Formulation study of duloxetine hydrochloride enteric-coated tablets

Abstract During storage, duloxetine hydrochloride may have an unexpected cross reaction with enteric coated acrylic resin, which may affect the product quality. Solve the problem of cross-reaction between the Duloxetine enteric-coated tablets core and coated enteric materials and improve the quality...

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Main Authors: Jiang Guowei, Cao Zhihui, Zhang Yuhan, Meng Yongjun, Yi Qingqing
Format: Article
Language:English
Published: Springer 2023-01-01
Series:SN Applied Sciences
Subjects:
Online Access:https://doi.org/10.1007/s42452-023-05290-2
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author Jiang Guowei
Cao Zhihui
Zhang Yuhan
Meng Yongjun
Yi Qingqing
author_facet Jiang Guowei
Cao Zhihui
Zhang Yuhan
Meng Yongjun
Yi Qingqing
author_sort Jiang Guowei
collection DOAJ
description Abstract During storage, duloxetine hydrochloride may have an unexpected cross reaction with enteric coated acrylic resin, which may affect the product quality. Solve the problem of cross-reaction between the Duloxetine enteric-coated tablets core and coated enteric materials and improve the quality of the products. Duloxetine enteric-coated tablets’ core formulation and isolation layer prescription were designed and compared with duloxetine enteric-coated tablets sold on the market. Then, we measured the dissolution rate, content, and releasing rate of prepared duloxetine enteric-coated tablets. In the formulation of tablets core, prescription 3 had advantages in particle mobility, disintegration time, and dissolution rate. Prescription 5 was stable during the coating process, and the dissolution residue in the cup was relatively good, showing obvious dissolution advantages. Thus, prescription 5 was selected as the isolation layer prescription. The most suitable adhesive for the preparation of Duloxetine hydrochloride enteric-coated tablets was povione K30 dissolved in ethanol solution with 1/2 of the prescription amount. When 1.3 g colloidal silica was added to the prescription and the dosage of magnesium stearate was 1.48 g, the dissolution rate of the drug could be relatively improved. The ratio of sucrose and talc was 138/8.7, which could effectively configure the coating solution with a solid content of 15–20% to make the coating smooth.
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spelling doaj.art-83aee1dd6d6e4e24aa03b6a4593481552023-01-29T12:19:06ZengSpringerSN Applied Sciences2523-39632523-39712023-01-01521810.1007/s42452-023-05290-2Formulation study of duloxetine hydrochloride enteric-coated tabletsJiang Guowei0Cao Zhihui1Zhang Yuhan2Meng Yongjun3Yi Qingqing4Pharmacy Department, Jiading District Central Hospital Affiliated Shanghai University of Medicine and Health SciencesPharmacy Department, Jiading District Central Hospital Affiliated Shanghai University of Medicine and Health SciencesSchool of Pharmacy, Shanghai University of Medicine and Health SciencesPharmacy Department, Jiading District Central Hospital Affiliated Shanghai University of Medicine and Health SciencesClinical Research Center, Jiading District Central Hospital Affiliated Shanghai University of Medicine and Health SciencesAbstract During storage, duloxetine hydrochloride may have an unexpected cross reaction with enteric coated acrylic resin, which may affect the product quality. Solve the problem of cross-reaction between the Duloxetine enteric-coated tablets core and coated enteric materials and improve the quality of the products. Duloxetine enteric-coated tablets’ core formulation and isolation layer prescription were designed and compared with duloxetine enteric-coated tablets sold on the market. Then, we measured the dissolution rate, content, and releasing rate of prepared duloxetine enteric-coated tablets. In the formulation of tablets core, prescription 3 had advantages in particle mobility, disintegration time, and dissolution rate. Prescription 5 was stable during the coating process, and the dissolution residue in the cup was relatively good, showing obvious dissolution advantages. Thus, prescription 5 was selected as the isolation layer prescription. The most suitable adhesive for the preparation of Duloxetine hydrochloride enteric-coated tablets was povione K30 dissolved in ethanol solution with 1/2 of the prescription amount. When 1.3 g colloidal silica was added to the prescription and the dosage of magnesium stearate was 1.48 g, the dissolution rate of the drug could be relatively improved. The ratio of sucrose and talc was 138/8.7, which could effectively configure the coating solution with a solid content of 15–20% to make the coating smooth.https://doi.org/10.1007/s42452-023-05290-2Duloxetine enteric-coated tabletsTablet coreCoating materialPrescription processDissolution rateDisintegration time
spellingShingle Jiang Guowei
Cao Zhihui
Zhang Yuhan
Meng Yongjun
Yi Qingqing
Formulation study of duloxetine hydrochloride enteric-coated tablets
SN Applied Sciences
Duloxetine enteric-coated tablets
Tablet core
Coating material
Prescription process
Dissolution rate
Disintegration time
title Formulation study of duloxetine hydrochloride enteric-coated tablets
title_full Formulation study of duloxetine hydrochloride enteric-coated tablets
title_fullStr Formulation study of duloxetine hydrochloride enteric-coated tablets
title_full_unstemmed Formulation study of duloxetine hydrochloride enteric-coated tablets
title_short Formulation study of duloxetine hydrochloride enteric-coated tablets
title_sort formulation study of duloxetine hydrochloride enteric coated tablets
topic Duloxetine enteric-coated tablets
Tablet core
Coating material
Prescription process
Dissolution rate
Disintegration time
url https://doi.org/10.1007/s42452-023-05290-2
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AT mengyongjun formulationstudyofduloxetinehydrochlorideentericcoatedtablets
AT yiqingqing formulationstudyofduloxetinehydrochlorideentericcoatedtablets