Andre G. Skirtach

Stimuli-responsive LbL capsules and nanoshells for drug delivery ☆

Review of basic principles and recent developments in the area of stimuli responsive polymeric capsules and nanoshells formed via layer-by-layer (LbL) is presented. The most essential attributes of the LbL approach are multifunctionality and responsiveness to a multitude of stimuli. The stimuli can be logically divided into three categories: physical (light, electric, magnetic, ultrasound, mechanical, and temperature), chemical (pH, ionic strength, solvent, and electrochemical) and biological (enzymes and receptors). Using these stimuli, numerous functionalities of nanoshells have been demonstrated: encapsulation, release including that inside living cells or in tissue, sensors, enzymatic reactions, enhancement of mechanical properties, and fusion. This review describes mechanisms and basic principles of stimuli effects, describes progress in the area, and gives an outlook on emerging trends such as theranostics and nanomedicine.

Near-IR Remote Release from Assemblies of Liposomes and Nanoparticles†

Set free by light: Near-IR (NIR) laser-initiated remote release of fluorescent dye from complexes of liposome-gold-nanoparticle aggregates is demonstrated (see fluorescence images). Complexes of the desired size are shown to be a viable approach to the construction of vesicle-based drug-delivery systems with light-triggered remote release characteristics. This opens up a new method to manipulate liposome-based drug-delivery systems in a biocompatible way by using the near-IR spectral range.

Encapsulation, release and applications of LbL polyelectrolyte multilayer capsules

Ever since their invention in 1998, polyelectrolyte multilayer micro- and nano-capsules have impacted various areas of biology, chemistry and physics. Here we highlight progress achieved since the millennium in the areas of encapsulation in and release from microcapsules, describe various structures including multicompartment and anisotropic constructs, and provide examples of several applications in biology. We also describe application areas such as drug delivery, intracellular trafficking, enzyme-catalyzed reactions, mechano-biology which benefited from recent developments in the area of polyelectrolyte multilayer capsules.

Polymeric microcapsules with light responsive properties for encapsulation and release.

This review is dedicated to recent developments on the topic of light sensitive polymer-based microcapsules. The microcapsules discussed are constructed using the layer-by-layer self-assembly method, which consists in absorbing oppositely charged polyelectrolytes onto charged sacrificial particles. Microcapsules display a broad spectrum of qualities over other existing microdelivery systems such as high stability, longevity, versatile construction and a variety of methods to encapsulate and release substances. Release and encapsulation of materials by light is a particularly interesting topic. Microcapsules can be made sensitive to light by incorporation of light sensitive polymers, functional dyes and metal nanoparticles. Optically active substances can be inserted into the shell during their assembly as a polymer complex or following the shell preparation. Ultraviolet-addressable microcapsules were shown to allow for remote encapsulation and release of materials. Visible- and infrared- addressable microcapsules offer a large array of release strategies for capsules, from destructive to highly sensitive reversible approaches. Besides the Introduction and Conclusions, this review contains in four sections reviewing the effects of light 1) on polymer-based microcapsules, 2) microcapsules containing metal nanoparticles and 3) functional dyes, as well as a fourth section that revisits the implications of light addressable polymeric microcapsules as a microdelivery system for biological applications.

Multicompartmental Micro- and Nanocapsules: Hierarchy and Applications in Biosciences

Multicompartmentalized micro- and nanocapsules allow simultaneous delivery of several vectors or biomolecules; they are the next generation of carriers with increased complexity. Here we overview multicompartment micro- and nanocapsules and present a road-map for future developments in the field. Four basic building block structures are demonstrated, three isotropic: concentric, pericentric, and innercentric, and one anisotropic: acentric. As an elaborate implementation of multicompartmentalization, an enzyme-catalyzed reaction inside the same capsule carrying both an enzyme and a substrate is shown. Applications of multicompartmentalized microcapsules for simultaneous multiple drug delivery in bio-medicine are discussed.

