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Biomedical subjects

C Shen

Publications and source records attributed to C Shen.

140 records · Page 8Linked to original sources
PubMed1981

Effect of K2SO4 and CaSO4 dihydrate solutions on crystallization and strength of gypsum.

Crystal formation obtained from evaporating clear filtrates of dental stone mixed with various solutions were examined with an optical and scanning electron microscope. It was found that when K2SO4 was present in any concentration, a spherulitic structure dissimilar to that of CaSO4. 2H2O and K2SO4 was dominant. It is concluded that syngenite (a complex compound of CaSO4 and K2SO4) forms at the center of the nuclei of crystallization and is responsible for spherulitic formation. The use of K2SO4 solution and saturated CaSO4 solution was also found to improve the strength both at one and 24 h.

Calcium Sulfate↗
PubMed1980

A 31P-NMR study of the cross-membrane pH gradient induced by ATP hydrolysis in mitochondria.

31P-NMR has been used to study the increase of delta pH in mitochondria by externally added ATP. Freshly prepared mitochondria was treated with N-ethylmaleimide to inhibit the exchange between internal and external P(i). Upon addition of ATP, phosphocreatine (30 mM) and creatine kinase to a NMR sample of mitochondria suspension (approx. 120 mg protein/ml) at 0 degrees C, an increase of delta pH by approx. 0.5 pH unit was observed. However the increased delta pH could not be maintained, but slowly decayed along with the increase of external ADP/ATP ratio. Further addition of valinomycin to the suspension induced a larger delta pH (approx. 1) which was maintained by the increased rate of internal ATP hydrolysis as seen in the growth of the internal P(i) peak intensity in NMR spectra and the concomitant decrease of the external phosphocreatine peak. The external P(i) and ATP peaks stayed virtually constant. When carboxyatractyloside was added to inhibit the ATP/ADP translocase, the internal P(i) increase was stopped and the delta pH decayed. These observations in conjunction with those made earlier in respiring mitochondria clearly show the reversible nature of the ATPase function in which the internal ATP hydrolysis is associated with outward pumping of protons.

Adenosine Diphosphate↗
PubMed1978

Sugar pucker geometries at the intercalation site of propidium diiodide into miniature RNA and DNA duplexes in solution.

We have evaluated the sugar pucker geometry at the intercalation site of propidium diiodide into the self-complementary dinucleoside monophosphate duplexes cytidylylguanosine and deoxycytidylyldeoxyguanosine as a function of the nucleotide/drug ratio in aqueous solution. Our solution results support the observation by Sobell and coworkers [Sobell, H.M., Tsai, C.C., Jain, S.C. & Gilbert, S.G. (1977) J. Mol. Biol. 114, 333--365] of a C3' endo (3'-5')C2' endo sugar pucker geometry in the 2:2 intercalation complex of ethidium bromide into the iodocytidylylguanosine duplex in the crystalline state. We demonstrate further that the mixed sugar pucker observed for the intercalation of propidium diiodide into the miniature RNA duplex in solution persists in the intercalative complex of this trypanocidal drug into the corresponding miniature DNA duplex in solution.

Deoxyribose↗
PubMed1977

Biogenic amine-ionophore interactions: Structure and dynamics of lasalocid (X537A) complexes with phenethylamines and catecholamines in nonpolar solution.

The ionophore lasalocid A forms 1:1 complexes with phenethylamines (1-amino-1-phenylethane and 1-amino-2-phenylethane) and catecholamines (dopamine and norepinephrine) in nonpolar solution. We have undertaken high-resolution proton nuclear magnetic resonance studies to deduce structural and kinetic information on the ionophore-biogenic amine complexes in chloroform solution. The coupling constant, chemical shift, and relaxation time data demonstrate that the lasalocid backbone conformation and the primary amine binding sites in the complexes are similar to those determined earlier for the alkali and alkaline earth complexes of this ionophore in solution. The exchange of lasalocid between the free acid (HX) and the primary amine complexes (RNH(3)X) in chloroform solution have been evaluated from the temperature-dependent line shapes at superconducting fields. The kinetic parameters associated with the unimolecular dissociation [Formula: see text] and the bimolecular exchange [Formula: see text] reactions have been deduced from an analysis of the lifetime of the complex as a function of the reactant concentrations. The relative stability of the complex decreases in the order phenyl > n-pentyl for substituents on the carbon alpha to the amino group (1-amino-1-phenylethane and 2-aminoheptane) and phenyl > 3,4-dihydroxyphenyl for substituents on the carbon beta to the amino group (1-amino-2-phenylethane and dopamine). These results suggest that nonpolar interactions between the biogenic amine side chain and the lasalocid molecule contribute to the stability of the complex in solution.

