Literature DB >> 20719477

Preparation and physicochemical characterization of naproxen-PLGA nanoparticles.

Yousef Javadzadeh1, Fatemeh Ahadi, Soodabeh Davaran, Ghobad Mohammadi, Araz Sabzevari, Khosro Adibkia.   

Abstract

Naproxen is a non-steroidal anti-inflammatory drug which can be used for the treatment of inflammatory disorders like uveitis and arthirit rheumatoid. The aim of the present study was to investigate the physicochemical characteristics of naproxen-PLGA nanoparticles. The nanoparticles of naproxen with PLGA were formulated using the solvent evaporation/extraction technique (the single emulsion technique). Several process parameters i.e., drug/polymer ratio, aqueous phase volume and speed of homogenization were considered with the aim of achieve optimal preparation conditions. The physicochemical characteristics of nanoparticles were studied applying particle size analysis, differential scanning calorimetry, X-ray crystallography, Fourier transform infrared spectroscopy and scanning electron microscopy. The release rate of naproxen from various drug/polymer nanoparticles was investigated as well. All the prepared formulations using PLGA resulted in nano-range size particles (352-571 nm) with spherical smooth morphology. The nanoparticles of naproxen-PLGA displayed lower crystallinity with no chemical interactions between the drug and polymer molecules. The nanoparticles exhibited the slower release of drug in comparison with the intact drug and the physical mixtures. According of these findings, formulation of the naproxen-PLGA nanoparticles was able to improve the physicochemical characteristics of the drug and possibly will increase the anti-inflammatory effects of drug following its ocular or intra-joint administration.
Copyright © 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 20719477     DOI: 10.1016/j.colsurfb.2010.07.047

Source DB:  PubMed          Journal:  Colloids Surf B Biointerfaces        ISSN: 0927-7765            Impact factor:   5.268


  15 in total

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3.  Novel PEG-graft-PLA nanoparticles with the potential for encapsulation and controlled release of hydrophobic and hydrophilic medications in aqueous medium.

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Review 4.  Nanosizing of drugs: Effect on dissolution rate.

Authors:  S Maleki Dizaj; Zh Vazifehasl; S Salatin; Kh Adibkia; Y Javadzadeh
Journal:  Res Pharm Sci       Date:  2015 Mar-Apr

5.  Preparation and In Vitro/Ex Vivo Evaluation of Moxifloxacin-Loaded PLGA Nanosuspensions for Ophthalmic Application.

Authors:  Meetali Mudgil; Pravin K Pawar
Journal:  Sci Pharm       Date:  2013-02-04

6.  Monitoring model drug microencapsulation in PLGA scaffolds using X-ray powder diffraction.

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Journal:  Saudi Pharm J       Date:  2015-03-21       Impact factor: 4.330

Review 7.  Concepts and practices used to develop functional PLGA-based nanoparticulate systems.

Authors:  Hongkee Sah; Laura A Thoma; Hari R Desu; Edel Sah; George C Wood
Journal:  Int J Nanomedicine       Date:  2013-02-21

8.  Cubic phase nanoparticles for sustained release of ibuprofen: formulation, characterization, and enhanced bioavailability study.

Authors:  Linghui Dian; Zhiwen Yang; Feng Li; Zhouhua Wang; Xin Pan; Xinsheng Peng; Xintian Huang; Zhefei Guo; Guilan Quan; Xuan Shi; Bao Chen; Ge Li; Chuanbin Wu
Journal:  Int J Nanomedicine       Date:  2013-02-26

9.  Novel multi-biotin grafted poly(lactic acid) and its self-assembling nanoparticles capable of binding to streptavidin.

Authors:  Hao Yan; Weimin Jiang; Yinxing Zhang; Ying Liu; Bin Wang; Li Yang; Lihong Deng; Gurinder K Singh; Jun Pan
Journal:  Int J Nanomedicine       Date:  2012-01-31

Review 10.  Particles from preformed polymers as carriers for drug delivery.

Authors:  K Miladi; D Ibraheem; M Iqbal; S Sfar; H Fessi; A Elaissari
Journal:  EXCLI J       Date:  2014-02-03       Impact factor: 4.068

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