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292  11  Electrospun Biopolymer Nanofibers and Their Composites for Drug Delivery Applications

                    protein encapsulation. In vitro release profiles measured using the Micro-BCA
                    assay indicated sustained release of BSA and lysozyme for more than 30 days.
                    The results of circular dichroism suggested that the secondary structure of
                    released BSA can be retained and the bioactivity of released lysozyme was found
                    to be more than 90%. Therefore, coaxial electrospray could be a very promising
                    approach to encapsulate biomacromolecules such as proteins, enzymes, DNA
                    plasmids, or living cells inside microparticles for controlled release drug delivery
                    applications [90].
                      With conventional methods for biodegradable particle production heavily rely-
                    ing on batch and emulsion preparation methods, Almería et al. developed a well-
                    controlled approach based on multiplexed electrospray to obtain a PLGA system
                    encapsulating amphiphilic agents such as doxorubicin, RHB, and RHB octadecyl
                    ester perchlorate. The results indicate that particles can be made encapsulating
                    the agent with high efficiency and be coated with emulsifiers in a single-step flow
                    process, which largely facilitates further functionalization for targeted drug deliv-
                    ery. Therefore, this synthesis technique is well suited for massive scale-up using
                    microfabricated, multiplexed arrays consisting of multiple electrospray nozzles
                    operating in parallel [91].



                    11.4
                    Conclusions and Outlook

                    Electrospinning has gained widespread interest as a potential polymer processing
                    technique for applications in drug delivery systems. By careful selection of
                    materials and processing conditions, either biodegradable or nondegradable
                    biopolymers can be used to control drug release via diffusion alone or diffusion
                    and scaffold degradation, and encapsulation of various suitable therapeutic
                    agents in electrospun nanofibers or nanoparticles has been effectively realized,
                    including antibiotics, anticancer drugs, proteins, and DNA. In addition, com-
                    bining different electrospinning techniques such as electrospraying, coaxial,
                    or emulsion electrospinning, a variety of different-structured drug/biopolymer
                    composites, for example, nanoparticle-encapsulated nanofibers and core/shell-
                    structured nanofibers or nanoparticles can be achieved to give finer control over
                    drug release kinetics, which show potential biomedical applications in wound
                    dressings, scaffolds, or devices for localized delivery of chemotherapeutics.
                      While electrospinning has emerged as a viable polymer processing technique
                    for applications in drug delivery systems, further investigations are required to
                    precisely characterize and optimize the pre-existing drug delivery systems and
                    develop new materials or methods for greatly improving the current product
                    properties. To date, most of the studies on drug release are performed in vitro,
                    while the capability of drug-loaded devices for clinical applications is essentially
                    needed to be confirmed in vivo. Therefore, it is urgently required for delivery of
                    therapeutic agents in a way very similar to the natural biological context through
                    electrospinning, especially for biomacromolecules such as DNA, RNA, or growth
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