Microstructure of colloidal liquid aphrons (CLAs) by freeze fracture transmission electron microscopy (FF-TEM)

Author(s):  
Yong-li Yan ◽  
Ning-sheng Zhang ◽  
Cheng-tun Qu ◽  
Li Liu
1992 ◽  
Vol 00 (7) ◽  
pp. 9-9
Author(s):  
Janet L. Burns ◽  
Richard J. Spontak

Traditional methods of sample preparation and analysis in conventional transmission electron microscopy (TEM) are not readily applicable to multicomponent complex liquids which may contain a wealth of microstructural information. Two techniques which facilitate the study of structure in such liquids are freeze-fracture (FF) TEM and cryo-TEM.


Parasitology ◽  
1993 ◽  
Vol 107 (5) ◽  
pp. 545-552 ◽  
Author(s):  
D. L. Lee ◽  
K. A. Wright ◽  
R. R. Shivers

SUMMARYThe surface of the cuticle of adult Nippostrongylus brasiliensis has been studied by means of the freeze-fracture technique and by transmission electron microscopy. Some of the surface coat appears to have been shed from the surface of the cuticle of adults fixed in situ in the intestine of its host and from the surface of individuals removed from the intestine and freeze-fractured. Freeze-fracturing the cuticle of individuals removed from the host has shown that this surface coat varies in thickness from 30 to 90 nm. The epicuticle is about 20 nm thick and cleaves readily to expose E- and P-faces. The P-face of the epicuticle possesses a small number of particles, similar to intra-membranous particles, whilst the E-face possesses a few, widely scattered depressions. Despite the presence of these particles the epicuticle is not considered to be a true membrane. Freeze-fracturing the remainder of the cuticle has confirmed its structure as described by conventional transmission electron microscopy. Clusters of particles on the P-face of the outer epidermal (hypodermal) membrane and corresponding depressions on the E-face of the membrane are thought to be associated with points of attachment of the cuticle to the epidermis (hypodermis). No differences in appearance of the cuticle and its surface layers were observed in individuals taken from 7-, 10-, 13- and 15-day infections.


Author(s):  
Janet L. Burns ◽  
Matthew H. Chestnut ◽  
Richard J. Spontak

Freeze-fracture transmission electron microscopy (FF/TEM) is a well-established and highly-valued technique, often employed in the study of biological systems which are extremely sensitive to structural alteration (e.g., membranes and tissues). The technique relies on rapid specimen cooling to immobilize detailed microstructure, usually in a hydrated environment, prior to fracture and subsequent surface replication. As Zasadzinski and Bailey point out, though, the principle governing this technique is general and can be applied with equal success to the study of “microstructured” or “complex” fluids, i.e., fluids consisting of self-organized supramolecular structures. In this vein, FF/TEM constitutes a powerful means of characterizing the structural attributes of dispersions, emulsions, gels, and liquid crystalline assemblies at relatively high spatial resolution. Such morphological information can prove valuable in the development of the structure-viscosity relationships needed in processing. Here, we demonstrate the utility of FF/TEM in elucidating the role of self-associated structures in three different systems: a chemical reaction environment, a high-internal-phase emulsion, and a nonaqueous gel.


Fuel ◽  
1981 ◽  
Vol 60 (7) ◽  
pp. 619-623 ◽  
Author(s):  
James E. Zajic ◽  
D.G. Cooper ◽  
J.A. Marshall ◽  
D.F. Gerson

Author(s):  
D. W. Coble ◽  
E. O. Kairinen

Examination of hair medulla by transmission electron microscopy (TEM) is difficult because of the keratinous composition of hair and because of sectioning problems that result from insufficient infiltration and nonmiscibility of hair with embedding resins, even those of low viscosity. Although longitudinally cutting or tearing fibers will expose the medulla for embedment or direct viewing, considerable disruption occurs in its structure. Less disruption results from the use of freeze fracture techniques for either transmission or scanning electron microscopy (SEM).Freshly plucked human scalp and beard hairs were submersed in liquid nitrogen for a minimum of three minutes, held at proximal and distal ends with Dumont #10 tweezers, and slowly bent to an arc until the specimens broke at the apex. Customarily, clean bevelled fractures occurred along the tips of the arcs and exposed not only the medulla but also the cortex and cuticle. The fractured specimens were then removed from liquid nitrogen.


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