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Mater."],"published-print":{"date-parts":[[2024,3,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:p>Nanofibers (NF) and nanoparticles are attractive for drug delivery to improve the drug bioavailability and administration. Easy manipulation of NF as macroscopic bulk material give rise to potential usages as implantable local drug delivery systems (LLDS) to overcome the failures of systemic drug delivery systems such as unmet personalized needs, side effects, suboptimal dosage. In this study, poly(ethylene glycol) polyethyleneimine (mPEG:PEI) copolymer blended poly <jats:italic>\u03f5<\/jats:italic>-caprolactone NFs, NF<jats:sub>blend<\/jats:sub> accommodating mesoporous silica nanoparticles (MSN) as the implantable LLDS was achieved by employing spin coating and cold atmospheric plasma (CAP) as the post-process for accommodation on NF<jats:sub>blend<\/jats:sub>. The macroporous morphology, mechanical properties, wettability, and <jats:italic>in vitro<\/jats:italic> cytocompatibility of NF<jats:sub>blend<\/jats:sub> ensured their potential as an implantable LLDS and superior features compared to neat NF. The electron microscopy images affirmed of NF<jats:sub>blend<\/jats:sub> random fiber (average diameter 832 \u00b1 321 nm) alignments and accessible macropores before and after MSN@Cur accommodation. The blending of polymers improved the elongation of NF and the tensile strength which is attributed as beneficial for implantable LLDS. CAP treatment could significantly improve the wettability of NF observed by the contact angle changes from \u223c126\u00b0 to \u223c50\u00b0 which is critical for the accommodation of curcumin-loaded MSN (MSN@Cur) and <jats:italic>in vitro<\/jats:italic> cytocompatibility of NF. The combined CAP and spin coating as the post-processes was employed for accommodating MSN@Cur on NF<jats:sub>blend<\/jats:sub> without interfering with the electrospinning process. The post-processing aided fine-tuning of curcumin dosing (\u223c3 \u00b5g to \u223c15 \u00b5g) per dose unit and sustained zero-order drug release profile could be achieved. Introducing of MSN@Cur to cells via LLDS promoted the cell proliferation compared to MSN@Cur suspension treatments and assigned as the elimination of adverse effects by nanocarriers by the dosage form integration. All in all, NF<jats:sub>blend<\/jats:sub>-MSN@Cur was shown to have high potential to be employed as an implantable LLDS. To the best of our knowledge, this is the first study in which mPEG:PEI copolymer blend NF are united with CAP and spin coating for accommodating nano-drug carriers, which allows for NF both tissue engineering and drug delivery applications.<\/jats:p>","DOI":"10.1088\/1748-605x\/ad1bb1","type":"journal-article","created":{"date-parts":[[2024,1,5]],"date-time":"2024-01-05T22:41:03Z","timestamp":1704494463000},"page":"025015","update-policy":"https:\/\/doi.org\/10.1088\/crossmark-policy","source":"Crossref","is-referenced-by-count":5,"title":["Mesoporous silica nanoparticles accommodating electrospun nanofibers as implantable local drug delivery system processed by cold atmospheric plasma and spin coating approaches"],"prefix":"10.1088","volume":"19","author":[{"given":"Nursu","family":"Erdo\u011fan","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-2368-9598","authenticated-orcid":true,"given":"Didem","family":"\u015een Karaman","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"\u00d6zlem","family":"Y\u0131ld\u0131z","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-3682-3733","authenticated-orcid":true,"given":"Gizem Dilara","family":"\u00d6zdemir","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-9762-2265","authenticated-orcid":true,"given":"Utku K\u00fcr\u015fat","family":"Ercan","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"266","published-online":{"date-parts":[[2024,1,24]]},"reference":[{"key":"bmmad1bb1bib1","doi-asserted-by":"publisher","first-page":"241","DOI":"10.1016\/C2017-0-00836-4","author":"Saka","year":"2019","edition":"ed"},{"key":"bmmad1bb1bib2","first-page":"560","article-title":"Personalized medicine: part 1: evolution and development into theranostics","volume":"35","author":"Vogenberg","year":"2010","journal-title":"Pharm. 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