Skip to main content

Evaluation and Formulation of Biodegradable Levodopa Microspheres Using 32 Factorial Design

  • Chapter
Biomedical Science and Technology

Abstract

The main neurochemial characteristic of the Parkinson’s disease is a marked degeneration of the nigrostriatal dopaminergic neurons which provide the dopaminergic striatal innervation. Due to the complex chemoarchitectiture of the Central Nervous System (CNS), drug delivery to a very restricted region of the brain is always required. The treatment of Parkinson’s disease patients with the dopamine biosynthetic precursor, levodopa in conjunction with a decarboxylase inhibitor 1 has received wide acceptance as an effective approach for the reduction of extrapyramidal symptoms in Parkinson’s disease. With the current convential medication levodopa can cause serious adverse effect reactions and its effectiveness decreases with time. However, implanted polymeric devices releasing the appropriate pharmacological agent could restore neurotransmission and lead to functional improvement.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 39.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 54.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. A. Barbeau, 1974, The clinical physiology of side effects in long-term 1-dopa therapy, Adv. Neurol 5:347–356

    PubMed  CAS  Google Scholar 

  2. WM. Pardridge, 1996 Brain drug delivery and blood-brain barrier transport. Drug Delivery 3: 99–115.

    Article  CAS  Google Scholar 

  3. M. Iwata and J.W. McGinity, 1992, Preparation of multiphase microspheres of poly(d,l-lactic-co-glycolic acid) containing a w/o emulsion by a multiple emulsion solvent evaporeation technique, J. Microencap 9:201–214

    Article  CAS  Google Scholar 

  4. R. Alex and R. Bodmeier, 1990, Encapsulation of water-soluble drugs by a modinea solvent evaporation method. I. Effect of process and formation variables on drug entrapment, J. Microencap 7:341–355

    Article  Google Scholar 

  5. B. Arıca, H.S. Kaş, M. Orman, H.H. Çelik and A.A. Hıncal, 1996, Proceed. 8th Inter. Pharm. Technol. Symp. (IPTS-96), Sept. 9–11, pp.167

    Google Scholar 

  6. P.K. Gupta, C.T. Hung and D.G. Perrier, 1986a, Albumin microspheres I: release characteristics of adriamycin. Int. J. Pharm 33:137–146

    Article  CAS  Google Scholar 

  7. P.K. Gupta, C.T. Hung and D.G. Perrier, 1986a, Albumin microspheres II: Effect of stabilization temperature on the release of adriamycin. Int. J. Pharm 33:147–153

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1998 Springer Science+Business Media New York

About this chapter

Cite this chapter

Arıca, B., Kaş, H.S., Hıncal, A.A. (1998). Evaluation and Formulation of Biodegradable Levodopa Microspheres Using 32 Factorial Design. In: Hıncal, A.A., Kaş, H.S. (eds) Biomedical Science and Technology. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-5349-6_4

Download citation

  • DOI: https://doi.org/10.1007/978-1-4615-5349-6_4

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4613-7440-4

  • Online ISBN: 978-1-4615-5349-6

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics