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Novel Extended-Release Multiple-Unit System of Imidafenacin Prepared by Fluid-Bed Coating Technique

Authors
Shin, Taek HwanIm, Sung HyunGoh, Min SuLee, Eun SeokHo, Myoung JinKim, Chang HyunKang, Myung JooChoi, Young Wook
Issue Date
Aug-2018
Publisher
SPRINGER
Keywords
imidafenacin; multiple-unit dosage form; controlled release; fluid-bed coating; drug release; pharmacokinetics
Citation
AAPS PHARMSCITECH, v.19, no.6, pp 2639 - 2645
Pages
7
Journal Title
AAPS PHARMSCITECH
Volume
19
Number
6
Start Page
2639
End Page
2645
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/1913
DOI
10.1208/s12249-018-1100-6
ISSN
1530-9932
1522-1059
Abstract
The objective of this study was to formulate once-a-day extended-release (ER) pellet system of imidafenacin (IDN), a recently approved urinary antispasmodic agent with twice-a-day dosing regimen. The sugar sphere pellets were firstly layered with IDN and hypromellose and then coated with Eudragit RS (copolymers of acrylic and methacrylic acid esters), employed as a release modifier, using a fluid-bed coater. Solid-state characterizations using solid-state X-ray diffraction and differential scanning calorimeter indicated that the antispasmodic agent was homogeneously layered onto the pellets in an amorphous state. Drug release from multiple-unit ER system was effectively retarded in proportion to the amount of Eudragit RS in the outer layer, with a high correlation value above 0.86. In a pharmacokinetic evaluation in beagle dogs, the plasma concentration profile of IDN was markedly protracted by ER pellets, exhibiting delayed the time needed to reach the maximum drug concentration and the elimination half-life in plasma, compared to the commercial immediate release form (UritosA (R) tablet, Kyorin Pharmaceutical Co., Ltd., Japan). Therefore, the novel ER pellets can be a promising tool for oral IDN therapy, providing a once-a-day dosing regimen, and thus, improving patient compliance.
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