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Table 1 Pharmacokinetic variables for doxycycline hyclate (Dox-h) in horses after the oral administration of three experimental formulations

From: Pharmacokinetics of a peroral single dose of two long-acting formulations and an aqueous formulation of doxycycline hyclate in horses

 

Dox-a

Dox-pol|

Dox-β

 

Mean ± SD

Mean ± SD

Mean ± SD

AUC (μg · h/mL)

3.1 ± 0.2 a

17.0 ± 2.2b

1.5 ± 0.1 c

AUMC (μg · h2/mL)

35.2 ± 1.2 a

208.3 ± 31.1b

12.3 ± 0.1 c

AUC0 -∞ (μg · h/mL)

3.0 ± 0.2 a

16.1 ± 4.8 b

1.5 ± 0.9 c

AUMC0 -∞ (μg · h2/mL)

31.2 ± 2.3 a

171.3 ± 5.8 b

12.3 ± 0.5 c

MRT (h)

11.3 ± 4.4 a

12.2 ± 4.2a

8.1 ± 2.1 a

MRT0 -∞ (h)

10.2 ± 2.6 a

10.7 ± 2.1 a

8.1 ± 1.2 a

T½β (h)

2.8 ± 0.9a

4.9 ± 1.0b

4.2 ± 0.9b

T½ab(h)

1.2 ± 0.2 a

3.5 ±1.2 b

1.4 ± 0.1 a

Kel (h-1)

0.2 ± 0.0 a

0.1 ± 0.1 a

0.2 ± 0.1 a

Kab (h-1)

1.6 ± 0.2 a

0.2 ± 0.2 b

0.5 ± 0.3 c

α (h-1)

1.2 ± 0.0

-

-

β (h-1)

9.2 ± 0.0

-

-

Cmax (μg/mL)

0.3 ± 0.1 a

1.3 ± 0.7 b

0.2 ± 0.0 c

Tmax (h)

2.2 ± 0.4 a

5.9 ± 1.7 b

3.4 ± 0.6 c

Frel (%)*

-

548% a

48% b

  1. a,b,c, The values within a row with no common superscript differ significantly (P < 0.05).
  2. * Mean of means.
  3. AUC, Area under the concentration-time curve; AUC 0 - ∞ , Area under the concentration –time to infinity; AUMC, Area under the first moment of the concentration-time curve; AUMC 0 - ∞ , Area under the first moment of the concentration-time curve to infinity; MRT, Mean residence time; MRT 0 - ∞ , Mean residence time to infinity; α, distribution hybrid rate constant; β, elimination hybrid rate constant; A, B,, zero time intercepts of the distribution and post-distribution phases; K el , Elimination rate constant from the central compartment; Kab, Absorption rate constant; T ½ab , Absorption half-life; T ½β , Elimination half-life; Cmax, Calculated maximum plasma concentration; Tmax, Time of maximum plasma concentration; Frel, Relative bioavailability.