Nanosized ethanolic vesicles loaded with econazole nitrate for the treatment of deep fungal infections through topical gel formulation

被引:164
作者
Verma, Poonam [1 ]
Pathak, Kamla [1 ]
机构
[1] Rajiv Acad Pharm, Dept Pharmaceut, Mathura 281001, Uttar Pradesh, India
关键词
Econazole nitrate; Ethosomes; Pharmacotechnical properties; Gels; Epidermal permeation; PERCUTANEOUS PENETRATION; DELIVERY; SKIN; RETENTION; LIPOSOMES; ACID;
D O I
10.1016/j.nano.2011.07.004
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
This project aimed at developing nanovesicles of econazole nitrate (EN) and formulating them as a suitable dermatological gel for improved therapeutic efficacy, better dispersity, and good storage stability. Ethosomes were prepared by cold method and evaluated for the mean diameter, surface charge, and entrapment efficiency. Optimized ethosomes with vesicle size and entrapment efficiency of 202.85 +/- 5.10 nm and 81.05 +/- 0.13%, respectively, were formulated as Carbopol 934 NF gels with varied permeation enhancers (G1-G7), and compared with liposomal and hydroethanolic gels. The pharmacotechnical evaluation of gels demonstrated G6 with a flux rate of 0.46 +/- 0.22 mu g/cm(2) hr(1/2) as the best formulation that was able to exhibit controlled release of EN for 12 hours across rat skin, and percent drug diffused from ethosomes was nearly twofold higher than liposomal and hydroethanolic gels. Confocal laser scanning microscopy demonstrated drug permeation as far as the last layer of epidermis (stratum basale). Stability profile of the prepared system assessed for 180 days revealed very low aggregation and insignificant growth in vesicular size. The results collectively suggest that because of the controlled drug release, better antifungal activity, and good storage stability, EN ethosomal gel has tremendous potential to serve as a topical delivery system. From the Clinical Editor: Ethosomal gel of econazole nitrate was found to have outstanding potential to serve as a topical delivery system, enabling controlled drug release, providing better antifungal activity, and good storage stability. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:489 / 496
页数:8
相关论文
共 28 条
  • [1] Polymer-lipid based mucoadhesive microspheres prepared by spray-congealing for the vaginal delivery of econazole nitrate
    Albertini, Beatrice
    Passerini, Nadia
    Di Sabatino, Marcello
    Vitali, Beatrice
    Brigidi, Patrizia
    Rodriguez, Lorenzo
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2009, 36 (4-5) : 591 - 601
  • [2] Transbuccal permeation, anti-inflammatory activity and clinical efficacy of piroxicam formulated in different gels
    Attia, MA
    El-Gibaly, I
    Shaltout, SE
    Fetih, GN
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2004, 276 (1-2) : 11 - 28
  • [3] Novel mechanisms and devices to enable successful transdermal drug delivery
    Barry, BW
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2001, 14 (02) : 101 - 114
  • [4] Enhanced Transdermal Delivery of Salbutamol Sulfate via Ethosomes
    Bendas, Ehab R.
    Tadros, Mina I.
    [J]. AAPS PHARMSCITECH, 2007, 8 (04)
  • [5] Bhalaria MK, 2009, INDIAN J EXP BIOL, V47, P368
  • [6] Ceve G, 2004, J ADV DRUG DEL, V56, P675
  • [7] Dennal and transdermal delivery of an anti-psoriatic agent via ethanolic liposomes
    Dubey, Vaibhav
    Mishra, Dinesh
    Dutta, Tathagata
    Nahar, Manoj
    Saraf, D. K.
    Jain, N. K.
    [J]. JOURNAL OF CONTROLLED RELEASE, 2007, 123 (02) : 148 - 154
  • [8] Melatonin loaded ethanolic liposomes: Physicochemical characterization and enhanced transdermal delivery
    Dubey, VaIbhav
    Mishra, Dinesh
    Jain, N. K.
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2007, 67 (02) : 398 - 405
  • [9] DYAS AM, 1994, ANAL PROF DRUG SUBST, V23, P125
  • [10] Lipid vesicles for skin delivery of drugs: Reviewing three decades of research
    Elsayed, Mustafa M. A.
    Abdallah, Ossama Y.
    Naggar, Viviane F.
    Khalafallah, Nawal M.
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2007, 332 (1-2) : 1 - 16