Abstract

On-demand drug-delivery systems using nanofibers are extensively applicable for customized drug release based on target location and timing to achieve the desired therapeutic effects. A nanofiber formulation is typically created for a certain medication and changing the drug may have a significant impact on the release kinetics from the same delivery system. Nanofibers have several distinguishing features and properties, including the ease with which they may be manufactured, the variety of materials appropriate for processing into fibers, a large surface area, and a complex pore structure. Nanofibers with effective drug-loading capabilities, controllable release, and high stability have gained the interest of researchers owing to their potential applications in on-demand drug delivery systems. Based on their composition and drug-release characteristics, we review the numerous types of nanofibers from the most recent accessible studies. Nanofibers are classified based on their mechanism of drug release, as well as their structure and content. To achieve controlled drug release, a suitable polymer, large surface-to-volume ratio, and high porosity of the nanofiber mesh are necessary. The properties of nanofibers for modified drug release are categorized here as protracted, stimulus-activated, and biphasic. Swellable or degradable polymers are commonly utilized to alter drug release. In addition to the polymer used, the process and ambient conditions can have considerable impacts on the release characteristics of the nanofibers. The formulation of nanofibers is highly complicated and depends on many variables; nevertheless, numerous options are available to accomplish the desired nanofiber drug-release characteristics.

Highlights

  • The development of on-demand drug delivery systems (DDSs) has received significant attention owing to the high demand for controlled delivery of various drugs to organs and cell tissues [1,2]

  • NF film containing RhB as a model drug was further modified with a hydrogel precursor solution containing N-isopropylacrylamide (NIPAAm), NIPMAAm, and BIS-AAm in a proportion of 1:0.05:0.03, respectively, with dispersed gold nanorods (GNRs) to obtain the mutual effects of temperature rise, water movement that triggers the release of molecules from the NFs, and photothermal therapy

  • Cho et al [71] have reported the use of electrospun nanostructures with topographical signals for neuronal differences in mesenchymal stem cells (MSCs) in combination with nerve growth factor (NGF)

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Summary

Introduction

The development of on-demand drug delivery systems (DDSs) has received significant attention owing to the high demand for controlled delivery of various drugs to organs and cell tissues [1,2]. The drugs that reach the market have potential side effects; for example, anticancer chemotherapeutics are a source of concern for both therapists and patients because of their inherent toxicity [9,10]. NFs offer unique qualities, of their immense potential for smart DDSs (Figure 1) [23,24]. NFs stabilize with active molecules on their surface [32,33,34] Because of their benefits, such as improving drug solubility and bioavailability or regulating the pace and location of administration, rapid dissolution and controlled release have become crucial for creating innovative properties, such asas protection of innovative drug drug delivery deliverymethods methods[35].

Types and Preparation of NFs as DDSs
Schematic
Blended NFs
Experiments on swelling and weight
Core-Shell NFs
A CS electrospun
Encapsulation
Chemical Immobilization
Schematic preparing NGF–conjugated
Physical Adsorption
Stimuli-Responsive on-Demand Drug Release
Temperature
11. Schematic
Electric and Magnetic Field
Multistimuli
Modes of Drug Administration
Oral Drug Delivery
Findings
Skin Treatment
Full Text
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