Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Stability analysis”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 217 records · Page 12Linked to original sources

Liposome formulation of poorly water soluble drugs: optimisation of drug loading and ESEM analysis of stability.

Liposomes due to their biphasic characteristic and diversity in design, composition and construction, offer a dynamic and adaptable technology for enhancing drug solubility. Starting with equimolar egg-phosphatidylcholine (PC)/cholesterol liposomes, the influence of the liposomal composition and surface charge on the incorporation and retention of a model poorly water soluble drug, ibuprofen was investigated. Both the incorporation and the release of ibuprofen were influenced by the lipid composition of the multi-lamellar vesicles (MLV) with inclusion of the long alkyl chain lipid (dilignoceroyl phosphatidylcholine (C24PC)) resulting in enhanced ibuprofen incorporation efficiency and retention. The cholesterol content of the liposome bilayer was also shown to influence ibuprofen incorporation with maximum ibuprofen incorporation efficiency achieved when 4 micromol of cholesterol was present in the MLV formulation. Addition of anionic lipid dicetylphosphate (DCP) reduced ibuprofen drug loading presumably due to electrostatic repulsive forces between the carboxyl group of ibuprofen and the anionic head-group of DCP. In contrast, the addition of 2 micromol of the cationic lipid stearylamine (SA) to the liposome formulation (PC:Chol - 16 micromol:4 micromol) increased ibuprofen incorporation efficiency by approximately 8%. However further increases of the SA content to 4 micromol and above reduced incorporation by almost 50% compared to liposome formulations excluding the cationic lipid. Environmental scanning electron microscopy (ESEM) was used to dynamically follow the changes in liposome morphology during dehydration to provide an alternative assay of liposome stability. ESEM analysis clearly demonstrated that ibuprofen incorporation improved the stability of PC:Chol liposomes as evidenced by an increased resistance to coalescence during dehydration. These finding suggest a positive interaction between amphiphilic ibuprofen molecules and the bilayer structure of the liposome.

Chemistry, Pharmaceutical↗

Spectral properties and synchronization in coupled map lattices.

Spectral properties of coupled map lattices are described. Conditions for the stability of spatially homogeneous chaotic solutions are derived using linear stability analysis. Global stability analysis results are also presented. The analytical results are supplemented with numerical examples. The quadratic map is used for the site dynamics with different coupling schemes such as global coupling, nearest neighbor coupling, intermediate range coupling, random coupling, small world coupling and scale free coupling.

Journal Article↗

Controlling chaos in a fast diode resonator using extended time-delay autosynchronization: Experimental observations and theoretical analysis.

We stabilize unstable periodic orbits of a fast diode resonator driven at 10.1 MHz (corresponding to a drive period under 100 ns) using extended time-delay autosynchronization. Stabilization is achieved by feedback of an error signal that is proportional to the difference between the value of a state variable and an infinite series of values of the state variable delayed in time by integral multiples of the period of the orbit. The technique is easy to implement electronically and it has an all-optical counterpart that may be useful for stabilizing the dynamics of fast chaotic lasers. We show that increasing the weights given to temporally distant states enlarges the domain of control and reduces the sensitivity of the domain of control on the propagation delays in the feedback loop. We determine the average time to obtain control as a function of the feedback gain and identify the mechanisms that destabilize the system at the boundaries of the domain of control. A theoretical stability analysis of a model of the diode resonator in the presence of time-delay feedback is in good agreement with the experimental results for the size and shape of the domain of control. (c) 1997 American Institute of Physics.

Journal Article↗

Modeling protein stability: a theoretical analysis of the stability of T4 lysozyme mutants.

Free energy calculations were conducted to determine the relative stability of the unnatural amino acid mutants of T4 lysozyme norvaline (Nvl) and O-methyl-serine (Mse) and of alanine at residue 133, which is leucine in the native sequence. These calculations were performed both to assess the validity of the methodology and to gain a better understanding of the forces which contribute to protein stability. Peptides of different length were used to model the denatured state. Restraints were employed to force sampling of the side chain chi1 dihedral of the perturbed side chain, and the effect of protein repacking in response to mutation was studied through the use of different constraint sets. In addition, the convergence behavior and hysteresis of the simulations in the folded and unfolded states were determined. The calculated results agree well with experiment, + 1.84 versus + 1.56 kcal/mol for Mse-->Nvl and -3.48 versus -2.2 to -3.6 kcal/mol for Nvl-->Ala. We find that free energy calculations can provide useful insights to protein stability when conducted carefully on a well chosen system. Our results suggest that loss of packing interactions in the native state is a major source of destabilization for mutants which decrease the amount of buried nonpolar surface area and that subtle responses of the backbone affect the magnitude of the loss of stability. We show that the conformational freedom of the chi1 dihedral has a noticeable effect on protein stability and that the solvation of amino acid side chains is strongly influenced by interactions with the peptide backbone.

