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Research Article

Evaluation of submicron emulsion as vehicles for rapid-onset intranasal delivery and improvement in brain targeting of zolmitriptan

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Pages 578-585 | Received 16 Jun 2011, Accepted 17 Jun 2011, Published online: 12 Aug 2011

Figures & data

Figure 1.  Animal model for pharmacokinetic study.

Figure 1.  Animal model for pharmacokinetic study.

Table 1.  Pharmacokinetic parameters of ZT after administration of ZTS (i.v.), ZTS (i.n.), ZTSE-1(i.n.) and ZTSE-2 (i.n.) to rats (n = 5).

Figure 2.  Section of the rat brain at the position for the probe inserted in.

Figure 2.  Section of the rat brain at the position for the probe inserted in.

Table 2.  Pharmacokinetic parameters of unbound ZT in CSF and values of AUCCSF/AUCPlasma after administration of ZTS (i.v.), ZTS (i.n.), ZTSE-1(i.n.) and ZTSE-2 (i.n.) to rats (n = 5).

Figure 3.  The mean concentration–time curves of unbound ZT in CSF in rats after intranasal and intravenous administration of the dosage forms at the dose of 0.9mg kg-1. (n = 5, mean ± SD).

Figure 3.  The mean concentration–time curves of unbound ZT in CSF in rats after intranasal and intravenous administration of the dosage forms at the dose of 0.9mg kg-1. (n = 5, mean ± SD).

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