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At least 91 records · Page 5Linked to original sources
PubMed2002

Estimation of initial dissolution rate of drug substance by thermal analysis: application for carbamazepine hydrate.

We have proposed a theory indicating the correlation between the dissolution rate and the heat of solution of drug substances. The initial dissolution rates of the drug substances containing amorphous were predicted accurately from their heats of solution. In this report, the possibility for the theory to estimate the dissolution rates of hydrate and polymorphs was examined using thermal analysis. The initial dissolution rates of carbamazepine dihydrate and polymorphs (forms I, II, and III) were measured by the rotating disk method. The heats of solution and the heats of fusion of samples were measured by microcalorimetry and Differential Scanning Calorimetry (DSC), respectively. The logarithm of the initial dissolution rate of the sample was correlated linearly with the heat of fusion as well as the heat of solution. The obtained correlation would be applicable for the quality control of the drug substances the contained hydrate and/or polymorphic forms.

Calorimetry, Differential Scanning↗
PubMed2001

Thermal analysis on the cure speed of dual cured resin cements under porcelain inlays.

The reaction kinetics of five commercial dual cured resin cements (Bistite, Dual, Scotchbond, Duolink and Duo) were investigated when cured under varying thicknesses of porcelain inlays by chemical or light activation. The effect of the porcelain disc on the rate of polymerization of dual cured resin cement during light exposure was evaluated using thermal analysis, thermogravimetric analysis and differential scanning calorimetry. Inorganic filler weight %, the heat of cure (Delta H), the maximum rate of heat output and the peak heat flow time were measured when the polymerization reaction occurred by chemical cure only or by light exposure through 1, 2 and 4-mm thick porcelain discs. In 4-mm thick porcelain discs, the exposure time was varied from 40 to 60 s to investigate the effect of the exposure time on polymerization reaction. Cure speed by light exposure was 5--20 times faster than by chemical cure. The dual cured resin cements differed markedly in their sensitivity to light and chemical activation. The peak heat flow time increased by 1.51, 1.87 and 3.24 times as light cure was carried out through 1, 2 and 4-mm thick porcelain discs, respectively. Exposure times recommended by the manufacturers were insufficient to compensate for the attenuation of light by the 4-mm thick porcelain disc.

Algorithms↗
PubMed2004

Effect of water structure on blood compatibility--thermal analysis of water in poly(meth)acrylate.

The purpose of this study is to clarify the main factor causing excellent blood compatibility of poly(2-methoxyethyl acrylate)(PMEA) by the comparison between PMEA and seven PMEA analogous polymers. The polymers have a typical functional group as ester side chains such as methoxyethyl, hydroxyethyl, phenoxyethyl, and alkyl groups. The properties of the polymers relating to water were investigated in terms of contact angle, equilibrium water content (EWC), and thermal analysis by differential scanning calorimetry. The water in PMEA could be classified into three types: nonfreezing water, freezing bound water, and free water while the water in the analogous polymers was classified into just two types: free and nonfreezing waters, regardless of the chemical structure of the side chain. The surface property represented by the contact angle of water corresponded to the content of the bound water (nonfreezing water + freezing bound water). The platelet compatibility in vitro did not depend on the contents of these waters, or on the contact angle. On the basis of the results of this work and the previous work on the platelet compatibility of poly(MEA-co-HEMA) (Tanaka et al. Biomacromolecules 2002;3;36-41), the main factor causing the excellent compatibility of PMEA is discussed.

Biocompatible Materials↗
PubMed2007

Reversibility of enantiotropically related polymorphic transformations from a practical viewpoint: thermal analysis of kinetically reversible/irreversible polymorphic transformations.

Although enantiotropically related polymorphic transitions are thermodynamically reversible with temperature and pressure, they may be observed as either reversible or irreversible in practical investigations. This behavior may be explained simply by a difference in the energy barrier for the transition. However, this difference may have a significant effect on strategy in formulation development. This article summarizes the characteristics of enantiotropic transitions with reference to the literature. Also provided are careful investigations of polymorphic transitions by thermal analysis, which is the most promising method to investigate transition behavior.

Calorimetry, Differential Scanning↗
PubMed2000

Temperature-controlled microscopy for imaging living cells: apparatus, thermal analysis and temperature dependency of embryonic elongation in Caenorhabditis elegans.

A new experimental apparatus for temperature-controlled microscopy has been developed for the study of the temperature dependency of developmental processes in the nematode Caenorhabditis elegans. However, the application of this apparatus is rather general and can be used for a wide range of temperatures between - 10 and 90 degrees C. The new apparatus is easy to use, inexpensive, simple to construct, and is designed for precise temperature control of oil-immersion microscopy using epifluorescence. Thermal analysis of the experimental apparatus shows the effects of each of its components, as well as the effects of uncertainty in temperature measurements. Finally, results of this study indicate that: (i) embryos incubated and imaged at temperatures of 8 degrees C and below do not elongate; (ii) the initial elongation rate is strongly temperature-dependent between 9 and 25 degrees C.

