{"title":"从静电纺混合聚乙烯醇和聚氧化物(PVA/PEO)纤维中快速输送褪黑素","authors":"Rachel Emerine, S. Chou","doi":"10.3934/bioeng.2022013","DOIUrl":null,"url":null,"abstract":"Water-soluble polymers possess great advantages in current drug delivery systems, such as fast delivery through polymer matrix dissolution as well as promoting solid dispersion of poorly water-soluble drugs. In this work, water-soluble polyvinyl alcohol (PVA) and polyethylene oxide (PEO) were blended (50/50) to electrospin with and without the incorporation of a model drug, melatonin (MLT), at various blend polymer concentrations. Results suggested that increasing blend PVA/PEO solution concentrations, up to 7 wt%, promoted the formation of smooth and defect-free drug-incorporating fibers with an average fiber diameter ranged from 300 to 700 nm. Mechanical properties of the blank and MLT-loaded PVA/PEO fibers showed dependence on fiber morphologies and fiber mat structures, due to polymer concentrations for electrospinning. Furthermore, the surface wettability of the blend PVA/PEO fibers were investigated and further correlated with the MLT release profile of the fibers. Results suggested that fiber mats with a more well-defined fiber structure promoted a linear release behavior within 10 minutes in vitro. These drug-incorporated fibers were compatible to human umbilical vein endothelial cells (HUVECs) up to 24 hours. In general, this work demonstrated the structure-property correlations of electrospun PVA/PEO fibers and their potential biomedical applications in fast delivery of small molecule drugs.","PeriodicalId":45029,"journal":{"name":"AIMS Bioengineering","volume":"16 1","pages":""},"PeriodicalIF":1.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"4","resultStr":"{\"title\":\"Fast delivery of melatonin from electrospun blend polyvinyl alcohol and polyethylene oxide (PVA/PEO) fibers\",\"authors\":\"Rachel Emerine, S. Chou\",\"doi\":\"10.3934/bioeng.2022013\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Water-soluble polymers possess great advantages in current drug delivery systems, such as fast delivery through polymer matrix dissolution as well as promoting solid dispersion of poorly water-soluble drugs. In this work, water-soluble polyvinyl alcohol (PVA) and polyethylene oxide (PEO) were blended (50/50) to electrospin with and without the incorporation of a model drug, melatonin (MLT), at various blend polymer concentrations. Results suggested that increasing blend PVA/PEO solution concentrations, up to 7 wt%, promoted the formation of smooth and defect-free drug-incorporating fibers with an average fiber diameter ranged from 300 to 700 nm. Mechanical properties of the blank and MLT-loaded PVA/PEO fibers showed dependence on fiber morphologies and fiber mat structures, due to polymer concentrations for electrospinning. Furthermore, the surface wettability of the blend PVA/PEO fibers were investigated and further correlated with the MLT release profile of the fibers. Results suggested that fiber mats with a more well-defined fiber structure promoted a linear release behavior within 10 minutes in vitro. These drug-incorporated fibers were compatible to human umbilical vein endothelial cells (HUVECs) up to 24 hours. In general, this work demonstrated the structure-property correlations of electrospun PVA/PEO fibers and their potential biomedical applications in fast delivery of small molecule drugs.\",\"PeriodicalId\":45029,\"journal\":{\"name\":\"AIMS Bioengineering\",\"volume\":\"16 1\",\"pages\":\"\"},\"PeriodicalIF\":1.0000,\"publicationDate\":\"2022-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"AIMS Bioengineering\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3934/bioeng.2022013\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"ENGINEERING, BIOMEDICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"AIMS Bioengineering","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3934/bioeng.2022013","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"ENGINEERING, BIOMEDICAL","Score":null,"Total":0}
Fast delivery of melatonin from electrospun blend polyvinyl alcohol and polyethylene oxide (PVA/PEO) fibers
Water-soluble polymers possess great advantages in current drug delivery systems, such as fast delivery through polymer matrix dissolution as well as promoting solid dispersion of poorly water-soluble drugs. In this work, water-soluble polyvinyl alcohol (PVA) and polyethylene oxide (PEO) were blended (50/50) to electrospin with and without the incorporation of a model drug, melatonin (MLT), at various blend polymer concentrations. Results suggested that increasing blend PVA/PEO solution concentrations, up to 7 wt%, promoted the formation of smooth and defect-free drug-incorporating fibers with an average fiber diameter ranged from 300 to 700 nm. Mechanical properties of the blank and MLT-loaded PVA/PEO fibers showed dependence on fiber morphologies and fiber mat structures, due to polymer concentrations for electrospinning. Furthermore, the surface wettability of the blend PVA/PEO fibers were investigated and further correlated with the MLT release profile of the fibers. Results suggested that fiber mats with a more well-defined fiber structure promoted a linear release behavior within 10 minutes in vitro. These drug-incorporated fibers were compatible to human umbilical vein endothelial cells (HUVECs) up to 24 hours. In general, this work demonstrated the structure-property correlations of electrospun PVA/PEO fibers and their potential biomedical applications in fast delivery of small molecule drugs.