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      Three EHDA Processes from a Detachable Spinneret for Fabricating Drug Fast Dissolution Composites

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          Abstract

          In this study, three kinds of electrohydrodynamic atomization (EHDA) processes (electrospraying, electrospinning, and coaxial electrospinning) are implemented to create hydroxypropyl methylcellulose (HPMC) based ultra‐thin products for providing the fast dissolution of a poorly water‐soluble drug ketoprofen (KET). An EHDA apparatus, characterized by a novel spinneret, is homemade for conducting the three processes. The three types of products are electrospun nanofibers E1, electrosprayed microparticles E2, and core‐shell nanofibers E3. SEM and TEM results indicate that they have the anticipated morphologies and inner structures. X‐ray diffraction and Fourier Transform Infrared results verify that KET is mainly amorphous in all the composites due to its fine compatibility with HPMC. In vitro dissolution tests demonstrate that the drug rapid release performances has an order of E3>E1>E2≫KET powders. The fast dissolution mechanisms are suggested and the advantages of the three products are compared. The super performance of E3 in furnishing the rapid release is attributed to a synergistic action of small size (of the shell thickness), high porosity, amorphous state of drug, and the solubility of HPMC. EHDA nanostructures can support the development of nano drug delivery systems (DDSs) through tailoring the spatial distribution of drug molecules within the nano products.

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          Electrospun tri-layer nanodepots for sustained release of acyclovir

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            Bio-mimic multichannel microtubes by a facile method.

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              Energy-Saving Electrospinning with a Concentric Teflon-Core Rod Spinneret to Create Medicated Nanofibers

              Although electrospun nanofibers are expanding their potential commercial applications in various fields, the issue of energy savings, which are important for cost reduction and technological feasibility, has received little attention to date. In this study, a concentric spinneret with a solid Teflon-core rod was developed to implement an energy-saving electrospinning process. Ketoprofen and polyvinylpyrrolidone (PVP) were used as a model of a poorly water-soluble drug and a filament-forming matrix, respectively, to obtain nanofibrous films via traditional tube-based electrospinning and the proposed solid rod-based electrospinning method. The functional performances of the films were compared through in vitro drug dissolution experiments and ex vivo sublingual drug permeation tests. Results demonstrated that both types of nanofibrous films do not significantly differ in terms of medical applications. However, the new process required only 53.9% of the energy consumed by the traditional method. This achievement was realized by the introduction of several engineering improvements based on applied surface modifications, such as a less energy dispersive air-epoxy resin surface of the spinneret, a free liquid guiding without backward capillary force of the Teflon-core rod, and a smaller fluid–Teflon adhesive force. Other non-conductive materials could be explored to develop new spinnerets offering good engineering control and energy savings to obtain low-cost electrospun polymeric nanofibers.
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                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                Macromolecular Materials and Engineering
                Macro Materials & Eng
                Wiley
                1438-7492
                1439-2054
                November 23 2023
                Affiliations
                [1 ] Fashion Institute Donghua University Shanghai 200051 China
                [2 ] Key Laboratory of Clothing Design & Technology Ministry of Education Donghua University Shanghai 200051 China
                [3 ] School of Materials and Chemistry University of Shanghai for Science and Technology Shanghai 200093 China
                [4 ] The Third Affiliated Hospital Naval Medical University Shanghai 200433 China
                Article
                10.1002/mame.202300361
                6a6a8396-538b-4430-b14c-3401217f80c5
                © 2023

                http://creativecommons.org/licenses/by/4.0/

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