In-vitro and in-vivo antileishmanial activity of inexpensive Amphotericin B formulations: Heated Amphotericin B and Amphotericin B-loaded microemulsion

被引:28
|
作者
do Vale Morais, Andreza Rochelle [1 ,3 ]
Silva, Andre Leandro [2 ,3 ,6 ]
Cojean, Sandrine [4 ]
Balaraman, Kaluvu [4 ,5 ]
Bories, Christian [4 ]
Pomel, Sebastien [4 ]
Barratt, Gillian [3 ]
Tabosa do Egito, Eryvaldo Socrates [1 ,2 ]
Loiseau, Philippe M. [4 ]
机构
[1] Univ Fed Rio Grande do Norte UFRN, Programa Posgrad Nanotecnol Farmaceut, Rua Gustavo Cordeiro de Farias SN, BR-59012570 Natal, RN, Brazil
[2] Univ Fed Rio Grande do Norte, Programa Posgrad Biotecnol RENORBIO, Ave Senador Salgado Filho,3000 Campus Univ, BR-59078970 Natal, RN, Brazil
[3] Univ Paris Sud, Inst Galien Paris Sud, UMR CNRS 8612, 5 Rue Jean Baptiste Clement, F-92296 Chatenay Malabry, France
[4] Univ Paris Sud, Fac Pharm, UMR CNRS BioCIS 8076, Chatenay Malabry, France
[5] IITM, Dept Biotechnol, Biol Chem Lab, Technol Madras, Madras, Tamil Nadu, India
[6] UFOB, Ctr Ciencias Biol & Saude, R Prof Jose Seabra de Lemos 316, BR-47808021 Barreiras, BA, Brazil
关键词
Visceral leishmaniasis; Amphotericin B; Microemulsion; Superaggregates; PHOSPHOLIPID-BASED MICROEMULSION; VISCERAL LEISHMANIASIS; DELIVERY-SYSTEM; DEOXYCHOLATE FUNGIZONE; INDUCED REFORMULATION; THERAPEUTIC-EFFICACY; ORAL DELIVERY; TOXICITY; DONOVANI; LIPOSOMES;
D O I
10.1016/j.exppara.2018.07.017
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Amphotericin B (AmB) is effective against visceral leishmaniasis (VL), but the renal toxicity of the conventional form, mixed micelles with deoxycholate (M-AmB), is often dose-limiting, while the less toxic lipid-based formulations such as AmBisome (R) are very expensive. Two different strategies to improve the therapeutic index of AmB with inexpensive ingredients were evaluated on this work: (i) the heat treatment of the commercial formulation (H-AmB) and (ii) the preparation of an AmB-loaded microemulsion (ME-AmB). M-AmB was heated to 70 degrees C for 20 min. The resulting product was characterized by UV spectrophotometry and circular dichroism, showing super-aggregates formation. ME-AmB was prepared from phosphate buffer pH 7.4, Tween 80 (R), Lipoid S100 (R) and Mygliol 812 (R) with AmB at 5 mg/mL. The droplet size, measured by dynamic light scattering, was about 40 nm and transmission electron microscopy confirmed a spherical shape. Rheological analysis showed low viscosity and Newtonian behavior. All the formulations were active in vitro and in vivo against Leishmania donovani (LV9). A selectivity index (CC50 on RAW/IC50 on LV9) higher than 10 was observed for ME-AmB, H-AmB and AmBisome (R). Furthermore, no important in vivo toxicity was observed for all the samples. The in-vivo efficacy of the formulations after IV administration was evaluated in Balb/C mice infected with LV9 (three doses of 1 mg/kg AmB) and no significant difference was observed between H-AmB, M-AmB, ME-AmB and AmBisome (R). In conclusion, these two inexpensive alternative formulations for AmB showing good efficacy and selectivity for Leishmania donovani merit further investigation.
引用
收藏
页码:85 / 92
页数:8
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