Animals↗
PubMed1999

Characterization of racemic species of chiral drugs using thermal analysis, thermodynamic calculation, and structural studies.

The identification of the racemic species, as a racemic compound, a racemic conglomerate, or a racemic solid solution (pseudoracemate), is crucial for rationalizing the potential for resolution of racemates by crystallization. The melting points and enthalpies of fusion of a number of chiral drugs and their salts were measured by differential scanning calorimetry. Based on a thermodynamic cycle involving the solid and liquid phases of the enantiomers and racemic species, the enthalpy, entropy and Gibbs free energy of the racemic species were derived from the thermal data. The Gibbs free energy of formation, is always negative for a racemic compound, if it can exist, and the contribution from the entropy of mixing in the liquid state to the free energy of formation is the driving force for the process. For a racemic conglomerate, the entropy of mixing in the liquid state is close to the ideal value of R ln 2 (1.38 cal.mol-1. K-1). Pseudoracemates behave differently from the other two types of racemic species. When the melting points of the racemic species is about 30 K below that of the homochiral species, is approximately zero, indicating that the racemic compound and racemic conglomerate possess similar relative stabilities. The powder X-ray diffraction patterns and 13C solid-state nuclear magnetic resonance spectra are valuable for revealing structural differences between a racemic compound and a racemic conglomerate. Thermodynamic prediction, thermal analysis, and structural study are in excellent agreement for identifying the nature of the racemic species.

Calorimetry, Differential Scanning↗
PubMed1993

Thermal analysis of rat bone tissue.

The paper describes thermoanalytical data obtained from rat limb bones by TG, DTG and DSC. Analyses were performed on bone samples from femurs, tibiae and humeri, either crude and extracted with acetone and/or sodium dodecylsulphate. The DSC curves show an endothermic reaction at 85 degrees C and a sharp exothermic peak at 337 degrees C, followed by an exothermic profile between 350 degrees-650 degrees C. Mean weight changes are: 34.28% total weight loss (25 degrees-800 degrees C); 7.33% water loss (25 degrees-200 degrees C); 26.21% organic loss (200 degrees-800 degrees C). Thermal analysis on diaphyseal and epiphyseal bone samples evidences an organic content of 24.54% for diaphyseal compact bone tissue and of 30.62% for epiphyseal trabecular bone tissue (p < .005). The values obtained from different bones and by different treatment of samples are compared.

Animals↗
PubMed1995

Temperature prediction of space flight experiments by computer thermal analysis.

Life sciences experiments are especially sensitive to temperature. A small temperature difference between otherwise identical samples can cause various differences in biological reaction rates. Knowledge of experimental temperatures and temperature histories help to distinguish the effects of microgravity and temperature on spaceflight experiments compared to ground based studies, and allow appropriate controls and sensitivity tests. Up to the present time, the Orbiter (Space Shuttle) has not generally provided temperature measurement instrumentation inside ambient lockers located in the Mid-deck of the Orbiter, or inside similar facilities such as Spacehab and Spacelab, but many pieces of hardware do have temperature recording capability. Most of these temperatures, however, have only been roughly measured or estimated. Such reported experimental temperatures, while accurate within a range of several degrees Celsius, are of limited utility to biological researchers. The temperature controlled lockers used in spaceflight, such as Commercial-Refrigeration Incubation Modules (C-R/IMs), severely reduce the mass and volume available for test samples and do not necessarily provide uniform thermal environments. While these test carriers avoid some of the experimental temperature variations of the ambient lockers, the number of samples which can be accommodated in these temperature controlled units is limited. In the present work, improved models of thermal prediction and control were sought. Temperatures are predicted by thermal analysis software using empirical temperatures recorded during STS-57. These temperatures are compared to data recorded throughout the mission using Ambient Temperature Recorders (ATRs) located within several payload lockers. Additional test cases are undertaken using controlled ground experiments to more precisely determine the reliability of the thermal model. The approach presented should increase the utility of various spaceflight carriers in the support of biological and material science research and ground control studies done in preparation for flight.

Air Conditioning↗
PubMed2005

Dynamic mechanical thermal analysis of two light-cured dental composites.

OBJECTIVES: Clinical observations suggest that some composite resins are more often linked to post-operative sensitivity than others. These differences may relate to differences in modulus of elasticity and polymerization rates among materials. The aim of this study was to identify viscoelastic behavior of two light curable composites and determine whether significant differences in viscoelastic behavior exist between the two materials when light cured at each of three different irradiance values. METHODS: Two composites (Z100 and Z250 by 3M ESPE) were evaluated. Six specimens per composite and irradiance value (250, 500 and 850 mW/cm2) were made. The curing times were chosen to produce a fixed energy value of 30 J/cm2 independent of irradiation value. Dynamic mechanical thermal analysis (DMTA) was performed in single cantilever clamped mode. RESULTS: There were significant differences in transition temperatures between the two materials and the three frequencies at their glass transition temperatures, while significant differences did not exist at the lower transitions. The glass transition of Z250 was lower and narrower than that of Z100. Z250 exhibited lower storage modulus values. The irradiance values did not affect any of the transition temperatures significantly. SIGNIFICANCE: The lower and more distinct T(g) of Z250 suggests that Z250 cures more efficiently than Z100. The lower storage modulus of Z250 suggests that Z250 develops less stress in the tooth than Z100 during curing if shrinkage is the same for the two materials. The findings suggest that the material chosen, rather than irradiance, determines the stress level developed during light curing.

