4.7 Article

Development of sulconazole-loaded nanoemulsions for enhancement of transdermal permeation and antifungal activity

期刊

INTERNATIONAL JOURNAL OF NANOMEDICINE
卷 14, 期 -, 页码 3955-3966

出版社

DOVE MEDICAL PRESS LTD
DOI: 10.2147/IJN.S206657

关键词

sulconazole; nanoemulsion; central composite design; transdermal delivery; antifungal activity

资金

  1. National Natural Science Foundation of China [81573613, 81873011]
  2. Science and Technology Commission of Shanghai Municipality [16401901900, 18401931500]
  3. Development Fund for Shanghai Talents [201658]
  4. Outstanding Talents Program of Shanghai Health and Family Planning Commission [2018BR27]
  5. Major Military Logistics Research Projects [AWS16023]
  6. Open Project Program of State Key Laboratory of Natural Medicines [SKLNMKF201809]

向作者/读者索取更多资源

Background: Sulconazole (SCZ) is a broad-spectrum transdermally administered antifungicidal agent. However, the therapeutic effect of SCZ is generally limited by its poor water solubility. This present study aimed to develop and evaluate sulconazole-loaded nanoemulsions (SCZ-NEs) for enhancement of the transdermal permeation and antifungal activity. Methods: A spontaneous titration method was applied to prepare the SCZ-NEs. And the optimized formulation of SCZ-NEs was screened by central composite design (CCD). In addition, the characteristics of the SCZ-NEs were evaluated, including particle size, zeta potential, drug loading (DL%) and encapsulation efficiency (EE%). The morphology of SCZ-NEs was observed by transmission electron microscopy (TEM). Franz diffusion cells were used to evaluate the transdermal permeability of the SCZ-NEs. The antifungal activity of the SCZ-NEs was measured by a zone of inhibition (ZOI) test. Results: The optimized SCZ-NEs possessed a moderate particle size of 52.3 +/- 3.8 nm, zeta potential of 23.3 +/- 1.2 mV, DL% of 0.47 +/- 0.05% and EE% of 87.1 +/- 3.2%. The ex vivo skin permeation study verified that the cumulative permeability (Qn) and penetration rate (Js) of the optimized SCZ-NEs were about 1.7-fold higher than that of a commercial reference, miconazole (MCZ) cream and 3-fold higher than that of SCZ-DMSO solution. The optimized SCZ-NEs exhibited zone of inhibition (ZOI) values of 23.5 +/- 2.4 and 20.4 +/- 2.5 mm against C. albicans and T. rubrum, which were larger compared with these of the MCZ cream and SCZ-DMSO solution. Conclusion: SCZ-NEs were effectively developed to overcome the poor solubility of SCZ, promote SCZ permeation through the skin and improve its antifungal activity. Thus, the SCZ-NEs are a promising percutaneous administration for skin fungal infections induced by C. albicans and T. rubrum.

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