scholarly journals Aging Process of Polyamidoamine Dendrimers: Effect of pH and Shaking in the Fluorescence Emission and Aggregation-State

2020 ◽  
Author(s):  
Igartua Daniela ◽  
David Ybarra ◽  
Dario Cabezas ◽  
Silvia del Valle Alonso ◽  
Fernando Alvira
Keyword(s):  
Aging Process ◽  
Aqueous Suspension ◽  
Chemical Change ◽  
Fluorescence Emission ◽  
Pamam Dendrimers ◽  
Aggregation State ◽  
Polyamidoamine Dendrimers ◽  
Ph Conditions ◽  
In Vivo Administration

In the last years, it has been discovered and intensely studied the non-traditional intrinsic fluorescence of PAMAM dendrimers. Nevertheless, their aging process in aqueous suspension is scarcely studied, being unknown the causes of the observed changes in their fluorescence properties. Hence, this work aims to characterize the PAMAM dendrimers of generation 4.0 (DG4.0) and 4.5 (DG4.5) through the aging process at three different pH conditions, stored with or without shaking. We studied, up to 16 days, the UV-Vis absorption, the fluorescence emission, and the size of dendrimers/aggregates. In a different way than the already published work, we demonstrated that there is no chemical change in dendrimers through the aging process, even though changes in fluorescence emission were observed. Besides, we have put in evidence that changes in the agglomeration patterns of dendrimers would not be related to change in the fluorescence emission thought aging. Moreover, we demonstrated that DG4.5 formed large aggregates in water that need to be disrupted by shaking previous to an in vivo administration. <br>

scholarly journals Aging Process of Polyamidoamine Dendrimers: Effect of pH and Shaking in the Fluorescence Emission and Aggregation-State

2020 ◽  
Author(s):  
Igartua Daniela ◽  
David Ybarra ◽  
Dario Cabezas ◽  
Silvia del Valle Alonso ◽  
Fernando Alvira
Keyword(s):  
Aging Process ◽  
Aqueous Suspension ◽  
Chemical Change ◽  
Fluorescence Emission ◽  
Pamam Dendrimers ◽  
Aggregation State ◽  
Polyamidoamine Dendrimers ◽  
Ph Conditions ◽  
In Vivo Administration

In the last years, it has been discovered and intensely studied the non-traditional intrinsic fluorescence of PAMAM dendrimers. Nevertheless, their aging process in aqueous suspension is scarcely studied, being unknown the causes of the observed changes in their fluorescence properties. Hence, this work aims to characterize the PAMAM dendrimers of generation 4.0 (DG4.0) and 4.5 (DG4.5) through the aging process at three different pH conditions, stored with or without shaking. We studied, up to 16 days, the UV-Vis absorption, the fluorescence emission, and the size of dendrimers/aggregates. In a different way than the already published work, we demonstrated that there is no chemical change in dendrimers through the aging process, even though changes in fluorescence emission were observed. Besides, we have put in evidence that changes in the agglomeration patterns of dendrimers would not be related to change in the fluorescence emission thought aging. Moreover, we demonstrated that DG4.5 formed large aggregates in water that need to be disrupted by shaking previous to an in vivo administration. <br>

Aging process of polyamidoamine dendrimers: Effect of pH and shaking in the fluorescence emission and aggregation‐state

2021 ◽  
Vol 138 (29) ◽  
pp. 50700
Author(s):  
Daniela E. Igartúa ◽  
David E. Ybarra ◽  
Darío M. Cabezas ◽  
Silvia del V. Alonso ◽  
Fernando C. Alvira
Keyword(s):  
Aging Process ◽  
Fluorescence Emission ◽  
Aggregation State ◽  
Effect Of Ph ◽  
Polyamidoamine Dendrimers

scholarly journals Use of Polyamidoamine Dendrimers in Brain Diseases

Molecules ◽  
2018 ◽  
Vol 23 (9) ◽  
pp. 2238 ◽  
Author(s):  
Maria Florendo ◽  
Alexander Figacz ◽  
Bhairavi Srinageshwar ◽  
Ajit Sharma ◽  
Douglas Swanson ◽  
...  
Keyword(s):  
Pamam Dendrimers ◽  
Brain Diseases ◽  
Surface Functional Groups ◽  
Polyamidoamine Dendrimers ◽  
Effective Delivery ◽  
The Right ◽  
The Brain ◽  
Reproducible Manner

