Sodium alginate microspheres containing multicomponent inclusion complex of domperidone

Sodium alginate microspheres of domperidone for intranasal systemic delivery were developed to eliminate first pass metabolism, improve patient compliance and obtain improved therapeutic efficacy in treatment of migraine, gastro-esophageal reflux and chemotherapy induced nausea and vomiting. Domp...

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Autores principales: Mali, Kailas K., Dias, Remeth J., Ghorpade, Vishwajeet S., Havaldar, Vijay D.
Formato: Articulo
Lenguaje:Inglés
Publicado: 2010
Materias:
Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/8049
http://www.latamjpharm.org/resumenes/29/7/LAJOP_29_7_1_22.pdf
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id I19-R120-10915-8049
record_format dspace
institution Universidad Nacional de La Plata
institution_str I-19
repository_str R-120
collection SEDICI (UNLP)
language Inglés
topic Farmacia
β-cyclodextrin; domperidone; microspheres; solubility; ternary inclusion complex
spellingShingle Farmacia
β-cyclodextrin; domperidone; microspheres; solubility; ternary inclusion complex
Mali, Kailas K.
Dias, Remeth J.
Ghorpade, Vishwajeet S.
Havaldar, Vijay D.
Sodium alginate microspheres containing multicomponent inclusion complex of domperidone
topic_facet Farmacia
β-cyclodextrin; domperidone; microspheres; solubility; ternary inclusion complex
description Sodium alginate microspheres of domperidone for intranasal systemic delivery were developed to eliminate first pass metabolism, improve patient compliance and obtain improved therapeutic efficacy in treatment of migraine, gastro-esophageal reflux and chemotherapy induced nausea and vomiting. Domperidone was encapsulated as ternary inclusion complex with β-cyclodextrin and citric acid to improve solubility. The phase solubility studies were performed in order to select suitable acid and ternary inclusion complex was prepared by kneading method. The complex was characterized by differential scanning calorimetry, X-ray diffraction and Fourier transform infrared spectroscopy. In vitro dissolution study was carried out in simulated nasal electrolyte solution, pH 6.4. The microspheres of optimised ternary inclusion complex were prepared by emulsification-cross-linking method and were evaluated for particle size, encapsulation efficiency, equilibrium swelling degree, in vitro mucoadhesion and in vitro drug release. The effect of various formulation variables such as drug loading, polymer concentration, crosslinking agent concentration and cross-linking time on microsphere characteristics were studied. The microspheres size range was 57.63-65.3 µm, whereas the percentage drug encapsulation was within the range 15-50 %. All microspheres showed good bioadhesive properties. The formulation variables influenced the drug release profile. The treatment of in vitro release kinetics with kinetic equations indicated that the domperidone release followed Higuchi's matrix model.
format Articulo
Articulo
author Mali, Kailas K.
Dias, Remeth J.
Ghorpade, Vishwajeet S.
Havaldar, Vijay D.
author_facet Mali, Kailas K.
Dias, Remeth J.
Ghorpade, Vishwajeet S.
Havaldar, Vijay D.
author_sort Mali, Kailas K.
title Sodium alginate microspheres containing multicomponent inclusion complex of domperidone
title_short Sodium alginate microspheres containing multicomponent inclusion complex of domperidone
title_full Sodium alginate microspheres containing multicomponent inclusion complex of domperidone
title_fullStr Sodium alginate microspheres containing multicomponent inclusion complex of domperidone
title_full_unstemmed Sodium alginate microspheres containing multicomponent inclusion complex of domperidone
title_sort sodium alginate microspheres containing multicomponent inclusion complex of domperidone
publishDate 2010
url http://sedici.unlp.edu.ar/handle/10915/8049
http://www.latamjpharm.org/resumenes/29/7/LAJOP_29_7_1_22.pdf
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AT ghorpadevishwajeets sodiumalginatemicrospherescontainingmulticomponentinclusioncomplexofdomperidone
AT havaldarvijayd sodiumalginatemicrospherescontainingmulticomponentinclusioncomplexofdomperidone
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