Hydrophilic End Research Articles

Safety, tolerability, and pharmacokinetics of adamgammadex sodium, a novel agent to reverse the action of rocuronium and vecuronium, in healthy volunteers

Neuromuscular blockers (NMBs) selectively block neuromuscular transmission at the N2-nicotinic receptor on motor neurons to paralyze skeletal muscles, and are mainly used to facilitate tracheal intubation and surgical procedures. Rapid reversal is necessary in clinical practice to avoid profound block and reduce recovery time. Adamgammadex sodium is a modified γ-cyclodextrin derivative consisting of a lipophilic core and a hydrophilic outer end that forms an inactive tight inclusion complex with free molecules of rocuronium and vecuronium. In preclinical study, adamgammadex produced a concentration-dependent reversion effect of neuromuscular blockade induced by rocuronium in beagle dogs. Furthermore, adamgammadex had a less potential side effects than sugammadex and other clinical used neuromuscular block antagonists. In this study, the objective was to assess the safety, tolerability, and pharmacokinetics of single intravenous injection of adamgammadex in healthy volunteers. Approved by the China Food and Drug Administration, 52 healthy volunteers (half male and half female) were enrolled in this single-center, randomized, double-blind placebo-controlled study. No serious adverse effects were happened in this study. The overall frequency of adverse effects in adamgammadex was similar for that in placebo, and there was no specific adverse effect in adamgammadex. All of the volunteers bearing the adverse effects were recovered to normal without any treatment or intervention. In pharmacokinetic study, the value of half-time, Tmax, and clearance were not changed significantly, and the Cmax and AUC0–∞ increased with a similar ratio of the escalating doses. For dose proportionality analysis of adamgammadex, the estimate of slope was close to 1, and it was not significantly different from 1 after doses (AUC0-∞, 0.9965 [90%CI, 0.9468, 1.046]; Cmax, 0.9462 [90%CI, 0.8800, 1.012]). Therefore, adamgammadex exposure in plasma increased in a dose- proportional manner. The urinary route is a significant excretory pathway for adamgammadex, and it is mostly completed at 8 h. All the results in this study showed that adamgammadex may be a novel safe neuromuscular blockade reversal agent .

Different factors determined the toxicokinetics of organic chemicals and nanomaterials exposure to zebrafish (Danio Rerio)

Little is known about how the chemical properties (molecular structure, such as the hydrophobic and hydrophilic end group for organic chemical, and particle size for nanomaterials (NMs)) quantitatively affect the toxicokinetics (TK) in organisms especially in short-term, single-species studies. A novel method based on a first-order one compartment TK model which described the monophasic uptake pattern and two-compartment TK model which adequately described the biphasic metabolism pattern was used to determine the bioconcentration and TK rate constants of organic compounds (n = 17) and nanomaterials (NMs, n = 7) in zebrafish. For both one and two compartment model, the uptake (kin) and elimination (kout) rate constants were fitted using a one- and two-compartment first-order kinetic model, and bioconcentration factors (BCF) and 95% depuration times (t95) for all tested chemicals were calculated, respectively. The results showed that there was significant difference in TK parameters kin, kout, and BCF between organic chemicals and nano metal oxides. For organic compounds, significant correlations were found between the kin and BCF and the octanol-water partition coefficient (Kow) and molecular mass. For nano metal oxides, there was a significant negative correlation between the kin or BCF and particle size, but a positive correlation between kin and Zeta potential of nanoparticles and also a significant positive correlation between kout and particle size or specific surface area. Those findings indicated that NMs particle size does matter in biological influx and efflux processes. Our results suggest that the TK process for organic compound and NMs are correlated by different chemical properties and highlight that the Kow, the absorption kin, metabolism k12 and k21, elimination rate kout, and all the parameters that enable the prediction and partitioning of chemicals need to be precisely determined in order to allow an effective TK modeling. It would therefore appear that the TK process of untested chemicals by a fish may be extrapolated from known chemical properties.

Foamy Urine: Is This a Sign of Kidney Disease?

