Self-assembled micelles loaded with itraconazole as anti-Acanthamoeba nano-formulation

被引:2
作者
Rao, Komal [1 ]
Abdullah, Muhammad [1 ]
Ahmed, Usman [2 ]
Wehelie, Hashi Isse [2 ]
Shah, Muhammad Raza [1 ]
Siddiqui, Ruqaiyyah [3 ,4 ]
Khan, Naveed A. [4 ]
Alawfi, Bader S. [5 ]
Anwar, Ayaz [2 ]
机构
[1] Univ Karachi, HEJ Res Inst Chem, Int Ctr Chem & Biol Sci, Karachi 75270, Pakistan
[2] Sunway Univ, Sch Med & Life Sci, Dept Biol Sci, Subang Jaya 47500, Selangor, Malaysia
[3] Heriot Watt Univ, Inst Biol Chem Biophys & Bioengn, Edinburgh EH14 4AS, Scotland
[4] Istinye Univ, Microbiota Res Ctr, TR-34010 Istanbul, Turkiye
[5] Taibah Univ, Coll Appl Med Sci, Dept Clin Lab Sci, Madinah 42353, Saudi Arabia
关键词
Micelles; Itraconazole; Acanthamoeba; Nanoformulation; Central nervous system; Infectious diseases; Free-living amoebae; Nanotechnology; RING-OPENING POLYMERIZATION; MIKTOARM STAR COPOLYMERS; DRUG; KERATITIS; POLYMERS; DISEASE; AGENTS; OPTIMIZATION; SOLUBILITY; TREAT;
D O I
10.1007/s00203-024-03854-3
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Acanthamoeba castellanii are opportunistic pathogens known to cause infection of the central nervous system termed: granulomatous amoebic encephalitis, that mostly effects immunocompromised individuals, and a sight threatening keratitis, known as Acanthamoeba keratitis, which mostly affects contact lens wearers. The current treatment available is problematic, and is toxic. Herein, an amphiphilic star polymer with AB(2) miktoarms [A = hydrophobic poly(-Caprolacton) and B = hydrophilic poly (ethylene glycol)] was synthesized by ring opening polymerization and Cu-I catalyzed azide-alkyne cycloaddition. Characterization by H-1 and C-13 NMR spectroscopy, size-exclusion chromatography and fluorescence spectroscopy was accomplished. The hydrophobic drug itraconazole (ITZ) was incorporated in self-assembled micellar structure of AB(2) miktoarms through co-solvent evaporation. The properties of ITZ loaded (ITZ-PCL-PEG(2)) and blank micelles (PCL-PEG(2)) were investigated through zeta sizer, scanning electron microscopy and Fourier-transform infrared spectroscopy. Itraconazole alone (ITZ), polymer (DPB-PCL), empty polymeric micelles (PCL-PEG(2)) alone, and itraconazole loaded in polymeric micelles (ITZ-PCL-PEG(2)) were tested for anti-amoebic potential against Acanthamoeba, and the cytotoxicity on human cells were determined. The polymer was able to self-assemble in aqueous conditions and exhibited low value for critical micelle concentration (CMC) 0.05-0.06 mu g/mL. The maximum entrapment efficiency of ITZ was 68%. Of note, ITZ, DPB, PCL-PEG(2) and ITZ-PCL-PEG(2) inhibited amoebae trophozoites by 37.34%, 36.30%, 35.77%, and 68.24%, respectively, as compared to controls. Moreover, ITZ-PCL-PEG(2) revealed limited cytotoxicity against human keratinocyte cells. These results are indicative that ITZ-PCL-PEG(2) micelle show significantly better anti-amoebic effects as compared to ITZ alone and thus should be investigated further in vivo to determine its clinical potential.
引用
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页数:15
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