Preparation and in vivo evaluation of a gel-based nasal delivery system for risperidone

The aim of this study was to prepare a nasal gel of risperidone and to investigate the pharmacokinetics and relative bioavailability of the drug in rats. Compared with oral dosing, the risperidone nasal gel exhibited very fast absorption and high bioavailability. Maximal plasma concentration (cmax)...

Full description

Saved in:
Bibliographic Details
Main Authors: Gu Fugen, Ma Weina, Meng Gendalai, Wu Chunzhi, Wang Yi
Format: Article
Language:English
Published: Sciendo 2016-12-01
Series:Acta Pharmaceutica
Subjects:
Online Access:https://doi.org/10.1515/acph-2016-0047
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832572505505660928
author Gu Fugen
Ma Weina
Meng Gendalai
Wu Chunzhi
Wang Yi
author_facet Gu Fugen
Ma Weina
Meng Gendalai
Wu Chunzhi
Wang Yi
author_sort Gu Fugen
collection DOAJ
description The aim of this study was to prepare a nasal gel of risperidone and to investigate the pharmacokinetics and relative bioavailability of the drug in rats. Compared with oral dosing, the risperidone nasal gel exhibited very fast absorption and high bioavailability. Maximal plasma concentration (cmax) and the time to reach cmax (tmax) were 15.2 μg mL-1 and 5 min for the nasal gel, 3.6 μg mL-1 and 30 min for the oral drug suspension, respectively. Pharmacokinetic parameters such as tmax′, cmax and AUC of oral and nasal routes were significantly different (p < 0.01). Relative bioavailability of the drug nasal preparation to the oral suspension was up to 1600.0 %. Further, the in vitro effect of the risperidone nasal gel on nasal mucociliary movement was also investigated using a toad palate model. The risperidone nasal formulation showed mild ciliotoxicity, but the adverse effect was temporary and reversible.
format Article
id doaj-art-bdd30ca33e8a4ace960fef1b5d56e208
institution Kabale University
issn 1846-9558
language English
publishDate 2016-12-01
publisher Sciendo
record_format Article
series Acta Pharmaceutica
spelling doaj-art-bdd30ca33e8a4ace960fef1b5d56e2082025-02-02T09:57:54ZengSciendoActa Pharmaceutica1846-95582016-12-0166455556210.1515/acph-2016-0047acph-2016-0047Preparation and in vivo evaluation of a gel-based nasal delivery system for risperidoneGu Fugen0Ma Weina1Meng Gendalai2Wu Chunzhi3Wang Yi4Department of Pharmaceutics Affiliated Hospital, Inner Mongolia Medical University, Hohhot 010050 , ChinaSchool of Pharmacy, Inner Mongolia Medical University, Hohhot 010110, ChinaDepartment of Pharmaceutics Affiliated Hospital, Inner Mongolia Medical University, Hohhot 010050 ChinaDepartment of Pharmaceutics Affiliated Hospital, Inner Mongolia Medical University, Hohhot 010050, ChinaDepartment of Pharmaceutics Affiliated Hospital, Inner Mongolia Medical University, Hohhot 010050, ChinaThe aim of this study was to prepare a nasal gel of risperidone and to investigate the pharmacokinetics and relative bioavailability of the drug in rats. Compared with oral dosing, the risperidone nasal gel exhibited very fast absorption and high bioavailability. Maximal plasma concentration (cmax) and the time to reach cmax (tmax) were 15.2 μg mL-1 and 5 min for the nasal gel, 3.6 μg mL-1 and 30 min for the oral drug suspension, respectively. Pharmacokinetic parameters such as tmax′, cmax and AUC of oral and nasal routes were significantly different (p < 0.01). Relative bioavailability of the drug nasal preparation to the oral suspension was up to 1600.0 %. Further, the in vitro effect of the risperidone nasal gel on nasal mucociliary movement was also investigated using a toad palate model. The risperidone nasal formulation showed mild ciliotoxicity, but the adverse effect was temporary and reversible.https://doi.org/10.1515/acph-2016-0047risperidonenasal gelformulationpharmacokineticsbioavailabilityciliotoxicity
spellingShingle Gu Fugen
Ma Weina
Meng Gendalai
Wu Chunzhi
Wang Yi
Preparation and in vivo evaluation of a gel-based nasal delivery system for risperidone
Acta Pharmaceutica
risperidone
nasal gel
formulation
pharmacokinetics
bioavailability
ciliotoxicity
title Preparation and in vivo evaluation of a gel-based nasal delivery system for risperidone
title_full Preparation and in vivo evaluation of a gel-based nasal delivery system for risperidone
title_fullStr Preparation and in vivo evaluation of a gel-based nasal delivery system for risperidone
title_full_unstemmed Preparation and in vivo evaluation of a gel-based nasal delivery system for risperidone
title_short Preparation and in vivo evaluation of a gel-based nasal delivery system for risperidone
title_sort preparation and in vivo evaluation of a gel based nasal delivery system for risperidone
topic risperidone
nasal gel
formulation
pharmacokinetics
bioavailability
ciliotoxicity
url https://doi.org/10.1515/acph-2016-0047
work_keys_str_mv AT gufugen preparationandinvivoevaluationofagelbasednasaldeliverysystemforrisperidone
AT maweina preparationandinvivoevaluationofagelbasednasaldeliverysystemforrisperidone
AT menggendalai preparationandinvivoevaluationofagelbasednasaldeliverysystemforrisperidone
AT wuchunzhi preparationandinvivoevaluationofagelbasednasaldeliverysystemforrisperidone
AT wangyi preparationandinvivoevaluationofagelbasednasaldeliverysystemforrisperidone