Historically, persistent foamy urine noticed upon voiding is considered a warning sign of kidney disease. Foamy urine is characterized by the appearance and persistence of multiple layers of small to medium bubbles in urine voided into a container, such as a toilet bowl (see [Figure 1][1]). The

Management of local anesthetic toxicity and importance of lipid infusion

Local anesthetics (LA) are one of the groups that block the transmission of sensory, motor and autonomic nerve impulses commonly used in clinical anesthesia. All local anesthetic molecules in clinical use consist of three parts: a lipophilic (aromatic) end, a hydrophilic (amine) end, and a chain that provides the connection between the ends. Physicochemical properties determine the clinical efficacy of local anaesthetics The part that determines the lipid solubility of local anesthetics is the aromatic ring. A higher dose of local anesthetics is required for cardiovascular system (CVS) toxicity. Hypertension, tachycardia and ventricular arrhythmia are the first of the diseases of CVS. Hypotension, arrhythmia, bradycardia and cardiac arrest develop as local anesthetics increase in blood. The symptoms of central nervous system (CNS) toxicity associated with LA are related to the plasma levels of drugs. Initially, there are drowsiness, dizziness, sedation, disorientation, tinnitus, nystagmus, metallic taste, nausea and vomiting. Then, restlessness, irritability, tremors and muscle twitches occur. After this, the tonic-clonic seizure and loss of consciousness develops, finally, apnea, cardiovascular collapse and coma. In the treatment of local anesthetic toxicity, it is recommended to provide airway, avoid the propofol if seizure occurs and treat with benzodiazepine. If cardiac arrest develops, it is recommended to switch to advanced life support, to reduce the given dose of adrenaline, to administer lipid emulsion (20%) and to respond to treatment if cardiopulmonary bypass is not provided.

Toxicokinetics of Perfluorinated Alkyl Acids Influences Their Toxic Potency in the Zebrafish Embryo ( Danio rerio).

Perfluorinated alkyl acids (PFAA) are highly persistent and bioaccumulative and have been associated with several adverse health effects. The chemical structure mainly differs in two ways: the length of the hydrophobic alkyl chain and the type of hydrophilic end group. Little is known how the chemical structure affects the toxicokinetics (TK) in different organisms. We studied the TK of four PFAA (PFOS, PFHxS, PFOA, and PFBA) with different chain lengths (4-8 carbons) and functional groups (sulfonic and carboxylic acid) in zebrafish ( Danio rerio) embryo. The time courses of the external (ambient water) and internal concentrations were determined at three exposure concentrations from 2 up to 120 h postfertilization (hpf). Three of the four PFAA showed a biphasic uptake pattern with slow uptake before hatching (around 48 hpf) and faster uptake thereafter. A two-compartment TK model adequately described the biphasic uptake pattern, suggesting that the chorion functions as an uptake barrier until 48 hpf. The bioconcentration factors (BCF) determined at 120 hpf varied widely between PFAA with averages of approximately 4000 (PFOS), 200 (PFHxS), 50 (PFOA), and 0.8 (PFBA) L kg dry weight-1, suggesting that both the alkyl chain length and the functional group influence the TK. The differences in toxic potency were reduced by 3 orders of magnitude when comparing internal effect concentrations instead of effective external concentrations.

Preparation of Soaps by using Different Oil and Analyze their Properties

The molecule of soap consists of two dissimilar ends, a hydrophilic end (polar head) which binds with water and another end which is hydrophobic end (non-polar hydrocarbon tail) that binds with oil. The soap is made by the saponification process, which reacts with the oil that contains triglycerides and lye (NaOH). Oils with different properties make them distinct from each other as the composition of fatty acids is incompatible. In the present study in the process of preparation of soaps, dissimilar oils of 5 types i.e., coconut oil, palm oil, castor oil, olive oil and gee oil were utilized. In order to prepare various soap samples, the oils were blended in different ratios which are then checked to analyze the soap’s quality. In this study amount of volatile matter and moisture content, total fatty mater content, alkali content and pH were determined. The obtained results were compared with some of commercially available soaps such as baby soap (BS-1), elder soap 1 (ES-1), elder soap 2 (ES-2), elder soap 3 (ES-3) and elder soap 4 (ES-4). With the observed studies, the soap made using olive oil was found to have better properties that the others. It has the good alkaline content, TFM value and pH values..

Callyspongidic Acids: Amphiphilic Diacids from the Tropical Eastern Pacific Sponge Callyspongia cf. californica.

