L-Carnitine ester of prednisolone: Pharmacokinetic and pharmacodynamic evaluation of a type I prodrug

被引:17
作者
Mo, Jingxin [1 ]
Lim, Lee Yong [1 ]
Zhang, Zhi-Rong [2 ]
机构
[1] Univ Western Australia, Sch Med & Pharmacol, Crawley, WA 6009, Australia
[2] Sichuan Univ, West China Sch Pharm, Minist Educ, Key Lab Drug Targeting & Drug Delivery Syst, Chengdu 610041, Sichuan, Peoples R China
关键词
Prednisolone; L-Carnitine; Prodrug; Asthma; Pharmacokinetics-pharmacodynamics; TRANSPORTER OCTN2; ASTHMA; MECHANISM;
D O I
10.1016/j.ijpharm.2014.08.049
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Purpose: To evaluate whether PDSC, an L-carnitine ester derivative of prednisolone and OCTN2 substrate, could provide a targeted delivery of the corticosteroid into the lung tissues of an asthmatic guinea pig model. Methods: PRED (prednisolone) and PDC (an L-carnitine prodrug of prednisolone not recognized by OCTN2) served as controls. Water solubility and log P values were determined, and PDSC and PDC in vivo were quantified by LC-MS/MS. Results: Unlike PRED, the intra-tracheal instillation of PDSC resulted in effective and prolonged accumulation of prednisolone in the lung tissues, leading to 3.8-fold higher reduction in inflammatory cell count in the bronchoalveolar fluid, and less severe lung and bronchial lesions in the asthmatic guinea pig. PDC showed similar pharmacokinetic profile to PRED, but exhibited higher efficiency (1.7-fold higher) at reducing the inflammatory cell count and the severity of lung histopathology, possibly due to the release of L-carnitine in vivo. Conclusions: The collective data suggest that PDSC has the potential to be an effective prodrug for the treatment of asthma with concomitant reduction in systemic side effects, and that novel prodrugs produced by L-carnitine conjugation can have useful applications in the targeted accumulation of drugs in the lungs. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:123 / 129
页数:7
相关论文
共 20 条
[1]   Micro-particle corrugation, adhesion and inhalation aerosol efficiency [J].
Adi, Santoso ;
Adi, Handoko ;
Tang, Patricia ;
Traini, Daniela ;
Chan, Hak-Kim ;
Young, Paul M. .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2008, 35 (1-2) :12-18
[2]  
AHMAD S, 1989, Kidney International Supplement, pS243
[3]  
AlBiltagi M., 2012, J Allergy
[4]   Solubility of Budesonide, Hydrocortisone, and Prednisolone in Ethanol plus Water Mixtures at 298.2 K [J].
Ali, Hany S. M. ;
York, Peter ;
Blagden, Nicholas ;
Soltanpour, Shahla ;
Acree, William E., Jr. ;
Jouyban, Abolghasem .
JOURNAL OF CHEMICAL AND ENGINEERING DATA, 2010, 55 (01) :578-582
[5]   CARNITINE - METABOLISM AND FUNCTIONS [J].
BREMER, J .
PHYSIOLOGICAL REVIEWS, 1983, 63 (04) :1420-1480
[6]   DETERMINATION OF PARTITION-COEFFICIENTS OF GLUCOCORTICOSTEROIDS BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
CARON, JC ;
SHROOT, B .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1984, 73 (12) :1703-1706
[7]   Global burden of allergic bronchopulmonary aspergillosis with asthma and its complication chronic pulmonary aspergillosis in adults [J].
Denning, David W. ;
Pleuvry, Alex ;
Cole, Donald C. .
MEDICAL MYCOLOGY, 2013, 51 (04) :361-370
[8]   An update on the role of leukotrienes in asthma [J].
Hallstrand, Teal S. ;
Henderson, William R., Jr. .
CURRENT OPINION IN ALLERGY AND CLINICAL IMMUNOLOGY, 2010, 10 (01) :60-66
[9]   Mechanism of the inhibitory effect of zwitterionic drugs (levofloxacin and grepafloxacin) on carnitine transporter (OCTN2) in Caco-2 cells [J].
Hirano, Takeshi ;
Yasuda, Satoru ;
Osaka, Yuki ;
Kobayashi, Masaki ;
Itagaki, Shirou ;
Iseki, Ken .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2006, 1758 (11) :1743-1750
[10]  
Kavukcu S, 1998, TURKISH J PEDIATR, V40, P79