Amino Acid Sequence↗

Numerical analysis for stability and self-excited oscillation in collapsible tube flow.

This paper describes numerical analysis of collapsible tube flow based on the one-dimensional distributed parameter model of Hayashi. In the present model the effect of flow separation at the collapsed part is replaced with simple viscous friction along the tube, so no ad-hoc modeling for flow separation in former studies is required. A stable semi-implicit numerical procedure based on the SIMPLE method is developed for the problem of flow and tube interaction. The numerical result for a characteristic self-excited oscillation agrees qualitatively with the experimental result. Nonlinear stability of the steady state dependent on the amplitude of the disturbance is numerically investigated and the result is compared with the linear stability analysis based on the former lumped parameter model. Finally, initiation of the self-excited oscillation is examined by applying the initial disturbance at the upstream end of the tube. The disturbance propagates in the downstream direction and is amplified to the self-excited oscillation.

Compliance↗

Cellular control models with linked positive and negative feedback and delays. II. Linear analysis and local stability.

An analysis of local behavior is made of two nonlinear models which incorporate both an induction or positive feedback control mechanism and a repression or negative feedback control mechanism. The systems of differential equations with delays are linearized about their equilibria. The related characteristic equations which are exponential polynomials are studied to determine the local stability of the models. Computer studies are included to show the range of stability for different parameter values, and the biological significance is discussed briefly.

Computers↗

Morphological instability and dynamics of fronts in bacterial growth models with nonlinear diffusion.

Depending on the growth condition, bacterial colonies can exhibit different morphologies. As argued by Ben-Jacob et al. there is biological and modeling evidence that a nonlinear diffusion coefficient of the type D(b)=D(0)b(k) is a basic mechanism that underlies almost all of the patterns and generates a long-wavelength instability. We study a reaction-diffusion system with a nonlinear diffusion coefficient and find that a unique planar traveling front solution exists whose velocity is uniquely determined by k and D=D(0)/D(n), where D(n) is the diffusion coefficient of the nutrient. Due to the fact that the bacterial diffusion coefficient vanishes when b-->0, in the front solution b vanishes in a singular way. As a result the standard linear stability analysis for fronts cannot be used. We introduce an extension of the stability analysis that can be applied to singular fronts, and use the method to perform a linear stability analysis of the planar bacteriological growth front. We show that a nonlinear diffusion coefficient generates a long-wavelength instability for k>0 and D 0 and k--> infinity the dynamics of the growth zone essentially reduces to that of a sharp interface problem that is reminiscent of a so-called one-sided growth problem where the growth velocity is proportional to the gradient of a diffusion field ahead of the interface. The moving boundary approximation that we derive in these limits is quite accurate but surprisingly does not become a proper asymptotic theory in the strict mathematical sense in the limit D-->0, due to lack of full separation of scales on all dynamically relevant length scales. Our linear stability analysis and sharp interface formulation will also be applicable to other examples of interface formation due to nonlinear diffusion, like in porous media or in the problem of vortex motion in superconductors.

Bacteria↗

The intercept method: a novel method for establishing consistency of M-wave recruitment curves.

The stability of the M-wave is an important component of experimental H-reflex methodology. Despite this importance, there is inconsistency in H-reflex literature on the most valid method of M-wave stability analysis. Further, there is currently no specific method for establishing the stability of an M-wave recruitment curve across various trials within an experiment. Therefore, the aim of this study was to investigate the most appropriate method of M-wave stability analysis for use with the recruitment curve methodology. Twenty-five healthy subjects participated in the study. Four M-wave recruitment curve recordings were made in various static positions that imposed stretch on the posterior structures of the back and leg. Four methods of post-data collection M-wave stability analysis were compared. Although on visual inspection, there was clear evidence of marked alterations to the M-wave recruitment curves between trials in some subject's data, analysis of variance of the Ms/p and Mmax found no significant difference. Evaluation of the percent deviation in Mmax found nine subjects with greater than ten percent deviation in their maximum M-wave across the four trials. The intercept method that utilises analysis of the 95% confidence interval of the intercept of the M-wave recruitment curve slope, excluded eight subjects that demonstrated variation. Comparison of the percent deviation and the intercept method revealed that the intercept method was the most appropriate method for M-wave stability analysis in conjunction with the recruitment curve methodology.

