2010
DOI: 10.1016/j.actbio.2009.10.028
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Manipulation of process parameters to achieve different ternary phase microparticle configurations

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Cited by 27 publications
(24 citation statements)
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References 31 publications
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“…In contrast, tri‐layered structure resulted when viscosity of PLGA was <<1.1 (Systems S2 and S3) and initial polymer concentrations were kept above cloud point keeping all other parameters same as System S1. Probably due to considerably lower viscosity and also more compatibility between DCM and PLGA compared to PLLA, more quantity of DCM may partition into PLGA phase. As a result of which, PLGA phase with more DCM content, may become more hydrophobic than PLLA–DCM droplet leading to the migration of PLGA–DCM droplet toward core and relatively hydrophilic PLLA–DCM droplet toward shell being attracted by surrounding aqueous PVA solution.…”
Section: Resultssupporting
confidence: 50%
See 1 more Smart Citation
“…In contrast, tri‐layered structure resulted when viscosity of PLGA was <<1.1 (Systems S2 and S3) and initial polymer concentrations were kept above cloud point keeping all other parameters same as System S1. Probably due to considerably lower viscosity and also more compatibility between DCM and PLGA compared to PLLA, more quantity of DCM may partition into PLGA phase. As a result of which, PLGA phase with more DCM content, may become more hydrophobic than PLLA–DCM droplet leading to the migration of PLGA–DCM droplet toward core and relatively hydrophilic PLLA–DCM droplet toward shell being attracted by surrounding aqueous PVA solution.…”
Section: Resultssupporting
confidence: 50%
“…This layer configuration can be reversed if mass ratios are also altered . In various articles, they have also reported the fabrication of ternary‐phase microparticles having PLGA core and PLLA shell impregnated with poly(ε‐caprolactone) particulates by changing the polymer content . The influences of these ternary phases on drug release have also been evaluated .…”
Section: Introductionmentioning
confidence: 99%
“…Proper drug administration requires a fine balance between time, dosage, and mode of delivery, and, more importantly, should aid in improving patient compliance and clinical outcomes. These factors have consequently led to the emergence of various drug delivery systems, such as liposomes, micelles, emulsions and micro/nanoparticles 7–12. However, monolithic particulate systems may suffer from burst release due to the presence of undissolved drug trapped on the particle surface.…”
Section: Methodsmentioning
confidence: 99%
“…Researchers are exerting efforts to widen the usage of this polymer, by copolymerizing with PLLA, PDLLA, PLGA, and so on. These copolymers should enhance degradation kinetics in drug delivery (21)(22)(23)(24). PCL composites have been used more in tissue engineering and medical implants compared to drug delivery (1).…”
Section: Poly(α-hydroxy Acids)mentioning
confidence: 98%