Bioavailability of Δ9-tetrahydrocannabinol following intranasal administration of a mucoadhesive gel spray delivery system in conscious rabbits

被引:14
作者
Al-Ghananeem, Abeer M. [1 ]
Malkawi, Ahmad H. [1 ]
Crooks, Peter A. [1 ]
机构
[1] Univ Kentucky, Coll Pharm, Dept Pharmaceut Sci, Lexington, KY 40536 USA
关键词
Chitosan; gel; LC-MS; nasal; pharmacokinetic; Delta(9)-tetrahydrocannabenol; CANNABINOIDS;
D O I
10.3109/03639045.2010.513009
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
Background: The purpose of this study was to investigate the potential of the intranasal route for systemic delivery of solubilized Delta(9)-tetrahydrocannabinol (THC). A further aim was to investigate the effect cf nasally administered chitosan-based nasal bioadhesive gel on THC bioavailability as a formulation strategy to decrease normal mucociliary drug clearance. Method: The THC formulations were administered intranasally and compared to intravenous administration utilizing conscious rabbits. Results: After nasal administration, the THC nasal solution afforded a C-max value of 20 +/- 3 ng/mL at 20 minutes. Interestingly, the THC loaded in chitosan gel formulation followed almost the same profile at early time points and subsequently afforded a higher C-max value of 31 +/- 4 ng/mL (T-max = 45 minutes). The absolute bioavailability of THC after nasal delivery was studied to compare plasma THC concentrations after nasal administration with those after intravenous injection. Absolute bioavailability values were 13.3 +/- 7.8% and 15.4 +/- 6.5% for the THC nasal solution and gel formulations, respectively. Conclusion: The results of the present study suggest that intranasal administration of THC in solution or in a chitosan-based nasal gel formulation could be an attractive modality for delivery of THC systemically.
引用
收藏
页码:329 / 334
页数:6
相关论文
共 23 条
[1]
ALGHANANEEM AM, 2002, AAPS PHARMSCITECH, V3, P5
[2]
Absorption of insulin from Pluronic F-127 gels following subcutaneous administration in rats [J].
Barichello, JM ;
Morishita, M ;
Takayama, K ;
Nagai, T .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 184 (02) :189-198
[3]
Pharmacokinetic and pharmacodynamic response after intranasal administration of diazepam to rabbits [J].
Bechgaard, E ;
Gizurarson, S ;
Hjortkjaer, RK .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1997, 49 (08) :747-750
[4]
Effects of physicochemical properties and other factors on systemic nasal drug delivery [J].
Behl, CR ;
Pimplaskar, HK ;
Sileno, AP ;
deMeireles, J ;
Romeo, VD .
ADVANCED DRUG DELIVERY REVIEWS, 1998, 29 (1-2) :89-116
[5]
Efficacy of two cannabis based medicinal extracts for relief of central neuropathic pain from brachial plexus avulsion: results of a randomised controlled trial [J].
Berman, JS ;
Symonds, C ;
Birch, R .
PAIN, 2004, 112 (03) :299-306
[6]
CYP2C-catalyzed delta(9)-tetrahydrocannabinol metabolism: Kinetics, pharmacogenetics and interaction with phenytoin [J].
Bland, TM ;
Haining, RL ;
Tracy, TS ;
Callery, PS .
BIOCHEMICAL PHARMACOLOGY, 2005, 70 (07) :1096-1103
[7]
Brenneisen R, 1996, INT J CLIN PHARM TH, V34, P446
[8]
CHIEN YW, 1987, CRC CR REV THER DRUG, V4, P67
[9]
Hall W, 2005, LANCET ONCOL, V6, P35, DOI 10.1016/S1470-2045(05)70024-3
[10]
Intranasal drug delivery [J].
Hussain, AA .
ADVANCED DRUG DELIVERY REVIEWS, 1998, 29 (1-2) :39-49