skip to main content
US FlagAn official website of the United States government
dot gov icon
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
https lock icon
Secure .gov websites use HTTPS
A lock ( lock ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

Explore Research Products in the PAR
It may take a few hours for recently added research products to appear in PAR search results.


Title: Hydrocortisone/cyclodextrin complex electrospun nanofibers for a fast-dissolving oral drug delivery system
The electrospinning of hydrocortisone/cyclodextrin complex nanofibers was performed in order to develop a fast-dissolving oral drug delivery system. Hydrocortisone is a water-insoluble hydrophobic drug, yet, the water solubility of hydrocortisone was significantly enhanced by inclusion complexation with hydroxypropyl-beta-cyclodextrin (HP-β-CyD). In this study, hydrocortisone/HP-β-CyD complexes were prepared in aqueous solutions having molar ratios of 1/1, 1/1.5 and 1/2 (hydrocortisone/HP-β-CyD). Highly concentrated aqueous solutions of HP-β-CyD (180%, w/v) were used for hydrocortisone/HP-β-CyD systems (1/1, 1/1.5 and 1/2) in order to perform electrospinning without the use of an additional polymer matrix. The turbidity of hydrocortisone/HP-β-CyD (1/1 and 1/1.5) aqueous solutions indicated the presence of some uncomplexed crystals of hydrocortisone whereas the aqueous solution of hydrocortisone/HP-β-CyD (1/2) was homogeneous indicating that hydrocortisone becomes totally water-soluble by inclusion complexation with HP-β-CyD. Nonetheless, the electrospinning of hydrocortisone/HP-β-CyD systems (1/1, 1/1.5 and 1/2) successfully yielded defect-free uniform nanofibrous structures. Moreover, the electrospinning process was quite efficient that hydrocortisone was completely preserved without any loss yielding hydrocortisone/HP-β-CyD nanofibers having the initial molar ratios (1/1, 1/1.5 and 1/2). The structural and thermal characterization of the hydrocortisone/HP-β-CyD nanofibers revealed that hydrocortisone was totally inclusion complexed with HP-β-CyD and was in the amorphous state in hydrocortisone/HP-β-CyD (1/2) nanofibers whereas some uncomplexed crystalline hydrocortisone was present in hydrocortisone/HP-β-CyD (1/1 and 1/1.5) nanofibers. Nevertheless, hydrocortisone/HP-β-CyD (1/1, 1/1.5 and 1/2) complex aqueous systems were electrospun in the form of nanofibrous webs having a free-standing and flexible nature. The hydrocortisone/HP-β-CyD (1/1, 1/1.5 and 1/2) nanofibrous webs have shown fast-dissolving behavior in water or when they were in contact with artificial saliva. Yet, the hydrocortisone/HP-β-CyD (1/2) nanofibrous web dissolved more quickly than the hydrocortisone/HP-β-CyD (1/1 and 1/1.5) nanofibrous webs due to the full inclusion complexation and the amorphous state of hydrocortisone in this sample. In short, the results suggest that polymer-free electrospun nanofibrous webs produced from hydrocortisone/HP-β-CyD could be quite applicable for fast-dissolving oral drug delivery systems.  more » « less
Award ID(s):
1719875
PAR ID:
10146821
Author(s) / Creator(s):
;
Date Published:
Journal Name:
RSC Medicinal Chemistry
Volume:
11
Issue:
2
ISSN:
2632-8682
Page Range / eLocation ID:
245 to 258
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. ; (, Food & Function)
    null (Ed.)
    The encapsulation of food/dietary supplements into electrospun cyclodextrin (CD) inclusion complex nanofibers paves the way for developing novel carrying and delivery substances along with orally fast-dissolving properties. In this study, CD inclusion complex nanofibers of Vitamin-A acetate were fabricated from polymer-free aqueous systems by using the electrospinning technique. The hydroxypropylated (HP) CD derivatives of HPβCD and HPγCD were used for both encapsulation of Vitamin-A acetate and the electrospinning of free-standing nanofibrous webs. The ultimate Vitamin-A acetate/CD nanofibrous webs (NWs) were obtained with a loading capacity of 5% (w/w). The amorphous distribution of Vitamin-A acetate in the nanofibrous webs by inclusion complexation and the unique properties of nanofibers ( e.g. high surface area and porosity) ensured the fast disintegration and fast dissolution/release of Vitamin-A acetate/CD-NW in a saliva simulation and aqueous medium. The enhanced solubility of Vitamin-A acetate in the case of Vitamin-A acetate/CD-NW also ensured an improved antioxidant property for the Vitamin-A acetate compound. Moreover, Vitamin-A acetate thermally degraded at higher temperature in Vitamin-A acetate/CD-NWs, suggesting the enhanced thermal stability of this active compound. Here, HPβCD formed inclusion complexes in a more favorable way when compared to HPγCD. Therefore, there were some uncomplexed Vitamin-A acetate crystals detected in Vitamin-A acetate/HPγCD-NW, while Vitamin-A acetate molecules loaded in Vitamin-A acetate/HPβCD-NW were completely in complexed and amorphous states. Depending on this, better solubilizing effect, higher release amount and enhanced antioxidant properties have been provided for the Vitamin-A acetate compound in the case of Vitamin-A acetate/HPβCD-NW. 
