Abstract

Polymeric multilayer capsules formed by the Layer-by-Layer (LbL) technique are interesting candidates for the purposes of storage, encapsulation, and release of drugs and biomolecules for pharmaceutical and biomedical applications. In the current study, cellulose-based core-shell particles were developed via the LbL technique alternating two cellulose derivatives, anionic carboxymethylcellulose (CMC), and cationic quaternized hydroxyethylcellulose ethoxylate (QHECE), onto a cationic vesicular template made of didodecyldimethylammonium bromide (DDAB). The obtained capsules were characterized by dynamic light scattering (DLS), ζ potential measurements, and high-resolution scanning electron microscopy (HR-SEM). DLS measurements reveal that the size of the particles can be tuned from a hundred nanometers with a low polydispersity index (deposition of 2 layers) up to micrometer scale (deposition of 6 layers). Upon the deposition of each cellulose derivative, the particle charge is reversed, and pH is observed to considerably affect the process thus demonstrating the electrostatic driving force for LbL deposition. The HR-SEM characterization suggests that the shape of the core-shell particles formed is reminiscent of the spherical vesicle template. The development of biobased nano- and micro-containers by the alternating deposition of oppositely charged cellulose derivatives onto a vesicle template offers several advantages, such as simplicity, reproducibility, biocompatibility, low-cost, mild reaction conditions, and high controllability over particle size and composition of the shell.

Highlights

  • IntroductionThe development of nanostructured materials (i.e., inorganic, organic, polymeric, and biological) with different composition, morphology, and sizes is of great scientific and technological interest due to their huge potential in many areas ranging from the encapsulation and controlled release of drugs, protection of biologically active species, and removal of pollutants, to the development of advanced materials suitable for cosmetics, inks, or catalysis [1,2,3,4,5]

  • The development of nanostructured materials with different composition, morphology, and sizes is of great scientific and technological interest due to their huge potential in many areas ranging from the encapsulation and controlled release of drugs, protection of biologically active species, and removal of pollutants, to the development of advanced materials suitable for cosmetics, inks, or catalysis [1,2,3,4,5]. These systems can be synthesized with well-defined structural features conferring control over different properties, such as mechanical, optical, electrical, and biological, among others [6]

  • The average hydrodynamic diameter and the ζ-potential values of the aggregates were determined by means of dynamic light scattering measurements and electrophoretic mobilities by laser Doppler velocimetry, respectively, using a Malvern UK Zetasizer-Nano

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Summary

Introduction

The development of nanostructured materials (i.e., inorganic, organic, polymeric, and biological) with different composition, morphology, and sizes is of great scientific and technological interest due to their huge potential in many areas ranging from the encapsulation and controlled release of drugs, protection of biologically active species, and removal of pollutants, to the development of advanced materials suitable for cosmetics, inks, or catalysis [1,2,3,4,5] These systems can be synthesized with well-defined structural features conferring control over different properties, such as mechanical, optical, electrical, and biological, among others [6]. Through alternating adsorption of cationic and anionic macromolecules, well-defined surface layers with variable thickness (from a few to hundreds of Å) can be created. Iler’s approach is conceptually interesting, but of limited use since the layers are not very stable and do not have molecular dimensions

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