Adult↗

[The bases of urodynamics: analysis of stability of the solutions for the equation defining detrusor behaviour].

OBJECTIVES: In this article we develop the analysis of stability of the solution(s) of the differential equation describing detrusor behaviour as a forced and overcushioned tensor. We followed the theories of Lyapunov about stability. Therefore, we used a matricial method which is more didactical and also analytically more graphic. Solutions are placed in the Trace-Determinant (T-D) plane. This work represents a previous study to the one about detrusor as a dispersing system. And about which we would have to perform an analysis, first from the point of view of the Hamiltonian systems, then from the point of view of chaos. METHODS/RESULTS: We worked on the equation which has been widely described in previous articles in the series of publications titled "the bases of urodynamics". In previous articles, we gave results after applying other methods different from the ones that are usually employed to solve differential equations. We used the matricial method for the analysis of stability of solutions because of its greater didactical clarity. CONCLUSIONS: We conclude that we are in an unstable balance until the moment right before to start voiding. Once voiding is initiated, we are in front of a system with a drain, which at the same time is a fountain. Then we pass from a Hamiltonian dispersing system to a chaotic one. But this is another question...

Humans↗

Selection of ovine housekeeping genes for normalisation by real-time RT-PCR; analysis of PrP gene expression and genetic susceptibility to scrapie.

BACKGROUND: Cellular prion protein expression is essential for the development of transmissible spongiform encephalopathies (TSEs), and in sheep, genetic susceptibility to scrapie has been associated to PrP gene polymorphisms. To test the hypothetical linkage between PrP gene expression and genetic susceptibility, PrP mRNA levels were measured by real-time RT-PCR in six ovine tissues of animals with different genotypes. RESULTS: Previous to the PrP gene expression analysis the stability of several housekeeping (HK) genes was assessed in order to select the best ones for relative quantification. The normalisation of gene expression was carried out using a minimum of three HK genes in order to detect small expression differences more accurately than using a single control gene. The expression stability analysis of six HK genes showed a large tissue-associated variation reflecting the existence of tissue-specific factors. Thereby, a specific set of HK genes was required for an accurate normalisation of the PrP gene expression within each tissue. Statistical differences in the normalised PrP mRNA levels were found among the tissues, obtaining the highest expression level in obex, followed by ileum, lymph node, spleen, cerebellum and cerebrum. A tendency towards increased PrP mRNA levels and genetic susceptibility was observed in central nervous system. However, the results did not support the hypothesis that PrP mRNA levels vary between genotypes. CONCLUSION: The results on PrP gene expression presented here provide valuable baseline data for future studies on scrapie pathogenesis. On the other hand, the results on stability data of several HK genes reported in this study could prove very useful in other gene expression studies carried out in these relevant ovine tissues.

Journal Article↗

Coexistence of regular and irregular dynamics in complex networks of pulse-coupled oscillators.

For general networks of pulse-coupled oscillators, including regular, random, and more complex networks, we develop an exact stability analysis of synchronous states. As opposed to conventional stability analysis, here stability is determined by a multitude of linear operators. We treat this multioperator problem exactly and show that for inhibitory interactions the synchronous state is stable, independent of the parameters and the network connectivity. In randomly connected networks with strong interactions this synchronous state, displaying regular dynamics, coexists with a balanced state exhibiting irregular dynamics. External signals may switch the network between qualitatively distinct states.

Biological Clocks↗

Content analysis and stability evaluation of selected commercial preparations of St. John's wort.

