Scholarly Works, Macromolecules Innovation Institute (MII)
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- Antibacterial efficacy of core-shell nanostructures encapsulating gentamicin against an in vivo intracellular Salmonella modelRanjan, Ashish; Pothayee, Nikorn; Seleem, Mohamed N.; Tyler, Ronald D.; Brenseke, Bonnie; Sriranganathan, Nammalwar; Riffle, Judy S.; Kasimanickam, Ramanathan K. (Dove Medical Press, 2009-01-01)Pluronic based core-shell nanostructures encapsulating gentamicin were designed in this study. Block copolymers of (PAA(+/-)Na-b-(PEO-b-PPO-b-PEO)-b-PAA(+/-)Na) were blended with PAA(-) Na(+) and complexed with the polycationic antibiotic gentamicin to form nanostructures. Synthesized nanostructures had a hydrodynamic diameter of 210 nm, zeta potentials of -0.7 (+/-0.2), and incorporated approximately 20% by weight of gentamicin. Nanostructures upon co-incubation with J774A.1 macrophage cells showed no adverse toxicity in vitro. Nanostructures administered in vivo either at multiple dosage of 5 microg g(-1) or single dosage of 15 microg g(-1) in AJ-646 mice infected with Salmonella resulted in significant reduction of viable bacteria in the liver and spleen. Histopathological evaluation for concentration-dependent toxicity at a dosage of 15 microg g(-1) revealed mineralized deposits in 50% kidney tissues of free gentamicin-treated mice which in contrast was absent in nanostructure-treated mice. Thus, encapsulation of gentamicin in nanostructures may reduce toxicity and improve in vivo bacterial clearance.
- Olefin cross-metathesis, a mild, modular approach to functionalized cellulose estersMeng, Xiangtao; Matson, John B.; Edgar, Kevin J. (The Royal Society of Chemistry, 2014-09-02)Olefin cross-metathesis has been demonstrated to be a modular pathway for synthesis of a series of functionalized cellulose esters. As a proof of concept, cellulose acetate was acylated with two terminally olefinic acid chlorides, pent-4-enoyl chloride and undec-10-enoyl chloride, providing olefin-terminated cellulose esters with different side-chain lengths. These ω-unsaturated cellulose esters were then reacted with a variety of cross-metathesis partners, including acrylic acid, methyl acrylate, 2-hydroxyethyl acrylate, poly(ethylene glycol) methyl ether acrylate, and allyl alcohols, using Hoveyda–Grubbs’ 2nd generation catalyst. Complete conversion to cross-metathesis products was achieved in reactions with acrylic acid or acrylates using 3–5 mol% catalyst at 40 °C within 1 h. We further demonstrate successful hydrogenation of these α,β-unsaturated esters and acids, thereby eliminating the potential for radical-induced crosslinking during storage.
- Nucleobase-functionalized acrylic ABA triblock copolymers and supramolecular blendsZhang, Keren; Aiba, Motohiro; Fahs, Gregory B.; Hudson, Amanda G.; Chiang, William D.; Moore, Robert Bowen; Ueda, Mitsuru; Long, Timothy E. (The Royal Society of Chemistry, 2015-01-30)Reversible addition-fragmentation chain transfer (RAFT) polymerization afforded the unprecedented synthesis of well-defined acrylic ABA triblock copolymers with nucleobase-functionalized external blocks and a central poly(n-butyl acrylate) (PnBA) block. Size exclusion chromatography (SEC) confirmed the molecular weight and molecular weight distribution of the central block. 1H NMR spectroscopy revealed the successful chain extension of the PnBA macro-chain transfer agent (CTA) using adenine or thymine-functionalized acrylic monomers. The acrylic monomer with a flexible spacer to the pendant nucleobases promoted intermolecular recognition of nucleobases and long range segmental motion of polymer main chains. The external block glass transition temperatures (Tg's) of thymine (T) and adenine (A) functionalized blocks were 52 °C and 76 °C, respectively. Thermomechanical and morphological analysis revealed the effect of processing conditions on self-assembly and microphase-separated morphology of nucleobase-functionalized ABA copolymers. Thymine and adenine-functionalized ABA triblocks formed a thermodynamically stable, hydrogen-bonded complex upon blending. The supramolecular blend exhibited a cylindrical microphase-separated morphology with an extended plateau window compared to the individual block copolymers. The complementary hydrogen bonding between adenine and thymine formed a thermally labile, physically crosslinked, network that exhibited enhanced mechanical performance with melt processability. Thus, these ABA nucleobase-functionalized block copolymers demonstrate potential as thermoplastic elastomers for hot melt adhesives and coatings.
