Literature DB >> 18395431

Dissolution rate enhancement of the novel antitumoral beta-lapachone by solvent change precipitation of microparticles.

Marcílio S S Cunha-Filho1, Ramón Martínez-Pacheco, Mariana Landín.   

Abstract

beta-Lapachone [betaLAP] is a novel antitumor drug, which was recently on clinical trials with promising preliminary results. Problems derived from its low water solubility, its instability in solution and its high therapeutic dose constitute some challenges for pharmaceutical researchers. The purpose of the present work is to enhance the limited dissolution rate of betaLAP by the design of particles using a solvent change precipitation process. The procedure induces the spontaneous crystalline growth of the betaLAP in the presence of a stabilizing polymer (Hydroxypropylmethylcellulose) that limits the size of the particles generated. Physicochemical characterization of microparticles and the betaLAP dissolution rate was carried out. The utility of the betaLAP microcrystals in the development of tablets with adequate dissolution properties was also stated. The procedure was optimized in order to obtain stable and homogeneous particles with a small mean particle size (approximately 3 microm) and a narrow particle size distribution. There were no differences between the drying methods evaluated (in an oven and freeze-drying) with regard to particle morphology or dissolution behaviour, which is almost instantaneous. Tablets having suitable mechanical properties were produced by dry granulation prior to compression. The compression process did not compromise betaLAP dissolution characteristics.

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Year:  2008        PMID: 18395431     DOI: 10.1016/j.ejpb.2008.02.014

Source DB:  PubMed          Journal:  Eur J Pharm Biopharm        ISSN: 0939-6411            Impact factor:   5.589


  5 in total

Review 1.  Rationale for faster oral delivery to overcome the pathophysiology associated with dental pain--biopharmaceutic and pharmacokinetic challenges.

Authors:  Nuggehally R Srinivas
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2009 Jan-Mar       Impact factor: 2.441

2.  Experimental Design to Predict Process Variables in the Microcrystals of Celecoxib for Dissolution Rate Enhancement Using Response Surface Methodology.

Authors:  Mitra Jelvehgari; Hadi Valizadeh; Seyed Hassan Montazam; Sanam Abbaszadeh
Journal:  Adv Pharm Bull       Date:  2015-06-01

Review 3.  Enhancing Oral Absorption of β-Lapachone: Progress Till Date.

Authors:  Marival Bermejo; Victor Mangas-Sanjuan; Isabel Gonzalez-Alvarez; Marta Gonzalez-Alvarez
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2017-02       Impact factor: 2.569

4.  Intestinal Permeability of β-Lapachone and Its Cyclodextrin Complexes and Physical Mixtures.

Authors:  Victor Mangas-Sanjuan; Jorge Gutiérrez-Nieto; Magdalena Echezarreta-López; Isabel González-Álvarez; Marta González-Álvarez; Vicente-Germán Casabó; Marival Bermejo; Mariana Landin
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2016-12       Impact factor: 2.569

5.  Preparation and Characterization of Fenofibrate Microparticles with Surface-Active Additives: Application of a Supercritical Fluid-Assisted Spray-Drying Process.

Authors:  Jeong-Soo Kim; Heejun Park; Eun-Sol Ha; Kyu-Tae Kang; Min-Soo Kim; Sung-Joo Hwang
Journal:  Pharmaceutics       Date:  2021-12-02       Impact factor: 6.321

  5 in total

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