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Pharmacokinetic and pharmacodynamic evaluation of a nanotechnological topical formulation of lidocaine/prilocaine (nanorap) in healthy volunteers.
Gagliano-Jucá, Thiago; Castelli, Maísa R; Mendes, Gustavo D; Arruda, André M M; Chen, Lu Shi; de Oliveira, Marco A; Costa, Sérgio F; Lopes, Anibal Gil; de Souza, Wanderley; De Nucci, Gilberto.
Afiliação
  • Gagliano-Jucá T; *Institute of Biophysics Carlos Chagas Filho, Federal University of Rio de Janeiro (UFRJ); †Galeno Research Unit, Campinas; ‡Department of Pharmacology, Faculty of Medical Sciences, State University of Campinas (UNICAMP); §Department of Surgery, Faculty of Odontology, University Camilo Castelo Branco (UNICASTELO); ¶Department of Surgery, Faculty of Odontology, University of Sao Francisco (USF), Braganca Paulista; ‖ECA-University of Sao Paulo; **Instituto Nacional de Metrologia, Qualidade e Tecno
Ther Drug Monit ; 37(3): 362-8, 2015 Jun.
Article em En | MEDLINE | ID: mdl-25525759
ABSTRACT

BACKGROUND:

Nanorap is a new nanotechnological formulation for topical anesthesia composed of lidocaine (2.5%) and prilocaine (2.5%). This study evaluated the pharmacokinetics of Nanorap. For the determination of lidocaine and prilocaine in human plasma, a new method using high-performance liquid chromatography coupled with tandem mass spectrometry was developed. Nanorap pharmacodynamic (PD) and its physical proprieties were also evaluated.

METHODS:

Nanorap was administered by topical application of 2 g to healthy volunteers, and blood samples were collected for the pharmacokinetics analysis. The drugs were extracted from plasma by liquid-liquid extraction with ether/hexane (80/20, vol/vol). The chromatography separation was performed on a Genesis C18 analytical column 4 µm (100 × 2.1 mm i.d.) with a mobile phase of methanol/acetonitrile/water (40/30/30, for lidocaine, and 50/30/20, for prilocaine, vol/vol/vol) + 2 mM of ammonium acetate and ropivacaine as internal standard. The drugs were quantified using a mass spectrometer with an electrospray source in the electrospray ionization positive mode configured for multiple reaction monitoring. The PD of Nanorap was evaluated with the use of a visual analog scale. Nanorap was characterized by cryofracture.

RESULTS:

The chromatography run-time was 5.5 minutes for lidocaine and 3.3 minutes for prilocaine, and the lower limit of quantification was 0.05 ng/mL for both drugs. Mean Cmax was 6.62 and 1.72 ng/mL for lidocaine and prilocaine, respectively. Median Tmax was 6.5 hours for both drugs. Nanocapsules had a mean size of 88 nm and mean drug association of 92.5% and 89% for lidocaine and prilocaine, respectively. The PD study showed that Nanorap has a sufficient analgesic effect (>30% reduction in pain) after 10 minutes of application.

CONCLUSIONS:

A new simple, selective, and sensitive method for determination of lidocaine and prilocaine in human plasma was developed. Nanorap generated safe plasma levels of the drugs and satisfactory analgesic effect.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Prilocaína / Nanocápsulas / Anestésicos Locais / Lidocaína Tipo de estudo: Clinical_trials Limite: Adolescent / Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Ther Drug Monit Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Prilocaína / Nanocápsulas / Anestésicos Locais / Lidocaína Tipo de estudo: Clinical_trials Limite: Adolescent / Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Ther Drug Monit Ano de publicação: 2015 Tipo de documento: Article
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