Preparation and characterization of itraconazole loaded nanomicelles based on dextran-behenic acid for cutaneous leishmaniasis treatment

被引:4
作者
Shahriyar, Sara [1 ,2 ]
Taymouri, Somayeh [1 ,2 ]
Saberi, Sedigheh [3 ]
Asadi, Parvin [4 ]
Tabbakhian, Majid [1 ,2 ]
机构
[1] Isfahan Univ Med Sci, Sch Pharm, Dept Pharmaceut, POB 81745-359, Esfahan, Iran
[2] Isfahan Univ Med Sci, Novel Drug Delivery Syst Res Ctr, POB 81745-359, Esfahan, Iran
[3] Isfahan Univ Med Sci, Sch Med, Dept Parasitol & Mycol, Esfahan, Iran
[4] Isfahan Univ Med Sci, Sch Pharm, Dept Med Chem, Esfahan, Iran
关键词
Cutaneous leishmania; itraconazole; polymeric micelle; dextran; J774; macrophage; anti-amastigotes effect; PLGA NANOPARTICLES; PARTICLE-SIZE; DRUG; MACROPHAGE; MICELLES; DELIVERY; RELEASE;
D O I
10.1080/03639045.2021.1890112
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Cutaneous leishmaniasis is known as the most prevalent clinical form of leishmaniasis. It needs the development of new therapies due to the serious side-effects promoted by taking the current drugs. In the present study, dextran-behenic acid (DEX-BA) based nanomicelles were developed to direct the delivery of itraconazole (ITZ) to the macrophages and enhance its toxic effects against Leishmania parasites. DEX-BA was synthesized through the esterification of dextran with behenic acid. The critical micelle concentration of the newly developed conjugate was evaluated using pyrene as the fluorescent probe. The nanomicelles were generated by the dialysis method; then they were optimized by applying a Box-Behnken design. The effects of the dialysis temperature, polymer content, and sonication time on the characteristics of micelles were subsequently studied. Furthermore, in vitro efficacy against Leishmania major promastigotes and parasite-infected macrophages was evaluated. The optimized formulation showed the particle size of 195.16 +/- 3.06 nm, the polydispersity index of 0.39 +/- 0.01, the zeta potential of -16.29 +/- 0.89 mV, the encapsulation efficiency % of 56.11 +/- 4.9, and the release efficiency % of 51.29 +/- 1.97. According to scanning electron microscopy, the nanomicelles were found to be nearly spherical in shape. ITZ-loaded nanomicelles showed the strongest anti-leishmanial activities when compared with the free ITZ and drug-free nanomicelles. It could be, therefore, concluded that ITZ-loaded nanomicelles might be useful as an alternative therapy for the treatment of cutaneous leishmania.
引用
收藏
页码:416 / 428
页数:13
相关论文
共 44 条
[1]   Th-1 biased immunomodulation and synergistic antileishmanial activity of stable cationic lipid-polymer hybrid nanoparticle: Biodistribution and toxicity assessment of encapsulated amphotericin B [J].
Asthana, Shalini ;
Jaiswal, Anil K. ;
Gupta, Pramod K. ;
Dube, Anuradha ;
Chourasia, Manish K. .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2015, 89 :62-73
[2]   Itraconazole encapsulated PLGA-nanoparticles covered with mannose as potential candidates against leishmaniasis [J].
Biswaro, Lubhandwa Sebastian ;
Garcia, Monica Pereira ;
da Silva, Jaqueline Rodrigues ;
Neira Fuentes, Laura Fernanda ;
Vera, Angelica ;
Escobar, Patricia ;
Azevedo, Ricardo Bentes .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART B-APPLIED BIOMATERIALS, 2019, 107 (03) :680-687
[3]   Mannose-conjugated chitosan nanoparticles loaded with rifampicin for the treatment of visceral leishmaniasis [J].
Chaubey, Pramila ;
Mishra, Brahmeshwar .
CARBOHYDRATE POLYMERS, 2014, 101 :1101-1108
[4]   Amphotericin B-incorporated polymeric micelles composed of poly(D,L-lactide-co-glycolide)/dextran graft copolymer [J].
Choi, Ki-Choon ;
Bang, Je-Yong ;
Kim, Pyoung-Il ;
Kim, Chan ;
Song, Chae-Eun .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2008, 355 (1-2) :224-230
[5]   Cutaneous leishmaniasis: successful treatment with itraconazole [J].
Consigli, J ;
Danielo, C ;
Gallerano, V ;
Papa, M ;
Guidi, A .
INTERNATIONAL JOURNAL OF DERMATOLOGY, 2006, 45 (01) :46-49
[6]   Sodium stibogluconate loaded nano-deformable liposomes for topical treatment of leishmaniasis: macrophage as a target cell [J].
Dar, M. Junaid ;
Din, Fakhar Ud ;
Khan, Gul Majid .
DRUG DELIVERY, 2018, 25 (01) :1595-1606
[7]   Nanotechnological Strategies for Treatment of Leishmaniasis-A Review [J].
de Almeida, Letcia ;
Fujimura, Andressa Terumi ;
Del Cistia, Mayara Lucia ;
Fonseca-Santos, Bruno ;
Imamura, Kely Braga ;
Michels, Paul A. M. ;
Chorilli, Marlus ;
Graminha, Marcia A. S. .
JOURNAL OF BIOMEDICAL NANOTECHNOLOGY, 2017, 13 (02) :117-133
[8]   In Vitro Activity of the Antifungal Azoles Itraconazole and Posaconazole against Leishmania amazonensis [J].
de Macedo-Silva, Sara Teixeira ;
Urbina, Julio A. ;
de Souza, Wanderley ;
Fernandes Rodrigues, Juliany Cola .
PLOS ONE, 2013, 8 (12)
[9]   Cutaneous Leishmaniasis: Recent Developments in Diagnosis and Management [J].
de Vries, Henry J. C. ;
Reedijk, Sophia H. ;
Schallig, Henk D. F. H. .
AMERICAN JOURNAL OF CLINICAL DERMATOLOGY, 2015, 16 (02) :99-109
[10]   Enhancing oral bioavailability of quercetin using novel soluplus polymeric micelles [J].
Dian, Linghui ;
Yu, Enjiang ;
Chen, Xiaona ;
Wen, Xinguo ;
Zhang, Zhengzan ;
Qin, Lingzhen ;
Wang, Qingqing ;
Li, Ge ;
Wu, Chuanbin .
NANOSCALE RESEARCH LETTERS, 2014, 9