Preparation, pharmacokinetics, biodistribution, antitumor efficacy and safety of Lx2-32c-containing liposome

• Published in: PloS one Vol. 9; no. 12; p. e114688
• Main Authors: Wang, Hongbo, Zhang, Jianqiao, Lv, Guangyao, Ma, Jinbo, Ma, Pengkai, Du, Guangying, Wang, Zongliang, Tian, Jingwei, Fang, Weishuo, Fu, Fenghua
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 15.12.2014; Public Library of Science (PLoS)
• Subjects: Animals; Anticancer properties; Antineoplastic Agents - administration & dosage; Antineoplastic Agents - pharmacokinetics; Antineoplastic Agents - therapeutic use; Antineoplastic Agents - toxicity; Antitumor activity; Bone marrow; Cancer therapies; Cardiotoxicity; Drug delivery systems; Education; Effectiveness; Heart; Hypersensitivity; Laboratories; Liposomes; Male; Medical research; Medicine and Health Sciences; Mice, Inbred C57BL; Nanoparticles; Neoplasms; Neoplasms - drug therapy; Paclitaxel; Paclitaxel - administration & dosage; Paclitaxel - analogs & derivatives; Paclitaxel - pharmacokinetics; Paclitaxel - therapeutic use; Paclitaxel - toxicity; Particle size; Pharmaceuticals; Pharmacokinetics; Pharmacology; Pharmacy; Rats, Sprague-Dawley; Safety; Solvents; Taxanes; Toxicity; Toxicology; Tumors; Beijing China; China
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0114688

Lx2-32c is a novel taxane that has been demonstrated to have robust antitumor activity against different types of tumors including several paclitaxel-resistant neoplasms. Since the delivery vehicles for taxane, which include cremophor EL, are all associated with severe toxic effects, liposome-based Lx2-32c has been developed. In the present study, the pharmacokinetics, biodistribution, antitumor efficacy and safety characteristics of liposome-based Lx2-32c were explored and compared with those of cremophor-based Lx2-32c. The results showed that liposome-based Lx2-32c displayed similar antitumor effects to cremophor-based Lx2-32c, but with significantly lower bone marrow toxicity and cardiotoxicity, especially with regard to the low ratio of hypersensitivity reaction. In comparing these two delivery modalities, targeting was superior using the Lx2-32c liposome formulation; it achieved significantly higher uptake in tumor than in bone marrow and heart. Our data thus suggested that the Lx2-32c liposome was a novel alternative formulation with comparable antitumor efficacy and a superior safety profiles to cremophor-based Lx2-32c, which might be related to the improved pharmacokinetic and biodistribution characteristics. In conclusion, the Lx2-32c liposome could be a promising alternative formulation for further development.