Formulation of metformin-loaded alginate microspheres by ionotropic gelationaerosolization technique
Metformin hydrochloric acid (HCl)-loaded alginate microspheres prepared using aerosolization method were subsequently evaluated for their physico-chemical characteristics in terms of particle size, morphology, drug loading, entrapment efficiency, yield and in vitro release. A two factorial Design...
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Main Authors: | , , , , , |
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Format: | Article |
Language: | English |
Published: |
Penerbit Universiti Kebangsaan Malaysia
2020
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Online Access: | http://journalarticle.ukm.my/15947/1/17.pdf http://journalarticle.ukm.my/15947/ http://www.ukm.my/jsm/malay_journals/jilid49bil10_2020/KandunganJilid49Bil10_2020.html |
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Summary: | Metformin hydrochloric acid (HCl)-loaded alginate microspheres prepared using aerosolization method were
subsequently evaluated for their physico-chemical characteristics in terms of particle size, morphology, drug
loading, entrapment efficiency, yield and in vitro release. A two factorial Design of Experiment (DoE) was used to
study the influence of polymer alginate and cross-linker calcium chloride (CaCl2
) concentrations on microparticle
characteristics. The results indicated that all microspheres were spherical in shape, while their particle size was
less than 5 µm, although this increased with the intensification of alginate and CaCl2 concentrations. Encapsulation
efficiency, loading, and yield were all enhanced by increasing alginate concentration and, conversely, decreasing
CaCl2 concentration. The highest encapsulation efficiency, loading, and yield were 40, 31, and 73%, respectively,
produced by a formula containing 1.75% alginate and 3% CaCl2
. The drug release of Metformin-loaded microparticles
in HCl pH 1.2 ranged from 22 to 28% during a two-hour period, while further drug release of PBS pH 7.4 increased
from 67 to 95% over ten hours. The total amount of drug released during a 12-h period increased by reducing alginate
concentration. Furthermore, a kinetic study of the dissolution data confirmed the prevalence of a diffusion-controlled
mechanism or Higuchi pattern of drug release. |
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