- Imidazole-containing triblock copolymers with a synergy of ether and imidazolium sitesJangu, Chainika; Wang, Jing-Han Helen; Wang, Dong; Fahs, Gregory B.; Heflin, James R.; Moore, Robert Bowen; Colby, Ralph H.; Long, Timothy E. (The Royal Society of Chemistry, 2015-03-06)Reversible addition-fragmentation chain transfer (RAFT) polymerization enabled the synthesis of well-defined A-BC-A triblock copolymers containing a synergy of pendant ether and imidazolium sites. The soft central BC block comprises low Tg di(ethylene glycol) methyl ether methacrylate (DEGMEMA) and 1-(4-vinylbenzyl) methyl imidazolium units. External polystyrene blocks provide mechanical reinforcement within a nanoscale morphology. Dynamic mechanical analysis (DMA) of the A-BC-A triblock copolymers exhibited a plateau region, which suggested the formation of a microphase-separated morphology. Atomic force microscopy (AFM) and small angle X-ray scattering (SAXS) collectively probed the morphology of the A-BC-A triblock copolymers, revealing long-range order at the nanoscale dimensions. Dielectric relaxation spectroscopy (DRS) examined the ion-transport properties of ionomeric A-BC-A triblock copolymers and random copolymers with different compositions. The role of morphology was demonstrated with block copolymer nanoscale structures providing superior ionic conductivity and mechanical performance compared to random copolymers. Under a 4 V direct current (DC) applied voltage, electromechanical transducers derived from these triblock copolymer membranes with added ionic liquid showed superior actuation performance compared to a benchmark Nafion[registered sign] membrane, suggesting potential for ionic polymer device applications. This was attributed to optimum modulus, improved ionic conductivity, and microphase-separated morphology of triblock copolymers.
- Imparting functional variety to cellulose ethers via olefin cross-metathesisDong, Yifan; Edgar, Kevin J. (The Royal Society of Chemistry, 2015-04-09)Olefin cross-metathesis is a valuable new approach for imparting functional variety to cellulose ethers. Starting from commercially available ethyl cellulose, terminally unsaturated alkyl groups were appended as metathesis handles by reaction with allyl chloride, 5-bromo-1-pentene, 7-bromo-1-heptene and 11-bromo-1-undecene, employing sodium hydride catalyst. These olefin-terminal ethyl cellulose derivatives were then subjected to olefin cross-metathesis with a variety of electron-poor olefin substrates, including acrylic acid and acrylate esters under optimized conditions (5–10 mol% Hoveyda-Grubbs’ 2nd generation catalyst, 37 °C, 2 h). The effects of varying the length of the ω-unsaturated alkyl handle, and of the solvent systems used were evaluated. Ethyl cellulose containing a pent-4-enyl substituent performed best in cross metathesis reactions and a hept-6-enyl substituent gave similarly good results. Ethyl cellulose with allyl substituents gave low to moderate metathesis conversion (<50%), possibly due to steric effects and the proximity of the ether oxygen to the terminal olefin. Interestingly, longer tethers (undec-10-enyl) gave high conversions (up to 90%) but relatively slow reactions (ca. 12 h needed for high conversion). While limited in this study by the relatively low DS (OH) of the starting commercial ethyl cellulose materials, this methodology has strong promise for introduction of diverse functionality to cellulose ethers in chemospecific and mild fashion, enabling amorphous solid dispersion and other applications.
- Peptide-based hydrogen sulphide-releasing gelsCarter, Jennifer M.; Qian, Yun; Foster, Jeffrey C.; Matson, John B. (The Royal Society of Chemistry, 2015-07-20)An aromatic peptide amphiphile was designed for delivery of the signaling gas H2S. The peptide self-assembled in water into nanofibers that gelled upon charge screening. The non-toxic gel slowly released H2S over 15 hours, and the presence of H2S in endothelial cells was verified using a fluorescent H2S probe.
