibercept in a controlled and extended manner for 6 months. The amount and rate of aflibercept release can be controlled by both the cross-linker concentration and microspheres load amount. The initial burst (release within 24 h) was from 37.35 ± 4.92 to 74.56 ± 6.16 µg (2 and 3 mM hydrogel, each loaded with 10 and 20 mg/ml of microspheres, respectively), followed by controlled drug release of 0.07-0.15 µg/day. Higher PEG-PLLA-DA concentration (3 mM) degraded faster than the lower concentration (2 mM). No significant cytotoxicity from degraded DDS byproducts was found for all investigated time points. Bioactivity of released drug was maintained at therapeutic level over entire release period.

conclusionsThe microsphere-hydrogel DDS is safe and can deliver bioactive aflibercept in a controlled manner. This may provide a significant advantage over current bolus injection therapies in the treatment of ocular neovascularization.

Indexed as

Absorbable ImplantsDrug Delivery SystemsAcrylamidesAcrylatesAngiogenesis InhibitorsAnimalsCells, CulturedCell SurvivalDelayed-Action PreparationsEnzyme-Linked Immunosorbent AssayHumansHuman Umbilical Vein Endothelial CellsHydrogelsImmunoblottingMicrospheresPolyethylene GlycolsAcrylamidesAcrylatesafliberceptAngiogenesis InhibitorsDelayed-Action PreparationsHydrogelsN-isopropylacrylamidepoly(ethylene glycol)-co-(L-lactic acid)diacrylatePolyethylene GlycolsReceptors, Vascular Endothelial Growth FactorRecombinant Fusion ProteinsVascular Endothelial Growth Factor AVEGFA protein, humanAnti-VEGF deliverybioactivityintravitreal injectionneovascularizationthermoresponsive hydrogel

Identifiers

PMID30295090
PMCPMC7216294

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.