Pharmacokinetics and oral bioavailability of cannabidiol in horses after intravenous and oral administration with oil and micellar formulations

被引:8
|
作者
de Medina, Antonia Sanchez [1 ,2 ]
Serrano-Rodriguez, Juan Manuel [3 ]
de Castro, Elisa Diez [1 ,2 ]
Garcia-Valverde, Maria Teresa [4 ]
Saitua, Aritz [1 ]
Becero, Mireia [1 ]
Munoz, Ana [2 ,5 ]
Ferreiro-Vera, Carlos [4 ]
de Medina, Veronica Sanchez [4 ]
机构
[1] Univ Cordoba, Vet Clin Hosp, Cordoba, Spain
[2] Univ Cordoba, Vet Fac, Dept Anim Med & Surg, Cordoba, Spain
[3] Univ Cordoba, Vet Fac, Dept Nursing Pharmacol & Physiotherapy, Cordoba, Spain
[4] Phytoplant Res SLU, Cordoba, Spain
[5] Univ Cordoba, Vet Fac, Equine Sport Med Ctr CEMEDE, Dept Anim Med & Surg, Cordoba, Spain
关键词
bioavailability; cannabidiol; horse; micellar; oil; pharmacokinetics; SIMULATION;
D O I
10.1111/evj.13923
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Background: Intravenous pharmacokinetics and oral bioavailability of cannabidiol (CBD) with different formulations have not been investigated in horses and may represent a starting point for clinical studies. Objectives: To describe pharmacokinetics after intravenous and oral administrations with oil and micellar formulations and simulate different treatments. Study design: Single intravenous experiment and two-way randomised oral experiments, Latin-square design. Methods: Eight healthy horses received intravenous CBD at 1.00 mg/kg dose, oral CBD in sesame oil and in micellar formulation, both at 10.00 mg/kg. Concentrations were measured using LC-MS/MS and fitted by nonlinear mixed effect modelling. Parameters obtained were used to simulate single and multiple treatments at steady state. Results: Intravenous and oral concentrations were simultaneously fitted using a three-compartment model. Final estimates indicate that CBD has a volume of distribution of 36 L/kg associated with a systemic clearance of 1.46 L/h/kg and half-lives ranged between 24 and 34 h. Oral bioavailability was close to 14% for both oral administrations. Simulated dose regimen of CBD every 12 and 24 h predicted similar percentages to reach effective plasma concentration with both oral formulation at 10.00 mg/kg. Main limitations: A small horse population was used (8 horses per trial). Conclusions and clinical importance: Oral bioavailability was low at the doses studied but fell within the range described for horse and other species. CBD had a high steady-state volume of distribution, a high clearance and long half-lives. No adverse reactions were detected at any dose or route. The micellar formulation showed a faster absorption and higher concentration peak, while the oil formulation presented lower levels, but more maintained over time. Simulations predicted that both could be useful in multiple oral dose treatments. These results indicated that CBD could be of interest, but further studies are needed to evaluate its clinical use in horses.
引用
收藏
页码:1094 / 1103
页数:10
相关论文
共 50 条
  • [41] Pharmacokinetics of vitexin in rats after intravenous and oral administration
    Wang, Yunjiao
    Han, Chunhui
    Leng, Aijing
    Zhang, Wenjie
    Xue, Hefei
    Chen, Yinghui
    Yin, Jingjing
    Lu, Dongrui
    Ying, Xixiang
    AFRICAN JOURNAL OF PHARMACY AND PHARMACOLOGY, 2012, 6 (31): : 2368 - 2373
  • [42] Pharmacokinetics of pefloxacin in goats after intravenous or oral administration
    Malik, JK
    Rao, GS
    Ramesh, S
    Muruganandan, S
    Tripathi, HC
    Shukla, DC
    VETERINARY RESEARCH COMMUNICATIONS, 2002, 26 (02) : 141 - 149
  • [43] THE PHARMACOKINETICS OF A SLOW-RELEASE THEOPHYLLINE PREPARATION IN HORSES AFTER INTRAVENOUS AND ORAL-ADMINISTRATION
    ERRECALDE, JO
    LANDONI, MF
    VETERINARY RESEARCH COMMUNICATIONS, 1992, 16 (02) : 131 - 138
  • [44] PHARMACOKINETICS OF VALPROIC ACID AFTER ORAL AND INTRAVENOUS ADMINISTRATION
    PERUCCA, E
    GATTI, G
    FRIGO, GM
    CREMA, A
    BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1978, 5 (04) : 313 - 318
  • [45] PHARMACOKINETICS OF PHENYLETHYLMALONAMIDE (PEMA) AFTER ORAL AND INTRAVENOUS ADMINISTRATION
    PISANI, F
    RICHENS, A
    CLINICAL PHARMACOKINETICS, 1983, 8 (03) : 272 - 276
  • [46] PHARMACOKINETICS OF FTORAFUR AFTER INTRAVENOUS AND ORAL-ADMINISTRATION
    ANTTILA, MI
    SOTANIEMI, EA
    KAIRALUOMA, MI
    MOKKA, RE
    SUNDQUIST, HT
    CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1983, 10 (03) : 150 - 153
  • [47] Pharmacokinetics of luxabendazole after oral and intravenous administration to sheep
    Ortiz, AI
    AlvarezBujidos, L
    Ferre, I
    Ordonez, D
    AMERICAN JOURNAL OF VETERINARY RESEARCH, 1997, 58 (11) : 1263 - 1266
  • [48] Pharmacokinetics of verproside after intravenous and oral administration in rats
    Park, Eun Jeong
    Lee, Hyun Sook
    Oh, Sei-Ryang
    Lee, Hyeong-Kyu
    Lee, Hye Suk
    ARCHIVES OF PHARMACAL RESEARCH, 2009, 32 (04) : 559 - 564
  • [49] Pharmacokinetics of doxycycline in sheep after intravenous and oral administration
    Castro, Luis J.
    Sahagun, Ana M.
    Jose Diez, M.
    Fernandez, Nelida
    Sierra, Matilde
    Garcia, Juan J.
    VETERINARY JOURNAL, 2009, 180 (03): : 389 - 395
  • [50] PHARMACOKINETICS OF ACYCLOVIR AFTER INTRAVENOUS AND ORAL-ADMINISTRATION
    DEMIRANDA, P
    BLUM, MR
    JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1983, 12 : 29 - 37