Title |
Probing insulin bioactivity in oral nanoparticles produced by ultrasonication-assisted emulsification/internal gelation
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Published in |
International Journal of Nanomedicine, September 2015
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DOI | 10.2147/ijn.s86313 |
Pubmed ID | |
Authors |
Marlene A Lopes, Bárbara Abrahim-Vieira, Claudia Oliveira, Pedro Fonte, Alessandra M T Souza, Tammy Lira, Joana A D Sequeira, Carlos R Rodrigues, Lúcio M Cabral, Bruno Sarmento, Raquel Seiça, Francisco Veiga, António J Ribeiro |
Abstract |
Alginate-dextran sulfate-based particles obtained by emulsification/internal gelation technology can be considered suitable carriers for oral insulin delivery. A rational study focused on the emulsification and particle recovery steps was developed in order to reduce particles to the nanosize range while keeping insulin bioactivity. There was a decrease in size when ultrasonication was used during emulsification, which was more pronounced when a cosurfactant was added. Ultrasonication add-on after particle recovery decreased aggregation and led to a narrower nanoscale particle-size distribution. Insulin encapsulation efficiency was 99.3%±0.5%, attributed to the strong pH-stabilizing electrostatic effect between insulin and nanoparticle matrix polymers. Interactions between these polymers and insulin were predicted using molecular modeling studies through quantum mechanics calculations that allowed for prediction of the interaction model. In vitro release studies indicated well-preserved integrity of nanoparticles in simulated gastric fluid. Circular dichroism spectroscopy proved conformational stability of insulin and Fourier transform infrared spectroscopy technique showed rearrangements of insulin structure during processing. Moreover, in vivo biological activity in diabetic rats revealed no statistical difference when compared to nonencapsulated insulin, demonstrating retention of insulin activity. Our results demonstrate that alginate-dextran sulfate-based nanoparticles efficiently stabilize the loaded protein structure, presenting good physical properties for oral delivery of insulin. |
X Demographics
Geographical breakdown
Country | Count | As % |
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Unknown | 3 | 100% |
Demographic breakdown
Type | Count | As % |
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Practitioners (doctors, other healthcare professionals) | 3 | 100% |
Mendeley readers
Geographical breakdown
Country | Count | As % |
---|---|---|
Unknown | 135 | 100% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Student > Bachelor | 49 | 36% |
Student > Ph. D. Student | 17 | 13% |
Student > Master | 14 | 10% |
Researcher | 7 | 5% |
Lecturer | 4 | 3% |
Other | 14 | 10% |
Unknown | 30 | 22% |
Readers by discipline | Count | As % |
---|---|---|
Pharmacology, Toxicology and Pharmaceutical Science | 50 | 37% |
Biochemistry, Genetics and Molecular Biology | 12 | 9% |
Chemistry | 11 | 8% |
Agricultural and Biological Sciences | 10 | 7% |
Medicine and Dentistry | 7 | 5% |
Other | 9 | 7% |
Unknown | 36 | 27% |