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1.
J Vet Pharmacol Ther ; 36(2): 122-9, 2013 Apr.
Article in English | MEDLINE | ID: mdl-22486358

ABSTRACT

Six adult male alpacas received one subcutaneous administration of ceftiofur crystalline free acid (CCFA) at a dosage of 6.6 mg/kg. After a washout period, the same alpacas received three subcutaneous doses of 6.6 mg/kg CCFA at 5-day intervals. Blood samples collected from the jugular vein before and at multiple time points after each CCFA administration were assayed for ceftiofur- and desfuroylceftiofur-related metabolite concentrations using high-performance liquid chromatography. Pharmacokinetic disposition of CCFA was analyzed by a noncompartmental approach. Mean pharmacokinetic parameters (± SD) following single-dose administration of CCFA were Cmax (2.7 ± 0.9 µg/mL); Tmax (36 ± 0 h); area under the curve AUC0→∞ (199.2 ± 42.1 µg·h/mL); terminal phase rate constant λz (0.02 ± 0.003/h); and terminal phase rate constant half-life t1/2λz (44.7 h; harmonic). Mean terminal pharmacokinetic parameters (±SD) following three administrations of CCFA were Cmax (2.0 ± 0.4 µg/mL); Tmax (17.3 ± 16.3 h); AUC0→∞ (216.8 ± 84.5 µg·h/mL); λz (0.01 ± 0.003/h); and t1/2λz (65.9 h; harmonic). The terminal phase rate constant and the Tmax were significantly different between single and multiple administrations. Local reactions were noted in two alpacas following multiple CCFA administrations.


Subject(s)
Anti-Bacterial Agents/pharmacokinetics , Camelids, New World/metabolism , Cephalosporins/pharmacokinetics , Animals , Anti-Bacterial Agents/administration & dosage , Area Under Curve , Bacteria/drug effects , Cephalosporins/administration & dosage , Drug Administration Schedule , Half-Life , Injections, Subcutaneous/veterinary , Male , Microbial Sensitivity Tests
2.
J Vet Pharmacol Ther ; 33(6): 605-9, 2010 Dec.
Article in English | MEDLINE | ID: mdl-21062314

ABSTRACT

Progesterone (P4)-impregnated intravaginal controlled internal drug-releasing devices (CIDRs) have been used worldwide for estrus synchronization in ruminants. CIDRs serve to place all treated animals in the luteal phase of the estrous cycle. The objectives of this study were to compare P4 concentrations in milk from normal reproductively cycling, CIDR-treated, and pregnant goats. CIDRs were placed in treatment goats on day 0 and removed on day 19. Milk was collected daily from day 0 to day 21 from control and CIDR-treated goats and for 5 consecutive days between 40 and 60 days of gestation from pregnant does. Milk P4 was plotted against time (in days) for each individual, and the area under the curve (AUC) was calculated as an estimate of total milk P4. The AUC(day 0-21) for control and CIDR-treated goats were 29.5 ± 11.9 and 33.7 ± 6.6 d·ng/mL, respectively (P = 0.77). The highest single-day and highest 5-day average P4 values for each animal were also compared among groups. Single-day peak P4 levels were 4.8 ± 1.5, 4.0 ± 1.0, and 6.0 ± 0.4 ng/mL for control, CIDR-treated, and pregnant goats (P = 0.42). The highest 5-day average P4 concentrations were 3.6 ± 1.3, 2.9 ± 1.8, and 4.2 ± 0.3 for control, CIDR-treated, and pregnant goats (P = 0.56). The results of this study show that intravaginal P4 CIDR devices inserted for 19 days in healthy goats resulted in milk P4 levels similar to or less than those endogenously produced during diestrus or pregnancy.


Subject(s)
Goats/metabolism , Milk/chemistry , Progesterone/administration & dosage , Animals , Drug Implants , Drug Residues/analysis , Estrus/drug effects , Female , Pregnancy , Pregnancy Outcome , Progesterone/analysis , Progesterone/pharmacokinetics , Radioimmunoassay/veterinary
3.
J Am Pharm Assoc (2003) ; 49(3): 446-52, 2009.
Article in English | MEDLINE | ID: mdl-19443327

ABSTRACT

OBJECTIVE: To describe how U.S. Public Health Service (PHS) pharmacists serving in jobs that are normal for them, but considerably different than those found in the private sector, are making a difference in advancing the nation's health. SUMMARY: Pharmacists who serve in the Commissioned Corps of PHS fill roles that are considerably different than their counterparts in the private sector. Their work takes them out from behind the counter and into the world. Pharmacy officers advance the health and safety of the nation by their involvement in the delivery of direct patient care to medically underserved people, national security, drug vigilance, research, and policy-making endeavors. PHS pharmacists fill essential public health leadership and service roles throughout the U.S. Department of Health and Human Services (HHS) and certain non-HHS federal agencies and programs. The Health Resources and Services Administration, National Institutes of Health, Federal Bureau of Prisons, Indian Health Service, Food and Drug Administration, and U.S. Coast Guard are among the many federal agencies in which pharmacy officers are assigned. CONCLUSION: In each setting, PHS pharmacists find traditional roles augmented with assignments and challenges that broaden the scope of their practice.


Subject(s)
Pharmaceutical Services/organization & administration , Pharmacists/organization & administration , United States Public Health Service/organization & administration , Career Choice , Delivery of Health Care/organization & administration , Humans , Professional Role , United States
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