Content analysis and stability studies were performed for the commercial products of St. John's wort. Six marketed formulations were analyzed for their hypericin and pseudohypericin content. These products were standardized to contain 0.3% hypericin. Results revealed total hypericin as 7.72-38.57% of the labeled claim with varying concentrations of pseudohypericin. Stability studies were carried out under three different storage conditions: 1) 25+/-2 degrees C, 60+/-5%RH for six months, 2) 40+/-2 degrees C, 75+/-5%RH for six months, and 3) 50 degrees C for one month. Tablet formulations were also analyzed for their hardness and friability. Stability studies revealed significant decrease in the content of the marker compounds with time.

Anthracenes↗

Influence of attractive van der Waals interactions on the optimal excitations in thermocapillary-driven spreading.

Recent investigations of microfluidic flows have focused on manipulating the motion of very thin liquid films by modulating the surface tension through an applied streamwise temperature gradient. The extent to which the choice of contact line model affects the flow and stability of such thermocapillary-driven films is not completely understood. Regardless of the contact line model used, the linearized disturbance operator corresponding to the evolution of the film height is non-normal, and a generalized non-modal stability analysis is required. Surprisingly, early predictions of frontal instability that stemmed from conventional modal analysis of thermocapillary flow on a flat, infinite precursor film showed excellent agreement with experiment. Within the more rigorous framework provided by a generalized stability analysis, this work investigates the transient dynamics and amplification of optimal disturbances subject to a finite precursor film generated by attractive van der Waals forces. Convergence of the disturbance growth rates and perturbed shapes to the asymptotic solutions obtained by conventional linear stability analysis occurs early in the spreading process. In addition, the level of transient disturbance amplification is minimal. The equations governing thermocapillary-driven spreading exhibit a small degree of non-normality, which explains the source of agreement between modal theory and experiment. The more rigorous generalized stability analysis presented here, however, affords critical insight into the types of disturbances leading to maximum unstable growth and the exact influence of the contact line model used.

Journal Article↗

Analysis and stability of carotenoids in the flowers of daylily (Hemerocallis disticha) as affected by various treatments.

The analysis and stability of carotenoids in the flowers of daylily (Hemerocallis disticha) as affected by soaking and drying treatments were studied. The various carotenoids in the flowers of daylily were analyzed using a reversed-phase C(30) HPLC column and a mobile phase of methanol/methylene chloride/2-propanol (89:1:10, v/v/v) with methanol/methylene chloride (45:55, v/v) as sample solvent. Twenty-one pigments were resolved, of which 14 carotenoids were identified, including neoxanthin, violaxanthin, violeoxanthin, lutein-5,6-epoxide, lutein, zeaxanthin, beta-cryptoxanthin, all-trans-beta-carotene, and their cis isomers, based on spectral characteristics and Q ratios. Prior to hot-air-drying (50 degrees C) or freeze-drying, some of the daylily flowers were subjected to soaking in a sodium sulfite solution (1%) for 4 h. Under either the hot-air- or the freeze-drying treatment, the amounts of most carotenoids were higher in the soaked daylily flowers than in those that were not soaked. With hot-air-drying, the amount of cis carotenoids showed a higher yield in soaked samples than in nonsoaked samples. However, with freeze-drying, only a minor change of each carotenoid was observed for both soaked and nonsoaked samples. Also, air-drying resulted in a higher loss of carotenoids than freeze-drying.

Air↗

Stability of parenteral nutrition admixtures containing organic phosphates.

The use of organic phosphates to avoid calcium phosphate precipitation in parenteral nutrition mixtures has been proposed. The purpose of this study was to evaluate the stability of total parenteral nutrition admixtures containing glucose-1-phosphate or glycerol phosphate as the phosphate source over 3 days. Three parenteral nutrition admixtures, each containing glucose-1-phosphate (30.0 mmol), glycerol phosphate (31.4 mmol) or inorganic phosphate (30.0 mmol), and their corresponding aqueous phases were prepared in 3-L ethylene vinyl acetate plastic bags and infusion bottles, and stored at 5 +/- 1 degrees C or 22 +/- 3 degrees C without light protection. Physical stability analysis and sampling for chemical analysis was performed at 0, 24, 48 and 72 h. Aqueous phases were subjected to physical stability analysis, including pH measurement, visual inspection and nephelometry. Admixtures were subjected to physical stability analysis consisting of pH measurement, and evaluation of emulsion stability by visual inspection, degree of creaming, phase contrast microscopy, zone sensing technique and photon correlation spectroscopy. Chemical analyses of amino-acids, dextrose, triglycerides, phospholipids, Na, K, Cl, Mg, Ca, glucose-1-phosphate, glycerolphosphate and inorganic phosphate were performed. No precipitation was detected in any of the aqueous phases. Admixtures remained acceptable with respect to visual and microscopic appearance, mean droplet diameter and droplet size distribution. All nutrient concentrations assayed in the three admixtures remained constant over the study period. Total parenteral nutrition admixtures for adult patients containing glucose-1-phosphate or glycerolphosphate are physically and chemically stable for 3 days when stored under refrigeration or controlled room temperature without light protection.