- Size dependent ion-exchange of large mixed-metal complexes into Nafion® membranesNaughton, Elise M.; Zhang, Mingqiang; Troya, Diego; Brewer, Karen J.; Moore, Robert Bowen (The Royal Society of Chemistry, 2015-08-18)Perfluorosulfonate ionomers have been shown to demonstrate a profound affinity for large cationic complexes, and the exchange of these ions may be used to provide insight regarding Nafion® morphology by contrasting molecular size with existing morphological models. The trimetallic complex, [{(bpy)2Ru(dpp)}2RhBr2]5+, is readily absorbed by ion-exchange into Na+-form Nafion® membranes under ambient conditions. The dimensions of three different isomers of the trimetallic complex were found to be: 23.6 Å × 13.3 Å × 10.8 Å, 18.9 Å × 18.0 Å × 13.7 Å, and 23.1 Å × 12.0 Å × 11.4 Å, yielding an average molecular volume of 1.2 × 103 Å3. At equilibrium, the partition coefficient for the ion-exchange of the trimetallic complex into Nafion® from a DMF solution was found to be 5.7 × 103. Furthermore, the total cationic charge of the exchanged trimetallic complexes was found to counterbalance 86 ± 2% of the anionic SO3− sites in Nafion®. The characteristic dimensions of morphological models for the ionic domains in Nafion® were found to be comparable to the molecular dimensions of the large mixed-metal complexes. Surprisingly, SAXS analysis indicated that the complexes absorbed into the ionic domains of Nafion® without significantly changing the ionomer morphology. Given the profound affinity for absorption of these large cationic molecules, a more open-channel model for the morphology of perfluorosulfonate ionomers is more reasonable, in agreement with recent experimental findings. In contrast to smaller monometallic complexes, the time dependent uptake of the large trimetallic cations was found to be biexponential. This behavior is attributed to a fast initial ion-exchange process on the surface of the membrane, accompanied by a slower transport-limited ion-exchange for exchange sites that are buried further in the ionomer matrix.
- Phosphonium-containing diblock copolymers from living anionic polymerization of 4-diphenylphosphino styreneSchultz, Alison R.; Fahs, Gregory B.; Jangu, Chainika; Chen, Mingtao; Moore, Robert Bowen; Long, Timothy E. (The Royal Society of Chemistry, 2015-11-20)Living anionic polymerization of 4-diphenylphosphino styrene (DPPS) achieved well-defined homopolymers, poly(DPPS-b-S) styrenic block copolymers, and poly(I-b-DPPS) diene-based diblock copolymers with predictable molecular weights and narrow polydispersities. In situ FTIR spectroscopy monitored the anionic polymerization of DPPS and tracked monomer consumption for kinetic analysis. Post-alkylation enabled controlled placement of phosphonium functionality in poly(I-b-DPPS) diblock copolymers, producing well-defined phosphonium-containing block copolymers with low degrees of compositional heterogeneity. Incorporating phosphonium charge disrupted the lamellar bulk morphology of the neutral diblock precursor and provided morphologies with interdigitated packing of alkyl chains on the phosphonium cation.
- Elucidating the Potential Biological Impact of Cellulose NanocrystalsCamarero-Espinosa, Sandra; Endes, Carola; Mueller, Silvana; Petri-Fink, Alke; Rothen-Rutishauser, Barbara; Weder, Christoph; Clift, Martin James David; Foster, Earl Johan (MDPI, 2016-07-08)Cellulose nanocrystals exhibit an interesting combination of mechanical properties and physical characteristics, which make them potentially useful for a wide range of consumer applications. However, as the usage of these bio-based nanofibers increases, a greater understanding of human exposure addressing their potential health issues should be gained. The aim of this perspective is to highlight how knowledge obtained from studying the biological impact of other nanomaterials can provide a basis for future research strategies to deduce the possible human health risks posed by cellulose nanocrystals.
- 3D printing vending machine(United States Patent and Trademark Office, 2016-08-16)A vending machine for creating a three-dimensional object having an enclosure having an exterior and interior. The interior receives and houses at least one three-dimensional printer. An interface for accepting an instruction associated with an object to be printed and transmitting the instruction to the printer. A storage section for storing a printed object that provides access to the printed part but limits or prohibits access to the interior.
