International audienceThe first purpose of this paper is to underline a relevant colorimetric co-ordinate characterizing the colour of ochres within their extremely wide range, from pale yellow to dark red. The second purpose is to link together quantitatively the variations of this colorimetric co-ordinate and the various chemical compositions of the samples, mainly hematite, goethite and white pigments. A group of 30 modern ochres and a group of 20 ancient ochres have been investigated. All these natural pigments have been commercialized. Diffuse reflectance spectrometry allows to calculate the colorimetric co-ordinates in the CIE-L*a*b* space and the position of the absorption band of each sample. Physico-chemical analysis has been obtained by quantitative X-ray diffraction, scanning and transmitting electronic microscopy and particle-size analysis by laser diffraction. The positive a* co-ordinate (redness) has been underlined, for the first time, to be the only relevant colorimetric parameter to characterize the colour of the ochres. Its variations are quantitatively connected to the shift of the absorption band due to the charge transfer between the ligand (OH− or O2−) and the Fe3+ ion contained in goethite and/or hematite. For ochres containing both hematite and goethite, the a* co-ordinate linearly increases with the relative amount of hematite while the absorption band progressively shifts towards the high wavelengths. Such a linear shift of the absorption band has never been underlined before. For ochres containing only one iron oxide, a* linearly decreases with the amount of white pigments, whatever the nature of the white charges. Moreover, this study gives the opportunity to show that only the nature, the amount and the size distribution of the white charges allow to discriminate the ochres according to their geographic origin
Highlights d We have developed a trained immunity-inducing nanobiologic therapeutic named MTP-HDL d MTP-HDL favorably accumulates in hematopoietic organs of mice and non-human primates d MTP-HDL nanotherapy induces trained immunity through bone marrow progenitors in vivo d MTP-HDL nanotherapy inhibits tumor growth and potentiates immune checkpoint inhibition
Parkinson's disease (PD) is an age-related neurodegenerative disorder characterized by the loss of dopaminergic neurons in the substantia nigra, associated with the accumulation of misfolded α-synuclein and lysosomal impairment, two events deemed interconnected. Protein aggregation is linked to defects in degradation systems such as the autophagy-lysosomal pathway, while lysosomal dysfunction is partly related to compromised acidification. We have recently proven that acidic nanoparticles (aNPs) can re-acidify lysosomes and ameliorate neurotoxin-mediated dopaminergic neurodegeneration in mice. However, no lysosome-targeted approach has yet been tested in synucleinopathy models in vivo. Here, we show that aNPs increase α-synuclein degradation through enhancing lysosomal activity in vitro. We further demonstrate in vivo that aNPs protect nigral dopaminergic neurons from cell death, ameliorate α-synuclein pathology, and restore lysosomal function in mice injected with PD patient-derived Lewy body extracts carrying toxic α-synuclein aggregates. Our results support lysosomal re-acidification as a disease-modifying strategy for the treatment of PD and other age-related proteinopathies.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.