• J. Pharm. Pharmacol. · Nov 2008

    Comparative Study

    Pharmacological and local toxicity studies of a liposomal formulation for the novel local anaesthetic ropivacaine.

    • Daniele Ribeiro de Araujo, Cíntia Maria Saia Cereda, Giovanna Bruschini Brunetto, Viviane Urbini Vomero, Amauri Pierucci, Humberto Santo Neto, Alexandre Leite Rodrigues de Oliveira, Leonardo Fernandes Fraceto, Angélica de Fátima de Assunção Braga, and Eneida de Paula.
    • Department of Biochemistry, Institute of Biology, State University of Campinas - UNICAMP, Campinas, SP, Brazil. draraujo2003@yahoo.com.br
    • J. Pharm. Pharmacol. 2008 Nov 1; 60 (11): 1449-57.

    AbstractThis study reports an investigation of the pharmacological activity, cytotoxicity and local effects of a liposomal formulation of the novel local anaesthetic ropivacaine (RVC) compared with its plain solution. RVC was encapsulated into large unilamellar vesicles (LUVs) composed of egg phosphatidylcholine, cholesterol and alpha-tocopherol (4:3:0.07, mole %). Particle size, partition coefficient determination and in-vitro release studies were used to characterize the encapsulation process. Cytotoxicity was evaluated by the tetrazolium reduction test using sciatic nerve Schwann cells in culture. Local anaesthetic activity was assessed by mouse sciatic and rat infraorbital nerve blockades. Histological analysis was performed to verify the myotoxic effects evoked by RVC formulations. Plain (RVC(PLAIN)) and liposomal RVC (RVC(LUV)) samples were tested at 0.125%, 0.25% and 0.5% concentrations. Vesicle size distribution showed liposomal populations of 370 and 130 nm (85 and 15%, respectively), without changes after RVC encapsulation. The partition coefficient value was 132 +/- 26 and in-vitro release assays revealed a decrease in RVC release rate (1.5 fold, P < 0.001) from liposomes. RVC(LUV) presented reduced cytotoxicity (P < 0.001) when compared with RVC(PLAIN). Treatment with RVC(LUV) increased the duration (P < 0.001) and intensity of the analgesic effects either on sciatic nerve blockade (1.4-1.6 fold) and infraorbital nerve blockade tests (1.5 fold), in relation to RVC(PLAIN). Regarding histological analysis, no morphological tissue changes were detected in the area of injection and sparse inflammatory cells were observed in only one of the animals treated with RVC(PLAIN) or RVC(luv) at 0.5%. Despite the differences between these preclinical studies and clinical conditions, we suggest RVC(LUV) as a potential new formulation, since RVC is a new and safe local anaesthetic agent.

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