New effective azelaic acid liposomal gel formulation of enhanced pharmaceutical bioavailability

被引:39
作者
Burchacka, E. [1 ]
Potaczek, P. [2 ]
Paduszynski, P. [2 ]
Karlowicz-Bodalska, K. [3 ]
Han, T. [3 ]
Han, S. [3 ]
机构
[1] Wroclaw Univ Technol, Dept Microbiol & Med Chem, Wyspianskiego Str 25, PL-50370 Wroclaw, Poland
[2] Res & Dev Ctr NOVASOME, Olsztynska Str 5, PL-51423 Wroclaw, Poland
[3] Wroclaw Med Univ, Dept Ind Pharm, Borowska Str 211, PL-50556 Wroclaw, Poland
关键词
Azelaic acid; Liposomal hydrogel; Pharmaceutical formulation; DRUG-DELIVERY; DERMAL DELIVERY; PARTICLE-SIZE; SKIN;
D O I
10.1016/j.biopha.2016.07.014
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Azelaic acid is a naturally occurring saturated C9-dicarboxylic acid which has been shown to be effective in the treatment of comedonal acne and inflammatory acne, as well as hiperpigmentary skin disorders. The aim of the present study is to compare new developed liposomal hydrogel (lipogel) and commercially available product in terms of the active substance-azelaic acid bioavailability. Topical formulations were evaluated for physical parameters, such as pH measurement, organoleptic evaluation and liposome size analysis in lipogel formulation. In addition, studies were performed on in vitro antimicrobial preservation, stability and accumulation in the stratum corneum according to guidelines established by European Pharmacopoeia and International Conferences on Harmonisation. The new formula for liposomal gel with azelaic acid has the stability required for pharmaceutical preparations. Moreover, presented formulation F2 reveals a very high accumulation (187.5 mu g/cm(2)) of an active substance in the stratum corneum, which results in opportunity to decrease of the API content to 10% in comparison to a reference formula: commercially available cream with 20% of azelaic acid. The study reveals that the final formula of lipogel F2 with azelaic acid had acceptable physical parameters that showed that they were compatible with the skin and in addition this formulation passed stability studies. In vitro antimicrobial preservation studies showed that the formulated lipogel F2 showed strong antibacterial activity; thus, no preservatives were added to the final composition of the preparation. The present study concludes that the formulated lipogel F2 with azelaic acid is stable, efficient in antimicrobial preservation and reveals improved active substance bioavailability. (C) 2016 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:771 / 775
页数:5
相关论文
共 22 条
[1]
Braun-Falco O, 2000, Dermatology, V2nd, P1101, DOI [10.1007/978-3-642-97931-6, DOI 10.1007/978-3-642-97931-6]
[2]
The skin: A pathway for systemic treatment with patches and lipid-based agent carriers [J].
Cevc, G ;
Blume, G ;
Schatzlein, A ;
Gebauer, D ;
Paul, A .
ADVANCED DRUG DELIVERY REVIEWS, 1996, 18 (03) :349-378
[3]
THE INFLUENCE OF PARTICLE-SIZE OF LIPOSOMES ON THE DEPOSITION OF DRUG INTO SKIN [J].
DUPLESSIS, J ;
RAMACHANDRAN, C ;
WEINER, N ;
MULLER, DG .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1994, 103 (03) :277-282
[4]
TOPICAL APPLICATION OF LIPOSOMALLY ENTRAPPED CICLOSPORIN EVALUATED BY INVITRO DIFFUSION STUDIES WITH HUMAN SKIN [J].
EGBARIA, K ;
RAMACHANDRAN, C ;
WEINER, N .
SKIN PHARMACOLOGY, 1991, 4 (01) :21-28
[5]
Liposomes and skin: From drug delivery to model membranes [J].
El Maghraby, G. M. ;
Barry, B. W. ;
Williams, A. C. .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2008, 34 (4-5) :203-222
[6]
Can drug-bearing liposomes penetrate intact skin? [J].
El Maghraby, GMM ;
Williams, AC ;
Barry, BW .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2006, 58 (04) :415-429
[7]
Lipid vesicles for skin delivery of drugs: Reviewing three decades of research [J].
Elsayed, Mustafa M. A. ;
Abdallah, Ossama Y. ;
Naggar, Viviane F. ;
Khalafallah, Nawal M. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2007, 332 (1-2) :1-16
[8]
Application of liposomes as potential cutaneous drug delivery systems. In vitro and in vivo investigation with radioactively labelled vesicles [J].
Fresta, M ;
Puglisi, G .
JOURNAL OF DRUG TARGETING, 1996, 4 (02) :95-101
[9]
Fresta M, 1997, J CONTROL RELEASE, V44, P141, DOI 10.1016/S0168-3659(96)01519-2
[10]
Liposome encapsulated of temozolomide for the treatment of glioma tumor: preparation, characterization and evaluation [J].
Gao, Jinhua ;
Wang, Zhonglan ;
Liu, Honghai ;
Wang, Longmei ;
Huang, Guihua .
DRUG DISCOVERIES AND THERAPEUTICS, 2015, 9 (03) :205-212