Maria Aurora Grimaudo

Dr. Maria Aurora Grimaudo

orcid

Research Focus & Metrics

Academic Career Length

10Years (2017-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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24 January 2018 in Molecular Pharmaceutics
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Journal Article
Closed access
MGMaria Aurora Grimaudo
Maria Aurora Grimaudo
Silvia PescinaSilvia Pescina
Silvia Pescina
CPCristina Padula
Cristina Padula
PSPatrizia Santi
Patrizia Santi
ACAngel Concheiro
Angel Concheiro
Sara NicoliSara Nicoli
Sara Nicoli

1 November 2019 in Journal of Controlled Release
Verified
Journal Article
Closed access
MGMaria Aurora Grimaudo
Maria Aurora Grimaudo
ACAngel Concheiro
Angel Concheiro
Carmen Alvarez-LorenzoCarmen Alvarez-Lorenzo
Carmen Alvarez-Lorenzo

1 March 2022 in Acta Biomaterialia
Verified
Journal Article
Closed access
MGMaria Aurora Grimaudo
Maria Aurora Grimaudo
GKG.S. Krishnakumar
G.S. Krishnakumar
EGE. Giusto
E. Giusto
FFFranco Furlani
Franco Furlani
GBGIADA BASSI
GIADA BASSI
SPSilvia Panseri
Silvia Panseri

17 March 2020 in Pharmaceutics
Verified
Journal Article
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MGMaria Aurora Grimaudo
Maria Aurora Grimaudo
ACAngel Concheiro
Angel Concheiro
Carmen Alvarez-LorenzoCarmen Alvarez-Lorenzo
Carmen Alvarez-Lorenzo
Electrospun nanofibers are gaining interest as ocular drug delivery platforms that may adapt to the eye surface and provide sustained release. The aim of this work was to design an innovative ophthalmic insert composed of hyaluronan (HA) nanofibers for the dual delivery of an antioxidant (ferulic acid, FA) and an antimicrobial peptide (ε-polylysine, ε-PL). Polyvinylpyrrolidone (PVP) was added to facilitate the electrospinning process. Fibers with diameters of approx. 100 nm were obtained with PVP 5%-HA 0.8% w/v and PVP 10%-HA 0.5% w/v mixtures in ethanol:water 4:6 v/v. An increase in PVP concentration to 20% w/v in both presence and absence of HA rendered fibers of approx. 1 µm. PVP 5%-HA 0.8% w/v fibers were loaded with 83.3 ± 14.0 µg FA per mg. After nanofibers crosslinking with ε-PL, blank and FA-loaded inserts showed a mean thickness of 270 ± 21 µm and 273 ± 41 µm, respectively. Blank and FA-loaded inserts completely released ε-PL within 30 min under sink conditions, whereas FA-loaded inserts released the antioxidant within 20 min. Both blank and FA-loaded inserts were challenged against Pseudomonas aeruginosa and Staphylococcus aureus, demonstrating their efficacy against relevant microbial species.

3 April 2019 in Expert Opinion on Drug Delivery
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Journal Article
Closed access
MGMaria Aurora Grimaudo
Maria Aurora Grimaudo
Silvia PescinaSilvia Pescina
Silvia Pescina
CPCristina Padula
Cristina Padula
PSPatrizia Santi
Patrizia Santi
ACAngel Concheiro
Angel Concheiro
Sara NicoliSara Nicoli
Sara Nicoli
Introduction: Polymeric micelles represent nowadays an interesting formulative approach for ocular drug delivery, as they act as solubility enhancers of poorly soluble drugs and promote drug transport across cornea and sclera. In particular, in the last 5 years polymeric nanomicelles have been increasingly investigated to overcome some of the important challenges of the topical treatment of ocular diseases. Areas covered: The aim of this review was to gather up-to-date information on the different roles that polymeric micelles (commonly in the nano-size scale) can play in ocular delivery. Thus, after a general description of ocular barriers and micelles features, the attention is focused on those properties that are relevant for ophthalmic application. Finally, their efficacy in improving the ocular delivery of different classes of therapeutics (anti-inflammatory, immunosuppresant, anti-glaucoma, antifungal, antiviral drugs) are reported. Expert opinion: Although still a few, in vivo experiments have clearly demonstrated the capability of polymeric nanomicelles to overcome a variety of hurdles associated to ocular therapy, notably increasing drug bioavailability. However, there are still some very important issues to be solved, such as tolerability and stability; additionally, the role of micelles in drug uptake by the ocular tissues and their potential for the treatment of posterior eye diseases still need to be clarified/verified.

Verified
Journal Article
Open access
PDF file
GBGIADA BASSI
GIADA BASSI
MGMaria Aurora Grimaudo
Maria Aurora Grimaudo
SPSilvia Panseri
Silvia Panseri
MMMonica Montesi
Monica Montesi
A hot topic in biomedical science is the implementation of more predictive in vitro models of human tissues to significantly improve the knowledge of physiological or pathological process, drugs discovery and screening. Bidimensional (2D) culture systems still represent good high-throughput options for basic research. Unfortunately, these systems are not able to recapitulate the in vivo three-dimensional (3D) environment of native tissues, resulting in a poor in vitro–in vivo translation. In addition, intra-species differences limited the use of animal data for predicting human responses, increasing in vivo preclinical failures and ethical concerns. Dealing with these challenges, in vitro 3D technological approaches were recently bioengineered as promising platforms able to closely capture the complexity of in vivo normal/pathological tissues. Potentially, such systems could resemble tissue-specific extracellular matrix (ECM), cell–cell and cell–ECM interactions and specific cell biological responses to mechanical and physical/chemical properties of the matrix. In this context, this review presents the state of the art of the most advanced progresses of the last years. A special attention to the emerging technologies for the development of human 3D disease-relevant and physiological models, varying from cell self-assembly (i.e., multicellular spheroids and organoids) to the use of biomaterials and microfluidic devices has been given.