Poly(lactide-co-glycolide) nanoparticles for peroral delivery of bioactives
β Scribed by C.N. Grama; D.D. Ankola; M.N.V. Ravi Kumar
- Publisher
- Elsevier Science
- Year
- 2011
- Tongue
- English
- Weight
- 652 KB
- Volume
- 16
- Category
- Article
- ISSN
- 1359-0294
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β¦ Synopsis
The benefits of increasing surface area to volume ratio have long been realized by the pharmaceutical industry for addressing the solubility limited oral bioavailability. In the recent past various excipients that include but not limited to polymers and lipids are used to engineer nanostructures that possess one or more of the following properties, improve oral bioavailability, improve therapeutic efficacy, sustain the release of the encapsulated bioactive, minimize toxicity, have the ability to target the pathological site of interest and also perform dual role of diagnosis and delivery of bioactives simultaneously. In this review, we attempt to discuss the use of poly(lactide-co-glycolide) (PLGA) nanoparticles in addressing the solubility/permeability limited bioavailability problems of various bioactives that include drugs as well as antioxidants.
π SIMILAR VOLUMES
Biodegradable poly(lactide-co-glycolide) (PLGA) particles have shown significant potential for sustained and targeted delivery of several pharmaceutical agents, including plasmid DNA (pDNA). Here, we survey current approaches to PLGA particle preparation for pDNA delivery and discuss recent progress
## Abstract The layerβbyβlayer (LbL) assembly technique was applied for the surface modification of biodegradable poly(lactideβ__co__βglycolide) nanoparticles (NPs), employing poly(acrylic acid) (PAA), and polyethylenimine (PEI) as building blocks. Amino terminated poly(ethylene glycol) (PEG) and f