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Physiological Hints for the Production of Artificial Microbubbles

Accordingly, a detailed series of tests in this laboratory revealed that aqueous solutions of saturated monoglycerides (with acyl chain lengths greater than 10 carbons) combined with [Pg.152]

2 LASER-BASED FLOW CYTOMETRY AND FORWARD-ANGLE LIGHT SCATTERING [Pg.153]

All experimental measurements were carried out with a Coulter EPICS V System. This instrument is a laser-based flow cytometer which, as one of its simpler analytical functions, utilizes light scatter measurements to accurately size cells or similar particles (e.g., artificial surfactant-stabilized microbubbles) suspended in aqueous media. The light scatter measurements are sensitive to particle sizes as small as 0.3 pm in diameter. [Pg.153]

An estimate of the actual concentration of synthetic microbubbles present in the (shaken) artificial-microbubble-surfactant solution, represented by Fig. 9.1(A), is given by the fact that 360-400 particles/sec were consistently detected at a flow rate of approximately 1 ml/30 min in order to produce the histogram shown. Therefore, the calculated approximate concentration of synthetic microbubbles in the sample is 7 x 105 microbubbles/ml. (A similar calculation for the distilled water sample shown in Fig. 9.1(B) results in an estimated concentration of only 5 x 103 microbubbles/ml.) [Pg.156]


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