The first chemical study of the marine sponge Callyspongia cf. californica widely distributed along the coasts of the Tropical Eastern Pacific led to the identification of a new family of amphiphilic derivatives called callyspongidic acids. The four isolated metabolites 1-4 feature a hydrophilic diacid end opposed to both an aromatic moiety and a long alkyl chain. They were evaluated against a panel of pathogenic microbes and seven tumoral cell lines, displaying moderate inhibitory properties against the A2058 melanoma cell line with an IC50 of 3.2 μM for callyspongidic acid C13:0 (2).

Preparation of gene drug delivery systems of cationic peptide lipid with 0G-PAMAM as hydrophilic end and its biological properties evaluation.

As an efficient gene delivery, non-viral vectors should have high transfection efficiency, excellent endosomal escape, low cytotoxicity, and the ability to rapidly release the gene into the cytoplasm.Cationic liposome have been widely used as efficient gene carriers, but the cytotoxicity, rapid degradation and low cellular uptake are major drawback impeding its further appolication. Herein, with double lauric acid as hydrophobic chains, tartaric acid as skeleton, 0 generation PAMAM modified with lysine as hydrophilic head, a new type cationic peptide lipid was synthetised. The alkyl chain promote lipid across cell membranes and with membrane fusion, 0 generation PAMAM modified with lysine hydrophilic end amino can contain a large number of protons which can change into ammonium and combine with the DNA negatively charge phosphate groups. It is expected that this carrier has low toxicity, high transfection efficiency and targeting property. By adjusting the cationic liposome/gene weight ratio, the transfection system was optimized to improved gene transfection efficiency, reduce cytotoxicity, and increase property and stability, etc.

Hierarchical Assembly of l-Phenylalanine-Terminated Bolaamphiphile with Porphyrin Show Tunable Nanostructures and Photocatalytic Properties.

Demands related to clean energy and environmental protection promote the development of novel supramolecular assemblies for photocatalysis. Because of the distinctive aggregation behaviors, bolaamphiphiles with two hydrophilic end groups could be theoretically the right candidates for the fabrication of high-performance photocatalysis. However, photocatalytic applications based on bolaamphiphilic assemblies were still rarely investigated. Especially, the relationship between diverse assembled nanostructures and the properties for different applications is urgently needed to be studied. Herein, we demonstrate that using the hierarchical assembly of bolaamphiphiles could correctly induce the porphyrin supramolecular architectures with much better photocatalytic performances than the aggregations containing 450 times of the porphyrin molecules, even though both molecular structures as well as the J-aggregations of porphyrin building blocks are same in two different systems. Thus, the co-assembly of l-phenylalanine terminated bolaamphiphile (Bola-F) and the porphyrin containing four hydroxyl groups (tetrakis-5,10,15,20-(4-hydroxyphenyl)porphyrin) can form microtube in methanol and forms fibers/spheres in methanol/water mixture. For catalyzing the photodegradation of rhodamine B, the small amount of J-aggregated porphyrin within Bola-F microtubes show much better photocatalytic performance comparing with that of huge porphyrin J-aggregations in fibers/spheres. The supramolecular assemblies as well as the photocatalysis were thoroughly characterized by different spectroscopies and electron microscopy. It is demonstrated that the co-assembly with bolaamphiphiles could inhibit the energy transfer of porphyrin aggregation and subsequently benefit the electron transfer and corresponding photocatalysis under photo-irradiation. This work is not only useful for further understanding the hierarchically supramolecular assembly but also provides a new strategy for making novel functional supramolecular architectures based on the assembly of bolaamphiphiles and porphyrins.

Diffusion of Gold Nanorods Functionalized with Thermoresponsive Polymer Brushes

Understanding the diffusion of gold nanorods (AuNRs) and their composites in dispersion is important at fundamental level and in fields as diverse as material science, nanobiotechnology to drug delivery. The translational and rotational diffusion of AuNRs decorated with thermoresponsive poly(N-isopropylacrylamide) brushes having hydrophilic and hydrophobic end groups was investigated in the dilute regime by dynamic light scattering. The same series of functionalized AuNRs were studied in the isotropic concentrated dispersions by high-resolution NMR diffusometry. The dependence of translational and rotational diffusivity upon molecular weight and polymer end group were measured as a function of temperature in the region of the brush phase transition. The effective hydrodynamic radius of AuNR composites proved to be the most sensitive quantity to the temperature-induced phase transition of brushes, allowing the evaluation of the brush thickness in the swollen and collapsed states.

