Laser-responsive liposome for selective tumor targeting of nitazoxanide nanoparticles

• Published in: European journal of pharmaceutical sciences 2018-01, Vol.111, p.526-533
• Main Authors: Darwish, Wael M., Bayoumi, Noha A., El-Kolaly, Mohamed T.
• Format: Article
• Language: English
• Subjects: Animals; Antiparasitic Agents - therapeutic use; Laser; Lasers; Liposomes; Liposomes - chemistry; Mice; Nanoparticles - chemistry; Neoplasms - drug therapy; Nitazoxanide nanoparticles; Particle Size; Phthalocyanine polymers; Radiolabeling; Thiazoles - chemistry; Thiazoles - pharmacology
• ISSN: 0928-0987; 1879-0720
• DOI: 10.1016/j.ejps.2017.10.038

Nitazoxanide [2-(Acetyloxy)-N-(5-nitro-2-thiazolyl)benzamide], usually referred as NTZ, is an antiparasites drug with a potential anti-cancer reactivity. However, the bioavailability of nitazoxanide is limited due to its poor water solubility. In this study, nitazoxanide could be successfully incorporated in a stable biocompatible liposome (NTZ-LP) using a modified thin film hydration technique. Further, a novel lipophilic phthalocyanine star polymer R4PcZn was prepared as photosensitizer and in situ incorporated with NTZ in the liposome formulation affording a laser-responsive liposome (NTZ-ZnPc-LP). Both (NTZ-LP) and (NTZ-ZnPc-LP) showed high entrapment efficiency (EE) and high in vitro drug release rates. Transmission electron microscope (TEM) images and dynamic light scattering (DLS) measurements of (NTZ-LP) and (NTZ-ZnPc-LP) showed unilamellar vesicles of mean diameter 192.2 and 87.4nm, respectively. In addition, NTZ nanoparticles (NTZ NPs) were prepared via membrane extrusion method using DMF and water as solvents. All formulations were similarly prepared using radiolabeled nitazoxanide 125I-NTZ. After induction of solid tumor in mices using Ehrlich Ascites Carcinoma, the prepared formulations were injected in the tail vein of the mices. Tumor sites of the animal injected with (125I–NTZ-ZnPc-LP) were illuminated with a HeNe laser (λ=630nm). Afterwards, the biodistriburtion of 125I–NTZ was tagged using γ counter. Results showed that the light-responsive formulation (125I–NTZ-ZnPc-LP) affords a higher accumulation of 125I NTZ in the tumor sites after illumination. This can be attributed to the rupture of liposome lipid bilayer as a result of the photosensitization process and the singlet oxygen species resulted thereof. Despite (NTZ NPs) formulation showed a rapid accumulation of NTZ in tumor, it showed unfavoured rapid blood clearance rate. [Display omitted]