Therapeutic applications of electrospun nanofibers for drug delivery systems

Electrospun nanofiber drug delivery systems have been studied using various techniques. Herein, we describe the fabrication of a drug-incorporating nanofiber. Drugs, such as proteins, peptide, antibodies, and small molecule drugs, can be loaded within or on the surface of nanofibers according to the...

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Published in	Archives of pharmacal research Vol. 37; no. 1; pp. 69 - 78
Main Authors	Son, Young Ju, Kim, Woo Jin, Yoo, Hyuk Sang
Format	Journal Article
Language	English
Published	Dordrecht Springer Netherlands 01.01.2014 대한약학회
Subjects	absorption Animals antibodies bioactive properties cell differentiation Delayed-Action Preparations Drug Carriers drug delivery systems Drug Delivery Systems - instrumentation drugs Humans hydrocolloids Hydrophobic and Hydrophilic Interactions hydrophobicity Medicine Nanofibers Nanomedicine - instrumentation Nanomedicine - methods nanoparticles Pharmaceutical Preparations - administration & dosage Pharmaceutical Preparations - chemistry Pharmacology/Toxicology Pharmacy polymers Polymers - chemistry proteins Review Solubility solvents Technology, Pharmaceutical - instrumentation Technology, Pharmaceutical - methods 약학 Electrospinning Nanofiber Drug delivery Tissue engineering
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ISSN	0253-6269 1976-3786 1976-3786
DOI	10.1007/s12272-013-0284-2

