• Je něco špatně v tomto záznamu ?

Pharmacokinetics of Ciclopirox Olamine after Buccal Administration in Rabbits

I. Lukášová, J. Muselík, D. Vetchý, J. Gajdziok, M. Gajdošová, J. Juřica, Z. Knotek, K. Hauptman, V. Jekl,

. 2017 ; 14 (1) : 99-108.

Jazyk angličtina Země Spojené arabské emiráty

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc17031764

Grantová podpora
NT14477 MZ0 CEP - Centrální evidence projektů

BACKGROUND: Prevalence of oral mucosal fungal infections increases with the frequent administration of antibiotics, corticosteroids and immunosuppressive drugs. Therapeutically used antifungals are usually associated with a variety of drug interactions. Furthermore, there has been a noticeable increase in microorganisms resistant to these preparations. Mucoadhesive buccal films represent a modern therapeutic system for the treatment of oral mucosal fungal infection paired with a high degree of patient compliance. Ciclopirox olamine applied directly onto the oral mucosa offers an attractive alternative to treatment with systemic antifungals thanks to its low incidence of resistance and side effects. OBJECTIVE: The aim of this work was to evaluate the pharmacokinetic parameters of ciclopirox olamine after the buccal application of mucoadhesive film prepared by the solvent casting method. METHOD: A chromatographic method using an internal standard was developed and validated for evaluation of ciclopirox olamine plasma concentrations. Method accuracy was 88.5-104.6% and 89.5-99.7% for interday and intraday assays, respectively. RESULTS: The pharmacokinetic properties of ciclopirox olamine were studied in New Zealand White rabbits. The mucoadhesive films containing ciclopirox olamine in a total dose of 34.4 (33.0; 35.9) mg kg-1 were applied to all the rabbits. Plasma ciclopirox olamine concentrations were determined during the 12 h following application. The time taken to reach maximum plasma concentration was 1.7 (1.1; 2.2) h after the drug administration with cmax 5.73 (4.18; 7.28) μg mL-1. Overall elimination half-life was 3.8 (1.9; 10.8) h. CONCLUSION: The experiment suggests that oral mucoadhesive film may be a valuable alternative ciclopirox olamine administration.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc17031764
003      
CZ-PrNML
005      
20190516150429.0
007      
ta
008      
171025s2017 ts f 000 0|eng||
009      
AR
024    7_
$a 10.2174/1567201813666160502142856 $2 doi
035    __
$a (PubMed)27138296
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a ts
100    1_
$a Lukášová, Ivana $7 _AN095711 $u Department of Pharmaceutics, Faculty of Pharmacy, University of Veterinary and Pharmaceutical Sciences Brno, Palackého tř. 1946/1, 612 42 Brno, Czech Republic
245    10
$a Pharmacokinetics of Ciclopirox Olamine after Buccal Administration in Rabbits / $c I. Lukášová, J. Muselík, D. Vetchý, J. Gajdziok, M. Gajdošová, J. Juřica, Z. Knotek, K. Hauptman, V. Jekl,
520    9_
$a BACKGROUND: Prevalence of oral mucosal fungal infections increases with the frequent administration of antibiotics, corticosteroids and immunosuppressive drugs. Therapeutically used antifungals are usually associated with a variety of drug interactions. Furthermore, there has been a noticeable increase in microorganisms resistant to these preparations. Mucoadhesive buccal films represent a modern therapeutic system for the treatment of oral mucosal fungal infection paired with a high degree of patient compliance. Ciclopirox olamine applied directly onto the oral mucosa offers an attractive alternative to treatment with systemic antifungals thanks to its low incidence of resistance and side effects. OBJECTIVE: The aim of this work was to evaluate the pharmacokinetic parameters of ciclopirox olamine after the buccal application of mucoadhesive film prepared by the solvent casting method. METHOD: A chromatographic method using an internal standard was developed and validated for evaluation of ciclopirox olamine plasma concentrations. Method accuracy was 88.5-104.6% and 89.5-99.7% for interday and intraday assays, respectively. RESULTS: The pharmacokinetic properties of ciclopirox olamine were studied in New Zealand White rabbits. The mucoadhesive films containing ciclopirox olamine in a total dose of 34.4 (33.0; 35.9) mg kg-1 were applied to all the rabbits. Plasma ciclopirox olamine concentrations were determined during the 12 h following application. The time taken to reach maximum plasma concentration was 1.7 (1.1; 2.2) h after the drug administration with cmax 5.73 (4.18; 7.28) μg mL-1. Overall elimination half-life was 3.8 (1.9; 10.8) h. CONCLUSION: The experiment suggests that oral mucoadhesive film may be a valuable alternative ciclopirox olamine administration.
650    _2
$a aplikace bukální $7 D000278
650    _2
$a zvířata $7 D000818
650    _2
$a antifungální látky $x aplikace a dávkování $x krev $x farmakokinetika $7 D000935
650    _2
$a vztah mezi dávkou a účinkem léčiva $7 D004305
650    _2
$a mužské pohlaví $7 D008297
650    _2
$a molekulární struktura $7 D015394
650    _2
$a pyridony $x aplikace a dávkování $x krev $x farmakokinetika $7 D011728
650    _2
$a králíci $7 D011817
655    _2
$a časopisecké články $7 D016428
700    1_
$a Muselík, Jan $u Department of Pharmaceutics, Faculty of Pharmacy, University of Veterinary and Pharmaceutical Sciences Brno, Palackého tř. 1946/1, 612 42 Brno, Czech Republic. $7 xx0100243
700    1_
$a Vetchý, David, $d 1972- $7 mzk2006368163
700    1_
$a Gajdziok, Jan $7 xx0126570
700    1_
$a Gajdošová, Markéta $7 ola20191054731
700    1_
$a Juřica, Jan $7 xx0085543
700    1_
$a Knotek, Zdeněk, $d 1956- $7 ola2004235496
700    1_
$a Hauptman, Karel $7 xx0035942
700    1_
$a Jekl, Vladimír $7 xx0044308
773    0_
$w MED00008817 $t Current drug delivery $x 1875-5704 $g Roč. 14, č. 1 (2017), s. 99-108
856    41
$u https://pubmed.ncbi.nlm.nih.gov/27138296 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20171025 $b ABA008
991    __
$a 20190516150536 $b ABA008
999    __
$a ok $b bmc $g 1255357 $s 992791
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2017 $b 14 $c 1 $d 99-108 $i 1875-5704 $m Current drug delivery $n Curr Drug Deliv $x MED00008817
GRA    __
$a NT14477 $p MZ0
LZP    __
$a Pubmed-20171025

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...