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

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          Abstract

          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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          Mechanisms of solute release from porous hydrophilic polymers

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            Modeling and comparison of dissolution profiles.

            Over recent years, drug release/dissolution from solid pharmaceutical dosage forms has been the subject of intense and profitable scientific developments. Whenever a new solid dosage form is developed or produced, it is necessary to ensure that drug dissolution occurs in an appropriate manner. The pharmaceutical industry and the registration authorities do focus, nowadays, on drug dissolution studies. The quantitative analysis of the values obtained in dissolution/release tests is easier when mathematical formulas that express the dissolution results as a function of some of the dosage forms characteristics are used. In some cases, these mathematic models are derived from the theoretical analysis of the occurring process. In most of the cases the theoretical concept does not exist and some empirical equations have proved to be more appropriate. Drug dissolution from solid dosage forms has been described by kinetic models in which the dissolved amount of drug (Q) is a function of the test time, t or Q=f(t). Some analytical definitions of the Q(t) function are commonly used, such as zero order, first order, Hixson-Crowell, Weibull, Higuchi, Baker-Lonsdale, Korsmeyer-Peppas and Hopfenberg models. Other release parameters, such as dissolution time (tx%), assay time (tx min), dissolution efficacy (ED), difference factor (f1), similarity factor (f2) and Rescigno index (xi1 and xi2) can be used to characterize drug dissolution/release profiles.
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              Electrospun tri-layer nanodepots for sustained release of acyclovir

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                Author and article information

                Journal
                Polymers (Basel)
                Polymers (Basel)
                polymers
                Polymers
                MDPI
                2073-4360
                20 October 2020
                October 2020
                : 12
                : 10
                : 2421
                Affiliations
                [1 ]School of Materials Science & Engineering, University of Shanghai for Science & Technology, 516 Jungong Road, Shanghai 200093, China; 182442511@ 123456st.usst.edu.cn (S.K.); 183762605@ 123456st.usst.edu.cn (S.H.); 1826418107@ 123456st.usst.edu.cn (X.C.); lixiaoyan@ 123456usst.edu.cn (X.L.)
                [2 ]Shanghai Institute of Technical Physics, Chinese Academy of Sciences, 500 Yutian Road, Shanghai 200083, China; wanglin@ 123456mail.sitp.ac.cn
                [3 ]UCL School of Pharmacy, University College London, 29-39 Brunswick Square, London WC1N 1AX, UK
                Author notes
                [* ]Correspondence: ydg017@ 123456usst.edu.cn (D.-G.Y.); g.williams@ 123456ucl.ac.uk (G.R.W.)
                [†]

                These two authors contribute equally to this work.

                Author information
                https://orcid.org/0000-0002-0764-6731
                https://orcid.org/0000-0001-7825-4498
                https://orcid.org/0000-0002-3066-2860
                Article
                polymers-12-02421
                10.3390/polym12102421
                7589577
                33092310
                90d0c21f-4862-4aad-95b1-f6e52471651c
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 25 September 2020
                : 19 October 2020
                Categories
                Article

                energy saving,electrospinning,engineering optimization,poorly water-soluble drug,fast dissolution

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