Composite Resins↗
PubMed2003

Effect of ER:YAG and diode laser irradiation on the root surface: morphological and thermal analysis.

BACKGROUND: The aim of the present study was to compare the effects of Er:YAG and diode laser treatments of the root surface on intrapulpal temperature after scaling and root planing with hand instruments. METHODS: Fifteen extracted single-rooted teeth were scaled and root planed with hand instruments. The teeth were divided into 3 groups of 5 each and irradiated on their buccal and lingual surfaces: group A: Er:YAG laser, 2.94 microm/100 mJ/10 Hz/30 seconds; group B: diode laser, 810 nm/1.0 W/0.05 ms/30 seconds; group C: diode laser, 810 nm/1.4 W/0.05 ms/30 seconds. The temperature was monitored by means of a type T thermocouple (copper-constantan) positioned in the pulp chamber to assess pulpal temperature during and before irradiation. Afterwards, the specimens were longitudinally sectioned, and the buccal and lingual surfaces of each root were analyzed by scanning electron microscopy. RESULTS: In the Er:YAG laser group, the thermal analysis revealed an average temperature of -2.2 +/- 1.5 degrees C, while in the diode laser groups, temperatures were 1.6 +/- 0.8 degrees C at 1.0 W and 3.3 +/- 1.0 degrees C at 1.4 W. Electronic micrographs revealed that there were no significant morphological changes, such as charring, melting, or fusion, in any group, although the specimens were found to be more irregular in the Er:YAG laser group. CONCLUSIONS: The application of Er:YAG and diode lasers at the utilized parameters did not induce high pulpal temperatures. Root surface irregularities were more pronounced after irradiation with an Er:YAG laser than with a diode laser.

Aluminum Silicates↗
PubMed2001

Selection of excipients for melt extrusion with two poorly water-soluble drugs by solubility parameter calculation and thermal analysis.

The aim of this study was to determine the miscibility of drug and excipient to predict if glass solutions are likely to form when drug and excipient are melt extruded. Two poorly water-soluble drugs, indomethacin and lacidipine, were selected along with 11 excipients (polymeric and non-polymeric). Estimation of drug/excipient miscibility was performed using a combination of the Hoy and Hoftzyer/Van Krevelen methods for Hansen solubility parameter calculation. Miscibility was experimentally investigated with differential scanning calorimetry (DSC) and hot stage microscopy (HSM). Studies were performed at drug/excipient ratios, 1:4, 1:1 and 4:1. Analysis of the glass transition temperature (T(g)) was performed by quench cooling drug/excipient melts in the DSC. Differences in the drug/excipient solubility parameters of <7.0 MPa(1/2) were predicted to indicate significant miscibility and, therefore, glass solution formation on melt extrusion. In comparison, differences of >10 MPa(1/2) were expected to indicate a lack of miscibility and not form glass solutions when melt extruded. Experimentally, miscibility was shown by changes in drug/excipient melting endotherms and confirmed by HSM investigations. Experimental results were in agreement with solubility parameter predictions. In addition, drug/excipient combinations predicted to be largely immiscible often exhibited more than one T(g) upon reheating in the DSC. Melt extrusion of miscible components resulted in amorphous solid solution formation, whereas extrusion of an "immiscible" component led to amorphous drug dispersed in crystalline excipient. In conclusion, combining calculation of Hansen solubility parameters with thermal analysis of drug/excipient miscibility can be successfully applied to predict formation of glass solutions with melt extrusion.

Calorimetry, Differential Scanning↗
PubMed1994

Thermal analysis.

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Calorimetry, Differential Scanning↗
PubMed1977

Determination of phase transitions in gutta-percha by differential thermal analysis.

Pure gutta-percha was heat-treated in a differential thermal analyzer. The high melting form crystallized on cooling when gutta-percha was heated to 70 C or less. Above 74 C, crystallization into the low melting form predominated. Either polymorph can be selectively crystallized by control of the heat-treatment temperature before cooling.

Chemical Phenomena↗
PubMed1991

Thermal analysis of water-containing systems.

Thermal analytical techniques offer many advantages in investigations of water-containing systems. This paper will review some of the methodologies used by us in studying food systems: 1) Differential Scanning Calorimetry (DSC): for determining freezable water, melting point, Tg' (see text), etc. 2) ThermoMechanical Analysis (TMA): for determining softening points as a function of water content, dilatometry and glass transition temperatures. 3) ThermoGravimetric Analysis (TGA): for investigating water uptake curves and water content determination. 4) Dynamic Mechanical Analysis (DMA): for the determination of low-energy transitions.

Calorimetry, Differential Scanning↗