Influence of molecular structure of extractor molecules on liquid-liquid extraction of oxide particles and properties of composites

Interest in particle extraction through liquid-liquid interface (PELLI) technology is motivated by the need to transfer particles directly from the synthesis medium to the device processing medium. This method avoids the difficulty encountered by conventional re-dispersion methods where particles agglomerate during the drying stage. We develop PELLI strategies to transfer MnO2, ZnO and CeO2 particles that are synthesized in aqueous media into 1-butanol using extractors containing phosphonate and carboxylic groups. We demonstrate that, in addition to head-tail (HT) surfactants, molecules containing two hydrophilic end groups (HTH) can also be employed as extractors, a finding that opens new PELLI applications. We demonstrate this new approach using multifunctional HTH molecules as both PELLI extractors, and charged dispersing agents for the electrophoretic deposition (EPD) of particles that are transferred to an EPD processing medium. Using the HTH extractors for PELLI, we fabricate MnO2-based bulk electrodes for electrochemical supercapacitors (ES) that exhibit superior electrochemical performance. These high active mass loading ES electrodes have a capacitance of 5.7 F cm−2 (157 F g−1) and 2.5 F cm−2 (67 F g−1) at 2 and 100 mV s−1 scan rates, respectively, with low impedance. In another strategy, the use of HTH extractor for particle transfer to screen printing processing medium facilitates the fabrication of efficient thin film SC electrodes. Measurements provide insight into the influence of anchoring groups and extractor molecule structure on the extraction efficiency and electrochemical performance.

Redefining Molecular Amphipathicity in Reversing the "Coffee-Ring Effect": Implications for Single Base Mutation Detection.

The "coffee ring effect" is a natural phenomenon wherein sessile drops leave ring-shaped structures on the solid surfaces upon drying. It drives a nonuniform deposition of suspended compounds on the substrates, which adversely affects many processes, including surface-assisted biosensing and molecular self-assembly. In this study, we describe how the coffee ring effect can be eliminated by controlling the amphipathicity of the suspended compounds, for example, DNA modified with hydrophobic dye. Specifically, nuclease digestion of the hydrophilic DNA end converts the dye-labeled molecule into an amphipathic molecule (one with comparably weighted hydrophobic and hydrophilic ends) and reverses the coffee ring effect and results in a uniform disk-shaped feature deposition of the dye. The amphipathic product decreases the surface tension of the sessile drops and induces the Marangoni flow, which drives the uniform distribution of the amphipathic dye-labeled product in the drops. As a proof of concept, this strategy was used in a novel enzymatic amplification method for biosensing to eliminate the coffee ring effect on a nitrocellulose membrane and increase assay reliability and sensitivity. Importantly, the reported strategy for eliminating the coffee ring effect can be extended to other sessile drop systems for potentially improving assay reliability and sensitivity.

Perovskites: Between the Grains

Defect reduction and device stabilization will continue to be two important thrusts toward efficient long-lasting polycrystalline perovskite solar cells. Recently in Chem, Zong et al. show that a complementary hydrophobic/hydrophilic triblock copolymer continuously incorporates into methylammonium lead tri-iodide grain boundaries. This improves solar cell stability and performance, resulting in a stabilized 19.4% power conversion efficiency, 92% of which is retained after 480 hr of continuous 1-sun illumination.

Polymers Diffusivity Encoded by Stimuli‐Induced Phase Transition: Theory and Application to Poly(N‐Isopropylacrylamide) with Hydrophilic and Hydrophobic End Groups

AbstractThe self‐diffusion of various nano‐objects investigated by high‐resolution nuclear magnetic resonance diffusometry proves to be an efficient method for the characterization of dynamics, aggregation kinetic, and matrix morphology. This study investigates how the two‐state model and Boltzmann function approach can be used for the evaluation of the thermodynamic parameters of temperature‐induced phase transition encoded in polymer diffusivity. The characteristics of the phase transition given by the transition temperature, change of entropy, and width of transition are obtained for poly(N‐isopropylacrylamide) (PNIPAm) linear polymers with hydrophilic and hydrophobic end‐group functionalization. The effect of end groups upon the polymer diffusivity is investigated as a function of molecular weight (M n), from which fractal dimensions and hydrodynamic drag coefficients are obtained. The PNIPAm diffusivity is affected strongly by the end groups, and it is reflected in the hydrodynamic radius dependence upon molecular weight that obeys different power‐law relations. In this study, the synthesis of α‐ω‐heterotelechelic PNIPAm of different molecular weights with a thiol end group and a hydrophilic NIPAm‐like as well as a hydrophobic benzyl end group are described by reversible addition–fragmentation chain‐transfer polymerization.

