Biodegradable Viral Nanoparticle/Polymer Implants Prepared via Melt-Processing
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作者:
Lee, Parker W.
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Case Western Reserve Univ, Case Sch Engn, Dept Macromol Sci & Engn, Cleveland, OH 44106 USACase Western Reserve Univ, Case Sch Engn, Dept Macromol Sci & Engn, Cleveland, OH 44106 USA
Lee, Parker W.
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Shukla, Sourabh
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Case Western Reserve Univ, Case Sch Engn, Dept Biomed Engn, Cleveland, OH 44106 USACase Western Reserve Univ, Case Sch Engn, Dept Macromol Sci & Engn, Cleveland, OH 44106 USA
Shukla, Sourabh
[2
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Wallat, Jaqueline D.
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Case Western Reserve Univ, Case Sch Engn, Dept Macromol Sci & Engn, Cleveland, OH 44106 USACase Western Reserve Univ, Case Sch Engn, Dept Macromol Sci & Engn, Cleveland, OH 44106 USA
Wallat, Jaqueline D.
[1
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Danda, Chaitanya
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Case Western Reserve Univ, Case Sch Engn, Dept Macromol Sci & Engn, Cleveland, OH 44106 USACase Western Reserve Univ, Case Sch Engn, Dept Macromol Sci & Engn, Cleveland, OH 44106 USA
Danda, Chaitanya
[1
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Steinmetz, Nicole F.
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Case Western Reserve Univ, Sch Med, Cleveland, OH 44106 USA
Case Western Reserve Univ, Case Comprehens Canc Ctr, Div Gen Med Sci Oncol, Cleveland, OH 44106 USACase Western Reserve Univ, Case Sch Engn, Dept Macromol Sci & Engn, Cleveland, OH 44106 USA
Steinmetz, Nicole F.
[3
,4
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Maia, Joao
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Case Western Reserve Univ, Case Sch Engn, Dept Macromol Sci & Engn, Cleveland, OH 44106 USACase Western Reserve Univ, Case Sch Engn, Dept Macromol Sci & Engn, Cleveland, OH 44106 USA
Maia, Joao
[1
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Pokorski, Jonathan K.
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Case Western Reserve Univ, Case Sch Engn, Dept Macromol Sci & Engn, Cleveland, OH 44106 USACase Western Reserve Univ, Case Sch Engn, Dept Macromol Sci & Engn, Cleveland, OH 44106 USA
Pokorski, Jonathan K.
[1
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机构:
[1] Case Western Reserve Univ, Case Sch Engn, Dept Macromol Sci & Engn, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Case Sch Engn, Dept Biomed Engn, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Sch Med, Cleveland, OH 44106 USA
[4] Case Western Reserve Univ, Case Comprehens Canc Ctr, Div Gen Med Sci Oncol, Cleveland, OH 44106 USA
Viral nanoparticles have been utilized as a platform for vaccine development and are a versatile system for the display of antigenic epitopes for a variety of disease states. However, the induction of a clinically relevant immune response often requires multiple injections over an extended period of time, limiting patient compliance. Polymeric systems to deliver proteinaceous materials have been extensively researched to provide sustained release, which would limit administration to a single dose. Melt-processing is an emerging manufacturing method that has been utilized to create polymeric materials laden with proteins as an alternative to typical solvent-based production methods. Melt-processing is advantageous because it is continuous, solvent-free, and 100% of the therapeutic protein is encapsulated. In this study, we utilized melt-encapsulation to fabricate-viral nanoparticle laden polymeric materials that effectively deliver intact particles and generate carrier specific antibodies in vivo. The effects of initial processing and postprocessing on particle integrity and aggregation were studied to develop processing windows for scale-up and the creation of more complex materials. The dispersion of particles within the PLGA matrix was studied, and the effect of additives and loading level on the release profile was determined. Overall, melt encapsulation was found to be an effective method to produce composite materials that can deliver viral nanoparticles over an extended period and elicit an immune response comparable to typical administration schedules.