Literature DB >> 12878396

PLGA-PEG microspheres of teverelix: influence of polymer type on microsphere characteristics and on teverelix in vitro release.

Delphine Mallardé1, François Boutignon, Fabien Moine, Edith Barré, Sandrine David, Hélène Touchet, Paolo Ferruti, Romano Deghenghi.   

Abstract

Teverelix microspheres were produced by coacervation using a new type of poly(ester-carbonates) made of block copolymers of poly(lactic-glycolic acid) (PLGA) and poly(ethylene glycol) (PEG). Five different PLGA-PEG copolymers and one PLGA were used. The 'stability window' has been determined for all polymers. It varied depending on the molecular weight and the weight percentage of PEG. With increasing core loading (from 9.4 to 34.2%), the microparticle size increased from 10-50 to 5-1000 micrometer. The core loading did not have any influence on encapsulation yield, which remained above 80%. The influence of polymer type on microsphere characteristics was studied at two different core loadings: 9.4 and 28%. At a low core loading, the nature of the polymer had no influence on microsphere characteristics whereas at 28%, only PLGA-PEG copolymers gave acceptable microparticles in term of particle size. At 28%, the glass transition temperature (T(g)) of loaded particles was 1-8 degrees C higher than the T(g) of the corresponding polymer. Increasing the core loading increased teverelix release whereas polymer degradation was decreased. All microparticles made of PLGA-PEG copolymers showed a faster release of teverelix than PLGA-based microspheres, whatever the core loading. One PLGA-PEG was selected on the basis of in vitro release rate for further in vivo investigations.

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Year:  2003        PMID: 12878396     DOI: 10.1016/s0378-5173(03)00272-2

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


  4 in total

1.  Preparation, characterization and in vitro release properties of morphine-loaded PLLA-PEG-PLLA microparticles via solution enhanced dispersion by supercritical fluids.

Authors:  Fu Chen; Guangfu Yin; Xiaoming Liao; Yi Yang; Zhongbing Huang; Jianwen Gu; Yadong Yao; Xianchun Chen; Hu Gao
Journal:  J Mater Sci Mater Med       Date:  2013-04-27       Impact factor: 3.896

2.  Stability of proteins encapsulated in injectable and biodegradable poly(lactide-co-glycolide)-glucose millicylinders.

Authors:  Jichao Kang; Oliver Lambert; Michael Ausborn; Steven P Schwendeman
Journal:  Int J Pharm       Date:  2008-02-14       Impact factor: 5.875

3.  Stealth Amphotericin B nanoparticles for oral drug delivery: In vitro optimization.

Authors:  Bushra T Al-Quadeib; Mahasen A Radwan; Lidija Siller; Benjamin Horrocks; Matthew C Wright
Journal:  Saudi Pharm J       Date:  2014-11-20       Impact factor: 4.330

Review 4.  Biodegradable polymers for microencapsulation of drugs.

Authors:  Jae Hyung Park; Mingli Ye; Kinam Park
Journal:  Molecules       Date:  2005-01-31       Impact factor: 4.411

  4 in total

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