Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: UMLS:C0344329 (collapse)
 28,634 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

In recent years, hydrogels have attracted attention as active components in microfluidic devices. Here, we present a demonstration of remote controlled flow regulation in a microfluidic device using a hydrogel nanocomposite valve. To create the nanocomposite hydrogel, magnetic nanoparticles were dispersed in temperature-responsive N-isopropylacrylamide (NIPAAm) hydrogels. The swelling and collapse of the resultant nanocomposite can be remotely controlled by application of an alternating magnetic field (AMF). A ceramic microfluidic device with Y-junction channels was fabricated using low temperature co-fired ceramic (LTCC) technology. The nanocomposite was incorporated as a valve in one of the channels of the device. An AMF of frequency 293 kHz was then applied to the device and ON-OFF control on flow was achieved. A pressure transducer was placed at the inlet of the channel and pressure measurements were done for multiple AMF ON-OFF cycles to evaluate the reproducibility of the valve. Furthermore, the effect of the hydrogel geometry on the response time was characterized by hydrogels with different dimensions. Magnetic hydrogel nanocomposite films of different thicknesses (0.5, 1, 1.5 mm) were subjected to AMF and the kinetics of collapse and recovery were studied.
 ...
PMID:Magnetic hydrogel nanocomposites as remote controlled microfluidic valves. 1949 62

An impedance analysis of quartz crystal microbalance data reveals the mass of water expelled by poly(N-isopropylacrylamide) brushes upon the thermo-induced collapse.
 ...
PMID:Real-time measurement of the mass of water expelled by poly(N-isopropylacrylamide) brushes upon thermo-induced collapse. 1950 93

The direct binding mechanism for urea-based denaturation of proteins was tested with a thermoresponsive polymer, poly(N-isopropylacrylamide) (PNIPAM). Thermodynamic measurements of the polymer's hydrophobic collapse were complemented by Fourier transform infrared (FTIR) spectroscopy, Stokes radius measurements, and methylated urea experiments. It was found that the lower critical solution temperature (LCST) of PNIPAM decreased as urea was added to the solution. Therefore, urea actually facilitated the hydrophobic collapse of the macromolecule. Moreover, these thermodynamic measurements were strongly correlated with amide I band data which indicated that the decrease in the LCST was coupled to the direct hydrogen bonding of urea to the amide moieties of the polymer. In addition, the hydrogen bonding was found to be highly cooperative, which is consistent with a cross-linking (bivalent binding) mechanism. Cross-linking was confirmed by Stokes radius measurements below the polymer's LCST using gel filtration chromatography. Finally, phase transition measurements with methylurea, dimethylurea, and tetramethylurea indicated that these substituted compounds caused the LCST of PNIPAM to rise with increasing methyl group content. No evidence could be found for the direct binding of any of these methylated ureas to the polymer amide moieties by FTIR. These results are inconsistent with a direct hydrogen-bonding mechanism for the urea-induced denaturation of proteins.
 ...
PMID:Investigating the hydrogen-bonding model of urea denaturation. 1952 28

Chemically cross-linked poly(N-isopropylacrylamide) (PNIPAM) microgels and PNIPAM with different amounts of acrylic acid groups (PNIPAM-co-PAA) were synthesized and the temperature-induced aggregation behaviors of aqueous suspensions of these microgels were investigated mainly with the aid of dynamic light scattering (DLS) and turbidimetry. The DLS results show that the particles at all conditions shrink at temperatures up to approximately the lower critical solution temperature (LCST), but the relative contraction effect is larger for the microgels without acid groups or for microgels with added anionic surfactant (SDS). A significant depression of the cloud point is found in suspensions of PNIPAM with very low concentrations of SDS. The compression of the microgels cannot be traced from the turbidity results, but rather the values of the turbidity increase in this temperature interval. This phenomenon is discussed in the framework of a theoretical model. At temperatures above LCST, the size of the microgels without attached charged groups in a very dilute suspension is unaffected by temperature, while the charged particles (pH 7 and 11) continue to collapse with increasing temperature over the entire domain. In this temperature range, low-charged particles of higher concentration and particles containing acrylic acid groups at low pH (pH 2) aggregate, and macroscopic phase separation is approached at higher temperatures. This study demonstrates how the stabilization of microgels can be affected by factors such as polymer concentration, addition of ionic surfactant to particles without charged acid groups, amount of charged groups in the polymer, and pH.
 ...
PMID:Effects of temperature and pH on the contraction and aggregation of microgels in aqueous suspensions. 1961 21

