AS1411aptamer conjugated liposomes for targeted delivery of arsenic trioxide in mouse xenograft model of melanoma cancer

• Published in: Journal of liposome research 2024-06, Vol.34 (2), p.288-302
• Main Authors: Shariat Razavi, Fatemeh, Kouchak, Maryam, Sistani Karampour, Neda, Mahdavinia, Masoud, Nazari Khorasgani, Zahra, Rezaie, Annahita, Rahbar, Nadereh
• Format: Article
• Language: English
• Subjects: Animals; Antineoplastic Agents - administration & dosage; Antineoplastic Agents - chemistry; Antineoplastic Agents - pharmacology; Aptamers, Nucleotide - chemistry; Aptamers, Nucleotide - pharmacology; Arsenic Trioxide - administration & dosage; Arsenic Trioxide - chemistry; Arsenic Trioxide - pharmacology; Cell Line, Tumor; Cell Survival - drug effects; Drug Delivery Systems; Humans; Liposomes - chemistry; Melanoma - drug therapy; Melanoma - pathology; Melanoma, Experimental - drug therapy; Melanoma, Experimental - pathology; Mice; Mice, Inbred C57BL; Oligodeoxyribonucleotides - administration & dosage; Oligodeoxyribonucleotides - chemistry; Oligodeoxyribonucleotides - pharmacology; Particle Size; Surface Properties; Xenograft Model Antitumor Assays
• ISSN: 0898-2104; 1532-2394
• DOI: 10.1080/08982104.2023.2271046

Development of AS1411aptamer-conjugated liposomes for targeted delivery of arsenic trioxide is the primary goal of this study. AS1411aptamer was used as ligand to target nucleolin, which is highly expressed on the surface of melanoma cancer cells. The targeted liposomes were constructed by the thin film method, and arsenic trioxide was loaded as cobalt (II) hydrogen arsenite (CHA) to increase the loading efficiency and stability of the liposomes. The liposomal structure was characterized by Fourier Transform Infrared Spectroscopy (FT-IR) and field emission scanning electron microscopy (FESEM). In addition, particle sizes and zeta potential of the CHA-loaded liposomes (CHAL) and aptamer-functionalized CHA-loaded liposomes (AP-CHAL) were determined. cytotoxicity of CHAL and AP-CHAL were evaluated using MTT assay in murine melanoma (B16) and mouse embryonic fibroblast (MEF) cell lines. The encapsulation efficiency of CHAL and AP-CHAL was reported as 60.2 ± 6.5% and 58.7 ± 4.2%, respectively. antitumor activity of CHAL and AP-CHAL in the B16 tumor-xenograft mouse model was dramatically observed. All mice of both groups survived until the end of treatment and showed body weight gain. The tumor protrusion completely disappeared in 50% of the mice in these groups. Furthermore, histopathology studies demonstrated that CHAL and AP-CHAL did not induce significant toxicity in healthy mice tissues. However, unlike the CHAL group, which showed an initial increase in tumor volume, a specific antitumor effect was observed in the AP-CHAL group from the beginning of treatment. The results showed that AP-CHAL can be used as an effective drug delivery system with high potential in the treatment of solid tumors.