A Comparison of the Penetration and Permeation of Caffeine into and through Human Epidermis after Application in Various Vesicle Formulations

被引:37
作者
Abd, Eman [1 ,3 ]
Roberts, Michael S. [1 ,2 ]
Grice, Jeffrey E. [1 ]
机构
[1] Univ Queensland, Translat Res Inst, Therapeut Res Ctr, Sch Med, Level 5,37 Kent St, Brisbane, Qld 4102, Australia
[2] Univ S Australia, Sch Pharm & Med Sci, Adelaide, SA 5001, Australia
[3] Coll Hlth & Med Technol, Baghdad, Iraq
关键词
Vesicle systems; Stratum corneum; Hair follicles; Encapsulation efficiency; TRANSDERMAL DRUG-DELIVERY; IN-VITRO; SKIN DELIVERY; PERFORMANCE EVALUATION; NONIONIC SURFACTANTS; VESICULAR CARRIER; HAIR FOLLICLE; LIPOSOMES; NIOSOMES; TRANSFERSOMES;
D O I
10.1159/000441040
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background/Aims: A range of vesicles is now widely used to carry various solutes into and through the epidermis. These usually have the active solute encapsulated within and may be modified to confer flexibility and skin penetration enhancement. Here, we compared the ability of five different vesicle systems to deliver a model hydrophilic drug, caffeine, into and through excised human skin. Methods: In addition to lipids, the vesicle excipients included eucalyptol or oleic acid as penetration enhancers, and decyl polyglucoside as a non-ionic surfactant. Vesicle particle sizes ranged between 135 and 158 nm, and caffeine encapsulation efficiencies were between 46 and 66%. Caffeine penetration and permeation were measured using high-performance liquid chromatography. Results: We found that niosomes, which are liposomes containing a non-ionic surfactant, and transferosomes (ultraflexible vesicles) showed significantly greater penetration into the skin and permeation across the stratum corneum. Significant enhancement of caffeine penetration into hair follicles was found for transferosomes and those liposomes containing oleic acid. Conclusions: We conclude that targeted delivery of the hydrophilic drug caffeine into the skin compartments can be modified using optimized vesicular formulations. (C) 2015 S. Karger AG, Basel
引用
收藏
页码:24 / 30
页数:7
相关论文
共 39 条
[1]   Proniosomes as a drug carrier for transdermal delivery of ketorolac [J].
Alsarra, IA ;
Bosela, AA ;
Ahmed, SM ;
Mahrous, GM .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2005, 59 (03) :485-490
[2]   Formulation and in vitro assessment of minoxidil niosomes for enhanced skin delivery [J].
Balakrishnana, Prabagar ;
Shanmugam, Srinivasan ;
Lee, Won Seok ;
Lee, Won Mo ;
Kim, Jong Oh ;
Oh, Dong Hoon ;
Kim, Dae-Duk ;
Kim, Jung Sun ;
Yoo, Bong Kyu ;
Choi, Han-Gon ;
Woo, Jong Soo ;
Yong, Chul Soon .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2009, 377 (1-2) :1-8
[3]   Human hair follicle: reservoir function and selective targeting [J].
Blume-Peytavi, U. ;
Vogt, A. .
BRITISH JOURNAL OF DERMATOLOGY, 2011, 165 :13-17
[4]  
Budai Livia, 2013, Sci Pharm, V81, P1151, DOI 10.3797/scipharm.1305-11
[5]   Ultraflexible vesicles, transfersomes, have an extremely low pore penetration resistance and transport therapeutic amounts of insulin across the intact mammalian skin [J].
Cevc, G ;
Gebauer, D ;
Stieber, J ;
Schätzlein, A ;
Blume, G .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1998, 1368 (02) :201-215
[6]   TRANSDERMAL DRUG CARRIERS - BASIC PROPERTIES, OPTIMIZATION AND TRANSFER EFFICIENCY IN THE CASE OF EPICUTANEOUSLY APPLIED PEPTIDES [J].
CEVC, G ;
SCHATZLEIN, A ;
BLUME, G .
JOURNAL OF CONTROLLED RELEASE, 1995, 36 (1-2) :3-16
[7]   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
[8]   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
[9]   Skin delivery of 5-fluorouracil from ultradeformable and standard liposomes in-vitro [J].
El Maghraby, GMM ;
Williams, AC ;
Barry, BW .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2001, 53 (08) :1069-1077
[10]   Skin delivery of oestradiol from lipid vesicles: importance of liposome structure [J].
El Maghraby, GMM ;
Williams, AC ;
Barry, BW .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2000, 204 (1-2) :159-169