We report on the fabrication of Cu2+-sensing thermoresponsive poly(N-isopropylacrylamide) (PNIPAM) microgels labeled with metal-chelating acceptor and fluorescent reporter moieties. Cu2+ detection sensitivity can be considerably enhanced via thermo-induced collapse of the sensing matrix, which can easily optimize the relative spatial distribution of Cu2+-binding sites and fluorescence readout functionalities. A novel picolinamine-containing monomer with Cu2+-binding capability, N-(2-(2-oxo-2-(pyridine 2-yl-methylamino)ethylamino)ethyl)acrylamide (PyAM, 3), was synthesized at first. Nearly monodisperse Cu2+-sensing microgels were prepared via emulsion polymerization of N-isopropylacrylamide (NIPAM) in the presence of a nonionic surfactant, N,N'-Methylene-bis(acrylamide) (BIS), PyAM (3), and fluorescent dansylaminoethyl- acrylamide (DAEAM, 5) monomers at around neutral pH and 70 degrees C. At 20 degrees C, as-synthesized microgels in their swollen state can selectively bind Cu2+ over other metal ions (Hg2+, Mg2+, Zn2+, Pb2+, Ag+, and Al3+), leading to prominent quenching of fluorescence emission intensity. Above the volume phase transition temperature, P(NIPAM-co-PyAM-co-DAEAM) microgels exhibit increased fluorescence intensity. It was observed that Cu2+ detection sensitivity can be dramatically enhanced via thermo-induced microgel collapse at elevated temperatures. At a microgel concentration of 3.0x10(-6) g/mL, the detection limit drastically improved from approximately 46 nM at 20 degrees C to approximately 8 nM at 45 degrees C. The underlying mechanism for this novel type of sensor with thermotunable detection sensitivity was tentatively proposed.
 ...
PMID:Metal-chelating and dansyl-labeled poly(N-isopropylacrylamide) microgels as fluorescent Cu2+ sensors with thermo-enhanced detection sensitivity. 1970 45

We report on reversible temperature-triggered swelling transitions in hydrogen-bonded multilayer films of a polycarboxylic acid and stimuli-responsive block copolymer micelles (BCMs). A neutral hydrogen-bonding temperature-responsive diblock copolymer, poly(N-vinylpyrrolidone)-b-poly(N-isopropylacrylamide) (PVPON-b-PNIPAM), was synthesized by macromolecular design via the interchange of xanthates (MADIX). The block copolymer exhibited reversible micellization, forming PNIPAM-core micelles with PVPON coronae in 0.01 M buffer solutions at temperatures higher than 34 degrees C, or in solutions with high salt concentrations (C(NaCl) > 0.4 M) at 20 degrees C. The PVPON-b-PNIPAM BCMs were then assembled with poly(methacrylic acid) (PMAA) at acidic pH and higher temperature using the layer-by-layer (LbL) technique. Within the hydrogen-bonded multilayer, BCMs were stabilized through hydrogen bonding between PVPON and PMAA units and, unlike in solution, did not dissociate into unimers in low-salt solution at T < 34 degrees C. Instead, PVPON-b-PNIPAM BCMs reversibly swelled within film in response to temperature- or salt-concentration variations, reflecting collapse and dissolution of the BCM PNIPAM cores. The capacity of BCM/PMAA films to retain hydrophobic molecules was also dramatically dependent on temperature and/or ionic strength. The characteristic release time of pyrene from a [BCM/PMAA](10) film decreased from 80 to 10 min upon a decrease in temperature from 37 to 20 degrees C. In addition, at 20 degrees C, ionic strength was also capable of controlling the collapse of PNIPAM micellar cores and the subsequent film swelling and pyrene release rate. Incorporation of stimuli-responsive BCM micelles within LbL films opens new opportunities in designing nanoscale films capable of controlling molecular swelling, transport, and diffusion in response to environmental stimuli.
 ...
PMID:Temperature-induced swelling and small molecule release with hydrogen-bonded multilayers of block copolymer micelles. 1979 44

