Literature DB >> 10205645

Development of 5-iodo-2'-deoxyuridine milling process to reduce initial burst release from PLGA microparticles.

A Gèze1, M C Venier-Julienne, D Mathieu, R Filmon, R Phan-Tan-Luu, J P Benoit.   

Abstract

The aim of this study was to prepare 5-iodo-2'-deoxyuridine (IdUrd) loaded poly(d,l-lactide-co-glycolide) (PLGA) microspheres with a reduced initial burst in the in vitro release profile, by modifying the drug grinding conditions. IdUrd particle size reduction has been performed using spray-drying or ball milling. Spray-drying significantly reduced drug particle size with a change of the initial crystalline form to an amorphous one and led to a high initial burst. Conversely, ball milling did not affect the initial IdUrd crystallinity. Therefore, the grinding process was optimized to emphasize the initial burst reduction. A first step allowed us to set qualitative parameters such as ball number (7) and cooling with liquid nitrogen to obtain a mean size reduction and a narrow distribution. In a second step, three parameters including milling speed, drug amount and time were studied by a response surface analysis. The interrelationship between drug amount and milling speed was the most significant factor. To reduce particle size it should be necessary to use a moderate speed associated with a sufficient drug amount (400-500 mg). IdUrd release from microparticles prepared by the o/w emulsion/extraction solvent evaporation process with the lowest crystalline particle size (15.3 microns) was studied. Burst effect could be reduced significantly. Concerning the first phase of drug release, the burst was 8.7% for 15.3 microns compared to 19% for 19.5 microns milled drug particles.

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Year:  1999        PMID: 10205645     DOI: 10.1016/s0378-5173(98)00380-9

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


  2 in total

1.  Optimization of the operating conditions of a lab scale Aljet mill using lactose and sucrose: a technical note.

Authors:  Neha B Vatsaraj; Danchen Gao; Donna L Kowalski
Journal:  AAPS PharmSciTech       Date:  2003       Impact factor: 3.246

2.  Enhanced solubility and functionality of valrubicin (AD-32) against cancer cells upon encapsulation into biocompatible nanoparticles.

Authors:  Nirupama Sabnis; Maya Nair; Mervyn Israel; Walter J McConathy; Andras G Lacko
Journal:  Int J Nanomedicine       Date:  2012-02-22
  2 in total

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