Solid-State Perturbation for Solubility Improvement: A Proof of Concept

ChemMedChem ◽  
2010 ◽  
Vol 6 (1) ◽  
pp. 60-62 ◽  
Author(s):  
Lars-Erik Briggner ◽  
Ramon Hendrickx ◽  
Lars Kloo ◽  
Jan Rosdahl ◽  
Per H. Svensson
ChemMedChem ◽  
2014 ◽  
Vol 9 (4) ◽  
pp. 724-726 ◽  
Author(s):  
Lars-Erik Briggner ◽  
Lars Kloo ◽  
Jan Rosdahl ◽  
Per H. Svensson

2015 ◽  
Vol 112 (7) ◽  
pp. 1995-1999 ◽  
Author(s):  
Sam Emaminejad ◽  
Mehdi Javanmard ◽  
Chaitanya Gupta ◽  
Shuai Chang ◽  
Ronald W. Davis ◽  
...  

The controlled immobilization of proteins on solid-state surfaces can play an important role in enhancing the sensitivity of both affinity-based biosensors and probe-free sensing platforms. Typical methods of controlling the orientation of probe proteins on a sensor surface involve surface chemistry-based techniques. Here, we present a method of tunably controlling the immobilization of proteins on a solid-state surface using electric field. We study the ability to orient molecules by immobilizing IgG molecules in microchannels while applying lateral fields. We use atomic force microscopy to both qualitatively and quantitatively study the orientation of antibodies on glass surfaces. We apply this ability for controlled orientation to enhance the performance of affinity-based assays. As a proof of concept, we use fluorescence detection to indirectly verify the modulation of the orientation of proteins bound to the surface. We studied the interaction of fluorescently tagged anti-IgG with surface immobilized IgG controlled by electric field. Our study demonstrates that the use of electric field can result in more than 100% enhancement in signal-to-noise ratio compared with normal physical adsorption.


2021 ◽  
Author(s):  
◽  
Nurul Akmar Binti Che Zaudin

<p>Efficient and effective delivery of fertilisers, herbicides, pesticides and growth regulating compounds to plants is the subject of much ongoing research. The objective of this research was to develop nano-formulations for delivery of compounds to plants. Two formulations were developed: the first was solution-based focused on encapsulation of the active ingredient in a nanoemulsion. Nanoemulsions should be ideal for facilitating transfer of compounds to plant leaves as their size correlates well with the nanoscale surface features of leaves, achieving significantly greater total contact area between the oil droplets and the leaves. The second nano-formulation was solid-state based, focused on locating the active ingredient within the tubules of a nanotube clay. For proof-of-concept two synthetic plant hormones, N-phenyl-N‘-(2-chloro-4-pyridyl)urea (CPPU) or forchlorfenuron, a synthetic cytokinin, and 2,4-dichlorophenoxyacetic acid (2,4-D), a synthetic auxin, were chosen for encapsulation. CPPU is a phenylurea derivative that shows strikingly strong cytokinin-like activity in plants, including delaying senescence. It is highly water insoluble, but soluble in organic solvents. It is widely used in a variety of crops, particularly kiwifruit and table grapes. Delivery of CPPU safely, efficiently and at the appropriate dosage is a priority as overdosing or incorrect timing of application causes detrimental effects on fruit firmness and other quality attributes. Auxins are also a group of plant hormone. 2,4-D is a synthetic auxin which has been widely used at high concentrations as a herbicide, at medium concentrations for fruit thinning, and at low concentrations promotes root initiation, but at even lower concentrations promote root elongation. Consequently, careful control of dosage is required to obtain the desired effect. The nanoemulsion system developed was water/polysorbate 80/glycerol/soybean oil. The active ingredient, CPPU, was incorporated into the nanoemulsion via the oil phase in a pre-concentrate which was then crash diluted to yield the final nanoemulsion. Nanoemulsions are created only when the concentrate is located in the bicontinuous or oil-in-water microemulsion regions of the phase diagram. The droplet size of the nanoemulsions was measured using dynamic light scattering with droplets ranging in size from 30 – 100 nm. The CPPU-loaded nanoemulsions were stable for more than three days. To determine if the nanoemulsion was an effective delivery system, a leaf senescence bioassay was conducted to test the senescence-delaying effect of the CPPU-loaded nanoemulsions when applied to explants. The nanoemulsions were applied directly to the leaves of dwarf bean explants. Chlorophyll was extracted from the leaves and measured spectrophotometrically before and several days following treatment. The CPPU-loaded nanoemulsions enhanced the effectiveness of CPPU in delaying leaf senescence compared with the control experiments, including direct application of CPPU. A >10-fold reduction in CPPU concentration was achieved. The second delivery method was a solid-state preparation, using halloysite clay nanotubes loaded with 2,4-D. A rooting bioassay using mung bean explants was used for proof of concept. Application of 2,4-D nanotubes to the cut end of a young stem, without roots, stimulated root formation compared to controls after 10 days and at a lower applied concentration. The retardation of root elongation, relative to controls after 13 days, potentially indicated continued slow release of the active ingredient from the nanotubes. Results obtained from this research indicate that nano-formulations have the potential to deliver biologically active compounds to plants in the horticultural and agricultural sectors at effective concentrations lower than in current usage.</p>


