Multiunit Particulate Systems: A Current Drug-Delivery Technology - Pharmaceutical Technology

Latest Issue
PharmTech

Latest Issue
PharmTech Europe

Multiunit Particulate Systems: A Current Drug-Delivery Technology
The current review describes the role and selection of excipients, pellet core, coating materials, and compression with various cushioning agents.


Pharmaceutical Technology
Volume 35, Issue 7, pp. 60-66

References

1. N.S. Dey, S. Majumdar, and M.E.B. Rao, Trop. J. Pharm. Res. 7 (3), 1067–1075 (2008).

2. N. Follonier and E. Doelker, S.T.P. Pharma Sci. 2 (2), 141–158 (1992).

3. A.S. Abdul, A.V. Chandewar, and S.B. Jaiswal, J. Control. Release 147 (1), 2–16 (2010).

4. FASS 2002, A.G. Hedstrand, Ed. (LINFO, Stockholm, 2002), pp. 853–854.

5. R. Bodmeier, Eur. J. Pharm. Biopharm. 43 (1), 1–8 (1997).

6. A.E.K. Lundqvist, F. Podczeck, and J.M. Newton, Eur. J. Pharm. Biopharm. 46 (3), 369–379 (1998).

7. H. Leuenberger, Int. J. Pharm. 12 (1), 41–55 (1982).

8. C. Sun and D.J.W. Grant, Pharm. Dev. Technol. 6 (2), 193–200 (2001).

9. J. Van der Zwan and C.A.M. Siskens, Powder Technol. 33 (1), 43–54 (1982).

10. B. Johansson and G. Alderborn, Int. J. Pharm. 132 (1–2), 207–220 (1996).

11. J.B. Schwartz, N.H. Nguyen, and R.L. Schnaare, Drug Dev. Ind. Pharm. 20 (20), 3105–3129 (1994).

12. F. Nicklasson and G. Alderborn, Eur. J. Pharm. Sci. 9 (1), 57–65 (1999).

13. C. Wang et al., Drug Dev. Ind. Pharm. 21 (7), 753–779 (1995).

14. N.O. Iloanusi and J.B. Schwartz, Drug Dev. Ind. Pharm. 24 (1), 37–44 (1998).

15. M. Salako, F. Podczeck, and J.M. Newton, Int. J. Pharm. 168 (1), 49–57 (1998).

16. M.E. Aulton, A.M. Dyer, and K.A. Khan, Drug Dev. Ind. Pharm. 20 (20), 3069–3104 (1994).

17. J.L. Haslam et al., Int. J. Pharm. 173 (1–2), 233–242 (1998).

18. B. Johansson, F. Nicklasson, and G. Alderborn, Int. J. Pharm. 163 (1–2), 35–48 (1998).

19. N Sarisuta and K. Punpreuk, J. Control. Release 31 (3), 215–222 (1994).

20. S.C. Porter, Drug Dev. Ind. Pharm. 15 (10), 1495–1521 (1989).

21. M.P. Flament et al., Pharm. Technol. Eur. 6 (2), 19–25 (1994).


ADVERTISEMENT

blog comments powered by Disqus
LCGC E-mail Newsletters

Subscribe: Click to learn more about the newsletter
| Weekly
| Monthly
|Monthly
| Weekly

Survey
FDASIA was signed into law two years ago. Where has the most progress been made in implementation?
Reducing drug shortages
Breakthrough designations
Protecting the supply chain
Expedited reviews of drug submissions
More stakeholder involvement
Reducing drug shortages
70%
Breakthrough designations
4%
Protecting the supply chain
17%
Expedited reviews of drug submissions
2%
More stakeholder involvement
7%
View Results
Eric Langerr Outsourcing Outlook Eric LangerTargeting Different Off-Shore Destinations
Cynthia Challener, PhD Ingredients Insider Cynthia ChallenerAsymmetric Synthesis Continues to Advance
Jill Wechsler Regulatory Watch Jill Wechsler Data Integrity Key to GMP Compliance
Sean Milmo European Regulatory WatchSean MilmoExtending the Scope of Pharmacovigilance Comes at a Price
From Generics to Supergenerics
CMOs and the Track-and-Trace Race: Are You Engaged Yet?
Ebola Outbreak Raises Ethical Issues
Better Comms Means a Fitter Future for Pharma, Part 2: Realizing the Benefits of Unified Communications
Better Comms Means a Fitter Future for Pharma, Part 1: Challenges and Changes
Source: Pharmaceutical Technology,
Click here