Development and Characterization of Eucalyptol Microemulsions for Topic Delivery of Curcumin

被引:70
作者
Liu, Chi-Hsien [1 ]
Chang, Fu-Yen [1 ]
机构
[1] Chang Gung Univ, Grad Inst Biochem & Biomed Engn, Kwei Shan Tao Yuan 333, Taiwan
关键词
eucalyptol microemulsion; transdermal delivery; curcumin; TRANSDERMAL DRUG-DELIVERY; IN-VITRO; DERMAL DELIVERY; SYSTEM; OIL; FORMULATION; SKIN; SOLUBILIZATION; PENETRATION; ENHANCERS;
D O I
10.1248/cpb.59.172
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Microemulsions have received great attention for applications in transdermal drug delivery. The use of curcumin for treating various skin diseases like scleroderma, psoriasis, and skin cancer was extensively reported. The solubility of curcumin in various oils, surfactants, and cosurfactants was studied herein in order to find the optimal components for a transdermal delivery vehicle. Microemulsion systems composed of eucalyptol, polysorbate 80, ethanol, and water were developed as transdermal delivery vehicles for curcumin. Effects of the microemulsion composition on transdermal curcumin delivery were studied using Franz diffusion cells. The transdermal curcumin flux, permeability coefficient, and enhancement ratio were analyzed to evaluate the effects of eucalyptol/water ratios in the microemulsions. Pseudo-ternary phase diagrams of the eucalyptol microemulsions with various surfactant/cosurfactant ratios (1: 1-1 : 3) were constructed to investigate their phase behaviors. Conductivity, interfacial tension, size, and viscosity data of the microemulsions were used to characterize the physicochemical properties of transdermal vehicles. The influence of the microemulsions on skin histology and on the delivery route was analyzed using hematoxylin/eosin staining and confocal laser scanning microscopy. In conclusion, microemulsions were successfully developed for transdermal curcumin delivery after screening various components and adjusting the oil/water ratios. The curcumin permeation rate of the microemulsion developed was 15.7-fold higher than that of the control (eucalyptol only). These results indicate that an eucalyptol microemulsion system is a promising tool for the percutaneous delivery of curcumin.
引用
收藏
页码:172 / 178
页数:7
相关论文
共 40 条
  • [31] Formation of fine emulsions by emulsification at high viscosity or low interfacial tension; A comparative study
    Sajjadi, Shahriar
    [J]. COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 2007, 299 (1-3) : 73 - 78
  • [32] Enhanced Oral Bioavailability of Daidzein by Self-Microemulsifying Drug Delivery System
    Shen, Qi
    Li, Xi
    Yuan, Dan
    Jia, Wei
    [J]. CHEMICAL & PHARMACEUTICAL BULLETIN, 2010, 58 (05) : 639 - 643
  • [33] Permeabilisation and solubilisation of soybean phosphatidylcholine bilayer vesicles, as membrane models, by polysorbate, Tween 80
    Simoes, SI
    Tapadas, JM
    Marques, CM
    Cruz, MEM
    Martins, MBF
    Cevc, G
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2005, 26 (3-4) : 307 - 317
  • [34] Phosphatidylcholine embedded micellar systems: Enhanced permeability through rat skin
    Spemath, Aviram
    Aserin, Abraham
    Sintov, Amnon C.
    Garti, Nissim
    [J]. JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2008, 318 (02) : 421 - 429
  • [35] Microemulsions as carriers for drugs and nutraceuticals
    Spernath, Aviram
    Aserin, Abraham
    [J]. ADVANCES IN COLLOID AND INTERFACE SCIENCE, 2006, 128 (47-64) : 47 - 64
  • [36] Thangapazham RL, 2007, ADV EXP MED BIOL, V595, P343
  • [37] Percutaneous penetration enhancers: An overview
    Thong, H.-Y.
    Zhai, H.
    Maibach, H. I.
    [J]. SKIN PHARMACOLOGY AND PHYSIOLOGY, 2007, 20 (06) : 272 - 282
  • [38] Overcoming the stratum corneum: The modulation of skin penetration - A review
    Trommer, H.
    Neubert, R. H. H.
    [J]. SKIN PHARMACOLOGY AND PHYSIOLOGY, 2006, 19 (02) : 106 - 121
  • [39] Vicentini E.T.M.C., 2008, BIOPHARM, V69, P948
  • [40] Formulation design of microemulsion for dermal delivery of penciclovir
    Zhu, Weiwei
    Yu, Aihua
    Wang, Weihong
    Dong, Ruiqian
    Wu, Jun
    Zhai, Guangxi
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2008, 360 (1-2) : 184 - 190