Investigation of the mechanism of enhanced skin penetration by ultradeformable liposomes

被引:36
作者
Subongkot, Thirapit [1 ]
Pamornpathomkul, Boonnada [1 ]
Rojanarata, Theerasak [1 ]
Opanasopit, Praneet [1 ]
Ngawhirunpat, Tanasait [1 ]
机构
[1] Silpakorn Univ, Fac Pharm, Muang 73000, Nakhon Pathom, Thailand
关键词
ultradeformable liposomes; mechanism of enhanced skin penetration; transmission electron microscopy; confocal laser scanning microscopy; HUMAN STRATUM-CORNEUM; TRANSDERMAL DELIVERY; LIPID VESICLES; DRUG-DELIVERY; CARRIERS; KETOPROFEN; TRANSPORT; TERPENES; INSULIN; SIZE;
D O I
10.2147/IJN.S65287
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
This study aimed to determine the mechanism by which ultradeformable liposomes (ULs) with terpenes enhance skin penetration for transdermal drug delivery of fluorescein sodium, using transmission electron microscopy (TEM) and confocal laser scanning microscopy (CLSM). Skin treated with ULs containing d-limonene, obtained from in vitro skin penetration studies, was examined via TEM to investigate the effect of ULs on ultrastructural changes of the skin, and to evaluate the mechanism by which ULs enhance skin penetration. The receiver medium collected was analyzed by TEM and CLSM to evaluate the mechanism of the drug carrier system. Our findings revealed that ULs could enhance penetration by denaturing intracellular keratin, degrading corneodesmosomes, and disrupting the intercellular lipid arrangement in the stratum corneum. As inferred from the presence of intact vesicles in the receiver medium, ULs are also able to act as a drug carrier system. CLSM images showed that intact vesicles of ULs might penetrate the skin via a transappendageal pathway, potentially a major route of skin penetration.
引用
收藏
页码:3539 / 3550
页数:12
相关论文
共 31 条
[1]   Novel mechanisms and devices to enable successful transdermal drug delivery [J].
Barry, BW .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2001, 14 (02) :101-114
[2]   LIPID-PROTEIN-PARTITIONING THEORY OF SKIN PENETRATION ENHANCEMENT [J].
BARRY, BW .
JOURNAL OF CONTROLLED RELEASE, 1991, 15 (03) :237-248
[3]   Water distribution and related morphology in human stratum corneum at different hydration levels [J].
Bouwstra, JA ;
de Graaff, A ;
Gooris, GS ;
Nijsse, J ;
Wiechers, JW ;
van Aelst, AC .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2003, 120 (05) :750-758
[4]   Degradation of corneodesmosome proteins by two serine proteases of the kallikrein family, SCTE/KLK5/hK5 and SCCE/KLK7/hK7 [J].
Caubet, C ;
Jonca, N ;
Brattsand, M ;
Guerrin, M ;
Bernard, D ;
Schmidt, R ;
Egelrud, T ;
Simon, M ;
Serre, G .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2004, 122 (05) :1235-1244
[5]   Transidermal drug delivery of insulin with ultradeformable carriers [J].
Cevc, G .
CLINICAL PHARMACOKINETICS, 2003, 42 (05) :461-474
[6]   LIPID VESICLES PENETRATE INTO INTACT SKIN OWING TO THE TRANSDERMAL OSMOTIC GRADIENTS AND HYDRATION FORCE [J].
CEVC, G ;
BLUME, G .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1104 (01) :226-232
[7]   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
[8]   Ultradeformable lipid vesicles can penetrate the skin and other semi-permeable barriers unfragmented.: Evidence from double label CLSM experiments and direct size measurements [J].
Cevc, G ;
Schätzlein, A ;
Richardsen, H .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2002, 1564 (01) :21-30
[9]   New, highly efficient formulation of diclofenac for the topical, transdermal administration in ultradeformable drug carriers, Transfersomes [J].
Cevc, G ;
Blume, G .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2001, 1514 (02) :191-205
[10]   Preclinical characterisation of NSAIDs in ultradeformable carriers or conventional topical gels [J].
Cevc, Gregor ;
Mazgareanu, Stefan ;
Rother, Matthias .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2008, 360 (1-2) :29-39