Polyamidoamine (PAMAM) dendrimers are one of the smallest and most precise nanomolecules available today, which have promising applications for the treatment of brain diseases. Each aspect of the dendrimer (core, size or generation, size of cavities, and surface functional groups) can be precisely modulated to yield a variety of nanocarriers for delivery of drugs and genes to brain cells in vitro or in vivo. Two of the most important criteria to consider when using PAMAM dendrimers for neuroscience applications is their safety profile and their potential to be prepared in a reproducible manner. Based on these criteria, features of PAMAM dendrimers are described to help the neuroscience researcher to judiciously choose the right type of dendrimer and the appropriate method for loading the drug to form a safe and effective delivery system to the brain.

Anticoagulant Properties of Three Mucopolysaccharides Used in Rheumatology

1983 ◽  
Vol 50 (03) ◽  
pp. 652-655 ◽  
Author(s):  
F Bauer ◽  
P Schulz ◽  
G Reber ◽  
C A Bouvier
Keyword(s):  
Factor Xa ◽  
Degenerative Joint Disease ◽  
Joint Disease ◽  
Thrombin Time ◽  
Coagulation Tests ◽  
Amplification System ◽  
Relative Potencies ◽  
In Vivo Administration

SummaryThree mucopolysaccharides (MPS) used in the treatment of degenerative joint disease were compared to heparin to establish their relative potencies on 3 coagulation tests, the aPTT, the antifactor X a activity and the dilute thrombin time. One of the compounds, Arteparon®, was one fourth as potent as heparin on the aPTT, but had little or no influence on the 2 other tests. Further in vitro studies suggested that Arteparon® acted at a higher level than factor Xa generation in the intrinsic amplification system and that its effect was independent of antithrombin III. In vivo administration of Arteparon® confirmed its anticoagulant properties, which raises the question of the clinical use of this MPS.

Isolierung von PS II-Partikeln mit in vivo Eigenschaften aus Euglena gracilis, Stamm Z / Isolation of PS II-Particels with in vivo Characteristics from Euglena gracilis, Stamm Z

1982 ◽  
Vol 37 (3-4) ◽  
pp. 256-259 ◽  
Author(s):  
F. Schuler ◽  
P. Brandt ◽  
W. Wießner
Keyword(s):  
Euglena Gracilis ◽  
Fluorescence Emission ◽  
Improved Method ◽  
Ps Ii ◽  
Ps I ◽  
Emission And Absorption Spectra ◽  
Chlorophyll Protein ◽  
Ps Ii Activity ◽  
Photosystem Ii Particles

Abstract An improved method for isolation of (photosystem II)-particles from Euglena gracilis, strain Z was established. PS II-particles isolated by ultrasonic treatment and following differential centrifugation show fluorescence emission and absorption spectra identical with in vivo properties of Euglena gracilis. These PS II-particles have only PS II-activity and contain CP a, the typical chlorophyll-protein-complex of PS II. No contamination of PS I-components are detectable.

scholarly journals Silica-Coated Fe3O4 Nanoparticles as a Bifunctional Agent for Magnetic Resonance Imaging and ZnII Fluorescent Sensing

