By successive enzymatic and chemical modifications, novel fluorinated polyhydroxyalkanoates were synthesized and characterized. Unsaturated polyhydroxyalkanoate, PHAU, was first produced by fermentation using marine bacteria , and a graft copolymer PHAU--CF was further prepared by controlled thiol-ene reaction in the presence of perfluorodecanethiol (PFDT). The PFDT grafting is realized by two different processes. In the first method, PHAU was previously solubilized in toluene. The grafting in solution is more efficient than the direct heterogeneous grafting onto a PHAU film. The degrees of grafting were determined by H NMR. The characterization of the microstructure by SEM-EDX and modulated and conventional DSC showed the formation of microdomains due to the organization of the hydrophobic segments of graft PFDT. Biomaterials prepared by 3D printing and coated by PHAU--CF have the potential to be used as novel contrast agents as shown by Hahn echo experiments.
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http://dx.doi.org/10.1021/acs.biomac.1c00770 | DOI Listing |
Biomacromolecules
November 2021
Univ. Paris-Est Créteil, CNRS, ICMPE, F-94010 Cretéil, France.
By successive enzymatic and chemical modifications, novel fluorinated polyhydroxyalkanoates were synthesized and characterized. Unsaturated polyhydroxyalkanoate, PHAU, was first produced by fermentation using marine bacteria , and a graft copolymer PHAU--CF was further prepared by controlled thiol-ene reaction in the presence of perfluorodecanethiol (PFDT). The PFDT grafting is realized by two different processes.
View Article and Find Full Text PDFBioengineering (Basel)
September 2021
ICMPE, CNRS, University Paris Est Creteil, F-94010 Creteil, France.
Nanoparticles have recently emerged as valuable tools in biomedical imaging techniques. Here PEGylated and fluorinated nanocapsules based on poly(3-hydroxyalkanoate) containing a liquid core of perfluorooctyl bromide PFOB were formulated by an emulsion-evaporation process as potential F MRI imaging agents. Unsaturated poly(hydroxyalkanoate), PHAU, was produced by marine bacteria using coprah oil and undecenoic acid as substrates.
View Article and Find Full Text PDFInt J Mol Sci
July 2021
Jerzy Haber Institute of Catalysis and Surface Chemistry, Polish Academy of Sciences, Niezapominajek 8, 30-239 Kraków, Poland.
Cancer is one of the deadliest illness globally. Searching for new solutions in cancer treatments is essential because commonly used mixed, targeted and personalized therapies are sometimes not sufficient or are too expensive for common patients. Sugar fatty acid esters (SFAEs) are already well-known as promising candidates for an alternative medical tool.
View Article and Find Full Text PDFAnalyst
March 2019
Department of Civil, Chemical, Environmental and Materials Engineering (DICAM), Università di Bologna, Via Terracini 28, 40131 Bologna, Italy. and Italian Consortium for Science and Technology of Materials (INSTM), Via Giusti 9, 50121 Firenze, Italy.
A new, facile and low-sample consuming technique for the determination of hydroxyl values (OHVs) in poly(hydroxyalkanoate)s (PHAs) is herein presented. After a fast, uncatalyzed and non-destructive trifluoroacetylation of all PHA hydroxyl groups, OHVs are calculated through F-NMR measurements, comparing integral values of the only two signals in the spectra: the fluorinated hydroxyl groups and the internal standard (trifluorotoluene) signals. Furthermore, the combined ex situ functionalization with a simple workup of the fluorinated polymer allowed to obtain spectra with an improved signal/noise ratio and short acquisition time if compared to H-NMR-based methods.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
October 2017
Departments of Chemistry and Molecular & Cell Biology, University of California, Berkeley, Berkeley, CA, 94720-1460, USA.
Fluorine has become an important element for the design of synthetic molecules for use in medicine, agriculture, and materials. Despite the many advantages provided by fluorine for tuning key molecular properties, it is rarely found in natural metabolism. We seek to expand the molecular space available for discovery through the development of new biosynthetic strategies that cross synthetic with natural compounds.
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