Multifunctional microbubbles for image-guided antivascular endothelial growth factor therapy
Open accessAbstract
We synthesize multifunctional microbubbles (MBs) for targeted delivery of antivascular endothelial growth factor (antiVEGF) therapy with multimodal imaging guidance. Poly-lactic-co-glycolic acid (PLGA) MBs encapsulating Texas Red dye are fabricated by a modified double-emulsion process. Simultaneous ultrasound and fluorescence imaging are achieved using Texas Red encapsulated MBs. The MBs are conjugated with Avastin, an antiVEGF antibody for treating neovascular age-related macular degeneration (AMD). The conjugation efficiency is characterized by enzyme-linked immunosorbent assay (ELISA). The efficiency for targeted binding of Avastin-conjugated MBs is characterized by microscopic imaging. Our work demonstrates the technical potential of using multifunctional MBs for targeted delivery of antiVEGF therapy in the treatment of exudative AMD.
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Multifunctional particles can be formulated from a component material to reduce side effects of the encapsulated drug.
“Such multifunctional particles can also be formulated from a component material to reduce side effects of the encapsulated drug [70].”
From Poly Lactic-co-Glycolic Acid (PLGA) as Biodegradable Controlled Drug Delivery Carrier (2011) · cites this paper as [70]
The paper describes multifunctional PLGA microbubbles made from a biocompatible, biodegradable material for targeted delivery (Abstract; page unavailable). It does not report reduced drug side effects; the encapsulated substance in this study was Texas Red dye, while the anti-VEGF drug Avastin was conjugated to the microbubble surface. (LLM, conf=0.87)
Experimental — accuracy not yet measuredThe high rate of clearance of micro/nanoparticles by the reticuloendothelial system and difficulty penetrating many tissue types may limit their use to the vascular space.
“However, the high rate clearance of micro/nanoparticles by the body’s reticuloendothelial system (RES) and the difficultyfor such particles to penetrate many tissue types may limit their use to the vascular space [69–71].”
From Poly Lactic-co-Glycolic Acid (PLGA) as Biodegradable Controlled Drug Delivery Carrier (2011) · cites this paper as [70]
The Abstract discusses micro- and nanobubbles for imaging and intraocular drug delivery, but does not address clearance by the reticuloendothelial system or difficulty penetrating tissue. Searches for those mechanisms and for confinement to the vascular space found no relevant passage in our copy. Page numbers were not provided. (LLM, conf=0.75)
Experimental — accuracy not yet measured
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- Authors
- Zhang, L., Xu, J. S., Sanders, V. E., Letson, A. D., Roberts, C. J., & Xu, R. X.
- Affiliations
- The Ohio State University (US)
- Los Alamos National Laboratory (US)
- Venue
- Journal of Biomedical Optics
- Publisher
- SPIE-Intl Soc Optical Eng
- Published
- 2010-05-01
- Volume
- 15
- Issue
- 03
- Pages
- 1-3
- ISSN
- 1083-3668 (ISSN-L)
- 1560-2281
- OpenAlex
- W2136036251
- Cited by
- 16
- References
- 14
- Citations by year
- 2024: 1 · 2023: 1 · 2021: 3 · 2016: 2 · 2015: 1 · 2014: 1 · 2013: 3 · 2012: 1
- FWCI
- 1.32
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Biomedical Optics (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Physical Sciences › Engineering › Biomedical Engineering › Ultrasound and Hyperthermia Applications
- Physical Sciences › Engineering › Biomedical Engineering › Photoacoustic and Ultrasonic Imaging
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advanced Drug Delivery Systems
- Keywords
- microbubbles, anti-VEGF therapy, bevacizumab, neovascular age-related macular degeneration, targeted drug delivery, Texas Red, ultrasonography, fluorescence imaging, antibody conjugation, image-guided therapy
- MeSH terms
- Bevacizumab, Antibodies, Monoclonal, Diagnostic Imaging, Enzyme-Linked Immunosorbent Assay, Humans, Macular Degeneration, Microscopy, Electron, Scanning, Logistic Models, Drug Delivery Systems, Angiogenesis Inhibitors, Vascular Endothelial Growth Factor A, Microbubbles, Antibodies, Monoclonal, Humanized
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