Controlled delivery systems for proteins based on poly(lactic/glycolic acid) microspheres
- PMID: 2062800
- DOI: 10.1023/a:1015841715384
Controlled delivery systems for proteins based on poly(lactic/glycolic acid) microspheres
Abstract
This paper describes an investigation of the use of poly(lactic/glycolic acid) polymers for long-term delivery of high molecular weight, water-soluble proteins. Poly(lactic/glycolic acid) (PLGA) microspheres, containing (fluorescein isothiocyanate)-labeled bovine serum albumin and (fluorescein isothiocyanate)-labeled horseradish peroxidase, were prepared by a modified solvent evaporation method using a double emulsion. The microspheres were spherical with diameters of 55-95 microns and encapsulated more than 90% of the protein. The preparation method was gentle and maintained enzyme activity and protein solubility. Stability studies showed that the encapsulation of an enzyme inside PLGA microspheres can protect them from activity loss. When not placed inside PLGA microspheres, (fluorescein isothiocyanate)-labeled horseradish peroxidase lost 80% of its activity in solution at 37 degrees C in a few days, whereas inside the PLGA microspheres it retained more than 55% of its activity after 21 days of incubation at 37 degrees C. In vitro release studies revealed that different release profiles (i.e., near-constant or biphasic) and release rates can be achieved by simply modifying factors in the preparation procedure such as mixing rate and volume of inner water and organic phases. Degradation studies by scanning electron microscopy and gel-permeation chromatography suggested that the mechanism responsible for protein release is mainly through matrix erosion.
Similar articles
-
Preparation and characterization of a composite PLGA and poly(acryloyl hydroxyethyl starch) microsphere system for protein delivery.Pharm Res. 2001 Nov;18(11):1600-6. doi: 10.1023/a:1013090700443. Pharm Res. 2001. PMID: 11758769
-
Brush-like branched biodegradable polyesters, part III. Protein release from microspheres of poly(vinyl alcohol)-graft-poly(D,L-lactic-co-glycolic acid).J Control Release. 2001 May 18;73(1):7-20. doi: 10.1016/s0168-3659(01)00231-0. J Control Release. 2001. PMID: 11337055
-
A heterogeneously structured composite based on poly(lactic-co-glycolic acid) microspheres and poly(vinyl alcohol) hydrogel nanoparticles for long-term protein drug delivery.Pharm Res. 1999 Sep;16(9):1430-5. doi: 10.1023/a:1018911411381. Pharm Res. 1999. PMID: 10496661
-
Protein delivery from poly(lactic-co-glycolic acid) biodegradable microspheres: release kinetics and stability issues.J Microencapsul. 1998 Nov-Dec;15(6):699-713. doi: 10.3109/02652049809008253. J Microencapsul. 1998. PMID: 9818948 Review.
-
Recent advances in the stabilization of proteins encapsulated in injectable PLGA delivery systems.Crit Rev Ther Drug Carrier Syst. 2002;19(1):73-98. doi: 10.1615/critrevtherdrugcarriersyst.v19.i1.20. Crit Rev Ther Drug Carrier Syst. 2002. PMID: 12046892 Review.
Cited by
-
Combination of the cationic surfactant dimethyl dioctadecyl ammonium bromide and synthetic mycobacterial cord factor as an efficient adjuvant for tuberculosis subunit vaccines.Infect Immun. 2004 Mar;72(3):1608-17. doi: 10.1128/IAI.72.3.1608-1617.2004. Infect Immun. 2004. PMID: 14977968 Free PMC article.
-
A review of the development of a vehicle for localized and controlled drug delivery for implantable biosensors.J Diabetes Sci Technol. 2008 Nov;2(6):1016-29. doi: 10.1177/193229680800200611. J Diabetes Sci Technol. 2008. PMID: 19885291 Free PMC article.
-
Effect of polymer porosity on aqueous self-healing encapsulation of proteins in PLGA microspheres.Macromol Biosci. 2013 Dec;13(12):1700-10. doi: 10.1002/mabi.201300323. Epub 2013 Nov 27. Macromol Biosci. 2013. PMID: 24285573 Free PMC article.
-
Highly loaded, sustained-release microparticles of curcumin for chemoprevention.J Pharm Sci. 2011 Jul;100(7):2599-609. doi: 10.1002/jps.22475. Epub 2011 Jan 14. J Pharm Sci. 2011. PMID: 21547911 Free PMC article.
-
Endostar-loaded PEG-PLGA nanoparticles: in vitro and in vivo evaluation.Int J Nanomedicine. 2010 Nov 24;5:1039-48. doi: 10.2147/IJN.S14753. Int J Nanomedicine. 2010. PMID: 21170352 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources