Pregled bibliografske jedinice broj: 1203299
Influence of β-cyclodextrin and its various derivatives on cinnarizine solubility in water
Influence of β-cyclodextrin and its various derivatives on cinnarizine solubility in water // 20th International Symposium and Summer School on Bioanalysis : Book of Abstracts / Kilár, Ferenc ; Nagy, Laura (ur.).
Pečuh, 2022. str. 73-73 (poster, međunarodna recenzija, sažetak, znanstveni)
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Naslov
Influence of β-cyclodextrin and its various
derivatives on cinnarizine solubility in water
Autori
Klarić, David ; Galić, Nives
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
20th International Symposium and Summer School on Bioanalysis : Book of Abstracts
/ Kilár, Ferenc ; Nagy, Laura - Pečuh, 2022, 73-73
Skup
20th International Symposium and Summer School on Bioanalysis
Mjesto i datum
Pečuh, Mađarska, 24.06.2022. - 30.06.2022
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
cinnarizine ; cyclodextrin ; inclusion complex
Sažetak
Cinnarizine (CIN) is a piperazine derivative with antihistaminic and calcium channel blocking activity which is widely used for the treatment of vertigo and prevention of motion sickness. Due to its extremely poor aqueous solubility, CIN is classified as a Class 2 drug substance according to The Biopharmaceutical Classification System [1]. β-Cyclodextrins (β-CDs) are cyclic oligosaccharides consisting of seven D- glucopyranose units which are α-(1, 4)-linked in a ring formation. It is already well known that β- CDs can interact with poorly soluble drugs by taking up lipophilic drug moieties into their central cavity hence forming inclusion complexes and thus enhancing drug aqueous solubility and bioavailability [2]. Our study aimed to evaluate the influence of β-CD and its randomly methylated (RMβCD), sulfobutylether (SBEβCD), and hydroxypropyl (HPβCD) derivatives on intrinsic solubility of CIN in water through phase- solubility studies according to existing Higuchi- Connors method [2]. To evaluate total drug solubility changes in the presence of increasing CD concentration phase- solubility diagrams were constructed. Quantitative determination of CIN was performed by developed and validated UV/Vis spectrophotometric and spectrofluorimetric methods. [1] S. Raghuvanshi, K. Pathak, J. Drug Delivery 2014, 2014, 479246. [2] P. Jansook, N. Ogawa, T. Loftsson, Int. J. Pharm. 2018, 535, 272– 284.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Ustanove:
Prirodoslovno-matematički fakultet, Zagreb