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Design and Optimization of 3D-Printed Gastroretentive Floating Devices by Central Composite Design.
Charoenying, Thapakorn; Patrojanasophon, Prasopchai; Ngawhirunpat, Tanasait; Rojanarata, Theerasak; Akkaramongkolporn, Prasert; Opanasopit, Praneet.
Affiliation
  • Charoenying T; Pharmaceutical Development of Green Innovations Group (PDGIG), Faculty of Pharmacy, Silpakorn University, Nakhon Pathom, 73000, Thailand.
  • Patrojanasophon P; Pharmaceutical Development of Green Innovations Group (PDGIG), Faculty of Pharmacy, Silpakorn University, Nakhon Pathom, 73000, Thailand.
  • Ngawhirunpat T; Pharmaceutical Development of Green Innovations Group (PDGIG), Faculty of Pharmacy, Silpakorn University, Nakhon Pathom, 73000, Thailand.
  • Rojanarata T; Pharmaceutical Development of Green Innovations Group (PDGIG), Faculty of Pharmacy, Silpakorn University, Nakhon Pathom, 73000, Thailand.
  • Akkaramongkolporn P; Pharmaceutical Development of Green Innovations Group (PDGIG), Faculty of Pharmacy, Silpakorn University, Nakhon Pathom, 73000, Thailand.
  • Opanasopit P; Pharmaceutical Development of Green Innovations Group (PDGIG), Faculty of Pharmacy, Silpakorn University, Nakhon Pathom, 73000, Thailand. opanasopit_p@su.ac.th.
AAPS PharmSciTech ; 22(5): 197, 2021 Jun 30.
Article in En | MEDLINE | ID: mdl-34191172
This study aimed to optimize the size of capsule-shaped 3D-printed devices (CPD) using an experimental design by the response surface methodology to provide a gastroretentive drug delivery system (GRDDS) with optimal floating time. The CPD was fabricated using a fused deposition modeling (FDM) 3D printer. The central composite design was employed for the optimization of the devices. The morphology of the CPD was observed using a digital microscope and scanning electron microscope (SEM). The in vitro floating time and drug release were evaluated using a USP dissolution apparatus II. Appropriate total floating time (TFT) of the devices (more than 3 h) was obtained with the device's body, cap, and bottom thickness of 1.2, 1.8, and 2.9 mm, respectively. The release kinetics of the drug from the devices fitted well with zero-order kinetics. In conclusion, the optimization of CPD for GRDDS using the experimental design provided the devices with desirable floating time and ideal drug release characteristics.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Drug Delivery Systems / Printing, Three-Dimensional Type of study: Prognostic_studies Language: En Journal: AAPS PharmSciTech Journal subject: FARMACOLOGIA Year: 2021 Document type: Article Affiliation country: Thailand Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Drug Delivery Systems / Printing, Three-Dimensional Type of study: Prognostic_studies Language: En Journal: AAPS PharmSciTech Journal subject: FARMACOLOGIA Year: 2021 Document type: Article Affiliation country: Thailand Country of publication: United States