2020 ◽  
Vol 117 (14) ◽  
pp. 7658-7664 ◽  
Author(s):  
Wilhelm Johannisson ◽  
Ross Harnden ◽  
Dan Zenkert ◽  
Göran Lindbergh

Structures that are capable of changing shape can increase efficiency in many applications, but are often heavy and maintenance intensive. To reduce the mass and mechanical complexity solid-state morphing materials are desirable but are typically nonstructural and problematic to control. Here we present an electrically controlled solid-state morphing composite material that is lightweight and has a stiffness higher than aluminum. It is capable of producing large deformations and holding them with no additional power, albeit at low rates. The material is manufactured from commercial carbon fibers and a structural battery electrolyte, and uses lithium-ion insertion to produce shape changes at low voltages. A proof-of-concept material in a cantilever setup is used to show morphing, and analytical modeling shows good correlation with experimental observations. The concept presented shows considerable promise and paves the way for stiff, solid-state morphing materials.


2019 ◽  
Vol 91 (9) ◽  
pp. 1471-1478 ◽  
Author(s):  
Francesco Papi ◽  
Giulia Targetti ◽  
Linda Cerofolini ◽  
Claudio Luchinat ◽  
Marco Fragai ◽  
...  

Abstract The fully characterization of tumor associated antigens (TAAs) and of tumor associated carbohydrate antigens (TACAs) have opened the avenue of cancer immunotherapy. The intrinsic poor immunogenicity of TACAs, however, spotlighted the importance of multivalent presentation of the antigen(s) to trigger an immune response. Nanoparticles are excellent scaffolds for this purpose. Here we reported on the easy glycosylation of iron-based and biocompatible dextran-based nanoparticles with 1, a mimetic of the TnThr antigen. The multivalent presentation of 1 induced the induction of TNF-α and IL-6/IL10, respectively. The multivalent glycosylation of silica nanoparticles (GSiNPs) was also performed and saccharide loading qualitative assessed by solid state NMR. Our results offer the proof of concept that biomolecules coating can also be investigated on solid system by NMR.


2020 ◽  
Author(s):  
Adrian Samkian ◽  
Gavin R. Kiel ◽  
Christopher G. Jones ◽  
Harrison Bergman ◽  
Julia Oktawiec ◽  
...  

Solid-state packing plays a defining role in the properties of a molecular organic material, but it is difficult to elucidate in the absence of single crystals that are suitable for X-ray diffraction. Here, we demonstrate the coupling of divergent synthesis with microcrystal electron diffraction (MicroED) for rapid assessment of solid-state packing motifs, using a class of chiral nanocarbons – expanded helicenes – as a proof of concept. Two highly selective oxidative dearomatizations of a readily-accessible helicene provided a divergent route to four electron-deficient analogues containing quinone or quinoxaline units. Crystallization efforts consistently yielded microcrystals that were unsuitable for single crystal X-ray diffraction, but ideal for MicroED. This technique facilitated the elucidation of solid-state structures of all five compounds with <1.1 Å resolution. The otherwise-inaccessible data revealed a range of notable packing behavior, including four different space groups, homochirality in a crystal for a helicene with an extremely low enantiomerization barrier, and nanometer scale cavities. The results of this study suggest that MicroED will soon become an indispensable tool for high-throughput investigations in pursuit of next-generation organic materials.


