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. Author manuscript; available in PMC: 2011 Dec 1.
Published in final edited form as: Pharm Res. 2010 Sep 25;27(12):2753–2765. doi: 10.1007/s11095-010-0277-5

Table II.

Characterization of fluorescein and thrombin emulsions. Thrombin precipitation, during the second emulsification step, and subsequent inactivation of thrombin during ADV was suspected in T2.

Formulation Mean diameter (μm) Percent of droplets > 6 μm diameter
Encapsulation (%) Volume percent vaporized Percent change in ACT upon ADV
Number Volume
F2 2.4 ± 0.2 2.6 ± 1.8 32.3 ± 15.4 3.8 ± 1.1 100 c NA
T1 1.6 ± 0.1 0.04 ± 0.02 6.7 ±3.0 76.3 ± 3.4 10.2 ± 4.2 −7.4 ± 1.6
T2 2.6 ± 0.2 6.5 ± 1.4 83.2 ± 1.0 63.7 ± 22.9 a 25.6 ± 7.1 63.0 ± 12.2 a,b
T3 27.4 ± 5.9 89.2 ± 1.1 99.9 ± 0.1 97.5 ± 0.6 100c −78.0 ± 13.5 b
T4 3.5 ± 0.1 15.5 ± 0.8 89.4 ± 4.5 98.8 ± 1.1 28.7 ± 10.2 −23.3 ± 5.9 b
T5 3.9 ± 0.1 17.6 ± 0.5 88.9 ± 3.1 97.2 ± 0.5 34.3 ± 15.9 −19.0 ± 4.9 b
a

T2 parameters that are potentially affected by thrombin precipitation

b

Statistically significant differences for the percent change in ACT upon ADV

c

Cases where complete vaporization was observed, and thus the number of droplets remaining in solution after ADV was below the noise threshold of the Coulter counter