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Polymeric carriers enhance targeted drug delivery by increasing efficacy while minimizing off-target effects. These carriers comprise a biodegradable polymeric backbone integrated with functional elements that enable targeting, improve physicochemical properties, and regulate drug release.Targeting MechanismsThe targeting ability of polymeric carriers is mediated by a homing device, which is a molecular recognition component designed to selectively bind to specific tissues or cells. Monoclonal...
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Biofunctionalized Prussian Blue Nanoparticles for Multimodal Molecular Imaging Applications
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Engineered BSA nanoparticles: Synthesis, drug loading, and advanced characterization.

Hemlata1, A Hariharan1, Nandan Murali2

  • 1Kusuma School of Biological Sciences, Indian Institute of Technology, Hauz Khas, New Delhi 110016, India.

Biology Methods & Protocols
|September 29, 2025
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Summary
This summary is machine-generated.

Bovine serum albumin (BSA) nanoparticles offer a versatile platform for drug delivery and biomedical applications. This study details reproducible methods for synthesizing and characterizing these nanoparticles for enhanced therapeutic potential.

Keywords:
bovine serum albumin nanoparticles (BSA NPs)controlled drug releasedesolvation methodnanoparticle characterization

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Area of Science:

  • Biomaterials Science
  • Nanotechnology
  • Pharmaceutical Sciences

Background:

  • Bovine serum albumin (BSA) nanoparticles are recognized for their biocompatibility and biodegradability.
  • They offer advantages like enhanced drug stability, solubility, non-toxicity, and surface modifiability.
  • Potential applications span cancer treatment, drug delivery, bioimaging, and theranostics.

Purpose of the Study:

  • To provide a detailed, reproducible, and adaptable protocol for synthesizing and characterizing BSA nanoparticles.
  • To explore the influence of synthesis parameters on nanoparticle properties.
  • To assess nanoparticle stability under physiological conditions.

Main Methods:

  • Synthesis via desolvation process followed by glutaraldehyde crosslinking.
  • Characterization using dynamic light scattering (DLS), electron microscopy (SEM, TEM), FTIR, and nanoparticle tracking analysis (NTA).
  • Stability assessment in phosphate-buffered saline (PBS) to simulate physiological conditions.

Main Results:

  • Established a reproducible method for BSA nanoparticle synthesis and drug encapsulation.
  • Demonstrated control over particle size, surface charge, and dispersity by adjusting crosslinking ratio, pH, and BSA content.
  • Confirmed nanoparticle stability under simulated physiological conditions.

Conclusions:

  • The presented protocol serves as a foundational reference for designing functionalized BSA nanoparticles for biomedical applications.
  • Standardized preparation and characterization techniques advance nanoparticle-based technology.
  • This work facilitates innovation in developing BSA nanoparticles for therapeutic and diagnostic purposes.