Journal Article↗

Secondary deletional recombination of rearranged switch region in Ig isotype-switched B cells. A mechanism for isotype stabilization.

Analysis of the Ig switch (S) region structure from many stable isotype-switched B cells reveals that the majority of the ultimate switch recombination sites are located at the 5' end, or even upstream of the 5' end of the Smu region. These findings strongly contrast with results from switch circle analysis which reveal that the primary switch recombination sites are preferentially distributed in the middle or at the 3' end of the Smu region. Secondary deletion within recombined chimeric S regions has been proposed as a mechanism to account for the different results. We directly tested whether secondary deletion of rearranged chimeric S regions indeed occurs in human cells. Circular DNAs representing secondary deletion events in gamma switched cells were isolated and characterized by using a specially designed PCR-based approach. Nucleotide sequence analysis revealed that all clones had the S gamma 1-Smu-S gamma 1 structure. Thus, these cloned fragments resulted from secondary deletion/recombination events within a chimeric Smu-S gamma 1 switch region, i.e., rearrangement between its 5' Smu and 3' S gamma 1. Analysis of the Smu region from stimulated B cells also revealed that some Smu regions undergo an internal deletion/rearrangement between the 5' and 3' ends. These results definitively demonstrate that secondary deletion/recombination of chimeric S regions of isotype-switched B cells occurs. Such secondary deletion/recombination events potentially can be responsible for isotype stabilization of switched B cells, as the active Ig gene may have an insufficient amount of retained chimeric switch sequence to serve as a substrate for further S-S recombination.

B-Lymphocytes↗

Developmental changes in the subcellular distribution of the 43K (v1) polypeptides in Torpedo marmorata electrocyte: support for a role in acetylcholine receptor stabilization.

Analysis of the relative amounts of the acetylcholine receptros (AChR) and of the 43K protein present in the membrane of developing electrocyte shows that massive accumulation of 43K protein is not required for induction of early AChR clustering. Furthermore, we demonstrate the existence o of cytosol- and membrane-associated 43K polypeptide pools in Torpedo electrocyte. Epitope analysis shows that both pools of 43K protein are related to the long mRNA transcript and share similar antigenic determinants distributed throughout the protein sequence. Their partition between the cytosol and membrane fractions abruptly increases in favor of the membrane during the postsynaptic maturation phase of development, supporting a role for 43K protein in the stabilization and maintenance of the postsynaptic domain.

Amino Acid Sequence↗

Aromatic-aromatic interaction: a mechanism of protein structure stabilization.

Analysis of neighboring aromatic groups in four biphenyl peptides or peptide analogs and 34 proteins reveals a specific aromatic-aromatic interaction. Aromatic pairs (less than 7 A between phenyl ring centroids) were analyzed for the frequency of pair type, their interaction geometry (separation and dihedral angle), their nonbonded interaction energy, the secondary structural locations of interacting residues, their environment, and their conservation in related molecules. The results indicate that on average about 60 percent of aromatic side chains in proteins are involved in aromatic pairs, 80 percent of which form networks of three or more interacting aromatic side chains. Phenyl ring centroids are separated by a preferential distance of between 4.5 and 7 A, and dihedral angles approaching 90 degrees are most common. Nonbonded potential energy calculations indicate that a typical aromatic-aromatic interaction has energy of between -1 and -2 kilocalories per mole. The free energy contribution of the interaction depends on the environment of the aromatic pair. Buried or partially buried pairs constitute 80 percent of the surveyed sample and contribute a free energy of between -0.6 and -1.3 kilocalories per mole to the stability of the protein's structure at physiologic temperature. Of the proteins surveyed, 80 percent of these energetically favorable interactions stabilize tertiary structure, and 20 percent stabilize quaternary structure. Conservation of the interaction in related molecules is particularly striking.

Amino Acids↗