Influence of application and formulation factors on the penetration of hypericin in normal mouse skin and UV induced skin tumors

被引:9
作者
Boiy, Annelies [1 ]
Roelandts, Rik [2 ]
De Witte, Peter A. M. [1 ]
机构
[1] Katholieke Univ Leuven, Fac Pharmaceut Sci, Lab Phamaceut Biol, B-3000 Louvain, Belgium
[2] Katholieke Univ Leuven, Univ Hosp, Photodermatol Unit, B-3000 Louvain, Belgium
关键词
hypericin; skin penetration; penetration enhancement; fluorescence microscopy; photodynamic therapy;
D O I
10.1016/j.jphotobiol.2007.10.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hypericin, a naturally occurring photosensitizer, is currently being investigated for topical use in photodynamic therapy (PDT). In a previous study, it was found that hypericin can be delivered in the epidermis of hairless mouse skin after a 4-h application in Beeler base. With the intention to further optimize the penetration conditions, the present study examines the effect of the concentration of hypericin in the cream, the application time, the presence of penetration enhancers and occlusion on the penetration of hypericin in the skin of hairless mice. Experiments with different hypericin concentrations and application times indicated that application of 0.1% hypericin for 12-24 h maximizes the accumulation of hypericin-related fluorescence in the skin, as estimated by fluorescence microscopy with image analysis. Depending on the formulation, the use of an occlusive dressing did not alter, or even reduced the accumulation of hypericin in the viable layers. Also, the addition of propylene glycol (30%) and oleic acid (5%) did not change hypericin fluorescence levels in the epidermis. Conversely, incorporation of ethanol (40%, integrated in a gel, and added to Beeler base) increased dramatically the fluorescence levels in all skin layers. Consequently, the optimized conditions were used to investigate the penetration of hypericin into UV induced skin tumors. It was found that application under occlusion of hypericin, formulated in the gelcrearn containing ethanol, during 24 h enabled the penetration of hypericin in the entire skin lesions with a relatively homogenous distribution. In conclusion, our results suggest the possible use of 0.1% hypericin in a gelcream containing ethanol for PDT of skin lesions. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:156 / 162
页数:7
相关论文
共 26 条
  • [1] Effect of penetration enhancers on the transdermal delivery of bupranolol through rat skin
    Babu, RJ
    Pandit, JK
    [J]. DRUG DELIVERY, 2005, 12 (03) : 165 - 169
  • [2] Is transdermal drug delivery research still important today?
    Barry, BW
    [J]. DRUG DISCOVERY TODAY, 2001, 6 (19) : 967 - 971
  • [3] INFLUENCE OF PROPYLENE-GLYCOL AS COSOLVENT ON MECHANISMS OF DRUG TRANSPORT FROM HYDROGELS
    BENDAS, B
    SCHMALFUSS, U
    NEUBERT, R
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1995, 116 (01) : 19 - 30
  • [4] Effect of vehicles and esterification on the penetration and distribution of hypericin in the skin of hairless mice
    Boiy, Annelies
    Roelandts, Rik
    Roskams, Tania
    de Witte, Peter A. M.
    [J]. PHOTODIAGNOSIS AND PHOTODYNAMIC THERAPY, 2007, 4 (02) : 130 - 139
  • [5] The 500 Dalton rule for the skin penetration of chemical compounds and drugs
    Bos, JD
    Meinardi, MMHM
    [J]. EXPERIMENTAL DERMATOLOGY, 2000, 9 (03) : 165 - 169
  • [6] Hypericin-based fluorescence diagnosis of bladder carcinoma
    D'Hallewin, MA
    Kamuhabwa, AR
    Roskams, T
    De Witte, PAM
    Baert, L
    [J]. BJU INTERNATIONAL, 2002, 89 (07) : 760 - 763
  • [7] DEGRUIJL FR, 1983, PHOTOCHEM PHOTOBIOL, V37, P53
  • [8] Photodynamic therapy for cancer
    Dolmans, DEJGJ
    Fukumura, D
    Jain, RK
    [J]. NATURE REVIEWS CANCER, 2003, 3 (05) : 380 - 387
  • [9] A CONVENIENT SEMISYNTHETIC ROUTE TO HYPERICIN
    FALK, H
    MEYER, J
    OBERREITER, M
    [J]. MONATSHEFTE FUR CHEMIE, 1993, 124 (03): : 339 - 341
  • [10] REGIONAL VARIATION IN PRECUTANEOUS PENETRATION OF 14C CORTISOL IN MAN
    FELDMANN, RJ
    MAIBACH, HI
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1967, 48 (02) : 181 - &