    more » « less
  2. ; ; ; ; ; (, RSC Medicinal Chemistry)
    Naproxen/Cyclodextrin inclusion complex nanofibrous films were generatedviaelectrospinning technique to develop fast-disintegrating oral drug delivery system. 
    more » « less
  3. (, Surfaces and interfaces)
    Co-axial electrospinning is an efficient technique to develop core-shell or hollow nanofibrous structures. In this study electrospun carbon nanofibers with three different morphologies, i.e. solid nanofibers with porous structure (P-ECNF), hollow nanofibers with solid wall (H-ECNF), and hollow nanofibers with porous wall (HP-ECNF) were developed through bicomponent electrospinning and co-axial electrospinning of polyacrylonitrile (PAN) and poly (methyl methacrylate) (PMMA) by varying proportion of the sacrificial PMMA. Through comparative electrochemical analyses, it is revealed that the primary factors for electrochemical performance, i.e. specific capacitance, of the electrospun carbon nanofibrous materials are mesopore volume and total pore volume. The hollow structure as well as ordered carbon structure and intact fiber structure also benefits electrolyte transfer and subsequent electrochemical performance but is secondary. Overall the porous carbon nanofibrous electrode material from electrospinning PAN/PMMA (50/50) solution (P-ECNF-50-50) outperformed those hollow and hollow-porous counterparts from co-axial electrospinning and demonstrated the largest specific capacitance due to the largest mesopore volume as well as the largest total pore volume. This electrode material also showed excellent cycling stability (without any loss of specific capacitance) after 3,000 cycles of charging and discharging. It even showed some increase of specific capacitance with cycling test due to its relatively large amount of micropores. 
    more » « less
  4. ; ; ; (, Macromolecular Rapid Communications)
    Abstract Electrospun fish gelatin (FGel) nanofibers (NF) mimic the natural bodies extracellular matrix's (ECM) structure and are an attractive material for many biomedical applications. However, FGel poor mechanical properties and rapid dissolution in an aqueous media paired with usually low productivity of the typical electrospinning process necessitate further effort in overcoming these issues. In this study, alternating field electrospinning (AFES) fabricates cold water fish skin gelatin nanofibrous materials (FGel NFM) with up to 10 wt.% Dextran (DEX) or acetyl glucosamine (AGA) from pure aqueous solutions at process productivity of 7.92–8.90 g∙h−1. Thermal crosslinking of as‐spun materials resulted in FGel‐based NFM with 125–325 nm fiber diameters. DEX (MW500k and MW75k) and AGA additives cause different effects on FGel fiber diameters, structure, tensile and degradation behavior, and in vitro performance. All tested materials reveal favorable, but not the same, cellular response through the formation of a confluent layer on the NFM surface regardless of the fibers’ composition despite the significant difference in FGel NFM structure and properties. Results show that AFES and thermal crosslinking of FGel‐based NFM can lead to a sustainable “green” fabrication technology of mono‐ and polysaccharide modified FGel‐based NFM scaffolds with the parameters attuned to targeted biomedical applications. 
    more » « less
  5. ; (, Analysis & Sensing)
    Abstract Phenolic acids are a class of poorly water‐soluble organic compounds with antioxidant properties that contain a carboxylic acid and a phenol group, common in plants. We used hydroxypropyl‐β‐cyclodextrin (HP‐β‐CD) as a supramolecular host to sense phenolic acids in water near physiological pH. The analytes’ complexation was monitored through changes in the optical absorption and emission properties of a series of six organic dyes, acting as indicators in a displacement assay, that were selected from screening a panel of 17 candidates. Binding constants between these dyes and the HP‐β‐CD were in the 102–104range. We showed that the nuanced differences in the dyes’ optical signatures associated with this displacement process, when analyzed and summarized using multivariate analysis algorithms such as principal component analysis (PCA), can be used to successfully discriminate among six phenolic acids, and to identify six unknown samples of such acids, down to a 0.02 mM concentration. 
    more » « less
  • Citation Formats
  • MLA
  • APA
  • Chicago
  • BibTeX
  • Save / Share this Record
  • Send to Email