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Abstract	Electrospun nanofiber drug delivery systems have been studied using various techniques. Herein, we describe the fabrication of a drug-incorporating nanofiber. Drugs, such as proteins, peptide, antibodies, and small molecule drugs, can be loaded within or on the surface of nanofibers according to their properties. Hydrophobic drugs are directly dissolved with a polymer in an organic solvent before electrospinning. However, it is preferred to surface-immobilize bioactive molecules on nanofibers by physical absorption or chemical conjugation. Especially, chemically surface-immobilized proteins on a nanofiber mesh stimulate cell differentiation and proliferation. Using a dual electrospinning nozzle to create nanofiber sheet layers, which are stacked on top of one another, the initial burst release is reduced compared with solid nanofibers because of the layers. Furthermore, hybridization of electrospun nanofibers with nanoparticles, microspheres, and hydrogels is indirect drug loading method into the nanofibers. It is also possible to produce multi-drug delivery systems with timed programmed release.
AbstractList	Electrospun nanofiber drug delivery systems have been studied using various techniques. Herein, we describe the fabrication of a drug-incorporating nanofiber. Drugs, such as proteins, peptide, antibodies, and small molecule drugs, can be loaded within or on the surface of nanofibers according to their properties. Hydrophobic drugs are directly dissolved with a polymer in an organic solvent before electrospinning. However, it is preferred to surface-immobilize bioactive molecules on nanofibers by physical absorption or chemical conjugation. Especially, chemically surface-immobilized proteins on a nanofiber mesh stimulate cell differentiation and proliferation. Using a dual electrospinning nozzle to create nanofiber sheet layers, which are stacked on top of one another, the initial burst release is reduced compared with solid nanofibers because of the layers. Furthermore, hybridization of electrospun nanofibers with nanoparticles, microspheres, and hydrogels is indirect drug loading method into the nanofibers. It is also possible to produce multi-drug delivery systems with timed programmed release.Electrospun nanofiber drug delivery systems have been studied using various techniques. Herein, we describe the fabrication of a drug-incorporating nanofiber. Drugs, such as proteins, peptide, antibodies, and small molecule drugs, can be loaded within or on the surface of nanofibers according to their properties. Hydrophobic drugs are directly dissolved with a polymer in an organic solvent before electrospinning. However, it is preferred to surface-immobilize bioactive molecules on nanofibers by physical absorption or chemical conjugation. Especially, chemically surface-immobilized proteins on a nanofiber mesh stimulate cell differentiation and proliferation. Using a dual electrospinning nozzle to create nanofiber sheet layers, which are stacked on top of one another, the initial burst release is reduced compared with solid nanofibers because of the layers. Furthermore, hybridization of electrospun nanofibers with nanoparticles, microspheres, and hydrogels is indirect drug loading method into the nanofibers. It is also possible to produce multi-drug delivery systems with timed programmed release. Electrospun nanofiber drug delivery systems have been studied using various techniques. Herein, we describe the fabrication of a drug-incorporating nanofiber. Drugs, such as proteins, peptide, antibodies, and small molecule drugs, can be loaded within or on the surface of nanofibers according to their properties. Hydrophobic drugs are directly dissolved with a polymer in an organic solvent before electrospinning. However, it is preferred to surface-immobilize bioactive molecules on nanofibers by physical absorption or chemical conjugation. Especially, chemically surface-immobilized proteins on a nanofiber mesh stimulate cell differentiation and proliferation. Using a dual electrospinning nozzle to create nanofiber sheet layers, which are stacked on top of one another, the initial burst release is reduced compared with solid nanofibers because of the layers. Furthermore, hybridization of electrospun nanofibers with nanoparticles, microspheres, and hydrogels is indirect drug loading method into the nanofibers. It is also possible to produce multi-drug delivery systems with timed programmed release. Electrospun nanofiber drug delivery systems have been studied using various techniques. Herein, we describe the fabrication of a drug-incorporating nanofiber. Drugs, such as proteins, peptide, antibodies, and small molecule drugs, can be loaded within or on the surface of nanofibers according to their properties. Hydrophobic drugs are directly dissolved with a polymer in an organic solvent before electrospinning. However, it is preferred to surface-immobilize bioactive molecules on nanofibers by physical absorption or chemical conjugation. Especially, chemically surface-immobilized proteins on a nanofiber mesh stimulate cell differentiation and proliferation. Using a dual electrospinning nozzle to create nanofiber sheet layers, which are stacked on top of one another, the initial burst release is reduced compared with solid nanofibers because of the layers. Furthermore, hybridization of electrospun nanofibers with nanoparticles, microspheres, and hydrogels is indirect drug loading method into the nanofibers. It is also possible to produce multi-drug delivery systems with timed programmed release. Electrospun nanofiber drug delivery systemshave been studied using various techniques. Herein, wedescribe the fabrication of a drug-incorporating nanofiber. Drugs, such as proteins, peptide, antibodies, and smallmolecule drugs, can be loaded within or on the surface ofnanofibers according to their properties. Hydrophobicdrugs are directly dissolved with a polymer in an organicsolvent before electrospinning. However, it is preferred tosurface-immobilize bioactive molecules on nanofibers byphysical absorption or chemical conjugation. Especially,chemically surface-immobilized proteins on ananofiber mesh stimulate cell differentiation and proliferation. Using a dual electrospinning nozzle to create nanofibersheet layers, which are stacked on top of one another,the initial burst release is reduced compared with solidnanofibers because of the layers. Furthermore, hybridizationof electrospun nanofibers with nanoparticles, microspheres,and hydrogels is indirect drug loading method intothe nanofibers. It is also possible to produce multi-drugdelivery systems with timed programmed release. KCI Citation Count: 126
Author	Kim, Woo Jin Son, Young Ju Yoo, Hyuk Sang
Author_xml	– sequence: 1 givenname: Young Ju surname: Son fullname: Son, Young Ju organization: Department of Biomedical Materials Engineering, Kangwon National University – sequence: 2 givenname: Woo Jin surname: Kim fullname: Kim, Woo Jin organization: Department of Internal Medicine, School of Medicine, Kangwon National University – sequence: 3 givenname: Hyuk Sang surname: Yoo fullname: Yoo, Hyuk Sang email: hsyoo@kangwon.ac.kr organization: Department of Biomedical Materials Engineering, Kangwon National University, Institute of Bioscience and Bioengineering, Kangwon National University
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PublicationCentury	2000
PublicationDate	20140100 2014-1-00 2014-Jan 20140101 2014-01
PublicationDateYYYYMMDD	2014-01-01
PublicationDate_xml	– month: 1 year: 2014 text: 20140100
PublicationDecade	2010
PublicationPlace	Dordrecht
PublicationPlace_xml	– name: Dordrecht – name: Korea (South)
PublicationTitle	Archives of pharmacal research
PublicationTitleAbbrev	Arch. Pharm. Res
PublicationTitleAlternate	Arch Pharm Res
PublicationYear	2014
Publisher	Springer Netherlands 대한약학회
Publisher_xml	– name: Springer Netherlands – name: 대한약학회
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Snippet	Electrospun nanofiber drug delivery systems have been studied using various techniques. Herein, we describe the fabrication of a drug-incorporating nanofiber.... Electrospun nanofiber drug delivery systemshave been studied using various techniques. Herein, wedescribe the fabrication of a drug-incorporating nanofiber....
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SubjectTerms	absorption Animals antibodies bioactive properties cell differentiation Delayed-Action Preparations Drug Carriers drug delivery systems Drug Delivery Systems - instrumentation drugs Humans hydrocolloids Hydrophobic and Hydrophilic Interactions hydrophobicity Medicine Nanofibers Nanomedicine - instrumentation Nanomedicine - methods nanoparticles Pharmaceutical Preparations - administration & dosage Pharmaceutical Preparations - chemistry Pharmacology/Toxicology Pharmacy polymers Polymers - chemistry proteins Review Solubility solvents Technology, Pharmaceutical - instrumentation Technology, Pharmaceutical - methods 약학
Title	Therapeutic applications of electrospun nanofibers for drug delivery systems
URI	https://link.springer.com/article/10.1007/s12272-013-0284-2 https://www.ncbi.nlm.nih.gov/pubmed/24234913 https://www.proquest.com/docview/1499144708 https://www.proquest.com/docview/1733513921 https://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART001902550
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