PLGA
Sign in to saveAlso known as Polylactic Acid-Polyglycolic Acid Copolymer
thumb|Structure of poly(lactic-co-glycolic acid). x= number of units of lactic acid; y= number of units of [[glycolic acid.]] PLGA, PLG, or 'poly(lactic-co-glycolic) acid' (CAS: ) is a copolymer which is used in a host of Food and Drug Administration (FDA) approved therapeutic devices, owing to its biodegradability and biocompatibility. PLGA is synthesized by means of ring-opening co-polymerization of two different monomers: glycolide and lactide, the cyclic dimers (1,4-dioxane-2,5-diones) of glycolic acid and lactic acid, respectively. Polymers can be synthesized as either random or block cop
Research
18,590 papers- PLGA-based biodegradable microspheres in drug delivery: recent advances in research and application.Drug delivery · 2021
- PLGA-Based Composites for Various Biomedical Applications.International journal of molecular sciences · 2022
- PEGylated PLGA nanoparticles: unlocking advanced strategies for cancer therapy.Molecular cancer · 2025
- Long-acting PLGA microspheres: Advances in excipient and product analysis toward improved product understanding.Advanced drug delivery reviews · 2023
- Exploiting PLGA-Based Biocompatible Nanoparticles for Next-Generation Tolerogenic Vaccines against Autoimmune Disease.International journal of molecular sciences · 2019
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8 sectionsContents
- Copolymer
- Degradation mechanism
- Biocompatibility
- Biodegradability
- Examples
- See also
- References
- External links
thumb|Structure of poly(lactic-co-glycolic acid). x= number of units of lactic acid; y= number of units of [[glycolic acid.]] PLGA, PLG, or 'poly(lactic-co-glycolic) acid' (CAS: ) is a copolymer which is used in a host of Food and Drug Administration (FDA) approved therapeutic devices, owing to its biodegradability and biocompatibility. PLGA is synthesized by means of ring-opening co-polymerization of two different monomers: glycolide and lactide, the cyclic dimers (1,4-dioxane-2,5-diones) of glycolic acid and lactic acid, respectively. Polymers can be synthesized as either random or block copolymers thereby imparting additional polymer properties. Common catalysts used in the preparation of this polymer include tin(II) 2-ethylhexanoate, tin(II) alkoxides, or aluminum isopropoxide. During polymerization, successive monomeric units of glycolic or lactic acid are linked together in PLGA by ester linkages, thus yielding a linear, polyester as a product. PLGA has also emerged as platform for advanced drug delivery systems, including nanoparticles, because of its tunable degradation behavior and ability to encapsulate different therapeutic agents. Recent research features its growing role in precision medicine and targeted therapies, specifically in cancer treatment and controlled release applications.
==Copolymer== Depending on the ratio of lactide to glycolide used for the polymerization, different forms of PLGA can be obtained: these are usually identified in regard to the molar ratio of the monomers used (e.g. PLGA 75:25 identifies a copolymer whose composition is 75% lactic acid and 25% glycolic acid). The crystallinity of PLGAs will vary from fully amorphous to fully crystalline depending on block structure and molar ratio. PLGAs typically show a glass transition temperature in the range of 40-60 °C. PLGA can be dissolved by a wide range of solvents, depending on composition. Higher lactide polymers can be dissolved using chlorinated solvents whereas higher glycolide materials will require the use of fluorinated solvents such as HFIP.