Journal Article↗
PubMed1977

Leucine aminopeptidase from swine kidney: purification, molecular weight, subunit and amino acid composition.

A homogeneous leucine aminopeptidase was obtained from mixed breed swine kidneys by means of chromatography on a special column. After coupling an inhibitor, N-sulfanilyl N'-butylcarbamide, to Sepharose 6B, the derivative did not absorb the enzyme, but absorbed a non-enzymatically active protein. The enzyme showed a single band on disc-gel electrophoresis. The molecular weight of the enzyme has 320,000 daltons. In 6 M guanidine solution containing 0.5% 2-mercaptoethanol at pH 8, the enzyme exhibited a molecular weight of 53,000 on equilibrium centrifugation. A similar value, 54,000, for the subunit of the enzyme was found on SDS-gel electrophoresis. The amino acid composition of the enzyme is also reported.

Amino Acids↗
PubMed1976

Free acid, anion, alkali, and alkaline earth complexes of lasalocid a (X537A) in methanol: structural and kinetic studies at the monomer level.

We report below on nuclear magnetic resonance investigations of the structure and exchange kinetics for the free acid, anion, sodium complex, and barium complex of the ionophore lasalocid A (X537A) in methanol solution. A comparison between the proton and carbon longitudinal relaxation times of lasalocid in nonpolar and polar solvents demonstrates that the free acid (HX) is a monomer in methanol solution. Parallel proton and carbon relaxation measurements demonstrate that the anion (X-), sodium complex (NaX), and barium complex (BaX+) are also monomeric in methanol solution. These results are in contrast to the Na2X2 dimer and the BaX2-H20 dimer observed in crystals and in nonpolar (cyclohexane and methylene chloride) solutions. Large downfield shifts on complex formation (X- to NaX and BaX+) are detected for protons located on the polar face of the ionophore with their C-H bonds directed towards and proximal to the metal ion. The exchange of lasalocid anion between free (X-) and complexed (BaX+) states in methanol can be monitored from the temperature-dependent line shapes of the proton resonances at superconducting fields. The exchange rates are independent of the reactant concentrations and are characteristic of a rate-determining dissociation of BaX+ in methanol solution with activation parameters delta H++ = 6.5 kcal mol-1 (25 degrees) and delta S++ = -20.0 cal mol-1 degree -1 (1 cal = 4.184 J). The rate constants for dissociation and formation of BaX+ complex in methanol, 25 degrees, are 5.2 X 10(3) sec-1 and 1.5 X 10(10) M-1 sec-1, respectively. These studies were extended to derive the activation parameters for the exchange of lasalocid anion between BaX+ and NaX and between BaX+ and HX in methanol, while the exchange among HX, X-, and NaX is too rapid to be monitored on the time scale of nuclear magnetic resonance.

Anti-Bacterial Agents↗
PubMed1976

Structural and kinetic studies of lasalocid A (X537A) and its silver, sodium, and barium salts in nonpolar solvents.

