Literature DB >> 24239996

Cinnarizine food-effects in beagle dogs can be avoided by administration in a Self Nano Emulsifying Drug Delivery System (SNEDDS).

Martin Lau Christiansen1, Rene Holm2, Jakob Kristensen3, Mads Kreilgaard1, Jette Jacobsen1, Bertil Abrahamsson4, Anette Müllertz5.   

Abstract

PURPOSE: To elucidate if a SNEDDS approach can eliminate the food-effect on cinnarizine absorption and to, investigate if a nutritional drink, Fresubin energy, could mimic food effect in dogs for the poorly soluble compound cinnarizine.
METHOD: A conventional tablet, a SNEDDS capsule or a SNEDDS tablet, containing cinnarizine, were dosed to beagles dogs in fed or fasted state (n=5), with a one week wash-out period between dosing. Dogs were pre-treated with pentagastrin. Fed state was induced by a nutritional drink (Fresubin Energy®). The food-effect was evaluated by comparing Tmax, Cmax and Bioavailability (F) for the different formulations.
RESULTS: Food effect was observed on all three parameters for the conventional tablet; Tmax was delayed 2.5times and bioavailability increased in fed state (from 20.9±5.7 to 53.8±30.1). Apart from an extended Tmax (2.5 and 3.3 times longer in fed state compared to fasted state for the SNEDDS tablets and SNEDDS capsules respectively), food effect on absorption for the SNEDDS capsules and SNEDDS tablets was not observed. The SNEDDS capsules had a higher bioavailability in both fed and fasted state compared to SNEDDS tablets (Ffasted=58.1±16.7, vs. 32.7±11.5), (Ffed=79.3±14.7 vs. 43.7±6.7) There were no significant differences in bioavailability between the conventional tablet in fed state and the SNEDDS capsules.
CONCLUSION: Food effect was observed when dosing cinnarizine with ingestion of the nutritional drink Fresubin Energy. Food effect on cinnarizine could be significantly reduced by dosing either as a SNEEDS capsule or a SNEDDS tablet, however, the SNEDDS tablet resulted in an overall lower absorption than the SNEDDS capsules in both fed and fasted state. The delay in fed state absorption could not be changed by dosing with SNEDDS formulations.
Copyright © 2014 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Dogs; Enabling formulations; Food interaction; Low soluble compounds; SNEDDS

Mesh:

Substances:

Year:  2013        PMID: 24239996     DOI: 10.1016/j.ejps.2013.11.003

Source DB:  PubMed          Journal:  Eur J Pharm Sci        ISSN: 0928-0987            Impact factor:   4.384


  7 in total

1.  Spontaneous emulsification of nifedipine-loaded self-nanoemulsifying drug delivery system.

Authors:  Yotsanan Weerapol; Sontaya Limmatvapirat; Mont Kumpugdee-Vollrath; Pornsak Sriamornsak
Journal:  AAPS PharmSciTech       Date:  2014-10-31       Impact factor: 3.246

2.  Supersaturated-Silica Lipid Hybrids Improve in Vitro Solubilization of Abiraterone Acetate.

Authors:  Hayley B Schultz; Paul Joyce; Nicky Thomas; Clive A Prestidge
Journal:  Pharm Res       Date:  2020-03-31       Impact factor: 4.200

Review 3.  Recent advances in delivery systems and therapeutics of cinnarizine: a poorly water soluble drug with absorption window in stomach.

Authors:  Smita Raghuvanshi; Kamla Pathak
Journal:  J Drug Deliv       Date:  2014-11-13

Review 4.  Understanding peroral absorption: regulatory aspects and contemporary approaches to tackling solubility and permeability hurdles.

Authors:  Prachi B Shekhawat; Varsha B Pokharkar
Journal:  Acta Pharm Sin B       Date:  2016-11-02       Impact factor: 11.413

5.  Stabilization benefits of single and multi-layer self-nanoemulsifying pellets: A poorly-water soluble model drug with hydrolytic susceptibility.

Authors:  Ahmad Abdul-Wahhab Shahba; Fars Kaed Alanazi; Sayed Ibrahim Abdel-Rahman
Journal:  PLoS One       Date:  2018-07-19       Impact factor: 3.240

6.  Development of self-nanoemulsifying drug delivery systems for the enhancement of solubility and oral bioavailability of fenofibrate, a poorly water-soluble drug.

Authors:  Kazi Mohsin; Rayan Alamri; Ajaz Ahmad; Mohammad Raish; Fars K Alanazi; Muhammad Delwar Hussain
Journal:  Int J Nanomedicine       Date:  2016-06-14

7.  The Influence of Fed State Lipolysis Inhibition on the Intraluminal Behaviour and Absorption of Fenofibrate from a Lipid-Based Formulation.

Authors:  Marlies Braeckmans; Joachim Brouwers; Danny Riethorst; Cécile Servais; Jan Tack; Patrick Augustijns
Journal:  Pharmaceutics       Date:  2022-01-04       Impact factor: 6.321

  7 in total

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