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Roberto Molinaro

Researcher at Houston Methodist Hospital

Publications -  51
Citations -  2934

Roberto Molinaro is an academic researcher from Houston Methodist Hospital. The author has contributed to research in topics: Drug delivery & Cancer. The author has an hindex of 22, co-authored 50 publications receiving 1944 citations. Previous affiliations of Roberto Molinaro include University of Padua & Vita-Salute San Raffaele University.

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The impact of nanoparticle protein corona on cytotoxicity, immunotoxicity and target drug delivery.

TL;DR: A survey of recent findings on the NP-PC interactions is provided and how the PC can be used to modulate both cytotoxicity and the immune response as well as to improve the efficacy of targeted delivery of nanocarriers is discussed.
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Biomimetic proteolipid vesicles for targeting inflamed tissues

TL;DR: A method is described that leverages the advantages of bottom-up and top-down strategies to incorporate proteins derived from the leukocyte plasma membrane into lipid nanoparticles that retained the versatility and physicochemical properties typical of liposomal formulations and enabled the selective and effective delivery of dexamethasone to inflamed tissues.
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Personalized protein corona on nanoparticles and its clinical implications

TL;DR: The same nanomaterial incubated with plasma proteins of patients with different pathologies adsorb protein coronas with different compositions, giving rise to the concept of personalized protein corona.
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Bio-inspired engineering of cell- and virus-like nanoparticles for drug delivery

TL;DR: The features and properties of biomimetic delivery systems that combine the intrinsic hallmarks of biological membranes with the delivery capabilities of synthetic carriers are described, recapitulating the distinctive traits and functions of viruses and cell-derived entities.
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Roles of PAD4 and NETosis in Experimental Atherosclerosis and Arterial Injury: Implications for Superficial Erosion

TL;DR: Results indicate that PAD4 from bone marrow-derived cells and NETs do not influence chronic experimental atherogenesis, but participate causally in acute thrombotic complications of intimal lesions that recapitulate features of superficial erosion.