Literature DB >> 34209066

3D Printing of Dapagliflozin Containing Self-Nanoemulsifying Tablets: Formulation Design and In Vitro Characterization.

Mohammed S Algahtani1, Abdul Aleem Mohammed1, Javed Ahmad1, M M Abdullah2, Ehab Saleh3.   

Abstract

The 3D printing techniques have been explored extensively in recent years for pharmaceutical manufacturing and drug delivery applications. The current investigation aims to explore 3D printing for the design and development of a nanomedicine-based oral solid dosage form of a poorly water-soluble drug. A self-nanoemulsifying tablet formulation of dapagliflozin propanediol monohydrate was developed utilizing the semisolid pressure-assisted microsyringe (PAM) extrusion-based 3D printing technique. The developed formulation system consists of two major components (liquid and solid phase), which include oils (caproyl 90, octanoic acid) and co-surfactant (PEG 400) as liquid phase while surfactant (poloxamer 188) and solid matrix (PEG 6000) as solid-phase excipients that ultimately self-nanoemulsify as a drug encapsulated nanoemulsion system on contact with aqueous phase/gastrointestinal fluid. The droplet size distribution of the generated nanoemulsion from a self-nanoemulsifying 3D printed tablet was observed to be 104.7 ± 3.36 nm with polydispersity index 0.063 ± 0.024. The FT-IR analysis of the printed tablet revealed that no drug-excipients interactions were observed. The DSC and X-RD analysis of the printed tablet revealed that the loaded drug is molecularly dispersed in the crystal lattice of the tablet solid matrix and remains solubilized in the liquid phase of the printed tablet. SEM image of the drug-loaded self-nanoemulsifying tablets revealed that dapagliflozin propanediol monohydrate was completely encapsulated in the solid matrix of the printed tablet, which was further confirmed by SEM-EDS analysis. The in vitro dissolution profile of dapagliflozin-loaded self-nanoemulsifying tablet revealed an immediate-release drug profile for all three sizes (8 mm, 10 mm, and 12 mm) tablets, exhibiting >75.0% drug release within 20 min. Thus, this study has emphasized the capability of the PAM-based 3D printing technique to print a self-nanoemulsifying tablet dosage form with an immediate-release drug profile for poorly water-soluble drug.

Entities:  

Keywords:  SEM-EDS analysis; dapagliflozin propanediol monohydrate; drug dissolution; nanoemulsion; self-nanoemulsifying tablet; semisolid extrusion-based 3D printing

Year:  2021        PMID: 34209066     DOI: 10.3390/pharmaceutics13070993

Source DB:  PubMed          Journal:  Pharmaceutics        ISSN: 1999-4923            Impact factor:   6.321


  30 in total

1.  A new solid self-microemulsifying formulation prepared by spray-drying to improve the oral bioavailability of poorly water soluble drugs.

Authors:  Tao Yi; Jiangling Wan; Huibi Xu; Xiangliang Yang
Journal:  Eur J Pharm Biopharm       Date:  2008-05-17       Impact factor: 5.571

Review 2.  Overview of solidification techniques for self-emulsifying drug delivery systems from industrial perspective.

Authors:  J Mandić; A Zvonar Pobirk; F Vrečer; M Gašperlin
Journal:  Int J Pharm       Date:  2017-05-18       Impact factor: 5.875

3.  Extrudability analysis of drug loaded pastes for 3D printing of modified release tablets.

Authors:  Ahmed Zidan; Alaadin Alayoubi; James Coburn; Sarah Asfari; Bahaa Ghammraoui; Celia N Cruz; Muhammad Ashraf
Journal:  Int J Pharm       Date:  2018-11-12       Impact factor: 5.875

4.  Self-emulsifying drug delivery systems (SEDDS) of coenzyme Q10: formulation development and bioavailability assessment.

Authors:  T R Kommuru; B Gurley; M A Khan; I K Reddy
Journal:  Int J Pharm       Date:  2001-01-16       Impact factor: 5.875

5.  Controlled release of a self-emulsifying formulation from a tablet dosage form: stability assessment and optimization of some processing parameters.

Authors:  Sami Nazzal; Mansoor A Khan
Journal:  Int J Pharm       Date:  2006-03-06       Impact factor: 5.875

6.  Evaluation of melt granulation and ultrasonic spray congealing as techniques to enhance the dissolution of praziquantel.

Authors:  Nadia Passerini; Beatrice Albertini; Beatrice Perissutti; Lorenzo Rodriguez
Journal:  Int J Pharm       Date:  2006-04-03       Impact factor: 5.875

7.  A Proof of Concept for 3D Printing of Solid Lipid-Based Formulations of Poorly Water-Soluble Drugs to Control Formulation Dispersion Kinetics.

Authors:  Kapilkumar Vithani; Alvaro Goyanes; Vincent Jannin; Abdul W Basit; Simon Gaisford; Ben J Boyd
Journal:  Pharm Res       Date:  2019-05-16       Impact factor: 4.200

8.  Improved pharmacokinetics and antihyperlipidemic efficacy of rosuvastatin-loaded nanostructured lipid carriers.

Authors:  Md Rizwanullah; Saima Amin; Javed Ahmad
Journal:  J Drug Target       Date:  2016-06-22       Impact factor: 5.121

Review 9.  Formulation of lipid-based delivery systems for oral administration: materials, methods and strategies.

Authors:  Colin W Pouton; Christopher J H Porter
Journal:  Adv Drug Deliv Rev       Date:  2007-11-04       Impact factor: 15.470

10.  Dissolution and powder flow characterization of solid self-emulsified drug delivery system (SEDDS).

Authors:  Vikas Agarwal; Akhtar Siddiqui; Hazem Ali; Sami Nazzal
Journal:  Int J Pharm       Date:  2008-09-10       Impact factor: 5.875

View more
  2 in total

1.  Three-Dimensional Printing of a Container Tablet: A New Paradigm for Multi-Drug-Containing Bioactive Self-Nanoemulsifying Drug-Delivery Systems (Bio-SNEDDSs).

Authors:  Vineet R Kulkarni; Mohsin Kazi; Ahmad Abdul-Wahhab Shahba; Aakib Radhanpuri; Mohammed Maniruzzaman
Journal:  Pharmaceutics       Date:  2022-05-18       Impact factor: 6.525

Review 2.  The Evolution of the 3D-Printed Drug Delivery Systems: A Review.

Authors:  Ildikó Bácskay; Zoltán Ujhelyi; Pálma Fehér; Petra Arany
Journal:  Pharmaceutics       Date:  2022-06-21       Impact factor: 6.525

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.