In situ generation of layered single- or double-hydroxide inorganic platelets (LSH and LDH) assisted by bola amphiphiles.

A novel preparation route for layered hydroxide based hybrid phases has been investigated combining the polyol route with the in situ generation of inorganic platelets, in the presence of an amphiphilic polymer as well as bola-amphiphiles. The polyol route consists of hydrolysis in an alcoholic medium containing acetate metal cations as precursor(s), to yield an LDH Zn2Al cation composition or LSH-Zn (layered single hydroxide). A bola amphiphile is described as hydrophobic polymer segment-telechelic-chains terminated by two anionic hydrophilic end groups, using volatile ammonium cations as counter ions. The impact of both process conditions as well as the chosen system with regard to the metal hydroxide framework on the morphology of the obtained hybrid phases is scrutinized by X-ray diffraction (XRD), small angle X-ray scattering (SAXS) and transmission electron microscopy (TEM), and compared to that of the corresponding physical mixture. For the ex situ approach, the diffusion of large cumbersome polymers or amphiphilic bolas between the inorganic platelets was found to be efficient, mostly driven by an anion exchange reaction between interleaved acetate anions and carboxylate functions of the molecular backbones, and keeping intact the inner sheet integrity through a topotactic process. In particular with LSH-Zn, a multi-stratified assembly has been observed combining an acetate pristine structure and a partly bola diffused structure, leading to a biphasic structure, aggregated and intercalated. To the best of our knowledge, observation of LSH-Zn single platelets has never been reported, making the combined process polyol/in situ an interesting new route to reach exfoliation. Indeed, it leads to the generation of either LSH or LDH platelets of lateral size ranging from 10 up to 200 nm. However, the platelets were found to be porous; it is considered as a drawback for barrier properties. It is our belief that such porosity may open new insights in "tectonic" architecture by intertwining 2D and 1D-type fillers. Rather counterintuitively, the ex situ approach based on a topotactic exchange reaction matches the in situ templating reaction in many cases as a function of the dispersion state regardless of the polymer or bolas as well as the platelet cation composition.

Effect of chain architecture on the swelling and thermal response of star-shaped thermo-responsive (poly(methoxy diethylene glycol acrylate)-block-polystyrene)3 block copolymer films.

The effect of chain architecture on the swelling and thermal response of thin films obtained from an amphiphilic three-arm star-shaped thermo-responsive block copolymer poly(methoxy diethylene glycol acrylate)-block-polystyrene ((PMDEGA-b-PS)3) is investigated by in situ neutron reflectivity (NR) measurements. The PMDEGA and PS blocks are micro-phase separated with randomly distributed PS nanodomains. The (PMDEGA-b-PS)3 films show a transition temperature (TT) at 33 °C in white light interferometry. The swelling capability of the (PMDEGA-b-PS)3 films in a D2O vapor atmosphere is better than that of films from linear PS-b-PMDEGA-b-PS triblock copolymers, which can be attributed to the hydrophilic end groups and limited size of the PS blocks in (PMDEGA-b-PS)3. However, the swelling kinetics of the as-prepared (PMDEGA-b-PS)3 films and the response of the swollen film to a temperature change above the TT are significantly slower than that in the PS-b-PMDEGA-b-PS films, which may be related to the conformation restriction by the star-shape. Unlike in the PS-b-PMDEGA-b-PS films, the amount of residual D2O in the collapsed (PMDEGA-b-PS)3 films depends on the final temperature. It decreases from (9.7 ± 0.3)% to (7.0 ± 0.3)% or (6.0 ± 0.3)% when the final temperatures are set to 35 °C, 45 °C and 50 °C, respectively. This temperature-dependent reduction of embedded D2O originates from the hindrance of chain conformation from the star-shaped chain architecture.

