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A time-dependent study of nano-mechanical and ultrastructural properties of internal limiting membrane under ocriplasmin treatment

Authors :
Mazzini, Alberto
Palermo, Francesca
Pagliei, Valeria
Romano', Sabrina
Papi, Massimiliano
Zimatore, Giovanna
Falsini, Benedetto
Rizzo, Stanislao
De Spirito, Marco
Ciasca, Gabriele
Minnella, Angelo Maria
Romanò, Sabrina
Papi, Massimiliano (ORCID:0000-0002-0029-1309)
Falsini, Benedetto (ORCID:0000-0002-3569-4968)
Rizzo, Stanislao (ORCID:0000-0001-6302-063X)
De Spirito, Marco (ORCID:0000-0003-4260-5107)
Ciasca, Gabriele (ORCID:0000-0002-3694-8229)
Minnella, Angelo (ORCID:0000-0001-5896-5313)
Mazzini, Alberto
Palermo, Francesca
Pagliei, Valeria
Romano', Sabrina
Papi, Massimiliano
Zimatore, Giovanna
Falsini, Benedetto
Rizzo, Stanislao
De Spirito, Marco
Ciasca, Gabriele
Minnella, Angelo Maria
Romanò, Sabrina
Papi, Massimiliano (ORCID:0000-0002-0029-1309)
Falsini, Benedetto (ORCID:0000-0002-3569-4968)
Rizzo, Stanislao (ORCID:0000-0001-6302-063X)
De Spirito, Marco (ORCID:0000-0003-4260-5107)
Ciasca, Gabriele (ORCID:0000-0002-3694-8229)
Minnella, Angelo (ORCID:0000-0001-5896-5313)
Publication Year :
2020

Abstract

Vitreomacular traction (VMT) syndrome has only been surgically treated for a long time. Recently,enzymatic vitreolysis with ocriplasmin has emerged as a possible option to release VMT and, in some cases, close full thickness macular holes (FTMHs). Despite its clinical relevance, gathering information about the ocriplasmin-induced alterations of the Inner Limiting Membrane (ILM) of the retina in a clinical study is a complex task, mainly because of the inter-individual variability among patients. To obtain more insights into the mechanism underlying the drug action, we studied in-vitro the mechanical and morphological changes of the ILM using Atomic Force Microscopy (AFM). To this aim, we measured the ILM average Young’s modulus (YM), hysteresis (H) and adhesion work (A) over time under ocriplasmin treatment. Our data unveil a time-dependent increase in the 34 membrane YM of 19% of its initial value, along with changes in its adhesive and dissipative behavior. Such modifications well correlate with the morphological alterations detected in the AFM imaging mode. Taken all together, the results here presented provide more insights into the mechanism underlying the ocriplasmin action in-vivo, suggesting that it is only able to alter the top-most layer of the vitreal side of the membrane, not compromising the inner ILM structure.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1196084047
Document Type :
Electronic Resource