2021 ◽  
Vol 20 ◽  
pp. 153303382110365
Author(s):  
Lin Qiu ◽  
Shuwen Zhou ◽  
Ying Li ◽  
Wen Rui ◽  
Pengfei Cui ◽  
...  
Keyword(s):  
Magnetic Resonance Imaging ◽  
Magnetic Resonance ◽  
Contrast Agent ◽  
Quantum Interference ◽  
Inductively Coupled Plasma ◽  
Fluorescence Emission ◽  
Mri Contrast Agent ◽  
Core Shell ◽  
Resonance Imaging

Bifunctional magnetic/fluorescent core-shell silica nanospheres (MNPs) encapsulated with the magnetic Fe3O4 core and a derivate of 8-amimoquinoline (N-(quinolin-8-yl)-2-(3-(triethoxysilyl) propylamino) acetamide) (QTEPA) into the shell were synthesized. These functional MNPs were prepared with a modified stöber method and the formed Fe3O4@SiO2-QTEPA core-shell nanocomposites are biocompatible, water-dispersible, and stable. These prepared nanoparticles were characterized by X-ray power diffraction (XRD), transmission electron microscopy (TEM), thermoelectric plasma Quad II inductively coupled plasma mass spectrometry (ICP-MS), superconducting quantum interference device (SQUID), TG/DTA thermal analyzer (TGA) and Fourier transform infrared spectroscopy (FTIR). Further application of the nanoparticles in detecting Zn2+ was confirmed by the fluorescence experiment: the nanosensor shows high selectivity and sensitivity to Zn2+ with a 22-fold fluorescence emission enhancement in the presence of 10 μM Zn2+. Moreover, the transverse relaxivity measurements show that the core-shell MNPs have T2 relaxivity (r2) of 155.05 mM−1 S−1 based on Fe concentration on the 3.0 T scanner, suggesting that the compound can be used as a negative contrast agent for MRI. Further in vivo experiments showed that these MNPs could be used as MRI contrast agent. Therefore, the new nanosensor provides the dual modality of magnetic resonance imaging and optical imaging.

scholarly journals Reaction of Chalcones with Cellular Thiols. The Effect of the 4-Substitution of Chalcones and Protonation State of the Thiols on the Addition Process. Diastereoselective Thiol Addition

Molecules ◽  
2021 ◽  
Vol 26 (14) ◽  
pp. 4332
Author(s):  
Fatemeh Kenari ◽  
Szilárd Molnár ◽  
Pál Perjési
Keyword(s):  
Biological Effects ◽  
Equilibrium Composition ◽  
Deprotonated Form ◽  
Degree Of Ionization ◽  
Thiol Reactivity ◽  
Michael Type Addition ◽  
Ph Conditions ◽  
The Difference ◽  
Initial Reactivity

Several biological effects of chalcones have been reported to be associated with their thiol reactivity. In vivo, the reactions can result in the formation of small-molecule or protein thiol adducts. Both types of reactions can play a role in the biological effects of this class of compounds. Progress of the reaction of 4-methyl- and 4-methoxychalcone with glutathione and N-acetylcysteine was studied by the HPLC-UV-VIS method. The reactions were conducted under three different pH conditions. HPLC-MS measurements confirmed the structure of the formed adducts. The chalcones reacted with both thiols under all incubation conditions. The initial rate and composition of the equilibrium mixtures depended on the ratio of the deprotonated form of the thiols. In the reaction of 4-methoxychalcone with N-acetylcysteine under strongly basic conditions, transformation of the kinetic adduct into the thermodynamically more stable one was observed. Addition of S-protonated N-acetylcysteine onto the polar double bonds of the chalcones showed different degrees of diastereoselectivity. Both chalcones showed a Michael-type addition reaction with the ionized and non-ionized forms of the investigated thiols. The initial reactivity of the chalcones and the equilibrium composition of the incubates showed a positive correlation with the degree of ionization of the thiols. Conversions showed systematic differences under each set of conditions. The observed differences can hint at the difference in reported biological actions of 4-methyl- and 4-methoxy-substituted chalcones.

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