We elucidate the sequence of events occurring during the collapse transition of thermoresponsive copolymer brushes based on poly(di(ethyleneglycol) methyl ether methacrylate) chains (PMEO2MA) grown by atom-transfer radical polymerization (ATRP). The collapse of the bulk of the brush is followed by quartz crystal microbalance measurements with dissipation monitoring (QCM-D), and the collapse of its outer surface is assessed by measuring equilibrium water contact angles in the captive bubble configuration. The bulk of the brush collapses over a broad temperature interval (approximately 25 degrees C), and the end of this process is signaled by a sharp first-order transition of the surface of the brush. These observations support theoretical predictions regarding the occurrence of a vertical phase separation during collapse, with surface properties of thermoresponsive brushes exhibiting a sharp variation at a temperature of T(br)(surf). In contrast, the bulk properties of the brush vary smoothly, with a bulk transition T(br)(bulk) occurring on average approximately 8 degrees C below T(br)(surf) and approximately 5 degrees C below the lower critical solution temperature (LCST) of free chains in solution. These observations should also be valid for planar brushes of other neutral, water-soluble thermoresponsive polymers such as poly(N-isopropylacrylamide) (PNIPAM). We also propose a way to analyze more quantitatively the temperature dependence of the QCM-D response of thermoresponsive brushes and deliver a simple thermodynamic interpretation of equilibrium contact angles, which can be of use for other complex temperature-responsive solvophilic systems.
 ...
PMID:Surface and bulk collapse transitions of thermoresponsive polymer brushes. 1984 35

The phase behavior of poly(N-isopropylacrylamide) nanoparticles dispersed in aqueous medium is investigated as a function of temperature using static and dynamic light scattering techniques. The diameter, d of the particles, as determined by dynamic light scattering measurements on dilute dispersion showed a decrease in size from 273 nm at 25 degrees C to 114 nm at 40 degrees C as function of temperature with a sudden collapse of particle volume (volume phase transition) at 32.4 degrees C. Further this nanoparticle dispersion is found to turn turbid beyond volume phase transition. Static light scattering measurements on samples with intermediate concentration and high concentration showed liquid-like order and crystalline order respectively. The intensity of the Bragg peak of the crystallized sample when monitored as a function of temperature showed crystal to liquid transition at 26.2 degrees C and a fluid to fluid transition at 31 degrees C. The occurrence of melting at a volume fraction of 0.85 and the absence of change in number density across the fluid-to-fluid transition suggest that interparticle interaction is repulsive soft-sphere below the volume phase transition. The reported results on the phase behavior of poly(N-isopropylacrylamide) nanogel suspensions are discussed in the light of the present results.
 ...
PMID:Phase behavior of poly(N-isopropylacrylamide) nanogel dispersions: temperature dependent particle size and interactions. 1992 22

We probe, using the surface forces apparatus, the thermal response of poly(N-isopropylacrylamide) (PNIPAM) brushes of various grafting densities, grown from plasma-activated mica by means of surface-initiated polymerization. We thus show that dense thermoresponsive brushes collapse gradually as temperature is increased and that grafting density greatly affects their ability to swell: the swelling ratio of the brushes, which characterizes the thickness variation between the swollen and the collapsed state, is found to decrease from approximately 7 to approximately 3 as the number of grafted chains per unit area increases. Such a result, obtained with an unprecedented resolution in grafting density, provides qualitative support to calculations by Mendez et al. [Macromolecules 2005, 38, 174]. We further show that, in contrast to swelling, adhesion between two PNIPAM brushes appears to be rather insensitive to their molecular structure.
 ...
PMID:Density effects on collapse, compression, and adhesion of thermoresponsive polymer brushes. 1996 Dec 8

We investigate in a hybrid material the interactions existing between magnetic nanoparticles of gamma-Fe(2)O(3) and the polymer matrix constituted by core-shell poly(N-isopropylacrylamide-sodium acrylate) microgels. These interactions provoke the shifting of the microgel volume phase transition to higher temperatures when the amount of gamma-Fe(2)O(3) increases. The study was performed using different techniques such as incoherent quasi-elastic neutron scattering (IQNS), infrared spectroscopy (FTIR-ATR), and dynamic light scattering (DLS). Below the low critical solution temperature (LCST) of the polymer, the IQNS data confirm that the presence of inorganic nanoparticles affects the PNIPAM chain motions. Thus, in the swollen state both the mean-square displacement of the polymer segments and the diffusive motion of the polymer chains decrease as the iron oxide content increases. The FTIR-ATR study indicates that the reduction of vibrational and diffusional motions of the polymer chains is due to the formation of hydrogen bonds between the amide groups of the polymer matrix and the OH groups of the magnetic nanoparticles. The creation of this hybrid complex would explain the reduction of the swelling capacity with increasing the iron content in the microgels. Furthermore, this interaction could also explain the shift of the polymer LCST to higher temperatures as due to the extra energy required by the system to break the hydrogen bonds prior to the PNIPAM collapse.
 ...
PMID:Investigation of the relationship between hydrogen bonds and macroscopic properties in hybrid core-shell gamma-Fe2O3-P(NIPAM-AAS) microgels. 2014 64


<< Previous 1 2 3 4 5 6 7 8 9 10 Next >>