Development of in situ gel containing CUR:HP-β-CD inclusion complex prepared for ocular diseases: Formulation, characterization, anti-inflammatory, antioxidant evaluation and comprehensive release kinetic studies

ArticleAçık Erişim

Özet

In this study, cyclodextrin (HP-β-CD) inclusion complexes were prepared with Curcumin (CUR) by cosolvency/lyophilization method. Characterization studies were performed with phase-solubility diagrams, scanning electron microscopy (SEM), FT-IR, FT-Raman, XRD, Differential scanning calorimetry (DSC). The prepared CUR:HP-βCD complexes were evaluated for their anti-oxidant and anti-inflammatory activities compared to free CUR and significantly higher activity was detected with the complexation. In addition, pre-formulation studies have been completed in order to develop an in situ gel formulation, containing CUR:HP-β-CD, suitable for use in ocular diseases. To prepare the in situ forming gels, different Pluronic F127 (PF127) concentrations were used. Chitosan was added to the formulations to improve the gel's mucoadhesive properties. The formulations were evaluated for their viscosity pH, clarity, and sol-gel transition temperature. It was established that the formulations were all clear, their pH was 6, their gelation temperature decreased with increasing PF127, and was between 26-35 °C. Viscosities of all formulations were found to be suitable for ocular application. For the selected formulation, CUR and CUR:HP-β-CD were loaded to in situ gelling systems. In vitro release experiments revealed that the CUR:HP-CD inclusion complex including NSL formulation released for 6 hours with a higher burst effect than the other formulation. At the end of the study, in situ gel formulations containing CUR:HP-β-CD were successfully prepared and characterized comprehensively. In addition, a detailed release kinetic study was conducted for the formulations and it was determined that the CUR release from the in situ gel formulations was compatible with the Weibull model. In conclusion, a mucoadhesive in situ gel formulation containing anti-oxidant and anti-inflammatory CUR:HP-β-CD complex for ocular diseases is presented as an innovative formulation approach. © 2023 Marmara University Press.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/12233Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.29228/jrp.296Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorÜnal, Sedat
dc.contributor.authorPolat, Heybet Kerem
dc.contributor.authorYuvali, Dönay
dc.contributor.authorKöngül Şafak, Esra
dc.date.accessioned2026-10-18T20:27:09.427473108Z
dc.date.available2026-10-18T20:27:09.427473108Z
dc.date.issued2023
dc.description.abstractIn this study, cyclodextrin (HP-β-CD) inclusion complexes were prepared with Curcumin (CUR) by cosolvency/lyophilization method. Characterization studies were performed with phase-solubility diagrams, scanning electron microscopy (SEM), FT-IR, FT-Raman, XRD, Differential scanning calorimetry (DSC). The prepared CUR:HP-βCD complexes were evaluated for their anti-oxidant and anti-inflammatory activities compared to free CUR and significantly higher activity was detected with the complexation. In addition, pre-formulation studies have been completed in order to develop an in situ gel formulation, containing CUR:HP-β-CD, suitable for use in ocular diseases. To prepare the in situ forming gels, different Pluronic F127 (PF127) concentrations were used. Chitosan was added to the formulations to improve the gel's mucoadhesive properties. The formulations were evaluated for their viscosity pH, clarity, and sol-gel transition temperature. It was established that the formulations were all clear, their pH was 6, their gelation temperature decreased with increasing PF127, and was between 26-35 °C. Viscosities of all formulations were found to be suitable for ocular application. For the selected formulation, CUR and CUR:HP-β-CD were loaded to in situ gelling systems. In vitro release experiments revealed that the CUR:HP-CD inclusion complex including NSL formulation released for 6 hours with a higher burst effect than the other formulation. At the end of the study, in situ gel formulations containing CUR:HP-β-CD were successfully prepared and characterized comprehensively. In addition, a detailed release kinetic study was conducted for the formulations and it was determined that the CUR release from the in situ gel formulations was compatible with the Weibull model. In conclusion, a mucoadhesive in situ gel formulation containing anti-oxidant and anti-inflammatory CUR:HP-β-CD complex for ocular diseases is presented as an innovative formulation approach. © 2023 Marmara University Press.
dc.identifier.doi10.29228/jrp.296
dc.identifier.eissn2630-6344
dc.identifier.endpage119
dc.identifier.issn2630-6344
dc.identifier.issue1
dc.identifier.scopus2-s2.0-85147267525
dc.identifier.startpage97
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/12233
dc.identifier.volume27
dc.identifier.wosWOS:000992608700009
dc.language.isoen
dc.publisherMarmara University
dc.relation.ispartofJournal of Research in Pharmacy
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectanti-inflammatory
dc.subjectanti-oxidant
dc.subjectCurcumin
dc.subjectHP-β-CD
dc.subjectocular diseases
dc.subjectrelease kinetics
dc.subject2 hydroxypropyl beta cyclodextrin
dc.subjectbenzalkonium chloride
dc.subjectchitosan
dc.subjectedetic acid
dc.subjectpoloxamer
dc.subjectsodium chloride
dc.subjectantiinflammatory activity
dc.subjectantioxidant activity
dc.subjectArticle
dc.subjectcomplex formation
dc.subjectcontrolled study
dc.subjectdifferential scanning calorimetry
dc.subjectdrug formulation
dc.subjectdrug release
dc.subjectdrug solubility
dc.subjectevaluation study
dc.subjecteye disease
dc.subjectFourier transform infrared spectroscopy
dc.subjectfreeze drying
dc.subjectgelation
dc.subjecthuman
dc.subjectin vitro study
dc.subjectkinetics
dc.subjectmathematical model
dc.titleDevelopment of in situ gel containing CUR:HP-β-CD inclusion complex prepared for ocular diseases: Formulation, characterization, anti-inflammatory, antioxidant evaluation and comprehensive release kinetic studies
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus7
rdl.citation.trdizin0
rdl.citation.wos6
rdl.departmentERCİYES ÜNİVERSİTESİ
rdl.departmentERZİNCAN BİNALİ YILDIRIM ÜNİVERSİTESİ
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexTRDIZIN
rdl.wos.indexEmerging Sources Citation Index (ESCI)