Science ◽  
2020 ◽  
Vol 368 (6495) ◽  
pp. 1091-1098 ◽  
Author(s):  
Cheng-Gong Han ◽  
Xin Qian ◽  
Qikai Li ◽  
Biao Deng ◽  
Yongbin Zhu ◽  
...  

Harvesting heat from the environment into electricity has the potential to power Internet-of-things (IoT) sensors, freeing them from cables or batteries and thus making them especially useful for wearable devices. We demonstrate a giant positive thermopower of 17.0 millivolts per degree Kelvin in a flexible, quasi-solid-state, ionic thermoelectric material using synergistic thermodiffusion and thermogalvanic effects. The ionic thermoelectric material is a gelatin matrix modulated with ion providers (KCl, NaCl, and KNO3) for thermodiffusion effect and a redox couple [Fe(CN)64–/Fe(CN)63–] for thermogalvanic effect. A proof-of-concept wearable device consisting of 25 unipolar elements generated more than 2 volts and a peak power of 5 microwatts using body heat. This ionic gelatin shows promise for environmental heat-to-electric energy conversion using ions as energy carriers.


2010 ◽  
Vol 99 (9) ◽  
pp. 3665-3675 ◽  
Author(s):  
Stephen R. Byrn ◽  
George Zografi ◽  
Xiaoming (Sean) Chen

2020 ◽  
Author(s):  
Zhaoyu Wang ◽  
Xinhui Zou ◽  
Yi Xie ◽  
Haoke Zhang ◽  
lianrui hu ◽  
...  

<p><b>Luminescent organic radicals have attracted much attention due to its distinctive open-shell structure and all-in-one properties on optoelectronics</b><b>, electronics</b><b>, and magnetics</b><b>. However, organic radicals are usually instable</b><b> and only very limited stable structures with π-radicals can </b><b>exhibit luminescent property</b><b> in the isolated state, most of which originate from the family of triphenylmethyl derivatives</b><b>. Here, we report an unusual radical luminescence phenomenon that nonconjugated radical polymer can readily emits red luminescence at ~635 nm in the solid state. A traditional luminescence quencher, 2,2,6,6-tetramethylpiperidine 1-oxyl (TEMPO)</b><b>, was turned into a red chromophore when grafted onto a polymer backbone. Experimental data confirms the emission is associated with the nitroxide radicals and is also affected by the packing of polymer. As a proof of concept, a biomedical application in intracellular ascorbic acid visualization is demonstrated. This work discloses a novel class of luminescent radicals and provides a distinctive and simple pathway for stable radical luminescence. </b></p>


2020 ◽  
Author(s):  
Adrian Samkian ◽  
Gavin R. Kiel ◽  
Christopher G. Jones ◽  
Harrison Bergman ◽  
Julia Oktawiec ◽  
...  

Solid-state packing plays a defining role in the properties of a molecular organic material, but it is difficult to elucidate in the absence of single crystals that are suitable for X-ray diffraction. Here, we demonstrate the coupling of divergent synthesis with microcrystal electron diffraction (MicroED) for rapid assessment of solid-state packing motifs, using a class of chiral nanocarbons – expanded helicenes – as a proof of concept. Two highly selective oxidative dearomatizations of a readily-accessible helicene provided a divergent route to four electron-deficient analogues containing quinone or quinoxaline units. Crystallization efforts consistently yielded microcrystals that were unsuitable for single crystal X-ray diffraction, but ideal for MicroED. This technique facilitated the elucidation of solid-state structures of all five compounds with <1.1 Å resolution. The otherwise-inaccessible data revealed a range of notable packing behavior, including four different space groups, homochirality in a crystal for a helicene with an extremely low enantiomerization barrier, and nanometer scale cavities. The results of this study suggest that MicroED will soon become an indispensable tool for high-throughput investigations in pursuit of next-generation organic materials.


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