- Remote Actuation of Magnetic Nanoparticles For Cancer Cell Selective Treatment Through Cytoskeletal DisruptionMaster, Alyssa M.; Williams, Philise N.; Pothayee, Nikorn; Pothayee, Nipon; Zhang, Rui; Vishwasrao, Hemant M.; Golovin, Yuri I.; Riffle, Judy S.; Sokolsky, Marina; Kabanov, Alexander V. (Springer Nature, 2016-09-20)Motion of micron and sub-micron size magnetic particles in alternating magnetic fields can activate mechanosensitive cellular functions or physically destruct cancer cells. However, such effects are usually observed with relatively large magnetic particles (> 250 nm) that would be difficult if at all possible to deliver to remote sites in the body to treat disease. Here we show a completely new mechanism of selective toxicity of superparamagnetic nanoparticles (SMNP) of 7 to 8 nm in diameter to cancer cells. These particles are coated by block copolymers, which facilitates their entry into the cells and clustering in the lysosomes, where they are then magneto-mechanically actuated by remotely applied alternating current (AC) magnetic fields of very low frequency (50 Hz). Such fields and treatments are safe for surrounding tissues but produce cytoskeletal disruption and subsequent death of cancer cells while leaving healthy cells intact.
- A critical review of the current knowledge regarding the biological impact of nanocelluloseEndes, Carola; Camarero-Espinosa, Sandra; Mueller, Silvana; Foster, Earl Johan; Petri-Fink, Alke; Rothen-Rutishauser, Barbara; Weder, Christoph; Clift, Martin James David (2016-12-01)Several forms of nanocellulose, notably cellulose nanocrystals and nanofibrillated cellulose, exhibit attractive property matrices and are potentially useful for a large number of industrial applications. These include the paper and cardboard industry, use as reinforcing filler in polymer composites, basis for low-density foams, additive in adhesives and paints, as well as a wide variety of food, hygiene, cosmetic, and medical products. Although the commercial exploitation of nanocellulose has already commenced, little is known as to the potential biological impact of nanocellulose, particularly in its raw form. This review provides a comprehensive and critical review of the current state of knowledge of nanocellulose in this format. Overall, the data seems to suggest that when investigated under realistic doses and exposure scenarios, nanocellulose has a limited associated toxic potential, albeit certain forms of nanocellulose can be associated with more hazardous biological behavior due to their specific physical characteristics.
- Oil-Impregnated Hydrocarbon-Based Polymer FilmsMukherjee, Ranit; Habibi, Mohammad; Rashed, Ziad T.; Berbert, Otacilio; Shi, Xiangke; Boreyko, Jonathan B. (Springer Nature, 2018-08-03)Porous surfaces impregnated with a liquid lubricant exhibit minimal contact angle hysteresis with immiscible test liquids, rendering them ideal as self-cleaning materials. Rather than roughening a solid substrate, an increasingly popular choice is to use an absorbent polymer as the "porous" material. However, to date the polymer choices have been limited to expensive silicone-based polymers or complex assemblies of polymer multilayers on functionalized surfaces. In this paper, we show that hydrocarbon-based polymer films such as polyethylene can be stably impregnated with chemically compatible vegetable oils, without requiring any surface treatment. These oil-impregnated hydrocarbon-based films exhibit minimal contact angle hysteresis for a wide variety of test products including water, ketchup, and yogurt. Our oil-impregnated films remain slippery even after several weeks of being submerged in ketchup, illustrating their extreme durability. We expect that the simple and cost-effective nature of our slippery hydrocarbon-based films will make them useful for industrial packaging applications.