The ionophore lasalocid A (X537A) and its metal salts have been investigated by high resolution (270 MHz and 360 MHz) proton nuclear magnetic resonance spectroscopy to obtain structural and kinetic information in nonpolar solution. The proton resonances were assigned from double resonance studies on lasalocid A and on its salts, homologs, isomers, and chemically modified derivatives. Studies of proton and carbon longitudinal relaxation time suggest that lasalocid A exists as a monomer, whereas the sodium and barium salts exist as dimers in nonpolar solvents. A study of the magnitude of the vicinal proton coupling constants and the chemical shifts and linewidths of the hydroxyl resonances suggest that the backbone conformation and intramolecular hydrogen bonds are similar for lasalocid A and its sodium and barium salts in nonpolar solvents. Nuclear magnetic resonance studies on the role of bound solvent molecules suggest a tightly bound water molecule in the barium complex dimer (crystallized from water-ethanol) and a weakly bound ethanol molecule in the lasalocid A monomer (crystallized from ethanol) in cyclohexane. The selective changes in proton chemical shift on complexation [where the polar faces of two lasalocid anions coordinate the metal cation(s) in nonpolar solvents have been analyzed in terms of the proximity of the resonances to the cation, their linkage to the coordinating oxygen atoms, and the magnetic anisotropy effects of the polar groups of one ligand on the resonances of its partner in the dimer. The nuclear magnetic resonance studies in solution are compared with earlier observations on lasalocid A and its salts in the crystalline state. Thus, the short Ag-C5 distance in the crystal structure of silver complex dimer is also observed in the solution structure. The kinetic parameters associated with the exchange between lasalocid A and its barium complex in chloroform have been measured from an analysis of the resonance line shapes as a function of temperature.

Anti-Bacterial Agents↗
PubMedDate not supplied

Placement and replacement of restorations in general dental practice in Iceland.

Ninety-one Icelandic practicing dentists (51% response rate) provided information related to the reasons for placement and replacement of 8,395 restorations and 741 sealants in 5,997 patients. Information included the patient's gender and age, the clinician's gender and experience in years since graduation, the defined criteria for replacement of restorations, the estimated past use of material in five-year increments and the records of 100 consecutively placed restorations. The materials used include composite (52.7%), amalgam (29.2%), glass ionomer (9.5%), resin-modified glass ionomer (7.1%) and other materials (1.4%). Although material selection was independent of the clinician's gender, female patients received more composite and fewer amalgam restorations than their male counterparts. Reasons for placing restorations comprised replacement of failed restorations (47.2%), primary caries (45.3%) and non-carious defects (7.5%). Secondary caries was the main reason for replacement for all types of restorations. Chi square analysis related to the dependence between the reasons for replacement and clinician's experience showed that more experienced clinicians recorded a lower frequency of secondary caries than less experienced ones (p<0.0001), while the diagnoses of discoloration and fracture of restorations increased with the clinicians' experience (p<0.0001).

Adolescent↗
PubMedDate not supplied

Characterization of treated porcelain surfaces via dynamic contact angle analysis.

Successful porcelain repair requires conditioning of porcelain surfaces. Conditioning is intended to facilitate wetting by repair materials and improve interfacial bonding. The objective of this investigation was to determine the effects of selected surface treatments upon the wettability of a representative feldspathic porcelain. Dynamic contact angle analysis and scanning electron microscopy were used to characterize the effects of such treatments. Standardized porcelain specimens were subjected to the following five treatment regimens: (1) control (no treatment); (2) airborne particle abrasion using 50 microns aluminum oxide; (3) etching with ammonium bifluoride gel; (4) etching with acidulated phosphate fluoride gel; and (5) etching with hydrofluoric acid gel. Following treatment, specimens were cleansed and dried. Advancing contact angles were quantified using dynamic contact angle analysis. Mean values and 95% confidence intervals were (in degrees): control, 63.8 +/- 2.7; ammonium bifluoride, 39.4 +/- 2.0; airborne particle abrading, 29.1 +/- 2.9; acidulated phosphate fluoride, 24.9 +/- 1.7; and hydrofluoric acid, 16.5 +/- 1.2. Significant differences were found between all treatment groups (P = .05). Subsequent scanning electron microscopy examination of treated surfaces indicated lesser contact angles were associated with surfaces displaying deeper and wider grooves. Apparently, the resultant increase in surface area produces increased wettability. It is inferred that an increase in surface area may correspond to enhanced resin-porcelain bonding.

Acidulated Phosphate Fluoride↗