4.7 Article

A novel gastroretentive porous microparticle for anti-Helicobacter pylori therapy: Preparation, in vitro and in vivo evaluation

Journal

INTERNATIONAL JOURNAL OF PHARMACEUTICS
Volume 463, Issue 1, Pages 10-21

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.ijpharm.2013.12.052

Keywords

Porous microparticles; Electrosp ray; Helicobacter pylori; Local delivery; SPECT/CT tomography

Funding

  1. National Natural Science Foundation of China [31200713]
  2. International Science and Technology Cooperation Base Construction of Chongqing [CSTC 201110005]
  3. Chongqing University Postgraduates' Innovative Team Building Project [201105A1001]

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Gastroretentive drug delivery system is a promising option for the treatment of Helicobacter pylori infection, which can prolong gastric residence time and supply high drug concentration in the stomach. In the present study, a low density system of metronidazole-loaded porous Eudragit RS microparticle with high drug loading capacity (>25%) was fabricated via electrospray method. The porous structure and size distribution of microparticles were affected by polymer concentration and flow rate of solution. FTIR and XRD analyses indicated that drug has been entrapped into the porous microparticles. In addition, sustained release profiles and slight cytotoxicity in vitro were detected. Gamma scintigraphy study in vivo demonstrated that 131I-labeled microparticles retained in stomach for over 8h, and about 65.50% radioactive counts were finally detected in the region of interest. The biodistribution study confirmed that hotspot of radioactivity was remaining in the stomach. Furthermore, metronidazole-loaded porous microparticles can eradicate H. pylon completely with lower dose and administration frequency of antibiotic compared with pure drug, which were also more helpful for the healing of mucosal damages. These results suggest that prepared porous microparticle has the potential to provide better treatment for H. pylon infection. (C) 2014 Elsevier B.V. All rights reserved.

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