- Ammonium Bisphosphonate Polymeric Magnetic Nanocomplexes for Platinum Anticancer Drug Delivery and Imaging with Potential Hyperthermia and Temperature-Dependent Drug ReleaseZhang, Rui; Fellows, Benjamin; Pothayee, Nikorn; Hu, Nan; Pothayee, Nipon; Jo, Ami; Bohórquez, Ana C.; Rinaldi, Carlos; Mefford, Olin Thompson; Davis, Richey M.; Riffle, Judy S. (Hindawi, 2018-08-05)Novel magnetite-ammonium bisphosphonate graft ionic copolymer nanocomplexes (MGICs) have been developed for potential drug delivery, magnetic resonance imaging, and hyperthermia applications. The complexes displayed relatively uniform sizes with narrow size distributions upon self-assembly in aqueous media, and their sizes were stable under simulated physiological conditions for at least 7 days. The anticancer drugs, cisplatin and carboplatin, were loaded into the complexes, and sustained release of both drugs was observed. The transverse NMR relaxivities (s) of the complexes were 244 s−1 (mM Fe)−1 which is fast compared to either the commercial T2-weighted MRI agent Feridex IV® or our previously reported magnetite-block ionomer complexes. Phantom MRI images of the complexes demonstrated excellent negative contrast effects of such complexes. Thus, the bisphosphonate-bearing MGICs could be promising candidates for dual drug delivery and magnetic resonance imaging. Moreover, the bisphosphonate MGICs generate heat under an alternating magnetic field of 30 kA·m−1 at 206 kHz. The temperature of the MGIC dispersion in deionized water increased from 37 to 41°C after exposure to the magnetic field for 10 minutes, corresponding to a specific absorption rate of 77.0 W·g−1. This suggests their potential as hyperthermia treatment agents as well as the possibility of temperature-dependent drug release, making MGICs more versatile in potential drug delivery applications.
- Prediction of Young’s Modulus for Injection Molded Long Fiber Reinforced ThermoplasticsChen, Hongyu; Baird, Donald G. (MDPI, 2018-08-06)In this article, the elastic properties of long-fiber injection-molded thermoplastics (LFTs) are investigated by micro-mechanical approaches including the Halpin-Tsai (HT) model and the Mori-Tanaka model based on Eshelby’s equivalent inclusion (EMT). In the modeling, the elastic properties are calculated by the fiber content, fiber length, and fiber orientation. Several closure approximations for the fourth-order fiber orientation tensor are evaluated by comparing the as-calculated elastic stiffness with that from the original experimental fourth-order tensor. An empirical model was developed to correct the fibers’ aspect ratio in the computation for the actual as-formed LFTs with fiber bundles under high fiber content. After the correction, the analytical predictions had good agreement with the experimental stiffness values from tensile tests on the LFTs. Our analysis shows that it is essential to incorporate the effect of the presence of fiber bundles to accurately predict the composite properties. This work involved the use of experimental values of fiber orientation and serves as the basis for computing part stiffness as a function of mold filling conditions. The work also explains why the modulus tends to level off with fiber concentration.
- Synthesis, characterization, and luminescent properties of two new Zr(IV) metal-organic frameworks based on anthracene derivativesRowe, Jennifer M.; Soderstrom, Erin M.; Zhu, Jie; Usov, Pavel M.; Morris, Amanda J. (2018-09)Metal-organic frameworks (MOFs) are crystalline materials constructed from metal ions or clusters, connected by multidentate organic ligands. Herein, we describe the synthesis and photophysical properties of two Zr-based, anthracene-containing MOFs, assembled from 2,6-anthracenedicarboxylic acid (2,6-ADCA and 2,6-MOF) and 1,4-anthracenedicarboxylic acid (1,4-ADCA and 1,4-MOF). The 2,6-ADCA analogue formed a highly crystalline octahedral structure that is isostructural with the well-known UiO-67 frameworks. Incorporation of the 1,4-ADCA ligand, on the other hand, resulted in large rod-shaped crystals. Both MOFs exhibit linker-based luminescence. The excited-state properties of the 2,6-MOF and 1,4-MOF were examined using stead-state diffuse reflectance and emission spectroscopies and time-correlated single photon counting (TCSPC) spectroscopy. The photophysical properties of the MOFs are compared with those of the corresponding ligand in solution.
