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Tissue biological

Microscopy had been the principal tool of biology in the 19th century but it fell from fashion around 1900. (Sir Andrew Huxley 1990) [Pg.160]

How are the mechanical properties related to the arrangement of macro-molecular structures and their functional significance  [Pg.160]


Sampling of biological tissue is done by removing the entire organ, which is then homogenized before smaller portions are taken for analysis. Alternatively, several small portions of tissue may be combined to form a composite sample. The composite sample is then homogenized and analyzed. [Pg.198]

Biosynthesis. Somatostatin exists in longer forms in several biological tissues (95,96). One of the longer forms, which has been isolated from porcine intestine, has been characterized as a 28-amino acid peptide (97). Somatostatin is derived from a precursor containing 116 amino acids (98,99). The precursor contains one copy of the somatostatin tetradecapeptide, which is contained within the sequence of the 28-amino acid peptide at the carboxy-terminal end of the precursor. The 28-amino acid somatostatin is preceded by a single Arg residue, while somatostatin 1-14 is preceded by a pair of basic residues. [Pg.203]

Poly(ethylene oxide)—Poly(ethylene terephthalate) Copolymers. The poly(ethylene oxide)-poly(ethylene terephthalate) (PEO/PET) copolymers were first described in 1954 (40). This group of polymers was developed in an attempt to simultaneously reduce the crystallinity of PET, and increase its hydrophilicity to improve dyeabiHty. PEO/PET copolymers with increased PEO contents produce surfaces that approach zero interfacial energy between the implant and the adjacent biological tissue. The coUagenous capsule formed around the implant is thinner as the PEO contents increase. The stmcture of a PEO/PET copolymer is shown below ... [Pg.191]

Hall22 at the Sloan-Kettering Institute for Cancer Research has approached the problem of determining trace metals in biological tissues in a way that has the following noteworthy features (1) X-ray... [Pg.301]

Table 11-5. X-ray Emission Spectrography of Biological Tissue Sections. Tabular Summary of Illustrative Information... Table 11-5. X-ray Emission Spectrography of Biological Tissue Sections. Tabular Summary of Illustrative Information...
Mineral elements in biological tissue sections, derivation and use of equation for determination, 301-305 Minerals, analysis, use of borax flux by Claisse in, 173, 207, 209 use of curved-crystal spectrograph for small samples in, 206, 207 assay by x-ray emission spectrography, 199-209... [Pg.348]

Typical areas where two phase samples commonly occur are foodstuffs, biological tissue and sludges from environmental tests. [Pg.228]

Compatibility with biological tissues or other materials... [Pg.169]

Rubinsky, B. Pegg, D.E. (1988). A mathematical model for the freezing process in biological tissue. Proc. Roy. Soc. London B 234, 343-358. [Pg.383]

The primary method for detecting methyl parathion and metabolites in biological tissues is gas chromatography (GC) coupled with electron capture (BCD), flame photometric (FPD), or flame ionization detection (FID). Sample preparation for methyl parathion analysis routinely involves extraction with an organic solvent (e g., acetone or benzene), centrifugation, concentration, and re suspension in a suitable solvent prior to GC analysis. For low concentrations of methyl parathion, further cleanup procedures, such as column chromatography on silica gel or Florisil are required. [Pg.175]

Table 7-1 summarizes the analytical methods used to detect methyl parathion and its metabolites in biological tissues and fluids. [Pg.175]

Methods for Determining Biomarkers of Exposure and Effect. GC/ECD, GC/MS, and GC/MC are analytical techniques used for measuring endosulfan in blood, urine, hand rinses, and various biological tissues and excreta at low- and sub-ppb levels (Coutselinis et al. 1976 Demeter and Heyndrickx 1978 Demeter et al. 1977 Griffith and Blanke 1974 Guardino et al. 1996 Kazen et al. [Pg.260]

Lundgren, 6. and Johansson, 6. "A Temperature-Controlled Graphite Tube Furnace for the Determination of Trace Metals in Solid Biological Tissue . Talanta (1974), 21, 257-264. [Pg.268]

There are many obstacles to permanent adhesion under oral conditions. The substrate is a biological tissue and subject to change, and the presence of moisture represents the worst kind of situation for adhesion. Water is the great barrier to adhesion. It competes for the polar surface of tooth material against any potential polymer adhesive. It also tends to hydrolyse any adhesive bond formed. These twin obstacles gave rise to considerable doubt as to whether materials adhesive to tooth material could be developed at all (Cornell, 1961). [Pg.93]

Interfaces between two different media provide a place for conversion of energy and materials. Heterogeneous catalysts and photocatalysts act in vapor or liquid environments. Selective conversion and transport of materials occurs at membranes of biological tissues in water. Electron transport across solid/solid interfaces determines the efficiency of dye-sensitized solar cells or organic electroluminescence devices. There is hence an increasing need to apply molecular science to buried interfaces. [Pg.103]


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Arsenic in biological tissue

Biological Tissue polymer adhesion

Biological behavior bone tissues

Biological cells and tissues

Biological characterization, tissue

Biological characterization, tissue engineering

Biological fluids and tissues

Biological functional properties tissue engineering

Biological hard tissues

Biological materials and tissues

Biological tissue adhesives

Biological tissue cobalt

Biological tissue, dielectric properties

Biological tissues, cavitation

Biological tissues, optical window

Biological tissues, surface behavior

Biological tissues, ultrasound effects

Detection of taurine in biological tissues

Half lives, biological tissue lead burdens

Imaging mass spectrometry biological tissues

Inactivated Biological Tissues and Extracts for Nanoparticle Synthesis

Mucoadhesion biological tissue

Nervous tissue biological significance

Osmium tetroxide biological tissue

Phospholipase biological tissue

Phospholipids biological tissue

Radiation and Biological Tissue

Surface biological tissues

Synthesis Using Extracts from Biological Tissues

Synthesis extracts from biological tissues

Synthesis inactivated biological tissues

Tissue analysis biological tissues

Tissue damage, rats, biological

Tissue engineering biologically active peptides

Tissue engineering cellular systems biology

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