Design and fabrication of low-cost microsystems for production of chitosan particles; [Kitosan parçacıklarının üretimi için düşük maliyetli mikrosistemlerin tasarımı ve fabrikasyonu]

MakaleAçık ErişimScopus SJRQ2
  • SDG 9 · Sanayi, Yenilikçilik ve Altyapı

Özet

Recent research has focused on the methods for administration of medications in a controlled manner while minimizing side effects. Cross-linked hydrogels have wide application area as nanocarriers. There are many approaches for developing suitable methods to produce ideal particles. Advances in microtechnology have been considered as a solution to produce controlled drug delivery systems, however, it is limited due to the necessity for specialized laboratories. In this study, a simple method to produce antibiotic-loaded chitosan particles is proposed. Production was carried out with two different designs, a syringe-based flow focusing system (outer diameter of 1 mm, inner diameter of 120 µm) and microchannel with 250 µm width and 100 µm height fabricated with the computer numerical control (CNC). Sodium Triphosphate (TPP) was used as cross-linking agent for the production of particles and the effects of the concentration and flow rates on the particle formation was investigated. It has been observed that particles can be produced in a syringe-based system, but the resulting particles are not homogeneous. In the studies carried out with CNC microchannel, it was determined by SEM analysis that the obtained particles ranged in size from 39 to 771 nm, and it was seen that the CNC microchannel was more effective at low and equal flow rates (25 µl/min). It has been found that increasing the flow rate and concentration of chitosan increases the particle size. It was determined that Ampicillin loaded particles synthesized with the CNC microchannel exhibited high inhibition against Gram positive and Gram negative bacteria. These results show that the proposed approaches for the design of microsystems can be used in the formation of drug carriers without the need for specialized laboratories and expertise.

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https://rdlopen.rawdatalibrary.net/r/gumushane/11400Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.17341/gazimmfd.1299367Yayıncı resmi DOI adresi
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AlanDeğerDil
dc.contributor.authorAkay, Seref
dc.contributor.authorÖzdilek, Hasret
dc.date.accessioned2026-10-22T10:18:59.128058327Z
dc.date.available2026-10-22T10:18:59.128058327Z
dc.date.issued2024
dc.description.abstractRecent research has focused on the methods for administration of medications in a controlled manner while minimizing side effects. Cross-linked hydrogels have wide application area as nanocarriers. There are many approaches for developing suitable methods to produce ideal particles. Advances in microtechnology have been considered as a solution to produce controlled drug delivery systems, however, it is limited due to the necessity for specialized laboratories. In this study, a simple method to produce antibiotic-loaded chitosan particles is proposed. Production was carried out with two different designs, a syringe-based flow focusing system (outer diameter of 1 mm, inner diameter of 120 µm) and microchannel with 250 µm width and 100 µm height fabricated with the computer numerical control (CNC). Sodium Triphosphate (TPP) was used as cross-linking agent for the production of particles and the effects of the concentration and flow rates on the particle formation was investigated. It has been observed that particles can be produced in a syringe-based system, but the resulting particles are not homogeneous. In the studies carried out with CNC microchannel, it was determined by SEM analysis that the obtained particles ranged in size from 39 to 771 nm, and it was seen that the CNC microchannel was more effective at low and equal flow rates (25 µl/min). It has been found that increasing the flow rate and concentration of chitosan increases the particle size. It was determined that Ampicillin loaded particles synthesized with the CNC microchannel exhibited high inhibition against Gram positive and Gram negative bacteria. These results show that the proposed approaches for the design of microsystems can be used in the formation of drug carriers without the need for specialized laboratories and expertise.
dc.description.sponsorshipGümüşhane Üniversitesi, GÜ, (F5119.0101)
dc.identifier.doi10.17341/gazimmfd.1299367
dc.identifier.eissn1304-4915
dc.identifier.endpage2372
dc.identifier.issn1300-1884
dc.identifier.issue4
dc.identifier.scopus2-s2.0-85195678431
dc.identifier.startpage2363
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/gumushane/11400
dc.identifier.volume39
dc.identifier.wosWOS:001265086400003
dc.language.isotr
dc.publisherGazi Universitesi
dc.relation.ispartofJournal of the Faculty of Engineering and Architecture of Gazi University
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAntimicrobial
dc.subjectchitosan
dc.subjectdrug delivery
dc.subjectmicrofabrication
dc.subjectmicrofluidic
dc.subject.classificationEngineering, Multidisciplinary
dc.subject.classificationEngineering
dc.subject.otherBacteria
dc.subject.otherComputer control systems
dc.subject.otherControlled drug delivery
dc.subject.otherCrosslinking
dc.subject.otherMicrochannels
dc.subject.otherMicrofluidics
dc.subject.otherParticle size
dc.subject.otherParticle size analysis
dc.subject.otherSodium compounds
dc.subject.otherSyringes
dc.subject.otherTargeted drug delivery
dc.subject.otherAntimicrobial
dc.subject.otherApplication area
dc.subject.otherChitosan particles
dc.subject.otherCross-linked hydrogels
dc.subject.otherLow-costs
dc.subject.otherMicro-fabrication
dc.subject.otherNanocarriers
dc.subject.otherNumerical control
dc.subject.otherRecent researches
dc.subject.otherSide effect
dc.subject.otherChitosan
dc.titleDesign and fabrication of low-cost microsystems for production of chitosan particles; [Kitosan parçacıklarının üretimi için düşük maliyetli mikrosistemlerin tasarımı ve fabrikasyonu]
dc.typeArticle
dspace.entity.typePublication
rdl.citation.openalex0
rdl.citation.scopus1
rdl.citation.trdizin0
rdl.citation.wos0
rdl.oa.statusgold
rdl.oa.urlhttps://doi.org/10.17341/gazimmfd.1299367
rdl.scopus.quartileQ2
rdl.sdgSDG09
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexTRDIZIN
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)