scholarly journals Curcumin micronization by supercritical fluid: In vitro and in vivo biological relevance

2022 ◽  
Vol 177 ◽  
pp. 114501
Author(s):  
Adrieli Sachett ◽  
Matheus Gallas-Lopes ◽  
Radharani Benvenutti ◽  
Matheus Marcon ◽  
Gean Pablo S. Aguiar ◽  
...  
Pharmaceutics ◽  
2019 ◽  
Vol 11 (2) ◽  
pp. 67 ◽  
Author(s):  
Fei Han ◽  
Wei Zhang ◽  
Ying Wang ◽  
Ziyue Xi ◽  
Lu Chen ◽  
...  

In this study, supercritical fluid (SCF) technology was applied to prepare reliable solid dispersions of pharmaceutical compounds with limited bioavailability using ibuprofen (IBU) as a model compound. Solid-state characterization of the dispersions was conducted by differential scanning calorimetry (DSC), powder X-ray diffraction (PXRD), and scanning electron microscopy (SEM). The PXRD and DSC results suggested that the amorphous form of IBU was maintained in the solid dispersions. Furthermore, in vitro dissolution and in vivo pharmacokinetic (PK) studies in rats were also performed. The dissolution performance of the SCF-prepared IBU dispersions was significantly improved compared to that of the physical mixtures of crystalline IBU and a polymer. In addition, the PK results revealed that the SCF-prepared IBU dispersions produced remarkably high blood drug concentrations (both the AUC and Cmax) and a rapid absorption rate (Tmax). Finally, molecular modeling was used to evaluate the binding energy of interactions between IBU and the polymers. The negative binding energy suggests a relatively stable system. Hence, SCF technology can be used as a very effective approach to prepare IBU solid dispersions with good physical stability and enhanced in vitro and in vivo performance.


2017 ◽  
Vol 130 ◽  
pp. 282-291 ◽  
Author(s):  
Gean Pablo S. Aguiar ◽  
Matheus Marcon ◽  
Ricieri Mocelin ◽  
Ana P. Herrmann ◽  
Lorenzo M.P.C. Chaves ◽  
...  

2021 ◽  
Vol 22 (15) ◽  
pp. 8312
Author(s):  
Daniela Valenti ◽  
Rosa Anna Vacca ◽  
Loredana Moro ◽  
Anna Atlante

Mitochondria are complex intracellular organelles traditionally identified as the powerhouses of eukaryotic cells due to their central role in bioenergetic metabolism. In recent decades, the growing interest in mitochondria research has revealed that these multifunctional organelles are more than just the cell powerhouses, playing many other key roles as signaling platforms that regulate cell metabolism, proliferation, death and immunological response. As key regulators, mitochondria, when dysfunctional, are involved in the pathogenesis of a wide range of metabolic, neurodegenerative, immune and neoplastic disorders. Far more recently, mitochondria attracted renewed attention from the scientific community for their ability of intercellular translocation that can involve whole mitochondria, mitochondrial genome or other mitochondrial components. The intercellular transport of mitochondria, defined as horizontal mitochondrial transfer, can occur in mammalian cells both in vitro and in vivo, and in physiological and pathological conditions. Mitochondrial transfer can provide an exogenous mitochondrial source, replenishing dysfunctional mitochondria, thereby improving mitochondrial faults or, as in in the case of tumor cells, changing their functional skills and response to chemotherapy. In this review, we will provide an overview of the state of the art of the up-to-date knowledge on intercellular trafficking of mitochondria by discussing its biological relevance, mode and mechanisms underlying the process and its involvement in different pathophysiological contexts, highlighting its therapeutic potential for diseases with mitochondrial dysfunction primarily involved in their pathogenesis.


2020 ◽  
Vol 7 (1) ◽  
pp. 17 ◽  
Author(s):  
Andreas M.A.O. Pollet ◽  
Jaap M.J. den Toonder

The development of Vasculature-on-Chip has progressed rapidly over the last decade and recently, a wealth of fabrication possibilities has emerged that can be used for engineering vessels on a chip. All these fabrication methods have their own advantages and disadvantages but, more importantly, the capability of recapitulating the in vivo vasculature differs greatly between them. The first part of this review discusses the biological background of the in vivo vasculature and all the associated processes. We then evaluate the biological relevance of different fabrication methods proposed for Vasculature-on-Chip, we indicate their possibilities and limitations, and we assess which fabrication methods are capable of recapitulating the intrinsic complexity of the vasculature. This review illustrates the complexity involved in developing in vitro vasculature and provides an overview of fabrication methods for Vasculature-on-Chip in relation to the biological relevance of such methods.


2013 ◽  
Vol 65 ◽  
pp. 1363-1377 ◽  
Author(s):  
Christian Opländer ◽  
Annika Deck ◽  
Christine M. Volkmar ◽  
Michael Kirsch ◽  
Jörg Liebmann ◽  
...  

2002 ◽  
Vol 28 (5) ◽  
pp. 483-490 ◽  
Author(s):  
Volker Liebe ◽  
Martina Brückmann ◽  
Karl-Georg Fischer ◽  
Karl Konstantin Haase ◽  
Martin Borggrefe ◽  
...  

2005 ◽  
Vol 284-286 ◽  
pp. 377-380
Author(s):  
Vincent Souillac ◽  
Jean Christophe Fricain ◽  
Y. Lepetitcorps ◽  
V. Bureau ◽  
Dominique Chauveaux

In this study we focus on the use of coral Porites Lutea and the various treatments used to remove proteins while assessing the impact of the various removal methods on the in vitro and in vivo coral behavior. No significant differences were observed in vitro among all materials. In vivo, no histological differences were observed between BiocoralÒ and samples treated by either hydrogen peroxide or a thermal procedure. The implants made from supercritical fluid treated coral were more resistant to resorption (50% more resistant after one month).


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