RETRACTED: Development and Optimization of Luliconazole Spanlastics to Augment the Antifungal Activity against Candida albicans (Retracted Article)

被引:10
|
作者
Alhakamy, Nabil A. [1 ,2 ,3 ]
Al-Rabia, Mohammed W. [4 ]
Md, Shadab [1 ,2 ,3 ]
Sirwi, Alaa [5 ]
Khayat, Selwan Saud [1 ]
AlOtaibi, Sahar Saad [1 ]
Hakami, Raghad Abkar [1 ]
Al Sadoun, Hadeel [6 ]
Eldakhakhny, Basmah Medhat [7 ]
Abdulaal, Wesam H. [8 ]
Aldawsari, Hibah M. [1 ,3 ]
Badr-Eldin, Shaimaa M. [1 ,9 ]
Elfaky, Mahmoud A. [5 ]
机构
[1] King Abdulaziz Univ, Fac Pharm, Dept Pharmaceut, Jeddah 21589, Saudi Arabia
[2] King Abdulaziz Univ, Fac Pharm, Adv Drug Delivery Res Grp, Jeddah 21589, Saudi Arabia
[3] King Abdulaziz Univ, Ctr Excellence Drug Res & Pharmaceut Ind, Jeddah 21589, Saudi Arabia
[4] King Abdulaziz Univ, Dept Med Microbiol & Parasitol, Fac Med, Jeddah 21589, Saudi Arabia
[5] King Abdulaziz Univ, Fac Pharm, Dept Nat Prod & Alternat, Med, Jeddah 21589, Saudi Arabia
[6] King Abdulaziz Univ, Fac Appl Med Sci, King Fahd Med Res Ctr, Dept Med Lab Technol, Jeddah 21589, Saudi Arabia
[7] King Abdulaziz Univ, Fac Med, Dept Clin Biochem, Jeddah 21589, Saudi Arabia
[8] King Abdulaziz Univ, Fac Sci, King Fahd Med Res Ctr, Dept Biochem, Jeddah 21589, Saudi Arabia
[9] Cairo Univ, Fac Pharm, Dept Pharmaceut & Ind Pharm, Cairo 11562, Egypt
关键词
luliconazole; spanlastics; particle size; Candida albicans infections; lesion score; IN-VITRO CHARACTERIZATION; DELIVERY; FORMULATION; RESISTANCE; ACTIVATOR; SYSTEM;
D O I
10.3390/pharmaceutics13070977
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Luliconazole is a new topical imidazole antifungal drug for the treatment of skin infections. It has low solubility and poor skin penetration which limits its therapeutic applications. In order to improve its therapeutic efficacy, spanlastics nanoformulation was developed and optimized using a combined mixture-process variable design (CMPV). The optimized formulation was converted into a hydrogel formula to enhance skin penetration and increase the efficacy in experimental cutaneous Candida albicans infections in Swiss mice wounds. The optimized formulation was generated at percentages of Span and Tween of 48% and 52%, respectively, and a sonication time of 6.6 min. The software predicted that the proposed formulation would achieve a particle size of 50 nm with a desirability of 0.997. The entrapment of luliconazole within the spanlastics carrier showed significant (p < 0.0001) antifungal efficacy in the immunocompromised Candida-infected Swiss mice without causing any irritation, when compared to the luliconazole treated groups. The microscopic observation showed almost complete removal of the fungal colonies on the skin of the infected animals (0.2 +/- 0.05 log CFU), whereas the control animals had 0.2 +/- 0.05 log CFU. Therefore, luliconazole spanlastics could be an effective formulation with improved topical delivery for antifungal activity against C. albicans.
引用
收藏
页数:11
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