Sodium hyaluronate dry powder inhalation in combination with sodium cromoglycate prepared using optimized spray drying conditions

ArticleAçık Erişim

Özet

Sodium hyaluronate (SHA) is an anti-inflammatory and protective agent against bronchoconstriction, and sodium cromoglicate (SCG) prevents exercise-induced bronchoconstriction and inflammation. Based on the pharmacological properties of both substances, this study aimed to develop a dry powder inhaler (DPI) of SHA alone and in combination with SCG. The target of the study was to develop flowable formulations without any surfactants by using the spray drying method. To obtain respirable SHA and SCG:SHA particles, variables of the spray dryer, such as inlet temperature, atomized air flow, and feed solution, were changed. The particles 1–8 μm in size were produced with high yield by spray drying and increasing the ethanol percentage of the feed solution (60%), which is the most remarkable parameter. After that, physicochemical characterizations were performed. The aerosol performance of DPI formulations prepared using lactose was evaluated using Handihaler® DPI. The fine particle fraction (FPF) was 36% for the SHA formulation, whereas it was 52 and 53% for SCG and SHA, respectively, in the SCG:SHA formulation. Consequently, both particles were produced reproducibly by spray drying, and inhaled SHA and SCG:SHA dry powder formulations were developed due to their high FPF and flowability with lactose. © 2023 Informa UK Limited, trading as Taylor & Francis Group.

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Tam Kayıt
AlanDeğerDil
dc.contributor.authorYildiz Türkyilmaz, Gülbeyaz
dc.contributor.authorÖzdokur, Kemal Volkan
dc.contributor.authorAlparslan, Levent
dc.contributor.authorKarasulu, Ercüment
dc.date.accessioned2026-10-18T20:27:07.883570603Z
dc.date.available2026-10-18T20:27:07.883570603Z
dc.date.issued2023
dc.description.abstractSodium hyaluronate (SHA) is an anti-inflammatory and protective agent against bronchoconstriction, and sodium cromoglicate (SCG) prevents exercise-induced bronchoconstriction and inflammation. Based on the pharmacological properties of both substances, this study aimed to develop a dry powder inhaler (DPI) of SHA alone and in combination with SCG. The target of the study was to develop flowable formulations without any surfactants by using the spray drying method. To obtain respirable SHA and SCG:SHA particles, variables of the spray dryer, such as inlet temperature, atomized air flow, and feed solution, were changed. The particles 1–8 μm in size were produced with high yield by spray drying and increasing the ethanol percentage of the feed solution (60%), which is the most remarkable parameter. After that, physicochemical characterizations were performed. The aerosol performance of DPI formulations prepared using lactose was evaluated using Handihaler® DPI. The fine particle fraction (FPF) was 36% for the SHA formulation, whereas it was 52 and 53% for SCG and SHA, respectively, in the SCG:SHA formulation. Consequently, both particles were produced reproducibly by spray drying, and inhaled SHA and SCG:SHA dry powder formulations were developed due to their high FPF and flowability with lactose. © 2023 Informa UK Limited, trading as Taylor & Francis Group.
dc.description.sponsorshipThe author(s) reported there is no funding associated with the work featured in this article. The authors acknowledge the support of NEUTEC ILAC SAN. TIC. A.S. (NEUTEC) for providing insight into the study, financial support, advice, and assistance on the use of the inhaler quality control laboratory. We are grateful to Ege University Planning and Monitoring Coordination of Organizational Development and Directorate of Library and Documentation for their support in editing and proofreading service of this study.
dc.identifier.doi10.1080/10837450.2023.2176517
dc.identifier.eissn1097-9867
dc.identifier.endpage247
dc.identifier.issn1083-7450
dc.identifier.issue2
dc.identifier.pmid36730066
dc.identifier.scopus2-s2.0-85147713715
dc.identifier.startpage240
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/12200
dc.identifier.volume28
dc.identifier.wosWOS:000929207700001
dc.language.isoen
dc.publisherTaylor and Francis Ltd.
dc.relation.ispartofPharmaceutical Development and Technology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectanti-inflammation
dc.subjectbronchoconstriction
dc.subjectdry powder inhaler
dc.subjectsodium cromoglycate
dc.subjectSodium hyaluronate
dc.subjectspray dryer
dc.subjectAdministration, Inhalation
dc.subjectAerosols
dc.subjectCromolyn Sodium
dc.subjectDry Powder Inhalers
dc.subjectHyaluronic Acid
dc.subjectLactose
dc.subjectParticle Size
dc.subjectPowders
dc.subjectSpray Drying
dc.subjectalcohol
dc.subjectcromoglycate disodium
dc.subjectsurfactant
dc.subjectaerosol
dc.subjectArticle
dc.subjectcapsule filling
dc.subjectchemical structure
dc.subjectcrystal structure
dc.subjectdifferential scanning calorimetry
dc.subjectdrug industry
dc.subjectdry powder
dc.subjectflow rate
dc.subjectFourier transform infrared spectroscopy
dc.subjectglass transition temperature
dc.subjecthigh performance liquid chromatography
dc.titleSodium hyaluronate dry powder inhalation in combination with sodium cromoglycate prepared using optimized spray drying conditions
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus1
rdl.citation.wos1
rdl.departmentDepartment of Chemistry, Faculty of Science and Letter, Erzincan Binali Yıldırım University, Erzincan, Türkiye.
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)