Abstract |
The rapidly growing applications of antibody-based therapeutics requires novel approaches to develop efficient drug delivery systems in which biodegradable polymeric nanoparticles are amongst the best candidates. In the present study bevacizumab loaded PLGA nanoparticles were formulated by water-in-oil-in-water emulsion method. Protein inactivation and aggregation are the major drawbacks of this technique. Therefore protective ability of various stabilizers was studied during entrapment process. Probable changes in VEGF₁₆₅ binding capability of bevacizumab was assayed by ELISA which portrays the antibody's bio-efficiency. Probable breakage of bevacizumab and its secondary and tertiary structural integrity upon entrapment were analyzed by SDS-PAGE and circular dichroism spectroscopy, respectively. In vitro and ex vivo released bevacizumab from the prepared nanoparticles was also investigated. Results revealed that the protein interfacial adsorption is the foremost destabilizing factor in the double emulsion method and incorporation of appropriate concentrations of albumin could protect bevacizumab against entrapment stress. Ex vivo release results, in rabbit vitreous, indicated the ability of prepared nanoparticles in prolonged release of the active antibody. Consequently this approach was an attempt to achieve sustained release PLGA nanoparticle formulation with the aim of protecting integrity and performance of entrapped bevacizumab.
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Authors | Reyhaneh Varshochian, Mahmood Jeddi-Tehrani, Ahmad Reza Mahmoudi, Mohammad Reza Khoshayand, Fatemeh Atyabi, Araz Sabzevari, Mohammad Riazi Esfahani, Rassoul Dinarvand |
Journal | European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences
(Eur J Pharm Sci)
Vol. 50
Issue 3-4
Pg. 341-52
(Nov 20 2013)
ISSN: 1879-0720 [Electronic] Netherlands |
PMID | 23933615
(Publication Type: Journal Article)
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Copyright | Copyright © 2013 Elsevier B.V. All rights reserved. |
Chemical References |
- Angiogenesis Inhibitors
- Antibodies, Monoclonal, Humanized
- Immunoglobulin G
- Serum Albumin
- VEGFA protein, human
- Vascular Endothelial Growth Factor A
- Polylactic Acid-Polyglycolic Acid Copolymer
- Polyglycolic Acid
- Bevacizumab
- Lactic Acid
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Topics |
- Angiogenesis Inhibitors
(chemistry, pharmacology)
- Animals
- Antibodies, Monoclonal, Humanized
(chemistry, pharmacology)
- Bevacizumab
- Choroidal Neovascularization
(drug therapy)
- Drug Stability
- Immunoglobulin G
(immunology)
- Lactic Acid
(chemistry)
- Nanoparticles
(chemistry)
- Polyglycolic Acid
(chemistry)
- Polylactic Acid-Polyglycolic Acid Copolymer
- Rabbits
- Retinal Neovascularization
(drug therapy)
- Serum Albumin
(chemistry)
- Vascular Endothelial Growth Factor A
(metabolism)
- Vitreous Body
(metabolism)
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