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


Autoria(s): de Araujo, Daniele Ribeiro; Saia Cereda, Cintia Maria; Brunetto, Glovanna Bruschini; Vomero, Viviane Urbini; Pierucci, Amauri; Santo Neto, Humberto; Rodrigues de Oliveira, Alexandre Leite; Fraceto, Leonardo Fernandes; de Assuncao Braga, Angelica de Fatima; de Paula, Eneida
Contribuinte(s)

Universidade Estadual Paulista (UNESP)

Data(s)

20/05/2014

20/05/2014

01/11/2008

Resumo

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Processo FAPESP: 01/12476-2

Processo FAPESP: 06/00121-9

This 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 a-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 (RVCPLAIN) and liposomal RVC (RVCLUV) 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. RVCLUV presented reduced cytotoxicity (P < 0.001) when compared with RVCPLAIN Treatment with RVCLUV 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 RVCPLAIN. 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 RVCPLAIN or RVCLUV at 0.5%. Despite the differences between these preclinical studies and clinical conditions, we suggest RVCLUV as a potential new formulation, since RVC is a new and safe local anaesthetic agent.

Formato

1449-1457

Identificador

http://dx.doi.org/10.1211/jpp.60.11.0005

Journal of Pharmacy and Pharmacology. London: Pharmaceutical Press-royal Pharmaceutical Soc Great Britian, v. 60, n. 11, p. 1449-1457, 2008.

0022-3573

http://hdl.handle.net/11449/212

10.1211/jpp/60.11.0005

WOS:000260921500005

Idioma(s)

eng

Publicador

Pharmaceutical Press-royal Pharmaceutical Soc Great Britian

Relação

Journal of Pharmacy and Pharmacology

Direitos

closedAccess

Tipo

info:eu-repo/semantics/article