Characterization of alkanoyl-10-O-minocyclines in micellar dispersions as potential agents for treatment of human neurodegenerative disorders

被引:11
作者
Di Stefano, Antonio [1 ]
Sozio, Piera [1 ]
Iannitelli, Antonio [1 ]
Cerasa, Laura Serafina [1 ]
Fontana, Antonella [1 ]
Di Biase, Giuseppe [1 ]
D'Amico, Guglielmo [1 ]
Di Giulio, Mara [2 ]
Carpentiero, Carmen [3 ]
Grumetto, Lucia [3 ]
Barbato, Francesco [3 ]
机构
[1] Univ G dAnnunzio, Dipartimento Sci Farm, I-66100 Chieti, Italy
[2] Univ G dAnnunzio, Dipartimento Sci Biomed, I-66100 Chieti, Italy
[3] Univ Naples Federico II, Dipartimento Chim Farm & Tossicol, I-80131 Naples, Italy
关键词
minocycline; micellar aggregates; brain targeting; lipophilicity; phospholipid partition; IAM;
D O I
10.1016/j.ejps.2008.02.123
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Minocycline is a widely used antibacterial agent. Moreover, it is also demonstrated to be effective in several neurodegenerative disorders, due to its antioxidant and anti-inflammatory activities. However, the last activity is only apparent at very high doses. in fact, minocycline poorly crosses the blood-brain barrier (BBB) due to its low lipophilicity and half-life. The present work details the physicochemical characterization of a series of alkanoyl-10-O-minocycline derivatives (2-6), which are able to produce self-assembled aggregates in aqueous solution. The n-octanol/aqueous phase lipophilicity of minocycline and its derivatives were assessed by theoretical calculation, by shake-flask method, and by reversed-phase HPLC. Moreover, we determined their affinity for membrane phospholipids measuring their HPLC retention on phospholipid-based stationary phases, the so-called "Immobilized Artificial Membranes" (IAMs). Our results indicate high lipophilicity values for the minocycline derivatives (compounds 2-6); these values and the corresponding phospholipid affinities increase with the length of the hydrocarbon moiety substituent. Furthermore, the ability of the investigated alkanoyl-10-O-minocycline derivatives to self-assemble could allow a direct administration by oral and intraperitoneal routes as supramolecular systems. The advantages are an enhancement of drug solubilization, a sustained release, and the consequent less frequent drug administration. Moreover, we can hypothesize the potential solubilization in the micellar core of other poorly water soluble drugs which could improve the therapeutic effects of the pharmaceutical formulation in a combined therapy. Given the high lipophilicity of the title derivatives, they can be supposed to offer higher half-life and a better BBB penetration than minocycline. Since the new derivatives retain the structural features related to the antioxidant and anti-inflammatory effects of minocycline, they can be regarded not only as long-acting antimicrobial agents but also as candidate drugs for a targeted treatment of mental illness. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:118 / 128
页数:11
相关论文
共 37 条
[1]  
ABATO P, 2007, Patent No. 2007014154
[2]   Chromatographic indexes on immobilized artificial membranes for local anesthetics: Relationships with activity data on closed sodium channels [J].
Barbato, F ;
La Rotonda, MI ;
Quaglia, F .
PHARMACEUTICAL RESEARCH, 1997, 14 (12) :1699-1705
[3]   Can protonated β-blockers interact with biomembranes stronger than neutral isolipophilic compounds?: A chromatographic study on three different phospholipid stationary phases (IAM-HPLC) [J].
Barbato, F ;
di Martino, G ;
Grumetto, L ;
La Rotonda, MI .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2005, 25 (4-5) :379-386
[4]   Prediction of drug-membrane interactions by IAM-HPLC: effects of different phospholipid stationary phases on the partition of bases [J].
Barbato, F ;
di Martino, G ;
Grumetto, L ;
La Rotonda, MI .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2004, 22 (04) :261-269
[5]   Chromatographic indices determined on an immobilized artificial membrane (IAM) column as descriptors of lipophilic and polar interactions of 4-phenyldihydropyridine calcium-channel blockers with biomembranes [J].
Barbato, F ;
LaRotonda, MI ;
Quaglia, F .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 1996, 31 (04) :311-318
[7]   Comparison between immobilized artificial membrane (IAM) HPLC data and lipophilicity in n-octanol for quinolone antibacterial agents [J].
Barbato, Francesco ;
Cirocco, Valentina ;
Grumetto, Lucia ;
La Rotonda, Maria Immacolata .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2007, 31 (05) :288-297
[8]   Clinical potential of minocycline for neurodegenerative disorders [J].
Blum, D ;
Chtarto, A ;
Tenenbaum, L ;
Brotchi, J ;
Levivier, M .
NEUROBIOLOGY OF DISEASE, 2004, 17 (03) :359-366
[9]   QUANTITATIVE STRUCTURE-ACTIVITY-RELATIONSHIPS FOR HERBICIDES - REVERSED-PHASE LIQUID-CHROMATOGRAPHIC RETENTION PARAMETER, LOG KW, VERSUS LIQUID-LIQUID PARTITION-COEFFICIENT AS A MODEL OF THE HYDROPHOBICITY OF PHENYLUREAS, S-TRIAZINES AND PHENOXYCARBONIC ACID-DERIVATIVES [J].
BRAUMANN, T ;
WEBER, G ;
GRIMME, LH .
JOURNAL OF CHROMATOGRAPHY, 1983, 261 (03) :329-343
[10]  
Buccafusco JJ, 2000, J PHARMACOL EXP THER, V295, P438