Particle size and distribution of biodegradable poly‐D,L‐lactide‐co‐poly(ethylene glycol) block polymer nanoparticles prepared by nanoprecipitation

A biodegradable block copolymer, poly-D,L-lactide (PLA)-co-poly(ethylene glycol) (PEG), was prepared by the ring-opening polymerization of lactide with stannous caprylate [Sn(Oct 2 )] as a catalyst; then, the PLA-PEG copolymer was made into nanoparticles by nanoprecipitation under different conditions. The average molecular weight and structure of PLA-PEG were detected by 1 H-NMR and gel permeation chromatography. The sizes and distributions of the nanoparticles were investigated with a laser particle-size analyzer. The morphologies of the nanoparticles were examined by transmission electron microscopy. The effects of the solvent-nonsolvent system, operation conditions, and dosage of span-80 on the sizes and distributions of the nanoparticles are discussed. The results show that acetone-water was a suitable solvent-nonsolvent system and the volume ratio of the nonsolvent phase to the solvent phase (O/W) (v/v), the concentration of PLA-PEG in the solvent phase, and the dosage of span-80 had important effects on the particle sizes and distributions.

[1]  E. Doelker,et al.  Influence of the microencapsulation method and peptide loading on poly(lactic acid) and poly(lactic-co-glycolic acid) degradation during in vitro testing. , 1998, Journal of controlled release : official journal of the Controlled Release Society.

[2]  Haixiong Ge,et al.  Synthesis and characterization of chitosan-poly(acrylic acid) nanoparticles. , 2002, Biomaterials.

[3]  E. Reverchon SUPERCRITICAL ANTISOLVENT PRECIPITATION OF MICRO- AND NANO-PARTICLES , 1999 .

[4]  Lisa Brannon-Peppas,et al.  Recent advances on the use of biodegradable microparticles and nanoparticles in controlled drug delivery , 1995 .

[5]  N. Elvassore,et al.  Production of insulin-loaded poly(ethylene glycol)/poly(l-lactide) (PEG/PLA) nanoparticles by gas antisolvent techniques. , 2001, Journal of pharmaceutical sciences.

[6]  T. Kissel,et al.  Sulfobutylated poly(vinyl alcohol)-graft-poly(lactide-co-glycolide)s facilitate the preparation of small negatively charged biodegradable nanospheres. , 2000, Journal of controlled release : official journal of the Controlled Release Society.

[7]  S. Davis,et al.  Drug delivery in poly(lactide-co-glycolide) nanoparticles surface modified with poloxamer 407 and poloxamine 908: in vitro characterisation and in vivo evaluation. , 2001, Journal of controlled release : official journal of the Controlled Release Society.

[8]  Shaobing Zhou,et al.  Synthesis and Characterization of Biodegradable Low Molecular Weight Aliphatic Polyesters and Their Use in Protein-Delivery Systems , 2004 .

[9]  Y. I. Kim,et al.  Preparation and characterization of nanoparticles containing an antihypertensive agent. , 1998, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[10]  Soriano,et al.  The role of PEG on the stability in digestive fluids and in vivo fate of PEG-PLA nanoparticles following oral administration. , 2000, Colloids and surfaces. B, Biointerfaces.

[11]  F. Mi,et al.  Chitin/PLGA blend microspheres as a biodegradable drug-delivery system: phase-separation, degradation and release behavior. , 2002, Biomaterials.

[12]  T. Chandy,et al.  Development of polylactide microspheres for protein encapsulation and delivery , 2002 .

[13]  F. Mi,et al.  Chitin/PLGA blend microspheres as a biodegradable drug delivery system: a new delivery system for protein. , 2003, Biomaterials.