Reversibly permeable nanomembranes of polymeric microcapsules.

Polymeric nanometer-thick membranes or nanomembranes possessing photocontrollable permeability are presented. Microcapsules are used as membrane model systems, while gold nanoparticle aggregates are used as active absorption centers. Upon laser light illumination the membranes change permeability reversibly because nanoparticles transiently affect the nearby polymeric network. Nanomembranes reseal to their impermeable state when the laser is switched off. This presents a novel and simple way of reversible permeability control of interest to intracellular signaling and membranes.

Ultrasound stimulated release and catalysis using polyelectrolyte multilayer capsules

Ultrasound has been used to trigger release of encapsulated material from polyelectrolyte multilayer capsules. Sonication was found to destroy both plain and nanoparticle-modified capsules. Cavitation occurs through the collapse of generated microbubbles and the resulting shear forces should cause the destruction of the polyelectrolyte capsules. Application in catalysis is demonstrated in this paper, while further potential usage of ultrasound triggered release is anticipated in bio-medical applications.

Controlled intracellular release of peptides from microcapsules enhances antigen presentation on MHC class I molecules.

To understand the time course of action of any small molecule inside a single cell, one would deposit a defined amount inside the cell and initiate its activity at a defined moment. An elegant way to achieve this is to encapsulate the molecule in a micrometer-sized reservoir, introduce it into a cell, remotely open its wall by a laser pulse, and then follow the biological response by microscopy. The validity of this approach is validated here using microcapsules with defined walls that are doped with metallic nanoparticles so as to enable them to be opened with an infrared laser. The capsules are loaded with a fluorescent antigenic peptide and introduced into mammalian cultured cells where, upon laser-induced release, the peptide binds to major histocompatibility complex (MHC) class I proteins and elicits their cell surface transport. The concept of releasing a drug inside a cell and following its action is applicable to many problems in cell biology and medicine.

Nanoplasmonics for dual-molecule release through nanopores in the membrane of red blood cells

A nanoplasmonics-based opto-nanoporation method of creating nanopores upon laser illumination is applied for inducing diffusion and triggered release of small and large molecules from red blood cells (RBCs). The method is implemented using absorbing gold nanoparticle (Au-NP) aggregates on the membrane of loaded RBCs, which, upon near-IR laser light absorption, induce release of encapsulated molecules from selected cells. The binding of Au-NPs to RBCs is characterized by Raman spectroscopy. The process of release is driven by heating localized at nanoparticles, which impacts the permeability of the membrane by affecting the lipid bilayer and/or trans-membrane proteins. Localized heating and temperature rise around Au-NP aggregates is simulated and discussed. Research reported in this work is relevant for generating nanopores for biomolecule trafficking through polymeric and lipid membranes as well as cell membranes, while dual- and multi-molecule release is relevant for theragnostics and a wide range of therapies.

Toward self-assembly of nanoparticles on polymeric microshells: Near-IR release and permeability

We present a novel approach to construct hollow polymeric microcontainers that can be remotely addressed using a low-power near-infrared laser to release encapsulated materials. Microshells possessing walls with aggregates of gold nanoparticles are found to release encapsulated materials upon near-IR irradiation, while shells containing the same amount of nonaggregated gold nanoparticles did not release their contents. The permeability of thermally shrunk microcapsules to dextran molecules is the lowest for shells containing nonaggregated nanoparticles and the highest for microcapsules with no nanoparticles. The wall thickness, roughness, influence of concentration of encapsulated materials, and general shrinking behavior of the microcapsules are studied. Aggregation of nanoparticles increases the absorption coefficient in the near-infrared part of electromagnetic spectrum. The temperature increase upon near-infrared laser illumination for different gold nanoparticle distributions is simulated. Important implications of this approach are expected in development of drug delivery systems as well as in temperature- and light-sensitive materials and membranes.