Sara LACERDA

Dr. Sara LACERDA

Center of Molecular Biophysics, CNRS, Orléans, France
orcid

Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

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

Representative Publications

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16 April 2020 in Angewandte Chemie International Edition
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DNDaouda Ndiaye
Daouda Ndiaye
MSMaryame Sy
Maryame Sy
APAgnès Pallier
Agnès Pallier
SMSandra Même
Sandra Même
ISIsidro de Silva
Isidro de Silva
ÉTÉva Tóth
Éva Tóth

20 May 2015 in Nano Research
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SKSlávka Kaščáková
Slávka Kaščáková
AGAlexandre Giuliani
Alexandre Giuliani
Sara LACERDASara LACERDA
Sara LACERDA
APAgnès Pallier
Agnès Pallier
PMPascal Mercère
Pascal Mercère
MRMatthieu Refregiers
Matthieu Refregiers
We report lanthanide-based micelles integrating hypericin (Hyp) for X-raytriggered photodynamic therapy (PDT). The lanthanide luminescence induced by X-ray irradiation excites the photosensitizer, which leads to the generation of singlet oxygen. This versatile approach can be extended to other photosensitizers or other types of liponanoparticles and can allow for magnetic resonance imaging (MRI) guidance.

1 July 2014 in Circulation: Cardiovascular Imaging
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RBRene Botnar
Rene Botnar
AWAndrea J. Wiethoff
Andrea J. Wiethoff
UEUllrich Ebersberger
Ullrich Ebersberger
Sara LACERDASara LACERDA
Sara LACERDA
UBUlrike Blume
Ulrike Blume
MMMarcus R. Makowski
Marcus R. Makowski
Background—: The incidence of abdominal aortic aneurysms (AAAs) has increased during the last decades. However, there is still controversy about the management of medium-sized AAAs. Therefore, novel biomarkers, besides aneurysmal diameter, are needed to assess aortic wall integrity and risk of rupture. Elastin is the key protein for maintaining aortic wall tensile strength and stability. The progressive breakdown of structural proteins, in particular, medial elastin, is responsible for the inability of the aortic wall to withstand intraluminal hemodynamic forces. Here, we evaluate the usefulness of elastin-specific molecular MRI for the in vivo characterization of AAAs. Methods and Results—: To induce AAAs, ApoE –/– mice were infused with angiotensin-II. An elastin-specific magnetic resonance molecular imaging agent (ESMA) was administered after 1, 2, 3, and 4 weeks of angiotensin-II infusion to assess elastin composition of the aorta (n=8 per group). The high signal provided by ESMA allowed for imaging with high spatial resolution, resulting in an accurate assessment of ruptured elastic laminae and the compensatory expression of elastic fibers. In vivo contrast-to-noise ratios and R1-relaxation rates after ESMA administration were in good agreement with ex vivo histomorphometry (Elastica van Gieson stain) and gadolinium concentrations determined by inductively coupled plasma mass spectroscopy. Electron microscopy confirmed colocalization of ESMA with elastic fibers. Conclusions—: Changes in elastin content could be readily delineated and quantified at different stages of AAAs by elastin-specific molecular magnetic resonance imaging. ESMA-MRI offers potential for the noninvasive detection of the aortic rupture site prior to dilation of the aorta and the subsequent in vivo monitoring of compensatory repair processes during the progression of AAAs.

30 May 2017 in ChemMedChem
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Sara LACERDASara LACERDA
Sara LACERDA
ÉTÉva Tóth
Éva Tóth


4 January 2016 in Journal of the American Chemical Society
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JHJiefang He
Jiefang He
Célia S.  BonnetCélia S. Bonnet
Célia S. Bonnet
SESvetlana V. Eliseeva
Svetlana V. Eliseeva
Sara LACERDASara LACERDA
Sara LACERDA
TCThomas Chauvin
Thomas Chauvin
PDPhilippe Durand
Philippe Durand