SUSTAINED RELEASE DOSAGE FORM: A CONCISE REVIEW

Authors

  • Darandale Abhishek S MES's College Of Pharmacy Sonai
  • Ghule Prashant J Mula Rural Institute of Pharmacy Sonai
  • Aher Abhijit A MES's College Of Pharmacy Sonai
  • Narwate B.M MES's College Of Pharmacy Sonai

Keywords:

Sustained release drug delivery system, Dose frequency, Biological half-life, physicochemical properties of drugs

Abstract

Now days as the expense and complications involved in marketing new drug entities are increased, with concomitant recognition of the therapeutic advantages of controlled drug delivery, greater attention has been focused on development of sustained or controlled release drug delivery systems (DDS). Hence we will change the area of focusing it is suitable to  designing sustained drug delivery is to reduce the frequency of dosing or to increase the effectiveness of the drug by localization at the site of action, reducing the dose required or providing uniform drug delivery. The design of oral sustained release DDS depends on various factors such as, physicochemical properties of drug, type of delivery system, disease being treated, and patient condition, and treatment duration, presence of food, gastrointestinal motility, and co-administration of other drugs.

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References

Jantzen GM, Robinson JR. Sustained and controlled release drug delivery system. In BankerGS, Rhodes CT, editors. Modern pharmaceutics. 3rd edition New york: Marcel dekkerInc;1996.p.575-09

Brahmankar D.M. and Jaiswal S.B. (1995): “Biopharmaceuticsand Pharmacokinetics” a Treatise. Val-labhPrakashan, FirstEdition; 336-337.

Lachman Leon, Lieberman Herbert A., Kanig Joseph L. (1996)“The theory and practice ofindustrial pharmacy” Secondedition, Varghese publishing house; Bombay, 171-196.

Gilbert S, Banker ; Christopher T; Rhodes; “ ModernPharmaceutical 3rd Edition” :576-578

Chein Y.W. Oral Drug delivery and delivery systems. In: Noveldrug delivery systems. Marcel Dekker, Inc., New York, 2002;50; 3rd edition: 139-96.

Lachman Leon, Lieberman Herbert A. Compression coatedand layer tablets. In: Pharmaceutical Dosage Forms: Tablets.Marcel Dekker, Inc., New York, 2002; vol 1; 2nd edition: 247-84.

Gennaro Alfonso R. Extended Release Dosage Forms. In:Remington: The Science and Practice of Phar-macy. LippincottWilliams and Wilkins, U.S.A, 2000; vol 1; 20th edition: 660-63.

Vyas S,P, KharRK.Controlled Drug delivery: Concepts andAdvances .Concepts and Advances.1st ed.vallabhprakashan,2002,p,156-189.

ShargelL,Yu ABC. Modified release drug products. In: AppliedBiopharmaceutics and Pharmacokinet-ics.4th ed.McGrawHill.1999;169-171.

Welling P. G. and Dobrinska M. R., Dosing considerationand bioavailability assessment of controlled drug deliverysystem, Chapter 7, Controlled drug delivery; fundamentalsand applications, 2nd edition, Robinson J.R. and Lee V. H. L.(Eds.), Marcel Dekker Inc., New York, 1978, 29,p. 254, 373

Ansel C.H., Pharmaceutical Dosage Forms and DrugDelivery Systems, 6th edition, B.I. Waverly Pvt. Ltd., NewDelhi, 1995, p. 213.

Parmar N. S. and Shivprakash, “Biopharmaceutical andpharmacokinetic consideration in development of controlledrelease drug product”, Chapter 1, Controlled and Novel DrugDelivery, 1st edition, Jain N. K. (Ed.), CBS Publisher andDistributor, New Delhi, 1997, p.1.

Vyas S.P. and Khare R. K., Controlled Drug Delivery Conceptand Advances 1st edition, VallabhPrakashan, New Delhi,2000, p.1, 54,155.

Chein Y.W. Oral Drug delivery and delivery systems. In: Noveldrug delivery systems. Marcel Dekker, Inc., New York, 2002;50; 3rd edition: 139-96.

Lachman Leon, Lieberman Herbert A. Compression coatedand layer tablets. In: Pharmaceutical Dosage Forms: Tablets.Marcel Dekker, Inc., New York,2002; vol 1; 2nd edition: 247-84.

Robinson J.R, Lee V.H.L. Controlled drug delivery andfundamentals applications. 2nd ed; 1987: 7.

Remington. The science and practice of pharmacy. 20th ed;vol.1: 2000; 903.

Ansel H.C, Allen L.V, Popovich N.G. Pharmaceutical dosageforms and drug delivery systems. 7th ed; 2000: 230.

Indian pharamacopeia. Government of India Ministry Healthand Family Welfare. Delhi: Controler of publication;2010

Subrahmanyam CVS. Textbook of physical pharmaceutics.2nd ed.Delhi: Vallaba praka-shan;2003.p.180-234.

Higuchi, W. I., Diffusional models useful in biopharmaceuticsdrug release rate processes. J. Pharm. Sci., 1967, 56: 315-324.

Published

2017-05-02
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How to Cite

Darandale Abhishek S, Ghule Prashant J, Aher Abhijit A, and Narwate B.M. “SUSTAINED RELEASE DOSAGE FORM: A CONCISE REVIEW”. International Journal of Pharmaceutics and Drug Analysis, vol. 5, no. 5, May 2017, pp. 153-60, https://ijpda.org/index.php/journal/article/view/283.

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