Literature DB >> 26386139

Development of flexible and dispersible oral formulations containing praziquantel for potential schistosomiasis treatment of pre-school age children.

Ramona Trastullo1, Luisa Stella Dolci2, Nadia Passerini1, Beatrice Albertini3.   

Abstract

Praziquantel (PZQ), an anthelmintic drug used in developing countries for the treatment of schistosome infections, was processed using the fluid bed wet granulation technology to prepare fast dispersible granules, as an appropriate and flexible dosage form for pre-school-aged children. Granulation experiments were performed incorporating PZQ either in the powder mixture, according to the traditional way, or in the liquid phase containing wetting agents. In the powder mixture several excipients were tested: Flowlac 100 as filler, Galeniq 721 (isomalt) and Neosorb P 100 T (D-sorbitol) as sweeteners and PVP K30 as binder; while in the liquid phase Lutrol F68, Cremophor RH 40 or Tween 80 as surfactants were investigated. Different formulations loaded with 10% w/w (batches 1-8) and 20% w/w of PZQ (batches 9-13) were produced The majority of granules displayed good flow properties and uniform drug content. X-ray powder diffraction showed that PZQ remained in its original crystalline state, while differential scanning calorimetry and Fourier transform-infrared analysis evidenced the formation of chemical interactions among the ingredients. The solubilisation test performed in non-sink condition to reproduce the actual condition in which a child of 4 years takes the medicine revealed that granules quickly formed a very fine suspension in water (dV90=39.9 μm). Although after the granulation process the solubility of raw PZQ was not increased, adding the aqueous suspension to 500 ml of buffer solution of pH 1.5, simulating the fasted state of a child, 50% of the drug was dissolved after 30 min. After granule manipulation with milk and fruit juices, no PZQ degradation was observed during time. Finally, the selected granule formulation provided evidence to be stable even at hot and very humid climate (30°C/75% RH), at least for the examined time.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Extemporaneous aqueous suspensions; Neglected tropical diseases; Paediatric dosage form; Praziquantel; Solid-state characterization; Stability; Wet granulation

Mesh:

Substances:

Year:  2015        PMID: 26386139     DOI: 10.1016/j.ijpharm.2015.09.019

Source DB:  PubMed          Journal:  Int J Pharm        ISSN: 0378-5173            Impact factor:   5.875


  4 in total

1.  Biopharmaceutical optimization in neglected diseases for paediatric patients by applying the provisional paediatric biopharmaceutical classification system.

Authors:  Jose Manuel Del Moral Sanchez; Isabel Gonzalez-Alvarez; Aaron Cerda-Revert; Marta Gonzalez-Alvarez; Andres Navarro-Ruiz; Gordon L Amidon; Marival Bermejo
Journal:  Br J Clin Pharmacol       Date:  2018-07-17       Impact factor: 4.335

2.  Ground Calcium Carbonate as a Low Cost and Biosafety Excipient for Solubility and Dissolution Improvement of Praziquantel.

Authors:  Ana Borrego-Sánchez; Rita Sánchez-Espejo; Beatrice Albertini; Nadia Passerini; Pilar Cerezo; César Viseras; C Ignacio Sainz-Díaz
Journal:  Pharmaceutics       Date:  2019-10-14       Impact factor: 6.321

3.  Investigation of Praziquantel/Cyclodextrin Inclusion Complexation by NMR and LC-HRMS/MS: Mechanism, Solubility, Chemical Stability, and Degradation Products.

Authors:  Tatjana Kezele Špehar; Marijana Pocrnić; David Klarić; Branimir Bertoša; Ana Čikoš; Mario Jug; Jasna Padovan; Snježana Dragojević; Nives Galić
Journal:  Mol Pharm       Date:  2021-10-21       Impact factor: 4.939

Review 4.  Safety of integrated preventive chemotherapy for neglected tropical diseases.

Authors:  Allan M Ciciriello; Jessica K Fairley; Emma Cooke; Paul M Emerson; Pamela J Hooper; Birgit Bolton; Genevieve LaCon; David G Addiss
Journal:  PLoS Negl Trop Dis       Date:  2022-09-29
  4 in total

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