- Capillary forces on a small particle at a liquid-vapor interface: Theory and simulationTang, Yanfei; Cheng, Shengfeng (American Physical Society, 2018-09-24)
- Folic Acid-Conjugated Cellulose Nanocrystals Show High Folate-Receptor Binding Affinity and Uptake by KB and Breast Cancer CellsBittleman, Katelyn Rose; Dong, Shuping; Roman, Maren; Lee, Yong Woo (American Chemical Society, 2018-10-24)The study evaluates cellulose nanocrystals (CNCs) as nanocarriers for targeted, intracellular delivery of molecular agents. CNCs were labeled with fluorescein-5′-isothiocyanate as an imaging agent and conjugated to folic acid (FA) as a targeting ligand. The CNC conjugates were characterized by UV–vis spectroscopy, ζ-potential analysis, dynamic light scattering, and atomic force microscopy. Cellular binding/uptake of the FA-conjugated CNCs by KB and MDA-MB-468 cells was quantified with cellular uptake assays. Internalization of the particles was confirmed by confocal microscopy. Uptake mechanisms were determined by inhibition studies with chlorpromazine and genistein. Binding affinity was qualitatively assessed with a free folate inhibition assay. Both KB and MDA-MB-468 cells exhibited significant and folate-receptor specific binding/uptake of FA-conjugated CNCs. Clathrin-mediated endocytosis was a significant uptake mechanism in both cell types, whereas caveolae-mediated endocytosis only played a significant role in MDA-MB-468 cells. Uptake inhibition of FA-conjugated CNCs by KB cells required high concentrations (>1 mM) of free FA. The observed FR-specific internalization of FA-conjugated CNCs by FR-positive cancer cells and tumors and their remarkable high affinity for the FR demonstrate the great potential of CNCs as novel nanocarriers for imaging agents and chemotherapeutics in the early detection and treatment of cancer.
- GSA Tomorrow: An Open Challenge to Promote the Future of GeoscienceDorfler, Kristin M.; Friedrich, Anke M. (Geological Society of America, 2018-11-20)The future of geoscience rests on your shoulders. Geologists are passionate about their science and discuss their interests with vigor, firmly understanding why geoscience is as important to society as physiology, agriculture, or engineering. In many cases, non-geologists don’t see the clear importance and implication of the profession, outside of natural disasters and events that have immediate and apparent human effects. Countless geoscientists1, including professionals, academics, and students, are already vocal self-advocates; however, in our currently digital world, where information can be instantly disseminated at the push of a button, it is time we took a collective effort as the Geological Society of America to actively emphasize the importance of science to the non-geologist, forming a movement to assertively advocate for our field. We invite you to contribute to this discussion by responding with succinct, measurable, and clear reasons on how what you do affects society. Our collective views could be used to guide non-geologists to advocate for geoscience just as non-physicians advocate for medical advances. GSA is as effective as its members, who make up 21 Scientific Divisions, which have numerous, tangible impacts on society. As GSA continues focusing efforts on the advancement of the Society into the twenty-first century, we are taking a critical look at what the Society is doing, whom it is doing it for, and how it could be doing it better.
- Nanoscale Bacteria‐Enabled Autonomous Drug Delivery System (NanoBEADS) Enhances Intratumoral Transport of NanomedicineSuh, SeungBeum; Jo, Ami; Traore, Mahama Aziz; Zhan, Ying; Coutermarsh-Ott, Sheryl; Ringel-Scaia, Veronica M.; Allen, Irving C.; Davis, Richey M.; Behkam, Bahareh (Wiley, 2018-12-05)Cancer drug delivery remains a formidable challenge due to systemic toxicity and inadequate extravascular transport of nanotherapeutics to cells distal from blood vessels. It is hypothesized that, in absence of an external driving force, the Salmonella enterica serovar Typhimurium could be exploited for autonomous targeted delivery of nanotherapeutics to currently unreachable sites. To test the hypothesis, a nanoscale bacteria‐enabled autonomous drug delivery system (NanoBEADS) is developed in which the functional capabilities of the tumor‐targeting S. Typhimurium VNP20009 are interfaced with poly(lactic‐co‐glycolic acid) nanoparticles. The impact of nanoparticle conjugation is evaluated on NanoBEADS' invasion of cancer cells and intratumoral transport in 3D tumor spheroids in vitro, and biodistribution in a mammary tumor model in vivo. It is found that intercellular (between cells) self‐replication and translocation are the dominant mechanisms of bacteria intratumoral penetration and that nanoparticle conjugation does not impede bacteria's intratumoral transport performance. Through the development of new transport metrics, it is demonstrated that NanoBEADS enhance nanoparticle retention and distribution in solid tumors by up to a remarkable 100‐fold without requiring any externally applied driving force or control input. Such autonomous biohybrid systems could unlock a powerful new paradigm in cancer treatment by improving the therapeutic index of chemotherapeutic drugs and minimizing systemic side effects.