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Preparation, Optimization and Activity Evaluation of PLGA/Streptokinase Nanoparticles Using Electrospray
Nasrin Yaghoobi1, Reza Faridi Majidi1, Mohammad Ali Faramarzi2
1Department of Medical Nanotechnology, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Advanced Pharmaceutical Bulletin
|May 17, 2017
Summary
Poly(lactic-co-glycolic acid) (PLGA) nanoparticles effectively encapsulated streptokinase (SK) using electrospray. This method offers a promising approach for protein delivery, though enzyme activity preservation requires further investigation.
Area of Science:
- Biomaterials Science
- Nanotechnology
- Drug Delivery
Background:
- Poly(lactic-co-glycolic acid) (PLGA) nanoparticles (NPs) are widely used for drug delivery.
- Streptokinase (SK) is a crucial enzyme for treating thrombotic diseases.
Purpose of the Study:
- To encapsulate streptokinase (SK) into PLGA NPs using electrospray.
- To evaluate the impact of electrospray parameters on NP size and size distribution (SD).
- To assess the activity and release profile of encapsulated SK.
Main Methods:
- Electrospray encapsulation of SK within PLGA NPs.
- Artificial Neural Networks (ANNs) for optimizing NP size and SD based on voltage, needle diameter, and polymer-to-protein ratio.
- In vitro drug release studies over 72 hours.
- Enzyme activity assays post-encapsulation.
Main Results:
- Optimized electrospray conditions yielded NPs with a mean size of 37 (12) nm and 90% encapsulation efficiency.
- Low polymer/enzyme ratio and needle ID favored smaller NP size.
- High voltage values minimized NP size distribution.
- Initial burst release of 20% SK within 30 minutes, followed by 41% over 72 hours.
- Encapsulated SK retained 19.2% activity immediately after preparation.
Conclusions:
- Electrospraying is a viable method for encapsulating enzymes like SK into PLGA NPs.
- Further research is needed to optimize electrospray conditions for maximum enzyme activity retention.