Mechanism of the formation of microphase separated water clusters in a water-mediated physical network of perfluoropolyether tetraol.

Perfluoropolyether tetraol (PFPE tetraol) possesses a hydrophobic perfluoropolyether chain in the backbone and two hydroxyl groups at each chain terminal, which facilitates the formation of hydrogen bonds with water molecules resulting in the formation an extended physical network. About 3 wt% water was required for the formation of the microphase separated physical network of PFPE tetraol. The mechanism responsible for the microphase separation of water clusters in the physical network was studied using a combination of techniques such as NMR spectroscopy, molecular dynamics (MD) simulations and DSC. MD simulation studies provided evidence for the formation of clusters in the PFPE tetraol physical network and the size of these clusters increased gradually with an increase in the extent of hydration. Both MD simulations and NMR spectroscopy studies revealed that these clusters position themselves away from the hydrophobic backbone or vice versa. The presence of intra- and inter-chain aggregation possibility among hydrophilic groups was evident. DSC results demonstrated the presence of tightly and loosely bound water molecules to the terminal hydroxyl groups of PFPE tetraol through hydrogen bonding. The data from all the three techniques established the formation of a physical network driven by hydrogen bonding between the hydrophilic end groups of PFPE tetraol and water molecules. The flexible nature of the PFPE tetraol backbone and its low solubility parameter favour clustering of water molecules at the terminal groups and result in the formation of a gel.

Retarding oxidation of copper nanoparticles without electrical isolation and the size dependence of work function

Copper nanoparticles (CuNPs) are attractive as a low-cost alternative to their gold and silver analogues for numerous applications, although their potential has hardly been explored due to their higher susceptibility to oxidation in air. Here we show the unexpected findings of an investigation into the correlation between the air-stability of CuNPs and the structure of the thiolate capping ligand; of the eight different ligands screened, those with the shortest alkyl chain, –(CH2)2–, and a hydrophilic carboxylic acid end group are found to be the most effective at retarding oxidation in air. We also show that CuNPs are not etched by thiol solutions as previously reported, and address the important fundamental question of how the work function of small supported metal particles scales with particle size. Together these findings set the stage for greater utility of CuNPs for emerging electronic applications.

An Environmental Friendly Fluorinated Oligoamide for Producing Nonwetting Coatings with High Performance on Porous Surfaces.

The changes in the surface wettability of many materials are receiving increased attention in recent years. It is not too hard to fabricate resistant hydrophobic surfaces through products bearing both hydrophobic and reactive hydrophilic end groups. More challenging is obtaining resistant nonwetting surfaces through noncovalent reversible bonds. In this work, a fluorinated oligo(ethylenesuccinamide), soluble in solvent benign for operators and environment, has been synthesized. It contains two opposite functional groups (perfluoropolyether segments and amidic groups) (SC2-PFPE) that provide water repellency while hydrophilicity is retained. Its performance has been tested on porous calcarenite and investigated by magnetic resonance imaging, water capillary absorption, and vapor diffusivity tests. The results demonstrate that SC2-PFPE modifies the wettability of porous substrates in a drastic and durable way and reduces the vapor condensation inside the pore space due to the perfluoropolyether segments that act at the air/surface interface.

Controlled Hydrolytic Degradation of Polyglycolide–Caprolactone-Based Bioabsorbable Copolymer

Polyglycolide–caprolactone (PGCL)-based copolymer was synthesized from glycolide and caprolactone by ring opening polymerization in the presence of stannous octoate catalyst and diethylene glycol initiator. The effects of prepolymerization time, monomer ratio, monomer-to-catalyst and monomer-to-initiator ratios on per cent weight conversion were optimized. The end-capped copolymer was synthesized to make absorbable sutures having controlled bioabsorbability at different pH levels. It was observed that endcapped absorbable copolymer was more stable at pH 10.0 compared to uncapped absorbable material. End-capped copolymer also retained higher tensile strength compared to uncapped copolymer after 21 days. This phenomenon of controlled hydrolytic degradation of PGCL-based bioabsorbable polymer having terminal group end-capping can be attributed to less availability of hydrophilic end groups facilitating hydrolytic degradation of polymers.